{"index_struct_id": "871d0d38-e0c3-43e7-b8d9-7abcb232ca80", "docstore": {"docs": {"871d0d38-e0c3-43e7-b8d9-7abcb232ca80": {"text": null, "doc_id": "871d0d38-e0c3-43e7-b8d9-7abcb232ca80", "embedding": null, "extra_info": null, "nodes_dict": {"3738475026862369325": {"text": "Nonalcoholic Fatty Liver Disease\nand Recent Guideline Updates\nYumi Ando, M.D.,* and Janice H. Jou, M.D., M.H.S.*,\u2020\n\nNonalcoholic fatty liver disease (NAFLD) is the most\ncommon chronic liver disease in the United States and\nin other industrialized nations. Its increase in prevalence and severity correlates with the rise in obesity and\nthe metabolic syndrome, and NAFLD now represents\na leading indication for liver transplantation in the\nUnited States.1 The rising clinical and economic burden\nof NAFLD has highlighted the need for a streamlined\napproach to prevention, diagnosis, and treatment of\nthe disease. In this review, we will summarize updated\nguideline and guidance recommendations for the management of adult NAFLD; highlight key difference between US, Asian, and European recommendations; and\nprovide key updates.\n\nKEY UPDATES TO US GASTROENTEROLOGY\nAND HEPATOLOGY SOCIETY\nRECOMMENDATIONS FOR ADULT NAFLD\nIn 2012, the American Association for the Study of Liver\nDiseases (AASLD), the American College of Gastroenterology,\nand the American Gastroenterological Association published a joint practice guideline on NAFLD.2 The diagnosis\nof NAFLD currently requires: (1) evidence of hepatic steatosis (HS) by imaging or histology, (2) no significant alcohol\nconsumption, (3) no competing causes of HS, and (4) no\ncoexisting causes of chronic liver disease. Research efforts\nhave led to significant progress in our understanding of the\ndisease. An updated practice guidance, based on expert\nconsensus rather than by systematic review of the literature,\n\nAbbreviations: AASLD, American Association for the Study of Liver Diseases; Asia-Pacific, Asia-Pacific Working Party on\nNonalcoholic Fatty Liver Disease; DM, diabetes mellitus; EASL, European Association for the Study of the Liver; ETOH, alcohol;\nF2, stage 2 fibrosis; F3, stage 3 fibrosis; FDA, US Food and Drug Administration; FIB-4, fibrosis-4 score; GRADE, grading of\nrecommendation assessment, development, and evaluation; HCC, hepatocellular carcinoma; HS, hepatic steatosis; IR, insulin\nresistance; MAFLD, metabolic (dysfunction)-associated fatty liver disease; MetS, metabolic syndrome; NAFL, nonalcoholic fatty\nliver; NAFLD, nonalcoholic fatty liver disease; NASH, nonalcoholic steatohepatitis; NFS, NAFLD fibrosis score; T2DM, type 2\ndiabetes mellitus; TBW, total body weight.\nFrom the * Division of Gastroenterology and Hepatology, Department of Medicine, Oregon Health & Science University Hospital,\nPortland, OR; and \u2020 Division of Gastroenterology and Hepatology, Department of Medicine, Portland VA Medical Center,\nPortland, OR.\nPotential conflict of interest: Nothing to report.\nReceived May 6, 2020; accepted September 20, 2020.\nView this article online at wileyonlinelibrary.com\n\u00a9 2021 by the American Association for the Study of Liver Diseases\n\n| Clinical Liver Disease, VOL 17, NO 1, JANUARY 2021\b\n23\u2003\u2009\n\nAn Official Learning Resource of AASLD\n\n20462484, 2021, 1, Downloaded from https://aasldpubs.onlinelibrary.wiley.com/doi/10.1002/cld.1045, Wiley Online Library on [21/02/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License\n\nReview\n\n\fwas published by AASLD in 2018 to help clinicians navigate\nthe most recent evidence into clinical practice.3 The guidance should be used in conjunction with the graded recommendations from previously published guidelines.\nOne notable change in guidance is a stronger emphasis\non assessment for metabolic risk factors in patients with\nincidental findings of HS and normal liver chemistries but\nlacking liver-related symptoms. Growing evidence supports\nthat patients with NAFLD have increased cardiovascular\nmorbidity and mortality.4 Moreover, advanced liver fibrosis\nis associated with increasing number of metabolic comorbidities.5 Thus, early identification and treatment of individual components of the metabolic syndrome are critical in\npreventing both cardiovascular and liver-related mortality.\nThe importance of identifying and staging the degree\nof fibrosis in patients with NAFLD is underscored in the\nupdated guidance because it is thought to be the main\ndriver of overall and liver-related mortality.6 In the original guideline, NAFLD fibrosis score was the only recommended tool to assess fibrosis noninvasively because\nimaging modalities were not yet readily available in the\nUnited States. Fibrosis-4 score (FIB-4), ultrasound-based\nelastography, and magnetic resonance elastography have\nnow been added to the arsenal of clinically useful tools to\nassess fibrosis staging. Accessibility to advanced imaging\ntools vary across institutions, and no guidance is provided\nfor the optimal sequence of diagnostic testing.\nMore recently, a consensus of international experts proposed changing the name of NAFLD to metabolic (dysfunction)-associated fatty liver disease (MAFLD).7 The paradigm\nshift to MAFLD would reflect the underlying pathogenesis, eliminate the \u201cnegative\u201d nomenclature, and allow for\nthe coexistence of other chronic liver diseases, including\nalcoholic liver disease. One concern of the use of MAFLD\nwould be an inclusive definition that would not specifically\naddress the population with nonalcoholic steatohepatitis\n(NASH) who are at highest risk for complications. Future\nresearch and guidelines will likely address this ongoing\nconversation within the field currently.\n\nSIMILARITIES AND DIFFERENCES IN\nGUIDELINES FROM EUROPE, ASIA, AND THE\nUNITED STATES\nIn today\u2019s increasingly globalized world, awareness\nof international differences in the approach to NAFLD\n\nNAFLD and Recent Guideline Updates Ando and Jou\n\nis important to provide high-quality care to patients of\nall backgrounds. The European Association for the Study\nof the Liver (EASL), in a joint effort with the European\nAssociation for the Study of Diabetes and European\nAssociation for the Study of Obesity, published a NAFLD\nclinical practice guideline in 2016.8 The Asia-Pacific\nWorking Party on NAFLD published its guideline in\n2017.9,10 Both the European and Asian guidelines use\nthe grading of recommendation assessment, development, and evaluation (GRADE) approach to rate the\nquality of evidence and the strength of each recommendation. Although many similarities exist across guidelines, there are several key areas of divergence that will\nbe outlined later (Table 1).\n\nWhat Is the Definition of \u201cSignificant\u201d Alcohol\nUse?\nAll society guidelines characterize NAFLD by the presence of HS in the absence of significant alcohol consumption. However, there is no international consensus as to\nthe amount of alcohol considered \u201csignificant.\u201d The Asian\nguideline has the most conservative alcohol threshold and\nmirrors the exclusion criteria for alcohol use defined in the\nNational Institutes of Health Nonalcoholic Steatohepatitis\nResearch Network database protocol. It is important to\nkeep in mind that alcohol thresholds are oversimplified because the duration of significant alcohol exposure, drinking pattern, and individual susceptibility all play a role in\nalcohol-induced liver injury.\n\nWho Should Be Screened for NAFLD?\nAll societies recommend against systematic screening\nfor NAFLD in the general population. AASLD currently recommends against screening even in high-risk populations\nbecause of the lack of effective drug treatment, cost-effectiveness analysis, and unclear long-term benefits to screening. A \u201chigh index of suspicion\u201d for NAFLD is advised in\npatients with type 2 diabetes.\nThe European guideline acknowledges the lack of validated cost-utility studies and the need to be cognizant of\nregional variations in available health care resources but\nrecommends that all patients with obesity or the metabolic\nsyndrome be screened for NAFLD because of the prognostic implications of progressive disease. The Asian guidelines\nstate that screening may be considered in at-risk groups,\nsuch as patients with diabetes and obesity. Lean NAFLD is\n\n| Clinical Liver Disease, VOL 17, NO 1, JANUARY 2021\b\n24\u2003\u2009\n\nAn Official Learning Resource of AASLD\n\n20462484, 2021, 1, Downloaded from https://aasldpubs.onlinelibrary.wiley.com/doi/10.1002/cld.1045, Wiley Online Library on [21/02/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License\n\nReview\n\n\f| Clinical Liver Disease, VOL 17, NO 1, JANUARY 2021\b\n25\u2003\u2009\n\nAsia-Pacific (2017)\n\n\u2022 Men: 21 standard drinks/week or 294 g/week\n\u2022 Men: 30 g/day\n\u2022 Men: 2 standard drinks/day or 140 g/week\n\u2022 Women: 14 standard drinks/week or 196 g/week\n\u2022 Women: 20 g/day\n\u2022 Women: 1 standard drink/day or 70 g/week\nSystematic screening of the general population not recommended\n\u2022 No screening recommended due to lack of evidence\n\u2022 Recommend screening in patients with obesity,\n\u2022 Consider screening in patients with obesity or T2DM\nof cost-effectiveness to support screening even in\nT2DM, MetS (A2)\n(B2)\nhigh-risk groups\n\u2022 Recommend screening in patients with persistently\n\u2022 \u201cVigilance\u201d in high-risk groups\nabnormal liver enzymes (A1)\n\u2022 NFS, FIB-4, and elastography\n\u2022 NFS and FIB-4 to risk-stratify low versus medium/high\n\u2022 No specific recommendation regarding preferred\n\u2022 No algorithm provided for preferred sequence of\nrisk for significant fibrosis\ntests or algorithm\ntesting\n\u2022 Hepatology referral for medium/high-risk patients\nfor further testing with elastography and identifying\nthose who need liver biopsy\nLiver biopsy remains the gold standard for differentiating NAFL from NASH and staging liver fibrosis. Proceed with liver biopsy if: (1) suspicion for NAFLD advanced fibrosis (2), or\nconcern for coexisting or competing etiology of chronic liver disease (B2).\nTarget weight loss of 7% to 10% TBW (B1). Achieve with 500-1000 daily caloric deficit and moderate-intensity exercise, preferably in a structured weight loss program (C2).\n\u2022 No specific recommendations related to specific\n\u2022 Mediterranean diet, avoidance of processed foods\n\u2022 No specific recommendations related to specific\nmacronutrient diets or exercise regimens\nand added fructose (B1)\nmacronutrient diets or exercise regimens\nThere are currently no approved drugs to treat NAFLD or NASH. However, multiple drugs are in phase 3 development. In patients with cardiovascular indications, statins can be\nsafely used in patients with NASH and compensated cirrhosis (B1)\n\u2022 Vitamin E 800 IU daily can be considered in non\u2022 Pharmacotherapy should be reserved for patients\n\u2022 Pioglitazone recommended only in patients with\ndiabetic patients with biopsy-proved NASH without\nwith NASH fibrosis (stage F2 or higher) or NASH\nprediabetic or diabetic NASH for short-term use (B2)\ncirrhosis\nwith high risk for disease progression (T2DM, MetS,\n\u2022 No firm recommendation can be made regarding\n\u2022 Pioglitazone 30 mg daily can be considered in\nelevated ALT) (B1)\nthe use of vitamin E due to insufficient evidence (A2)\npatients with and without T2DM with biopsy-proved\n\u2022 No firm recommendations can be made for the use\nNASH\nof pioglitazone or vitamin E (B2)\n\nEASL (2016)\n\nNAFLD and Recent Guideline Updates Ando and Jou\n\nAn Official Learning Resource of AASLD\n\n20462484, 2021, 1, Downloaded from https://aasldpubs.onlinelibrary.wiley.com/doi/10.1002/cld.1045, Wiley Online Library on [21/02/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License\n\nGRADE scores, when available, are listed in parentheses.\n\nPharmacological intervention\n\nLifestyle intervention\n\nFibrosis assessment\n\nDefinition of significant alcohol\nconsumption\nScreening for NAFLD\n\nAASLD (2018)\n\nTABLE 1.\u2002SIMILARITIES AND DIFFERENCES IN GUIDELINES FROM EUROPE, ASIA, AND THE UNITED STATES\n\nReview\n\n\fprevalent in Asia, where almost a quarter of patients with\nNAFLD are not obese.11 Thus, insulin resistance (IR) and altered body fat distribution rather than body mass index per\nse may be better indicators of NAFLD in such patients. In\npatients without diabetes, the homeostatic model assessment for IR (HOMA-IR) provides an acceptable estimate\nof IR. Ultrasound remains the first-line assessment for HS\nbecause of its wide availability and low cost. However, it\nis less reliable when HS is <20%12 and raises concerns of\nunderestimating the prevalence of NAFLD. Magnetic resonance imaging\u2013derived proton density fat fraction is highly\nsensitive but is not widely available outside of research settings. Controlled attenuation parameter is available with\nthe FibroScan system and may be more sensitive than ultrasound. Its point-of-care nature makes it appealing as\na tool to monitor disease progression and treatment response, but more studies are needed to assess its validity.\n\nHow Should NAFLD Be Diagnosed, and How\nShould It Be Monitored?\nLiver histology remains the gold standard for differentiating steatohepatitis from simple steatosis and for\nassessing fibrosis staging. Due to its invasive nature\nand associated costs, all guidelines agree that liver biopsy should be considered only in select individuals. The\nAmerican and European guidelines agree that patients\nwith NAFLD and suspicion for advanced fibrosis should\nhave a liver biopsy to confirm findings because this\nwould have prognostic", "doc_id": "231fd3ec-ec79-4b4c-8314-0ec37abf8b20", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "f8b6d6f3-e734-4f62-a93f-3672b5b3c7dc", "node_info": {"start": 0, "end": 13396}}, "5409451774554091213": {"text": "Controlled attenuation parameter is available with\nthe FibroScan system and may be more sensitive than ultrasound. Its point-of-care nature makes it appealing as\na tool to monitor disease progression and treatment response, but more studies are needed to assess its validity.\n\nHow Should NAFLD Be Diagnosed, and How\nShould It Be Monitored?\nLiver histology remains the gold standard for differentiating steatohepatitis from simple steatosis and for\nassessing fibrosis staging. Due to its invasive nature\nand associated costs, all guidelines agree that liver biopsy should be considered only in select individuals. The\nAmerican and European guidelines agree that patients\nwith NAFLD and suspicion for advanced fibrosis should\nhave a liver biopsy to confirm findings because this\nwould have prognostic implications and lead to management changes. The Asian guidelines differ in that they\nrecommend biopsy only if the presence and/or the severity of coexisting chronic liver disease cannot be excluded\nor if assessment of fibrosis using noninvasive testing is\ninconclusive. All guidelines agree that noninvasive tools\nshould be used to stratify patients as low or high risk for\nadvanced fibrosis, but a preferred sequence of testing is\nnot provided in the American and Asian guidelines. The\nEuropean guideline provides a proposed diagnostic algorithm with suggestions to guide referral to hepatology.\nIn addition, it provides a proposed follow-up strategy to\nmonitor for disease progression with the caveat that optimal follow-up has yet to be determined.\nThe identification of NASH is clinically important because it indicates an increased risk for fibrosis progression and the need for aggressive treatment and closer\nfollow-up. There are currently no acceptable noninvasive\nmodalities to differentiate between bland steatosis and\n\nNAFLD and Recent Guideline Updates Ando and Jou\n\nsteatohepatitis. The presence of the metabolic syndrome\nincreases the risk for steatohepatitis, and the US guidelines\nsuggest performing liver biopsy in these patients. However,\nbecause most patients with NAFLD have at least one component of the metabolic syndrome, such an approach is\nclinically impractical. Furthermore, without the availability\nof a US Food and Drug Administration (FDA)\u2013approved\npharmacological therapy for NASH, many clinicians remain\nhesitant to proceed with biopsy.\nOnce NASH is diagnosed, therapies recommended by\nthe AASLD guidelines include vitamin E for patients with\nadvanced fibrosis and without diabetes mellitus (DM)\nand pioglitazone, a thiazolidinedione that may be used\nin patients with NASH and diabetes. More recently, liraglutide, a glucagon-like peptide-1 receptor agonist, was\nshown to be of benefit in patients with NASH and DM.\nPharmacological therapy for NASH is an area of significant\nongoing investigation.\n\nKEY OUTCOMES OF CONSIDERATION IN\nPATIENTS WITH NAFLD\nHepatocellular carcinoma (HCC) related to NAFLD is\nof growing concern, particularly because it can occur in\nthe absence of cirrhosis.13 Obesity, type 2 diabetes, advanced age, male sex, and certain gene polymorphisms\nare associated with increased risk for HCC. However, the\nmortality benefit and cost-effectiveness of surveillance for\nHCC in patients with noncirrhotic NAFLD is yet to be determined and is not recommended at this time by any of\nthe guidelines.\nEarly recognition and intervention are key to improving\nclinical outcomes and reducing the economic and health\ncare burden of NAFLD. Despite this, widespread awareness\nof NAFLD in the primary care setting is lacking and remains\nunderdiagnosed in real-world settings.14,15\nOnce drugs specifically targeting NAFLD obtain FDA\napproval, there will most likely be a surge of interest in\nNAFLD by the key health care stakeholders: patients, providers, payors, and policymakers. NAFLD is a fast-moving field, and current guidelines will soon be outdated.\nFuture guideline updates should outline a practical\nstrategy for the identification of high-risk patients with\nNAFLD who would benefit most from hepatology referral\nand targeted therapy (Fig. 1). There remains a pressing\nneed to establish the optimal assessment of steatosis,\n\n| Clinical Liver Disease, VOL 17, NO 1, JANUARY 2021\b\n26\u2003\u2009\n\nAn Official Learning Resource of AASLD\n\n20462484, 2021, 1, Downloaded from https://aasldpubs.onlinelibrary.wiley.com/doi/10.1002/cld.1045, Wiley Online Library on [21/02/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License\n\nReview\n\n\fNAFLD and Recent Guideline Updates Ando and Jou\n\nFIG 1 Proposed diagnostic and risk stratification algorithm for patients with suspected NAFLD. 1HBV and HCV serological workup should\nbe completed in the primary care setting, with subsequent workup tailored to the individual patient by hepatology. Note that NAFLD may\ncoexist with other chronic liver diseases. 2Evidence-based optimal follow-up of patients with NAFLD has not been established. The EASL\nrecommends monitoring low-risk patients with NAFLD without worsening metabolic risk factors every 2 to 3 years. 3Biopsy should also be\nconsidered in patients with increasing number of metabolic diseases who are at high risk for steatohepatitis.\n\nsteatohepatitis, and fibrosis in a cost-effective and minimally invasive manner.\nCORRESPONDENCE\nJanice H. Jou, M.D., Division of Gastroenterology and Hepatology,\nDepartment of Medicine, 3181 SW Sam Jackson Park Road, L-461,\nPortland, OR 97239. E-mail: jou@ohsu.edu\n\nREFERENCES\n1) Wong RJ, Aguilar M, Cheung R, et al. Nonalcoholic steatohepatitis\nis the second leading etiology of liver disease among adults awaiting liver transplantation in the United States. Gastroenterology\n2015;148:547-555.\n2) Chalasani N, Younossi Z, Lavine JE, et al. The diagnosis and management of non-alcoholic fatty liver disease: practice Guideline by\nthe American Association for the Study of Liver Diseases, American\nCollege of Gastroenterology, and the American Gastroenterological\nAssociation. Hepatology 2012;55:2005-2023.\n3) Chalasani N, Younossi Z, Lavine JE, et al. The diagnosis and management of nonalcoholic fatty liver disease: Practice guidance from the\nAmerican Association for the Study of Liver Diseases. Hepatology\n2018;67:328-357.\n\n4) Targher G, Byrne CD, Lonardo A, et al. Non-alcoholic fatty liver disease and risk of incident cardiovascular disease: a meta-analysis. J\nHepatol 2016;65:589-600.\n5) Wong RJ, Tran T, Kaufman H, et al. Increasing metabolic co-morbidities are associated with higher risk of advanced fibrosis in nonalcoholic steatohepatitis. PLoS One 2019;14:e0220612.\n6) Angulo P, Kleiner DE, Dam-Larsen S, et al. Liver fibrosis, but no\nother histologic features, is associated with long-term outcomes\nof patients with nonalcoholic fatty liver disease. Gastroenterology\n2015;149:389-397.e10.\n7) Eslam M, Sanyal AJ, George J, International Consensus Panel. MAFLD:\na consensus-driven proposed nomenclature for metabolic associated\nfatty liver disease. Gastroenterology 2020;158:1999-2014.e1.\n8) European Association for the Study of the Liver, European\nAssociation for the Study of Diabetes, European Association for\nthe Study of Obesity. EASL-EASD-EASO Clinical Practice Guidelines\nfor the management of non-alcoholic fatty liver disease. J Hepatol\n2016;64:1388-1402.\n9) Wong VW, Chan WK, Chitturi S, et al. Asia-Pacific Working Party on\nNon-alcoholic Fatty Liver Disease guidelines 2017-Part 1: definition,\nrisk factors and assessment. J Gastroenterol Hepatol 2018;33:70-85.\n\n| Clinical Liver Disease, VOL 17, NO 1, JANUARY 2021\b\n27\u2003\u2009\n\nAn Official Learning Resource of AASLD\n\n20462484, 2021, 1, Downloaded from https://aasldpubs.onlinelibrary.wiley.com/doi/10.1002/cld.1045, Wiley Online Library on [21/02/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License\n\nReview\n\n\fNAFLD and Recent Guideline Updates Ando and Jou\n\n10) Chitturi S, Wong VW, Chan WK, et al. The Asia-Pacific Working\nParty on Non-alcoholic Fatty Liver Disease guidelines 2017-Part\n2: management and special groups. J Gastroenterol Hepatol\n2018;33:86-98.\n\n13) Mittal S, El-Serag HB, Sada YH, et al. Hepatocellular carcinoma\nin the absence of cirrhosis in united states veterans is associated\nwith nonalcoholic fatty liver disease. Clin Gastroenterol Hepatol\n2016;14:124-131.e1.\n\n11) Liu CJ. Prevalence and risk factors for non-alcoholic fatty liver disease in Asian people who are not obese. J Gastroenterol Hepatol\n2012;27:1555-1560.\n\n14) Blais P, Husain N, Kramer JR, et al. Nonalcoholic fatty liver disease\nis underrecognized in the primary care setting. Am J Gastroenterol\n2015;110:10-14.\n\n12) Dasarathy S, Dasarathy J, Khiyami A, et al. Validity of real time ultrasound in the diagnosis of hepatic steatosis: a prospective study. J\nHepatol 2009;51:1061-1067.\n\n15) Alexander M, Loomis AK, Fairburn-Beech J, et al. Real-world data reveal a diagnostic gap in non-alcoholic fatty liver disease. BMC Med\n2018;16:130.\n\n| Clinical Liver Disease, VOL 17, NO 1, JANUARY 2021\b\n28\u2003\u2009\n\nAn Official Learning Resource of AASLD\n\n20462484, 2021, 1, Downloaded from https://aasldpubs.onlinelibrary.wiley.com/doi/10.1002/cld.1045, Wiley Online Library on [21/02/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License\n\nReview\n\n\f", "doc_id": "2c396776-1fa2-4a5a-b199-5aa0b5111036", "embedding": null, "extra_info": null, "index": 1, "child_indices": [], "ref_doc_id": "f8b6d6f3-e734-4f62-a93f-3672b5b3c7dc", "node_info": {"start": 12598, "end": 22193}}, "4392219367997839596": {"text": "\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f\f", "doc_id": "11e89965-8471-4d7b-9739-ea3eb38a7830", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "67c2fd00-63d6-404c-9af6-d25bbea1e8c7", "node_info": {"start": 0, "end": 64}}, "2232762506725266668": {"text": "Nonalcoholic Fatty Liver Disease\nand Recent Guideline Updates\nYumi Ando, M.D.,* and Janice H. Jou, M.D., M.H.S.*,\u2020\n\nNonalcoholic fatty liver disease (NAFLD) is the most\ncommon chronic liver disease in the United States and\nin other industrialized nations. Its increase in prevalence and severity correlates with the rise in obesity and\nthe metabolic syndrome, and NAFLD now represents\na leading indication for liver transplantation in the\nUnited States.1 The rising clinical and economic burden\nof NAFLD has highlighted the need for a streamlined\napproach to prevention, diagnosis, and treatment of\nthe disease. In this review, we will summarize updated\nguideline and guidance recommendations for the management of adult NAFLD; highlight key difference between US, Asian, and European recommendations; and\nprovide key updates.\n\nKEY UPDATES TO US GASTROENTEROLOGY\nAND HEPATOLOGY SOCIETY\nRECOMMENDATIONS FOR ADULT NAFLD\nIn 2012, the American Association for the Study of Liver\nDiseases (AASLD), the American College of Gastroenterology,\nand the American Gastroenterological Association published a joint practice guideline on NAFLD.2 The diagnosis\nof NAFLD currently requires: (1) evidence of hepatic steatosis (HS) by imaging or histology, (2) no significant alcohol\nconsumption, (3) no competing causes of HS, and (4) no\ncoexisting causes of chronic liver disease. Research efforts\nhave led to significant progress in our understanding of the\ndisease. An updated practice guidance, based on expert\nconsensus rather than by systematic review of the literature,\n\nAbbreviations: AASLD, American Association for the Study of Liver Diseases; Asia-Pacific, Asia-Pacific Working Party on\nNonalcoholic Fatty Liver Disease; DM, diabetes mellitus; EASL, European Association for the Study of the Liver; ETOH, alcohol;\nF2, stage 2 fibrosis; F3, stage 3 fibrosis; FDA, US Food and Drug Administration; FIB-4, fibrosis-4 score; GRADE, grading of\nrecommendation assessment, development, and evaluation; HCC, hepatocellular carcinoma; HS, hepatic steatosis; IR, insulin\nresistance; MAFLD, metabolic (dysfunction)-associated fatty liver disease; MetS, metabolic syndrome; NAFL, nonalcoholic fatty\nliver; NAFLD, nonalcoholic fatty liver disease; NASH, nonalcoholic steatohepatitis; NFS, NAFLD fibrosis score; T2DM, type 2\ndiabetes mellitus; TBW, total body weight.\nFrom the * Division of Gastroenterology and Hepatology, Department of Medicine, Oregon Health & Science University Hospital,\nPortland, OR; and \u2020 Division of Gastroenterology and Hepatology, Department of Medicine, Portland VA Medical Center,\nPortland, OR.\nPotential conflict of interest: Nothing to report.\nReceived May 6, 2020; accepted September 20, 2020.\nView this article online at wileyonlinelibrary.com\n\u00a9 2021 by the American Association for the Study of Liver Diseases\n\n| Clinical Liver Disease, VOL 17, NO 1, JANUARY 2021\b\n23\u2003\u2009\n\nAn Official Learning Resource of AASLD\n\n20462484, 2021, 1, Downloaded from https://aasldpubs.onlinelibrary.wiley.com/doi/10.1002/cld.1045, Wiley Online Library on [21/02/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License\n\nReview\n\n\fwas published by AASLD in 2018 to help clinicians navigate\nthe most recent evidence into clinical practice.3 The guidance should be used in conjunction with the graded recommendations from previously published guidelines.\nOne notable change in guidance is a stronger emphasis\non assessment for metabolic risk factors in patients with\nincidental findings of HS and normal liver chemistries but\nlacking liver-related symptoms. Growing evidence supports\nthat patients with NAFLD have increased cardiovascular\nmorbidity and mortality.4 Moreover, advanced liver fibrosis\nis associated with increasing number of metabolic comorbidities.5 Thus, early identification and treatment of individual components of the metabolic syndrome are critical in\npreventing both cardiovascular and liver-related mortality.\nThe importance of identifying and staging the degree\nof fibrosis in patients with NAFLD is underscored in the\nupdated guidance because it is thought to be the main\ndriver of overall and liver-related mortality.6 In the original guideline, NAFLD fibrosis score was the only recommended tool to assess fibrosis noninvasively because\nimaging modalities were not yet readily available in the\nUnited States. Fibrosis-4 score (FIB-4), ultrasound-based\nelastography, and magnetic resonance elastography have\nnow been added to the arsenal of clinically useful tools to\nassess fibrosis staging. Accessibility to advanced imaging\ntools vary across institutions, and no guidance is provided\nfor the optimal sequence of diagnostic testing.\nMore recently, a consensus of international experts proposed changing the name of NAFLD to metabolic (dysfunction)-associated fatty liver disease (MAFLD).7 The paradigm\nshift to MAFLD would reflect the underlying pathogenesis, eliminate the \u201cnegative\u201d nomenclature, and allow for\nthe coexistence of other chronic liver diseases, including\nalcoholic liver disease. One concern of the use of MAFLD\nwould be an inclusive definition that would not specifically\naddress the population with nonalcoholic steatohepatitis\n(NASH) who are at highest risk for complications. Future\nresearch and guidelines will likely address this ongoing\nconversation within the field currently.\n\nSIMILARITIES AND DIFFERENCES IN\nGUIDELINES FROM EUROPE, ASIA, AND THE\nUNITED STATES\nIn today\u2019s increasingly globalized world, awareness\nof international differences in the approach to NAFLD\n\nNAFLD and Recent Guideline Updates Ando and Jou\n\nis important to provide high-quality care to patients of\nall backgrounds. The European Association for the Study\nof the Liver (EASL), in a joint effort with the European\nAssociation for the Study of Diabetes and European\nAssociation for the Study of Obesity, published a NAFLD\nclinical practice guideline in 2016.8 The Asia-Pacific\nWorking Party on NAFLD published its guideline in\n2017.9,10 Both the European and Asian guidelines use\nthe grading of recommendation assessment, development, and evaluation (GRADE) approach to rate the\nquality of evidence and the strength of each recommendation. Although many similarities exist across guidelines, there are several key areas of divergence that will\nbe outlined later (Table 1).\n\nWhat Is the Definition of \u201cSignificant\u201d Alcohol\nUse?\nAll society guidelines characterize NAFLD by the presence of HS in the absence of significant alcohol consumption. However, there is no international consensus as to\nthe amount of alcohol considered \u201csignificant.\u201d The Asian\nguideline has the most conservative alcohol threshold and\nmirrors the exclusion criteria for alcohol use defined in the\nNational Institutes of Health Nonalcoholic Steatohepatitis\nResearch Network database protocol. It is important to\nkeep in mind that alcohol thresholds are oversimplified because the duration of significant alcohol exposure, drinking pattern, and individual susceptibility all play a role in\nalcohol-induced liver injury.\n\nWho Should Be Screened for NAFLD?\nAll societies recommend against systematic screening\nfor NAFLD in the general population. AASLD currently recommends against screening even in high-risk populations\nbecause of the lack of effective drug treatment, cost-effectiveness analysis,", "doc_id": "ebfbab0b-ea89-4034-974d-84e25522c449", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "9ecdfb29-da7d-40df-b0c2-5b4fb302ad15", "node_info": {"start": 0, "end": 7428}}, "3751959691413948309": {"text": "populations\nbecause of the lack of effective drug treatment, cost-effectiveness analysis, and unclear long-term benefits to screening. A \u201chigh index of suspicion\u201d for NAFLD is advised in\npatients with type 2 diabetes.\nThe European guideline acknowledges the lack of validated cost-utility studies and the need to be cognizant of\nregional variations in available health care resources but\nrecommends that all patients with obesity or the metabolic\nsyndrome be screened for NAFLD because of the prognostic implications of progressive disease. The Asian guidelines\nstate that screening may be considered in at-risk groups,\nsuch as patients with diabetes and obesity. Lean NAFLD is\n\n| Clinical Liver Disease, VOL 17, NO 1, JANUARY 2021\b\n24\u2003\u2009\n\nAn Official Learning Resource of AASLD\n\n20462484, 2021, 1, Downloaded from https://aasldpubs.onlinelibrary.wiley.com/doi/10.1002/cld.1045, Wiley Online Library on [21/02/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License\n\nReview\n\n\f| Clinical Liver Disease, VOL 17, NO 1, JANUARY 2021\b\n25\u2003\u2009\n\nAsia-Pacific (2017)\n\n\u2022 Men: 21 standard drinks/week or 294 g/week\n\u2022 Men: 30 g/day\n\u2022 Men: 2 standard drinks/day or 140 g/week\n\u2022 Women: 14 standard drinks/week or 196 g/week\n\u2022 Women: 20 g/day\n\u2022 Women: 1 standard drink/day or 70 g/week\nSystematic screening of the general population not recommended\n\u2022 No screening recommended due to lack of evidence\n\u2022 Recommend screening in patients with obesity,\n\u2022 Consider screening in patients with obesity or T2DM\nof cost-effectiveness to support screening even in\nT2DM, MetS (A2)\n(B2)\nhigh-risk groups\n\u2022 Recommend screening in patients with persistently\n\u2022 \u201cVigilance\u201d in high-risk groups\nabnormal liver enzymes (A1)\n\u2022 NFS, FIB-4, and elastography\n\u2022 NFS and FIB-4 to risk-stratify low versus medium/high\n\u2022 No specific recommendation regarding preferred\n\u2022 No algorithm provided for preferred sequence of\nrisk for significant fibrosis\ntests or algorithm\ntesting\n\u2022 Hepatology referral for medium/high-risk patients\nfor further testing with elastography and identifying\nthose who need liver biopsy\nLiver biopsy remains the gold standard for differentiating NAFL from NASH and staging liver fibrosis. Proceed with liver biopsy if: (1) suspicion for NAFLD advanced fibrosis (2), or\nconcern for coexisting or competing etiology of chronic liver disease (B2).\nTarget weight loss of 7% to 10% TBW (B1). Achieve with 500-1000 daily caloric deficit and moderate-intensity exercise, preferably in a structured weight loss program (C2).\n\u2022 No specific recommendations related to specific\n\u2022 Mediterranean diet, avoidance of processed foods\n\u2022 No specific recommendations related to specific\nmacronutrient diets or exercise regimens\nand added fructose (B1)\nmacronutrient diets or exercise regimens\nThere are currently no approved drugs to treat NAFLD or NASH. However, multiple drugs are in phase 3 development. In patients with cardiovascular indications, statins can be\nsafely used in patients with NASH and compensated cirrhosis (B1)\n\u2022 Vitamin E 800 IU daily can be considered in non\u2022 Pharmacotherapy should be reserved for patients\n\u2022 Pioglitazone recommended only in patients with\ndiabetic patients with biopsy-proved NASH without\nwith NASH fibrosis (stage F2 or higher) or NASH\nprediabetic or diabetic NASH for short-term use (B2)\ncirrhosis\nwith high risk for disease progression (T2DM, MetS,\n\u2022 No firm recommendation can be made regarding\n\u2022 Pioglitazone 30 mg daily can be considered in\nelevated ALT) (B1)\nthe use of vitamin E due to insufficient evidence (A2)\npatients with and without T2DM with biopsy-proved\n\u2022 No firm recommendations can be made for the use\nNASH\nof pioglitazone or vitamin E (B2)\n\nEASL (2016)\n\nNAFLD and Recent Guideline Updates Ando and Jou\n\nAn Official Learning Resource of AASLD\n\n20462484, 2021, 1, Downloaded from https://aasldpubs.onlinelibrary.wiley.com/doi/10.1002/cld.1045, Wiley Online Library on [21/02/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License\n\nGRADE scores, when available, are listed in parentheses.\n\nPharmacological intervention\n\nLifestyle intervention\n\nFibrosis assessment\n\nDefinition of significant alcohol\nconsumption\nScreening for NAFLD\n\nAASLD (2018)\n\nTABLE 1.\u2002SIMILARITIES AND DIFFERENCES IN GUIDELINES FROM EUROPE, ASIA, AND THE UNITED STATES\n\nReview\n\n\fprevalent in Asia, where almost a quarter of patients with\nNAFLD are not obese.11 Thus, insulin resistance (IR) and altered body fat distribution rather than body mass index per\nse may be better indicators of NAFLD in such patients. In\npatients without diabetes, the homeostatic model assessment for IR (HOMA-IR) provides an acceptable estimate\nof IR. Ultrasound remains the first-line assessment for HS\nbecause of its wide availability and low cost. However, it\nis less reliable when HS is <20%12 and raises concerns of\nunderestimating the prevalence of NAFLD. Magnetic resonance imaging\u2013derived proton density fat fraction is highly\nsensitive but is not widely available outside of research settings. Controlled attenuation parameter is available with\nthe FibroScan system and may be more sensitive than ultrasound. Its point-of-care nature makes it appealing as\na tool to monitor disease progression and treatment response, but more studies are needed to assess its validity.\n\nHow Should NAFLD Be Diagnosed, and How\nShould It Be Monitored?\nLiver histology remains the gold standard for differentiating steatohepatitis from simple steatosis and for\nassessing fibrosis staging. Due to its invasive nature\nand associated costs, all guidelines agree that liver biopsy should be considered only in select individuals. The\nAmerican and European guidelines agree that patients\nwith NAFLD and suspicion for advanced fibrosis should\nhave a liver biopsy to confirm findings because this\nwould have prognostic implications and lead to management changes. The Asian guidelines differ in that they\nrecommend biopsy only if the presence and/or the severity of coexisting chronic liver disease cannot be excluded\nor if assessment of fibrosis using noninvasive testing is\ninconclusive. All guidelines agree that noninvasive tools\nshould be used to stratify patients as low or high risk for\nadvanced fibrosis, but a preferred sequence of testing is\nnot provided in the American and Asian guidelines. The\nEuropean guideline provides a proposed diagnostic algorithm with suggestions to guide referral to hepatology.\nIn addition, it provides a proposed follow-up strategy to\nmonitor for disease progression with the caveat that optimal follow-up has yet to be determined.\nThe identification of NASH is clinically important because it indicates an increased risk for fibrosis progression and the need for aggressive treatment and closer\nfollow-up. There are currently no acceptable noninvasive\nmodalities to differentiate between bland steatosis and\n\nNAFLD and Recent Guideline Updates Ando and", "doc_id": "9ec55804-4dfc-4d60-86db-86050aca9d6a", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "63f3673c-1a6d-4318-8cf8-5a8843fb3b19", "node_info": {"start": 0, "end": 7132}}, "1883151682849727311": {"text": "steatosis and\n\nNAFLD and Recent Guideline Updates Ando and Jou\n\nsteatohepatitis. The presence of the metabolic syndrome\nincreases the risk for steatohepatitis, and the US guidelines\nsuggest performing liver biopsy in these patients. However,\nbecause most patients with NAFLD have at least one component of the metabolic syndrome, such an approach is\nclinically impractical. Furthermore, without the availability\nof a US Food and Drug Administration (FDA)\u2013approved\npharmacological therapy for NASH, many clinicians remain\nhesitant to proceed with biopsy.\nOnce NASH is diagnosed, therapies recommended by\nthe AASLD guidelines include vitamin E for patients with\nadvanced fibrosis and without diabetes mellitus (DM)\nand pioglitazone, a thiazolidinedione that may be used\nin patients with NASH and diabetes. More recently, liraglutide, a glucagon-like peptide-1 receptor agonist, was\nshown to be of benefit in patients with NASH and DM.\nPharmacological therapy for NASH is an area of significant\nongoing investigation.\n\nKEY OUTCOMES OF CONSIDERATION IN\nPATIENTS WITH NAFLD\nHepatocellular carcinoma (HCC) related to NAFLD is\nof growing concern, particularly because it can occur in\nthe absence of cirrhosis.13 Obesity, type 2 diabetes, advanced age, male sex, and certain gene polymorphisms\nare associated with increased risk for HCC. However, the\nmortality benefit and cost-effectiveness of surveillance for\nHCC in patients with noncirrhotic NAFLD is yet to be determined and is not recommended at this time by any of\nthe guidelines.\nEarly recognition and intervention are key to improving\nclinical outcomes and reducing the economic and health\ncare burden of NAFLD. Despite this, widespread awareness\nof NAFLD in the primary care setting is lacking and remains\nunderdiagnosed in real-world settings.14,15\nOnce drugs specifically targeting NAFLD obtain FDA\napproval, there will most likely be a surge of interest in\nNAFLD by the key health care stakeholders: patients, providers, payors, and policymakers. NAFLD is a fast-moving field, and current guidelines will soon be outdated.\nFuture guideline updates should outline a practical\nstrategy for the identification of high-risk patients with\nNAFLD who would benefit most from hepatology referral\nand targeted therapy (Fig. 1). There remains a pressing\nneed to establish the optimal assessment of steatosis,\n\n| Clinical Liver Disease, VOL 17, NO 1, JANUARY 2021\b\n26\u2003\u2009\n\nAn Official Learning Resource of AASLD\n\n20462484, 2021, 1, Downloaded from https://aasldpubs.onlinelibrary.wiley.com/doi/10.1002/cld.1045, Wiley Online Library on [21/02/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License\n\nReview\n\n\fNAFLD and Recent Guideline Updates Ando and Jou\n\nFIG 1 Proposed diagnostic and risk stratification algorithm for patients with suspected NAFLD. 1HBV and HCV serological workup should\nbe completed in the primary care setting, with subsequent workup tailored to the individual patient by hepatology. Note that NAFLD may\ncoexist with other chronic liver diseases. 2Evidence-based optimal follow-up of patients with NAFLD has not been established. The EASL\nrecommends monitoring low-risk patients with NAFLD without worsening metabolic risk factors every 2 to 3 years. 3Biopsy should also be\nconsidered in patients with increasing number of metabolic diseases who are at high risk for steatohepatitis.\n\nsteatohepatitis, and fibrosis in a cost-effective and minimally invasive manner.\nCORRESPONDENCE\nJanice H. Jou, M.D., Division of Gastroenterology and Hepatology,\nDepartment of Medicine, 3181 SW Sam Jackson Park Road, L-461,\nPortland, OR 97239. E-mail: jou@ohsu.edu\n\nREFERENCES\n1) Wong RJ, Aguilar M, Cheung R, et al. Nonalcoholic steatohepatitis\nis the second leading etiology of liver disease among adults awaiting liver transplantation in the United States. Gastroenterology\n2015;148:547-555.\n2) Chalasani N, Younossi Z, Lavine JE, et al. The diagnosis and management of non-alcoholic fatty liver disease: practice Guideline by\nthe American Association for the Study of Liver Diseases, American\nCollege of Gastroenterology, and the American Gastroenterological\nAssociation. Hepatology 2012;55:2005-2023.\n3) Chalasani N, Younossi Z, Lavine JE, et al. The diagnosis and management of nonalcoholic fatty liver disease: Practice guidance from the\nAmerican Association for the Study of Liver Diseases. Hepatology\n2018;67:328-357.\n\n4) Targher G, Byrne CD, Lonardo A, et al. Non-alcoholic fatty liver disease and risk of incident cardiovascular disease: a meta-analysis. J\nHepatol 2016;65:589-600.\n5) Wong RJ, Tran T, Kaufman H, et al. Increasing metabolic co-morbidities are associated with higher risk of advanced fibrosis in nonalcoholic steatohepatitis. PLoS One 2019;14:e0220612.\n6) Angulo P, Kleiner DE, Dam-Larsen S, et al. Liver fibrosis, but no\nother histologic features, is associated with long-term outcomes\nof patients with nonalcoholic fatty liver disease. Gastroenterology\n2015;149:389-397.e10.\n7) Eslam M, Sanyal AJ, George J, International Consensus Panel. MAFLD:\na consensus-driven proposed nomenclature for metabolic associated\nfatty liver disease. Gastroenterology 2020;158:1999-2014.e1.\n8) European Association for the Study of the Liver, European\nAssociation for the Study of Diabetes, European Association for\nthe Study of Obesity. EASL-EASD-EASO Clinical Practice Guidelines\nfor the management of non-alcoholic fatty liver disease. J Hepatol\n2016;64:1388-1402.\n9) Wong VW, Chan WK, Chitturi S, et al. Asia-Pacific Working Party on\nNon-alcoholic Fatty Liver Disease guidelines 2017-Part 1: definition,\nrisk factors and assessment. J Gastroenterol Hepatol 2018;33:70-85.\n\n| Clinical Liver Disease, VOL 17, NO 1, JANUARY 2021\b\n27\u2003\u2009\n\nAn Official Learning Resource of AASLD\n\n20462484, 2021, 1, Downloaded from https://aasldpubs.onlinelibrary.wiley.com/doi/10.1002/cld.1045, Wiley Online Library on [21/02/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License\n\nReview\n\n\fNAFLD and Recent Guideline Updates Ando and Jou\n\n10) Chitturi S, Wong VW, Chan WK, et al. The Asia-Pacific Working\nParty on Non-alcoholic Fatty Liver Disease guidelines 2017-Part\n2: management and special groups. J Gastroenterol Hepatol\n2018;33:86-98.\n\n13) Mittal S, El-Serag HB, Sada YH, et al. Hepatocellular", "doc_id": "426ca369-c039-4677-8158-191cea3fa06d", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "79f32302-a385-4928-a1e9-61bba994bc3f", "node_info": {"start": 0, "end": 6534}}, "514734408579139799": {"text": "El-Serag HB, Sada YH, et al. Hepatocellular carcinoma\nin the absence of cirrhosis in united states veterans is associated\nwith nonalcoholic fatty liver disease. Clin Gastroenterol Hepatol\n2016;14:124-131.e1.\n\n11) Liu CJ. Prevalence and risk factors for non-alcoholic fatty liver disease in Asian people who are not obese. J Gastroenterol Hepatol\n2012;27:1555-1560.\n\n14) Blais P, Husain N, Kramer JR, et al. Nonalcoholic fatty liver disease\nis underrecognized in the primary care setting. Am J Gastroenterol\n2015;110:10-14.\n\n12) Dasarathy S, Dasarathy J, Khiyami A, et al. Validity of real time ultrasound in the diagnosis of hepatic steatosis: a prospective study. J\nHepatol 2009;51:1061-1067.\n\n15) Alexander M, Loomis AK, Fairburn-Beech J, et al. Real-world data reveal a diagnostic gap in non-alcoholic fatty liver disease. BMC Med\n2018;16:130.\n\n| Clinical Liver Disease, VOL 17, NO 1, JANUARY 2021\b\n28\u2003\u2009\n\nAn Official Learning Resource of AASLD\n\n20462484, 2021, 1, Downloaded from https://aasldpubs.onlinelibrary.wiley.com/doi/10.1002/cld.1045, Wiley Online Library on [21/02/2023]. See the Terms and Conditions (https://onlinelibrary.wiley.com/terms-and-conditions) on Wiley Online Library for rules of use; OA articles are governed by the applicable Creative Commons License\n\nReview\n\n\f", "doc_id": "ab4776d6-4629-4785-9082-a5b97503ace2", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "e772c18e-2497-4cfb-a258-f2d66111c1ef", "node_info": {"start": 0, "end": 1289}}, "6710055391404016423": {"text": "1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nDiabetic Macular Edema\neyewiki.aao.org/Diabetic_Macular_Edema\n\nAssigned editor:\nNeelakshi Bhagat, MD, FACS\nReview:\nAssigned status Update Pending\nby Neelakshi Bhagat, MD, FACS on June 6, 2022.\n3 Further reading\n4 References\n\nDisease Definition\nDiabetic macular edema (DME) is the accumulation of excess fluid in the extracellular\nspace within the retina in the macular area, typically in the inner nuclear, outer\nplexiform, Henle\u2019s fiber layer, and subretinal space.[1][2]\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n1/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nPathophysiology\n\nFigure 1: Diabetic macular edema. A: Schematic diagram\nof DME. Microaneurysms or damaged capillaries resulting from\nthe breakdown of the blood-retina barrier leak fluid to the\nextracellular space, resulting in a swollen retina. Resorption of\nDME is dependent on the adjacent capillaries and retinal\npigment epithelium. Resorption of fluid may leave behind\nlipoprotein residues seen as exudates. B: Optical Coherence\nTomography image of DME. Published online with permission\nfrom the AAO.\n\nChronic hyperglycemia-related accumulation of advanced glycated end products (AGEs)\ndisrupts the blood retinal barrier (BRB) characterized by endothelial cell junction\nbreakdown and pericyte loss. The inner BRB is composed of endothelial cells in the\nretinal capillaries, while the outer BRB is composed of retinal pigment epithelium (RPE)\ncells. Altered BRB leads to interstitial fluid accumulation within and underneath the\nretina through leakage of molecules dependent on intact cell to cell junctions (Figure 1).\n[3] Evidence also shows that DME has an inflammatory component to the disease, with\nseveral chemokines and cytokines involved in its development. These factors include\nvascular endothelial growth factor (VEGF), interleukins (ILs), matrix metalloproteinases\n(MMPs), and tumor necrosis factor (TNF). Upregulation of multiple pathways leads to\nincreased inflammation, oxidative stress, and vascular dysfunction.[4] There are also\nsignificant changes in the neurovascular unit, altering the homeostasis between\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n2/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nastrocytes, ganglion cells, M\u00fcller cells, retinal vascular endothelial cells, and amacrine\ncells.[5] Retinal vascular permeability changes also involve the kallikrein-kinin system,\nwhich induces vasorelaxation via bradykinin and nitric oxide.[6][7][8]\n\nNatural History\nDME can develop at any stage of diabetic retinopathy (DR), from mild nonproliferative\ndiabetic retinopathy (NPDR) to proliferative diabetic retinopathy (PDR), but is more\nfrequent as the severity of DR increases. DME threatening or at the fovea is more likely to\nresult in blurred vision and metamorphopsia. When the DME involves or threatens the\nfovea, the risk of moderate visual loss (MVL, defined as a three-line or more decrease of\nvisual acuity, equivalent to a doubling of the visual angle) over 3 years in the Early\nTreatment of Diabetic Retinopathy Study (ETDRS) was 24% without treatment.[9] The\ndisease course is variable, with some eyes having chronic persistent DME spanning\nseveral years, while other eyes have rapid spontaneous resolution, although the risk of\nrecurrence is always present.\n\nPrevalence\nThe Wisconsin Epidemiologic Study of Diabetic Retinopathy (WESDR) found that DME\nincidence over 25 years among people with type 1 DM (T1DM) was 29%.[10] The Diabetes\nControl and Complications Trial (DCCT) reported that 27% of people with T1DM had\nDME within 9 years of onset of diabetes.[11] For people with type 2 DM (T2DM), the\nWESDR found that 25.4% of those who used insulin and 13.9% of those who did not use\ninsulin had DME.[10] Yau et al. estimated the global prevalence of DME at 6.8% among\npeople with DM. Estimates in the United States are between 2.7% to 3.8%, with nonHispanic whites less likely to have DME versus non-Hispanic blacks.[12][13][14]\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n3/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nFigure 2: Circinate exudates. A: Blue arrows - Circinate\nexudates, defined as exudates arranged in a circular appearance.\nB: OCT b-scan across the fovea confirming the presence of DME\nassociated with an elevated foveal contour. The patient\u2019s bestcorrected vision was 20/32.\n\nRisk Factors\nRisk factors for DME and DR are similar. These risks include a longer duration of\ndiabetes mellitus (DM), poor control of DM with elevated hemoglobin A1c (HbA1c),\nhypertension, and hyperlipidemia. Other secondary risk factors include impaired renal\nfunction and the use of thiazolidinediones.[15][16][17]\n\nPrevention\nPrimary prevention of DME involves intensive control of DM, blood glucose,\nhypertension, blood lipids, and other systemic risk factors. The Diabetic Retinopathy\nClinical Research (DRCR) Protocol W investigated whether aflibercept injections in eyes\nwith baseline moderate to severe NPDR could prevent the eventual development of\ncenter-involved DME (ci-DME) with vision loss.[18] Vision loss was defined as a 10 letter\nor more decrease in visual acuity (VA) at 1 visit, or a 5 to 9 letter decrease at 2 consecutive\nvisits, with the decrease in vision attributed to the ci-DME. The 2-year cumulative\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n4/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nprobability of developing ci-DME with vision loss was 14.8% in the sham group versus\n4.1% in the aflibercept group. However, there was no significant difference in mean\nchange of visual acuity (VA) between both groups. From baseline to the 2-year checkup,\neyes treated with sham had a mean (SD) change of -2.0 (6.1) letters, while aflibercept\ntreated eyes had a -0.9 (5.8) letter change (adjusted mean difference 0.5 letters, [97.5%\nCI: -1.0 to 1.9 letters, p=0.47]. At present, the use of anti-VEGF injections for the\nprevention of ci-DME is still not the standard of care.\n\nDiagnosis\nHistory\nDME is suspected in patients with any level of DR who present with blurred vision or\nmetamorphopsias. A detailed history including the approximate date of onset of diabetes,\nthe use of insulin versus oral antihyperglycemic agents, and the quality of metabolic\ncontrol (e.g., HbA1c level) should be elicited. Any associated medical problems such as\nhypertension, hypercholesterolemia, renal disease, and thyroid disease should be\nidentified, along with a thorough review of medications. It should be noted that mild to\nextensive DME may be present without symptoms evident to the patient.\n\nFigure 3: Dense macular exudates involving the", "doc_id": "4eec6e94-115a-4d9a-b9ac-1546dd91b9f5", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "2103623e-c00e-4b0b-b283-b16cad1c464c", "node_info": {"start": 0, "end": 6662}}, "7512979820905562967": {"text": "to the patient.\n\nFigure 3: Dense macular exudates involving the fovea.\nA: Blue arrow\u2013 Dense foveal exudates. B: Red arrow\u2013 OCT bscan across the fovea confirming the presence of DME and the\ndense foveal exudate. The patient\u2019s best-corrected vision was\n20/200.\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n5/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nPhysical Examination\nPatients undergo a detailed biomicroscopic examination using the slit lamp\nbiomicroscope and indirect ophthalmoscope. Historically, DME classifications were\nbased on the ETDRS definitions of clinically significant macular edema (CSME). The\nspecific criteria for diagnosing CSME were:\n1. Retinal thickening at or within 500 \u03bcm of the center of the fovea\n2. Hard exudates at or within 500 \u03bcm of the center of the fovea if adjacent to an area\nof retinal thickening\n3. Retinal thickening of at least 1 disc area any portion of which is within 1500 \u03bcm\n(approximately 1 disc diameter) from the center of the fovea\n\nThus, CSME as defined by the ETDRS in the 1980s is a clinical diagnosis made by slitlamp examination using a contact lens. While clinical examinations remain essential for\nthe full evaluation of DME, Optical Coherence Tomography (OCT) is now routinely used\nto complement physical examination in the diagnosis of DME.\n\nSigns\nMacular thickening with or without hard exudates may be seen with stereo\nbiomicroscopy. However, some eyes may present without apparent signs of retinal\nthickening on clinical examination despite significant DME as observed using OCT.\nThickening can occur in various patterns: focal, multifocal, and diffuse areas of retina\nthickening. Despite these terms being frequently used, there are no well-established\nstandard definitions, and different authors use them inconsistently.[19] In the ETDRS,\nfocal leakage results from microaneurysms that may be treated with fluorescein\nangiography (FA) guided focal laser, while diffuse capillary leakage is from a more\nwidespread breakdown of the BRB, which may be treated with grid laser.[20] Hard\nexudates in various patterns may also be seen, including circinate rings and focal\naggregations of exudates (Figures 2-3). Hard exudates consist of lipoprotein residues of\nserous leakage from damaged vessels, serving as biomarkers for DME.\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n6/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nFigure 4: Basic structural changes seen in OCT with\nDME. Yellow bracket\u2013 Generalized retinal swelling. Blue\narrow\u2013 Cystoid macular edema. Red arrow\u2013 Subretinal fluid.\n\nSymptoms\nDME may present with decreased visual acuity (VA), metamorphopsia, changes in color\nperception, and difficulty reading, although it may also present asymptomatically.\nVision and DME\nStudies show a poor to modest correlation between visual acuity and central subfoveal\nthickness (CST) on OCT, within the range of 0.3-0.5.[21][22] Over two years, only around\n12-14% of the change in VA can be attributed to the change in OCT thickness for eyes with\nDME. In a study by the DRCR Network, the slope of the best fit line shows an\napproximately 4.4 letter improvement (95% CI: 3.5, 5.3) for every 100-micron decrease in\nCST at baseline.[22] Interestingly, on follow-up after treatment with macular laser\nphotocoagulation, there were some eyes with paradoxical improvement in VA with\nincreased CST (7-17% at different time points) and paradoxical worsening of VA with\ndecreased CST (18-26% at different time points). These findings highlight how OCT\nmeasurements cannot be used as a perfect surrogate for visual acuity; however, in clinical\nand research settings, the technology remains an important tool. The DRCR has\nrecommended a 10% change in CST to indicate a real change that can be considered in\nclinical decision-making.\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n7/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nDiagnostic Procedures\n1. Optical Coherence Tomography (OCT)\n\nFigure 5: Montage of center-involved versus non-center involved DME. Top Row A: Noncenter involved DME. Retinal thickening does not involve the central 1-mm subfield zone (innermost\ncircle) per the en-face OCT heatmap, as seen on b-scan. Bottom Row B: Center-involved DME.\nRetinal thickening involves the central 1-mm subfield zone (innermost circle) per the en-face OCT\nheatmap and b-scan. Published online with permission from the AAO.\n\nOCT within recent years has quickly become an important ancillary procedure in the\ndiagnosis and treatment of DME. Three basic structural changes can be seen: retinal\nswelling, cystoid macular edema, and subretinal fluid (Figure 4). Macular scans can\nquickly and accurately identify even subtle areas of thickening, along with quantitative\nmetrics for different areas. Changes in the anatomic distribution of DME can be\nmonitored over time, especially the fluid\u2019s relationship to the fovea. This information has\nproven crucial regarding clinical and research implications for the evaluation and\nmanagement of DME. More recently, the International Council of Ophthalmology (ICO)\nguidelines for diabetic eye care in 2018 have adopted the clinical entity of center-involved\nDME (ci-DME) versus non-center involved DME (non-ciDME) for the evaluation of\nmacular fluid (Figure 5). The classification is:\n1. Center-involved DME: Retinal thickening in the macula that involves the central\nsubfield zone (1 mm in diameter)\n2. Non-center involved DME: Retinal thickening in the macula that does not\ninvolve the central subfield zone (1 mm in diameter)\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n8/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nAside from the location of the swelling, the DRCR retina network has given\nrecommendations on CST treatment thresholds based on sex-matched standards.[23] The\nthresholds were different per OCT machine since thickness measurements cannot be\ncompared between different devices, with each device having its own normative database\nand algorithms. In DRCR Protocol T, in conjunction with visual acuity, treatment\neligibility thresholds per machine were:\n1. Heidelberg Spectralis - 320 \u03bcm for men or 305 \u03bcm for women\n2. Zeiss Cirrus OCT - 305 \u03bcm for men or 290 \u03bcm for women\n3. Zeiss Stratus OCT - 250 \u03bcm for both men and women\n\nMoreover, OCT is a more sensitive method for objective evaluation of vitreomacular\ninterface abnormalities (VMIA), which include vitreomacular adhesion (VMA),\nvitreomacular traction (VMT), and epiretinal membrane (ERM). Identifying VMIA is\ncrucial when diagnosing the etiology of macular edema, whether it is primarily from\nDME, from secondary causes of VMIA, or combined mechanism macular edema.\n\nFigure 6: Disorganization of the retinal inner layers. OCT images showing\ncombinations of presence or absence of DRIL and DME. The central 1-mm area is\nenclosed in the box. Upper images show segmentation of inner retinal layers, with the\nwhite lines demarcating the boundaries between IPL-INL and the", "doc_id": "7f7da798-ff62-420e-845c-84f8fd6b4a7b", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "11685734-5d4f-47c1-878e-5868711241f2", "node_info": {"start": 0, "end": 6979}}, "6692861175815638226": {"text": "with the\nwhite lines demarcating the boundaries between IPL-INL and the INL-OPL. Image\ncredit to: Barham et al., Association of Macular Nonperfusion, Leakage, and DRIL\n(ARVO poster, 2016)\n\nOCT Biomarkers for DME\nDME's different OCT features have been associated with disparate prognostic outcomes\nand treatment responses.\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n9/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\n1. Disorganization of the retinal inner layers (DRIL) is thought to represent damaged\ncells within the inner retinal layers, indicating a disruption in the normal visual\npathway from the photoreceptors to the ganglion cells.[24] DRIL is identified on\nOCT when there is disruption of the demarcating interface lines between the\nganglion cell-inner plexiform complex (GCL-IPL), inner nuclear layer (INL), outer\nplexiform layer (OPL), and outer nuclear layer (ONL). Eyes with DRIL have a worse\nbaseline and final VA despite anti-Vascular Endothelial Growth Factor (VEGF)\ninjections and have almost eight times greater risk for poor visual recovery. In\ncontrast, the resolution of DRIL has resulted in better visual outcomes (Figure 6).\n[25][26][27]\nDRIL was better correlated to VA when compared to glycemic status and\n[24]\nCST.\n2. External limiting membrane (ELM) and ellipsoid zone (EZ) disruption strongly\ncorrelate with baseline and final BCVA. At the same time, restoration of the EZ was\na requirement for good visual recovery in some studies (Figure 7).[28][29][30][31][32]\nThe ELM connects a row of zonular adherents to the photoreceptor cell bodies,\nwhile the EZ represents the isthmus between the outer and inner segments of\nphotoreceptors.[33]\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n10/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\n3. DME associated with vitreomacular interface abnormalities (VMIA), notably ERM\nand VMT, has poorer visual outcomes (Figure 8).[34][35] VMIA have been observed\nin 7%-16% of eyes with DME, with an annual incidence of up to 4.5%.[36][37] For\nVMA, the READ-3 trial showed that eyes with VMA still had a good response to\nanti-VEGF therapy.[38] Presence of posterior vitreous detachment (PVD) has been\nassociated with improved visual outcomes. Nasrallah et al. reported that DME was\npresent in 55% of eyes with an attached hyaloid, compared to only 20% of eyes with\nPVD.[39] Hikishi et al. reported only a 25% rate of spontaneous resolution in eyes\nwith attached posterior hyaloid, compared to a 55% resolution rate in eyes with\nPVD.[40] The role of the vitreous and VMIA concerning DME, which may be related\nto changes in transvitreal oxygenation, hyalocyte proliferation from vitreous\nremnants on the ILM, and the present growth factors in the premacular hyaloid, is\nstill being investigated.[41][42][43][44]\n\nFigure 7: External limiting membrane and ellipsoid zone disruption. A: DME\nwith large cystic spaces (blue arrow) and exudates (green arrows). Despite anti-VEGF\ntreatment, DME persisted. The EZ and ELM were still intact, with BCVA of 20/32. B:\nFive years after photo A, extensive ELM and EZ disruption (red bracket) developed\nwhich involved the fovea. A few chronic parafoveal cysts can still be seen. BCVA dropped\nto 20/63.\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n11/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\n2. Fluorescein Angiography\n\nFigure 8: Epiretinal membrane associated with DME. Dense epiretinal\nmembrane overlying the retinal surface, with an elevated foveal contour and\nsignificant intraretinal cystic spaces in a patient with diabetes. Published online\nwith permission from the AAO.\n\nFigure 9: Focal and diffuse DME. A and B: Fundus photo showing\ncircinate exudates, with adjacent microaneurysms and leakage seen on FA. C\nand D: Fundus photo with subtle signs of macular thickening, with diffuse,\npoorly demarcated capillary leakage seen on FA. Published online with\npermission from the AAO.\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n12/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nFluorescein angiography (FA) is performed to identify leaking microaneurysms or\ncapillaries to guide laser treatment, and areas of retinal ischemia. Leakage on the\nangiogram is not synonymous with retinal edema. Focal DME is characterized by focal\nleakage from microaneurysms or capillaries. In contrast, diffuse DME is diagnosed when\npoorly demarcated areas of capillary leakage are present (Figure 9). Recently, there has\nbeen a decreasing trend in the use of FA in the management of DME, likely due to the\nprocedure being more invasive and time-consuming compared to OCT.[45]\nContraindications to the use of FA include pregnancy and allergy associated with the\ncontrast dye.\n\nLaboratory Testing\nPrimary: HbA1c (Glycated Hemoglobin), Blood pressure, Lipid Profile. Secondary:\nHemoglobin (anemia exacerbates diabetic retinopathy and may be associated with\ndiabetic nephropathy), Fasting Blood Sugar (FBS), Post Prandial Blood Sugar (PPBS),\nUrea, Creatinine, Urine microalbumin levels, Thyroid panel.\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n13/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nDifferential Diagnosis\n\nFigure 10: Pseudophakic cystoid macular edema/Irvine-Gass\nSyndrome. A: Color fundus photograph of an optic nerve head and macula 3\nmonths after complex cataract surgery. A small incidental grayish-yellow adult\nvitelliform dystrophy lesion is present in the subfoveal region (circled). B: A\nmid-phase fluorescein angiography image demonstrates cystic\nhyperfluorescence, with a classic petaloid pattern. As is typical in eyes with\npseudophakic CME, there is mild hyperfluorescence of the nasal portion of the\noptic nerve head. C: OCT shows cystic retinal thickening and a subfoveal\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n14/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nvitelliform lesion. D: Following 8 weeks of topical steroidal and nonsteroidal\nanti-inflammatory therapy, OCT shows that the CME has fully resolved.\nPublished online with permission from the AAO.\n\nOther causes of macular edema include retinal vein occlusion, ruptured macroaneurysm,\nIrvine-Gass syndrome, radiation retinopathy, hypertensive retinopathy, subfoveal\nchoroidal neovascularization, retinal vein occlusion, and VMIA. OCT and FA ancillary\ndiagnostics can help differentiate between these differential diagnoses (Figures 10-11).\n\nFigure 11: Vitreo-macular traction with secondary macular edema. A:\nColor fundus photograph of the right eye with pseudohole and", "doc_id": "14032852-58c5-41dd-8708-81db1c1ea201", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "00cd7c2b-cfff-4f63-9979-9184dd733c58", "node_info": {"start": 0, "end": 6519}}, "57614952976131457": {"text": "A:\nColor fundus photograph of the right eye with pseudohole and epiretinal\nmembrane with tractional macular edema. B: Optical coherence tomography\nimage of same patient showing vitreomacular traction, epiretinal membrane,\nand resulting macular edema. C: Optical coherence tomography of the same eye\nafter vitrectomy surgery with epiretinal membrane peeling. Published online\nwith permission from the AAO.\n\nManagement\nMedical therapy\nStrict control of diabetes, blood glucose, hypertension, and hypercholesterolemia[46]\nDiet Modification\nWeight Loss\nExercise\n\nPharmacotherapy\nAt present, anti-VEGF agents are the first-line treatment for DME requiring treatment.\nSince 2005, intravitreal bevacizumab has been used off-label for ocular conditions. FDA\napproved ranibizumab for DME in 2012, Aflibercept in 2014 and Brolucizumab and\nFaricimab in 2022.\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n15/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nDRCR Retina Network anti-VEGF treatment algorithm\nSix monthly injections are given unless VA is 20/20 or better, and CST is <320\u03bcm for\nmen or <305\u03bcm for women on the Heidelberg Spectralis, in which case treatment may be\nwithheld starting the 4th month. At the 6th monthly visit, if stability is achieved in vision\nor CST from the previous 2 or more visits, or DME has resolved, further treatment may be\nwithheld. Stability is defined as:\n1. Lack of improvement\nNo BCVA increase of \u22655 letters (approximately 1 line on a Snellen chart)\nNo decrease in OCT CST \u226510%\n2. No worsening\nBCVA decreases \u22655 letters (approximately 1 line on a Snellen chart) in the\nsetting of persistent DME\nOCT CST increases \u226510%\n\nIf there is worsening on follow-up, anti-VEGF injections are resumed. In general, eyes\nshowing stability may be followed-up in 3-4 months, and sooner as needed. Withholding\ninjections does not require 20/20 vision or a dry macula, only evidence of stability over\nthe previous 2 or more visits. DRCR Protocol I published the first anti-VEGF PRN\ntreatment algorithm for DME. Long-term data show that even without using a monthly\ntreatment protocol, eyes with persistent DME often maintain good BCVA over the long\nterm in clinical trial settings.[47] Outside of trial settings, the five-year extension study of\nProtocol I showed that CST remained stable among eyes given anti-VEGF; however, mean\nBCVA worsened between the 5th and 2nd-year time points.[48] On average, patients are\ngiven 6-8 injections in the first year, 2-4 injections in the second year, and 0-1 injections\nbeginning the third year.[49]\nClinical considerations in the anti-VEGF treatment of DME\nObservation is recommended for eyes with ci-DME and visual acuity of 20/25 or better.\nThis recommendation is based on the findings of DRCR Protocol V, where patients were\nrandomized to receive either aflibercept injections, macular laser, or observation. At the\n2-year endpoint, the mean BCVA was 20/20, and the rates of \u2265 5 letter vision loss (1619%) were similar among all three groups. Given the risks of ocular infection and the\ncosts associated with intravitreal injections, observation is a viable treatment option in\nthese patients if they can reliably follow up and receive appropriate therapy when there is\nclinical deterioration. In contrast, among eyes with ci-DME presenting with 20/50 vision\nor worse, Protocol T results showed that aflibercept was superior to both ranibizumab\nand bevacizumab, with area under the curve analysis showing better visual outcomes over\n1 year.[50] However, the superiority of aflibercept over ranibizumab was not maintained at\nthe 2-year checkup.[23] Bevacizumab thinned the retina the least; however, all 3\nmedications had similar visual outcomes among eyes with baseline vision of 20/40 or\nbetter.\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n16/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nNot all treatment results in complete resolution of DME, with 40% of eyes still showing\npersistent DME (defined as never having a CST < 250\u03bcm through 6 months on timedomain OCT) in Protocol I over 2 years.[47] Eyes given bevacizumab were more likely to\nhave persistent DME than eyes given aflibercept. The percentage of eyes with complete\nresolution increases with each ranibizumab or aflibercept injection.[51] At the 3-year\nfollow-up, eyes with chronic persistent DME still had a significant 7 letter mean\nimprovement compared to baseline, lower than the 13 letter mean improvement in eyes\nwith complete DME resolution.[52] Importantly, only 3.4% of eyes with chronic persistent\nDME lost \u2265 2 lines of vision over 2 years regardless of the type of anti-VEGF they\nreceived.[53] To summarize, in clinical trial settings, a substantial proportion of eyes with\npersistent DME still have \u2265 2 lines of improvement in vision over the long term, with very\nfew eyes developing considerable vision loss.\nFor eyes that do not respond optimally, switching to another anti-VEGF drug is a\ntreatment option. The switch is typically from bevacizumab to either ranibizumab or\naflibercept, or ranibizumab to aflibercept. The rationale for switching is that aflibercept\nhas 100 times more affinity to VEGF-A than bevacizumab or ranibizumab, while\nconcurrently binding placental growth factor (PIGF) and VEGF-B.[54] Aflibercept also has\na longer half-life and can negate more cytokines that promote DME development. Most\nstudies looking at switching are retrospective and show a significant reduction in CST;\nhowever, visual outcomes vary.[55][56][57][58][59][60][61][62][63][64][65][66][67][68] Some eyes\nmay be delayed responders to anti-VEGF. These eyes need more than the initial 3-6\nmonthly injections to show significant improvement but eventually catch up with\nimmediate responders.[69][70] It may be viable to continue treatment with the same\nmedication if there is at least a trend of continued improvement, as bevacizumab and\nranibizumab are more cost-effective options. Caution is warranted for switching, as any\nclinical improvement may be due to continued treatment among delayed responders\ninstead of the shift in medications.\nDRCR protocol AC was a randomized controlled trial evaluating the relative efficacy of\nadministering aflibercept monotherapy compared with bevacizumab first with a switch to\naflibercept (step therapy) in eyes with suboptimal response despite treatment. A total of\n312 eyes with moderate vision loss from ci-DME were enrolled. Over a 2-year period, the\nmean improvement in VA was 14.0 letters in the bevacizumab-first group and 15.0 letters\nin the aflibercept-monotherapy group (adjusted difference, 0.8 letters; 95% confidence\ninterval, \u22120.9 to 2.5; P=0.37). At 2 years, the mean changes in VA and retinal CST were\nsimilar in the two groups.[71]\nSteroids\nIntravitreal steroids improve vision and decrease retinal thickness, as there is an\ninflammatory component to DME. Steroids have powerful anti-edematous and antiinflammatory effects as they decrease several pro-inflammatory mediators (IL-6, IL-8,\nTNF-\u03b1, MCP-1, ICAM-1, VEGF, etc).[72] However, long-term results have not shown\nmaintenance of", "doc_id": "e70b3b03-801f-4b05-b956-7725c68ebc41", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "1288eae1-ad79-48b8-b807-7554fc10e525", "node_info": {"start": 0, "end": 7088}}, "3451629399861619015": {"text": "VEGF, etc).[72] However, long-term results have not shown\nmaintenance of initial clinical improvement. In DRCR Protocol I, although the group\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n17/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\ngiven intravitreal triamcinolone had a similar response with ranibizumab in the first 6\nmonths, vision declined due to cataracts. Even with cataract surgery, the final vision did\nnot recover to the levels comparable to the group given ranibizumab.[47] In Protocol U\neyes with persistent DME despite at least 6 ranibizumab injections were randomized to\ncontinue ranibizumab monotherapy, or shift to ranibizumab plus dexamethasone\n(Ozurdex).[73] At 6 months average visual gain was similar in both groups, although the\nimprovement in CST was greater in the combination group. Phakic eyes given intravitreal\nsteroids often develop cataracts needing surgery, and are at risk for intraocular pressure\n(IOP) elevations leading to glaucoma.\n\nPharmacotherapy Landmark Studies\nAnti-VEGF\nBevacizumab: Bevacizumab is a recombinant humanized monoclonal IgG1\nantibody that binds VEGF. Bevacizumab is given off-label for the treatment of DME,\nand remains the most cost-effective treatment option among anti-VEGF\nmedications.[74] In the BOLT study, intravitreal Bevacizumab (1.25 mg) at 6-week\nintervals was reported to be more effective than modified ETDRS focal/grid laser in\nterms of improvement in visual acuity at 12 months.[75] In DRCR Protocol T, a\ncomparison between bevacizumab, ranibizumab, and aflibercept, 1-year results\nshowed that bevacizumab thinned the retina the least.[23] However, all 3\nmedications had similar visual outcomes among eyes with baseline vision of 20/40\nor better.[53] Intravitreal bevacizumab doses of 1.25 to 2.5mg have shown\nimprovement in best-corrected visual acuity and reduced macular thickness on OCT\nat 24 months in The Pan-American Collaborative Retina Study Group.[76]\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n18/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nRanibizumab: Ranibizumab is a recombinant humanized IgG1 monoclonal\nantibody fragment that binds and inhibits VEGF-A.[77] It is FDA approved for the\ntreatment of DME.\n1. DRCR Protocol I was the first definitive phase III study demonstrating the\neffectiveness of ranibizumab for DME treatment.[47] Four treatment arms\nwere compared: ranibizumab with immediate grid/focal laser, ranibizumab\nwith macular laser given only for at least 6 months of persistent DME,\nintravitreal triamcinolone with immediate macular laser, and macular laser\nwith sham injections. Results showed that ranibizumab in an as-needed\ntreatment protocol was superior to laser therapy. Eyes treated with\nranibizumab gained an average of 8-9 letters, versus an average of only 3\nletters gained with laser therapy at the 1-year endpoint. Protocol I\nrevolutionized the treatment protocol for DME when it was published in 2011.\nBefore this study, macular laser was considered the 1st line therapy for DME, a\ntreatment protocol originating from the original ETDRS papers first published\nin 1985.\n2. RISE and RIDE - The two-year results for ranibizumab in DME showed that\n98% of patients maintained vision (lost less than 15 letters) with 0.3mg\nmonthly injections, 34-45% of patients gained at least 15 letters, and mean\nvisual acuity gain was 10.9 to 12.5 letters.[78] Only 45-49% of patients needed\nmacular laser compared with 91-94% in the control group. No additional\nbenefit was seen with 0.5mg monthly versus 0.3mg ranibizumab monthly.[79]\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n19/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nAflibercept: Aflibercept is a soluble decoy receptor that binds VEGF-A, VEGF-B,\nand placental growth factor with high affinity.[79] It is termed a decoy receptor or a\n\u201cVEGF-trap\u201d as VEGF mistakenly binds with aflibercept instead of the body\u2019s native\nreceptors, reducing VEGF\u2019s activity. It is FDA approved for the treatment of DME.\nIn the Da Vinci study, DME patients were assigned randomly to 1 of 5 treatment\nregimens: Aflibercept 0.5mg every 4 weeks (0.5q4); 2mg every 4 weeks (2q4); 2mg\nevery 8 weeks after 3 initial monthly doses (2q8); or 2mg dosing as needed after 3\ninitial monthly doses (2prn), or macular laser photocoagulation.[80] Mean\nimprovements in BCVA in the aflibercept groups at week 52 were 11.0, 13.1, 9.7, and\n12.0 letters for 0.5q4, 2q4, 2q8, and 2prn regimens, respectively, versus -1.3 letters\nfor the laser group. The proportion of eyes with gains in BCVA of 15 or more ETDRS\nletters at week 52 in the aflibercept groups were 40.9%, 45.5%, 23.8%, and 42.2%\nversus 11.4% for laser. Mean reductions in CST in the aflibercept groups at week 52\nwere -165.4\u03bcm, -227.4\u03bcm, -187.8\u03bcm, and -180.3\u03bcm versus -58.4\u03bcm for laser.[79]\nThe PHOTON trial evaluated the use of high-dose 8mg aflibercept every 12 (8q12)\nor 16 (8q16) weeks, compared with conventional dosing of 2mg every 8 weeks.[81]\nResults showed that the 8mg extended interval dosage was non-inferior to\nconventional treatment when comparing gains in BCVA and retinal thinning at 48\nweeks. There was an increase of 9.2, 8.8, and 7.9 letters, and a mean CST reduction\nof -165\u03bcm, -172\u03bcm, and -148\u03bcm, for the 2q8, 8q12, and 8q16 groups at 48 weeks,\nrespectively. Patients in the high-dose group with a 50\u03bcm increase in CST or a 10letter loss from week 12 onwards had their dosing schedule shortened to either 12 or\n8 weeks, but 93% of patients remained on dosing intervals of 12 weeks or more.\nThere was no increase in hypertension in the high-dose group.\nFaricimab: Farcimab is a novel combined mechanism inhibitor that binds both\nAngiopoietin-2 (Ang-2) and VEGF-A with high specificity and affinity. The 1-year\nresults from the phase II BOULEVARD study show that in patients given the 6.0mg\ndose, there was a statistically significant gain of 3.6 letters over ranibizumab.[82]\nMoreover, faricimab showed improvement in DR severity, reduced CST, and had a\nlonger time to retreatment than ranibizumab. There were no unexpected safety\nconcerns noted. The phase III YOSEMITE and RHINE non-inferiority trials\ncompared faricimab with aflibercept in patients with DME.[83] The non-inferiority\nprimary endpoint of BCVA was achieved with faricimab given every 8 weeks. More\nthan 50% of patients achieved", "doc_id": "78239d23-baa2-49bb-8d04-e7992a1a517d", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "4194bfd1-6cfa-4ffe-b2c8-5d7d856d5ba1", "node_info": {"start": 0, "end": 6340}}, "4872224928877324632": {"text": "faricimab given every 8 weeks. More\nthan 50% of patients achieved dosing of every 16 weeks, and more than 70%\nachieved dosing of every 12 weeks or longer. These results demonstrate the\npotential of faricimab to decrease the treatment burden on patients by extending\nthe intraocular durability of anti-VEGF. FDA approved the use of faricimab for\nDME as 4 monthly loading doses followed by injections every 1-4 months, or a\nloading dose of 6 monthly injections followed up with injections every 2 months.\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n20/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nBrolucizumab: Brolucizumab is a single-chain antibody fragment with a high\naffinity for VEGF. Brolucizumab\u2019s low molecular weight of 26kDa allows more of\nthe drug to be delivered intraocularly per injection, with the potential for increased\ndurability and effective tissue penetration in the eye. The phase III KESTREL and\nKITE 52 week results showed that brolucizumab was non-inferior to aflibercept in\nthe mean improvement of BCVA, more patients had CST <280\u03bcm without\npersistent macular fluid, and >50% of brolucizumab 6mg patients were maintained\non q12 weekly dosage after loading.[84] However, reports of retinal vascular\nocclusion (RVO) and retinal vasculitis (RV) with intraocular inflammation (IOI)\nhave been reported.[85][86] Risk factors for developing these adverse reactions\ninclude a prior history of IOI or RVO in the 12 months before brolucizumab\ninitiation, female sex, and same-day bilateral injections.[87][88] FDA approved use of\nBrolucimab 6 mg for the treatment of DME in June 2022 for an injection every 8-12\nweeks after a loading dose of 5 injections 6 weeks apart.\nSteroids\nTriamcinolone (1 mg or 4 mg) preservative-free intravitreal injection was less\neffective and had more side-effects for most patients with DME than focal/grid\nphotocoagulation at 2-years follow-up (Protocol B).[89]\nDexamethasone (Ozurdex) 0.7 mg biodegradable implant improved vision by at\nleast 15 letters in 22% of patients at 3 years in the phase III MEAD study.[90] The\nFDA approved the 0.7 mg implant for DME, and at this dose, 41.5% of patients\nneeded anti-glaucoma medications, with 0.6% needing glaucoma surgery. Around\n60% of eyes in the 0.7 mg implant group had cataract surgery. The implant is\neffective for approximately 3-6 months intraocularly.\nFluocinolone acetonide (Iluvien) 0.19 mg non-biodegradable implant is a sustained\nrelease device effective for up to 3 years intraocularly. It is FDA approved to treat\nDME in patients who have been previously treated with a course of corticosteroids\nand did not have a clinically significant rise in IOP.[91][92] At the 0.2 \u03bcg/day dosage\nBCVA improvement of at least 15 letters was found in 28.7% of patients, with 38.4%\nneeding anti-glaucoma medications and 4.8% needing glaucoma surgery. The latter\nfigure was reduced to 0% among eyes that did not have a history of IOP elevation\nwith a prior steroid challenge. The implant can have complications like the\ndexamethasone implant, including cataracts and implant migration.\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n21/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nLaser Photocoagulation\n\nFigure 12: Focal laser for focal CSME. A: Planning of focal laser for focal\nCSME. Note the identified treatment areas, specifically the leakingmicroaneurysms that would be highlighted on FA. B: Focal laser-treated areas\nwith parameters. Published online with permission from the AAO.\n\nBefore developing anti-VEGF for DME, the standard treatment for CSME was macular\nlaser photocoagulation since the ETDRS was published in 1985. In \u201cfocal\u201d CSME, a focal\nlaser pattern is used to treat leaking microaneurysms identified on the FA that contribute\nto the retinal edema (Figure 12). In \u201cdiffuse\u201d CSME, intraretinal leakage is noted on the\nFA from dilated retinal capillary beds or intraretinal microvascular abnormalities (IRMA)\nwithout isolated, discrete foci of leakage. Macular grid is done for diffuse macular edema\n(Figure 13). Laser photocoagulation has been shown to decrease the risk of moderate\nvisual loss (loss of 15 or more ETDRS letters) from 24% to 12% by 3 years.[9] After laser\ntreatment, the follow-up examination is at three months. If residual CSME is noted, OCT\nand FA may be performed to evaluate the benefit and location of repeat laser treatment.\nWith the FDA approval of anti-VEGF for DME, focal/grid laser is only indicated in\npatients with non-ciDME. Especially in resource-limited countries with decreased access\nto anti-VEGF agents, macular laser remains a viable treatment option for patients with\nDME.\n\nFigure 13: Grid laser for diffuse CSME. A: Planning of grid laser for diffuse\nCSME. Note the identified treatment area, specifically the outlined region with\ndiffuse edema that would be highlighted on FA. B: Grid laser-treated area with\nparameters. Published online with permission from the AAO.\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n22/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nCombined Therapy\nIntravitreal ranibizumab with laser: Intravitreal ranibizumab with prompt\n(within 1 week) or deferred (after 24 weeks) laser is more effective compared to\nfocal/grid laser alone for the treatment of ci-DME (Protocol I).[47] Ranibizumab is\ninjected intravitreally at baseline with prompt laser, followed by monthly\nranibizumab injections for 4 months followed by the continuation of injections at 16\nweeks if the OCT central subfield thickness is \u2265250 um with visual acuity worse\nthan 20/20.\nSteroid with laser: Intravitreal triamcinolone (IVT, 4 mg) with focal/grid laser\nwithin a week is more effective than laser alone at 4 months (Protocol B). However,\nlong-term benefit with this combined therapy was not seen, with mean BCVA better\nin the laser monotherapy group than the combined therapy group from the 16month timepoint until the 2-year endpoint. Complications of steroid therapy\nincluded cataracts, ocular hypertension, and glaucoma. The difference in BCVA\ncould not be attributed fully to the development of cataracts. In DRCR Protocol I,\nvisual acuity improvement in eyes given IVT with prompt laser were comparable to\neyes given ranibizumab at 6 months, but vision declined afterward until the 2-year\ntimepoint.[47][93] Subgroup analysis in pseudophakic eyes given IVT showed visual\nimprovement was significantly better than in phakic eyes, with results comparable\nto pseudophakic eyes given ranibizumab at the 1 and 2-year time points.\nIntravitreal ranibizumab with peripheral targeted retinal\nphotocoagulation (TRP): The DAVE study was a phase I/II clinical trial that\nevaluated if ranibizumab with TRP could reduce the number of required", "doc_id": "fe714995-2a3e-4d86-8a6c-1b0d3e18e3e4", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "46c99f92-994c-4cac-ab4a-1ebbb03866a0", "node_info": {"start": 0, "end": 6724}}, "8656308487412474790": {"text": "that\nevaluated if ranibizumab with TRP could reduce the number of required anti-VEGF\ninjections compared to ranibizumab monotherapy.[94] Peripheral TRP was defined\nas retinal photocoagulation administered outside the macula to areas of retinal\ncapillary nonperfusion identified on widefield FA. The nonperfused hypoxic retina\nis thought to upregulate hypoxia-inducible factors and cytokines, including VEGF\nand erythropoietin, with small studies suggesting that TRP can decrease the antiVEGF treatment burden.[95][96][97][98][99] At the 3-year endpoint, there was no\nevidence that combined ranibizumab plus TRP reduced treatment burden or\nimproved vision outcomes compared to ranibizumab alone.\n\nSurgery\nNo well-constructed studies show a definitive benefit of pars plana vitrectomy (PPV) for\nmanaging DME. The theoretical basis for PPV as a treatment option comes from reports\nthat it increases vitreous oxygenation in ischemia, leading to decreased VEGF production,\nand from the observation that DME is less common among eyes with PVD.[100][101][102]\n[103][104][105]\nVitreous viscosity also significantly decreases, which may bring about a\ngreater diffusion of pro-inflammatory cytokines away from the macula.[106] Other authors\nsuggest PPV plus internal limiting membrane (ILM) peeling should be attempted, as its\nremoval brings better resolution of the tractional forces at the vitreoretinal interface\nknown to worsen DME. This procedure also prevents proliferating astrocytes from using\nthe ILM as a scaffold which may lead to ERM.[107] In a systematic review looking at PPV\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n23/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nfor DME, CST was significantly decreased by 102 \u03bcm, and a non-significant VA increase\nof 2 letters was observed.[108] However, the anatomic benefit was not maintained by the\n12-month timepoint. A similar meta-analysis looking at PPV plus ILM peeling versus PPV\nalone showed no significant difference in postoperative vision and macular thickness.[109]\nDRCR Protocol D, a prospective study of eyes with DME and VMT, found that at 6\nmonths postop, 43% of eyes had a reduction in central subfield thickness to <250 \u03bcm.[110]\nHowever, the median VA did not change at 6 months. In 38% of eyes the median visual\nacuity improved by \u226510 letters, and in 22% the median VA decreased by \u226510 letters.\nPosthoc analysis of DRCR Protocol I showed that previously vitrectomized eyes given\nanti-VEGF for ci-DME had no improved clinical outcomes compared to nonvitrectomized eyes.[111]\n\nTreatment Complications\nComplications, listed below, may arise from the various treatment modalities. The perinjection risk of developing complications is also listed below, when available.\nIntravitreal injections\nLaser Photocoagulation\nSubretinal fibrosis\nExtension of the laser scar into the fovea\nChoroidal neovascular membrane\nParacentral scotoma\nDecreased visual acuity\nPPV\nRetinal tears and retinal detachment\nVitreous hemorrhage\nElevated intraocular pressure\nEndophthalmitis\nCataract\n\nPrognosis\nClinical factors associated with better visual outcomes with anti-VEGF treatment include\nlower hemoglobin A1c, younger age, less severe DR, absence of ERM, quick and\nconsistent CST decreases with anti-VEGF therapy, and absence of prior panretinal\nphotocoagulation (PRP).[122][123] In terms of anatomic outcomes, eyes with hard exudates\nwithin the 6mm foveal center had a larger CST decrease at the end of 1 year. The presence\nof exudates may be a marker of BRB abnormalities typical of DME responsive to antiVEGF. Eyes that lack exudates may have other underlying mechanisms of retinal\nthickening, including cystoid degeneration, traction, or ischemia. In contrast, eyes with\nhigh baseline CST \u2265 570\u03bcm had a significantly higher chance of developing persistent\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n24/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nDME despite monthly ranibizumab therapy.[124] In terms of response to macular laser\ntherapy, the ETDRS reported that worse clinical outcomes were associated with higher\nblood lipid levels, presence of hard exudates, and diffuse edema.[125]\nMatsunaga et al. looked at eyes with DME treated with at least 1 dose of anti-VEGF, and\nthen afterward were lost to follow-up (LTFU) for at least 6 months before returning to the\nclinic.[126] Their vision worsened significantly at the initial return visit to ~20/69 from\n~20/52, however at the 3, 6, and 12-month follow-up, and final checkup, their vision\nrecovered and had no significant difference with their baseline vision. OCT CST also\nshowed similar trends. Gao et al. found that 25% of patients with NPDR and DME had no\nfollow-up for at least 1 year after receiving 1 anti-VEGF injection.[127] Factors associated\nwith LTFU included being Hispanic (OR 1.66), American Indian, Pacific Islander,\nmultiple races (OR 2.6), and unknown race (OR 1.59) compared to whites. Lower\nadjusted gross income and decreasing baseline vision were also factors significantly\nassociated with LTFU.\n\nFuture Directions\nNumerous pharmacotherapy trials for DME treatment are underway. The development of\na long-acting anti-VEGF that could remain effective in the vitreous for multiple months or\nyears would significantly decrease the treatment burden for patients needing monthly\ninjections. Novel pharmacotherapies based on different mechanisms of action include\nanti-VEGF designed ankyrin repeat proteins (DARPins), growth factor inhibitors, antiinflammatory medications, hormone modulators, acetylcholine receptor blockers, IGF-1\nreceptor blockers, and neuroprotective/antiapoptotic agents.[128] Port delivery systems\nFDA approved for wet AMD are in development to treat DR and DME.[129] These\nexperimental therapies have the potential to significantly decrease the burden of\ntreatment while restoring vision to DME patients in the coming years ahead.\n\nFurther reading\n1. Bhagat N, Grigorian RA, Tutela A, Zarbin MA. Diabetic macular edema:\npathogenesis and treatment. 2009 Jan-Feb;54(1):1-32\n2. Diabetic Retinopathy Clinical Research Network Randomized trial evaluating\nranibizumab plus prompt or deferred laser or triamcinolone plus prompt laser for\ndiabetic macular edema. Ophthalmology June 2010; 117(6):1064-1077.\n3. Early Treatment Diabetic Retinopathy Study: Photocoagulation for diabetic macular\nedema. Early Treatment Diabetic Retinopathy Study report number 1. Early\nTreatment Diabetic Retinopathy Study research group. Arch Ophthalmol 103:17961806, 1985.\n4. Michaelides M, Kaines A et al A prospective randomized trial of intravitreal\nbevacizumab or laser therapy in the management of diabetic macular edema (BOLT\nstudy) 12 month data. Ophthalmology June 2010; 117(6):1059-1060.\n5. Schachat AP. A new approach to the management of diabetic macular edema.\nOphthalmology 2010 June;117(6):1059-1060.\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n25/34\n\n\f1/4/23, 8:18", "doc_id": "d8d9f4a4-4469-4806-976c-4dd0142f1d9f", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "99dde055-d214-4c5c-81fd-2124ba89460f", "node_info": {"start": 0, "end": 6928}}, "5225354482783333180": {"text": "8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\nReferences\n1. \u2191 Otani T, Kishi S, Maruyama Y. Patterns of diabetic macular edema with optical\ncoherence tomography. American journal of ophthalmology. 1999;127(6):688-693.\n2. \u2191 Yanoff M, Fine BS, Brucker AJ, et al. Pathology of human cystoid macular edema.\nSurvey of ophthalmology. 1984;28:505-511.\n3. \u2191 Xu H-Z, Le Y-Z. Significance of outer blood\u2013retina barrier breakdown in diabetes\nand ischemia. Investigative Ophthalmology & Visual Science. 2011;52(5):21602164.\n4. \u2191 Brownlee M. The pathobiology of diabetic complications: a unifying mechanism.\ndiabetes. 2005;54(6):1615-1625.\n5. \u2191 Del Zoppo G. The neurovascular unit in the setting of stroke. Journal of internal\nmedicine. 2010;267(2):156-171.\n6. \u2191 Gao B-B, Clermont A, Rook S, et al. Extracellular carbonic anhydrase mediates\nhemorrhagic retinal and cerebral vascular permeability through prekallikrein\nactivation. Nature medicine. 2007;13(2):181-188.\n7. \u2191 Jeppesen P, Aalkj\u00e6r C, Bek T. Bradykinin relaxation in small porcine retinal\narterioles. Investigative ophthalmology & visual science. 2002;43(6):1891-1896.\n8. \u2191 Parpura V, Basarsky TA, Liu F, et al. Glutamate-mediated astrocyte\u2013neuron\nsignalling. Nature. 1994;369(6483):744-747.\n9. \u2191 White NH, Sun W, Cleary PA, et al. Effect of prior intensive therapy in type 1\ndiabetes on 10-year progression of retinopathy in the DCCT/EDIC: comparison of\nadults and adolescents. Diabetes. 2010;59(5):1244-1253.\n10. \u2191 Varma R, Bressler NM, Doan QV, et al. Prevalence of and risk factors for diabetic\nmacular edema in the United States. JAMA ophthalmology. 2014;132(11):13341340.\n11. \u2191 Wong TY, Klein R, Islam FA, et al. Diabetic retinopathy in a multi-ethnic cohort in\nthe United States. American journal of ophthalmology. 2006;141(3):446-455. e441.\n12. \u2191 Yau JW, Rogers SL, Kawasaki R, et al. Global prevalence and major risk factors of\ndiabetic retinopathy. Diabetes care. 2012;35(3):556-564.\n13. \u2191 Ishibazawa A, Nagaoka T, Takahashi K, et al. Association between diabetic\nmacular edema and chronic kidney disease in patients with type 2 diabetes.\nInvestigative Ophthalmology & Visual Science. 2013;54(15):2400-2400.\n14. \u2191 Hsieh Y-T, Tsai M-J, Tu S-T, et al. Association of abnormal renal profiles and\nproliferative diabetic retinopathy and diabetic macular edema in an Asian\npopulation with type 2 diabetes. JAMA ophthalmology. 2018;136(1):68-74.\n15. \u2191 Fong DS, Contreras R. Glitazone use associated with diabetic macular edema.\nAmerican journal of ophthalmology. 2009;147(4):583-586. e581.\n16. \u2191 Maturi RK, Glassman AR, Josic K, et al. Effect of Intravitreous Anti\u2013Vascular\nEndothelial Growth Factor vs Sham Treatment for Prevention of VisionThreatening Complications of Diabetic Retinopathy: The Protocol W Randomized\nClinical Trial. JAMA ophthalmology. 2021.\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n26/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\n17. \u2191 Browning DJ, Altaweel MM, Bressler NM, et al. Diabetic macular edema: what is\nfocal and what is diffuse? American journal of ophthalmology. 2008;146(5):649655. e646.\n18. \u2191 Early Treatment Diabetic Retinopathy Study Research Group. Treatment\ntechniques and clinical guidelines for photocoagulation of diabetic macular edema:\nEarly Treatment Diabetic Retinopathy Study report number 2. Ophthalmology.\n1987;94(7):761-774.\n19. \u2191 Sun JK, Jampol LM. The Diabetic Retinopathy Clinical Research Network (DRCR.\nnet) and its contributions to the treatment of diabetic retinopathy. Ophthalmic\nresearch. 2019;62(4):225-230.\n20. \u2191 Jump up to: 24.0 24.1 Sun JK, Lin MM, Lammer J, et al. Disorganization of the retinal\ninner layers as a predictor of visual acuity in eyes with center-involved diabetic\nmacular edema. JAMA ophthalmology. 2014;132(11):1309-1316.\n21. \u2191 Santos AR, Costa M\u00c2, Schwartz C, et al. Optical coherence tomography baseline\npredictors for initial best-corrected visual acuity response to intravitreal antivascular endothelial growth factor treatment in eyes with diabetic macular edema:\nthe CHARTRES study. Retina. 2018;38(6):1110-1119.\n22. \u2191 Radwan SH, Soliman AZ, Tokarev J, et al. Association of disorganization of retinal\ninner layers with vision after resolution of center-involved diabetic macular edema.\nJAMA ophthalmology. 2015;133(7):820-825.\n23. \u2191 Das R, Spence G, Hogg RE, et al. Disorganization of inner retina and outer retinal\nmorphology in diabetic macular edema. JAMA ophthalmology. 2018;136(2):202208.\n24. \u2191 Maheshwary AS, Oster SF, Yuson RM, et al. The association between percent\ndisruption of the photoreceptor inner segment\u2013outer segment junction and visual\nacuity in diabetic macular edema. American journal of ophthalmology.\n2010;150(1):63-67. e61.\n25. \u2191 Otani T, Yamaguchi Y, Kishi S. Correlation between visual acuity and foveal\nmicrostructural changes in diabetic macular edema. Retina. 2010;30(5):774-780.\n26. \u2191 Shin HJ, Lee SH, Chung H, et al. Association between photoreceptor integrity and\nvisual outcome in diabetic macular edema. Graefe's Archive for Clinical and\nExperimental Ophthalmology. 2012;250(1):61-70.\n27. \u2191 Lai K, Huang C, Li L, et al. Anatomical and functional responses in eyes with\ndiabetic macular edema treated with \u201c1+ PRN\u201d ranibizumab: one-year outcomes in\npopulation of mainland China. BMC ophthalmology. 2020;20(1):1-7.\n28. \u2191 Mori Y, Suzuma K, Uji A, et al. Restoration of foveal photoreceptors after\nintravitreal ranibizumab injections for diabetic macular edema. Scientific reports.\n2016;6(1):1-11.\n29. \u2191 Bunt-Milam A, Saari JC, Klock IB, et al. Zonulae adherentes pore size in the\nexternal limiting membrane of the rabbit retina. Investigative ophthalmology &\nvisual science. 1985;26(10):1377-1380.\n30. \u2191 Ercalik NY, Imamoglu S, Kumral ET, et al. Influence of the epiretinal membrane\non ranibizumab therapy outcomes in patients with diabetic macular edema.\nArquivos brasileiros de oftalmologia. 2016;79:373-375.\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n27/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema -", "doc_id": "66b5f9b9-3e0f-4a4f-85c3-7a1d6dbb4adc", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "85da3e76-5c3c-4eff-9e65-1ddb004e70ea", "node_info": {"start": 0, "end": 5991}}, "6448166473482900554": {"text": "8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\n31. \u2191 Maryam AK, Tafgeh M, Mahmoud M, et al. Short term effect of intravitreal\nbevacizumab for diabetic macular edema associated with epiretinal membrane.\nRomanian journal of ophthalmology. 2018;62(3):212.\n32. \u2191 Kim NR, Kim YJ, Chin HS, et al. Optical coherence tomographic patterns in\ndiabetic macular oedema: prediction of visual outcome after focal laser\nphotocoagulation. British journal of ophthalmology. 2009;93(7):901-905.\n33. \u2191 Chang C-K, Cheng C-K, Bai C-H, et al. Development of vitreomacular interface\nabnormality in patients with diabetic macular edema. Taiwan Journal of\nOphthalmology. 2012;2(3):93-98.\n34. \u2191 Sadiq MA, Soliman MK, Sarwar S, et al. Effect of vitreomacular adhesion on\ntreatment outcomes in the ranibizumab for edema of the macula in diabetes\n(READ-3) study. Ophthalmology. 2016;123(2):324-329.\n35. \u2191 Nasrallah FP, Jalkh AE, Van Coppenolle F, et al. The role of the vitreous in\ndiabetic macular edema. Ophthalmology. 1988;95(10):1335-1339.\n36. \u2191 Hikichi T, Fujio N, Akiba J, et al. Association between the short-term natural\nhistory of diabetic macular edema and the vitreomacular relationship in type II\ndiabetes mellitus. Ophthalmology. 1997;104(3):473-478.\n37. \u2191 Stef\u00e1nsson E. The therapeutic effects of retinal laser treatment and vitrectomy. A\ntheory based on oxygen and vascular physiology. Acta Ophthalmologica\nScandinavica. 2001;79(5):435-440.\n38. \u2191 Stolba U, Binder S, Gruber D, et al. Vitrectomy for persistent diffuse diabetic\nmacular edema. American journal of ophthalmology. 2005;140(2):295. e291-295.\ne299.\n39. \u2191 Stef\u00e1nsson E. Ocular oxygenation and the treatment of diabetic retinopathy.\nSurvey of ophthalmology. 2006;51(4):364-380.\n40. \u2191 Bu S-C, Kuijer R, Li X-R, et al. Idiopathic epiretinal membrane. Retina.\n2014;34(12):2317-2335.\n41. \u2191 Bailey C, Sparrow J, Grey R, et al. The national diabetic retinopathy laser\ntreatment audit. I. Maculopathy. Eye. 1998;12(1):69-76.\n42. \u2191 Tripathy K, Raj Sharma Y, Chawla R, et al. Recent advances in management of\ndiabetic macular edema. Current diabetes reviews. 2015;11(2):79-97.\n43. \u2191 Jump up to: 47.0 47.1 47.2 47.3 47.4 47.5 Elman MJ, Bressler NM, Qin H, et al. Expanded\n2-year follow-up of ranibizumab plus prompt or deferred laser or triamcinolone\nplus prompt laser for diabetic macular edema. Ophthalmology. 2011;118(4):609614.\n44. \u2191 Glassman AR, Wells III JA, Josic K, et al. Five-year outcomes after initial\naflibercept, bevacizumab, or ranibizumab treatment for diabetic macular edema\n(Protocol T Extension Study). Ophthalmology. 2020;127(9):1201-1210.\n45. \u2191 Elman MJ, Ayala A, Bressler NM, et al. Intravitreal ranibizumab for diabetic\nmacular edema with prompt versus deferred laser treatment: 5-year randomized\ntrial results. Ophthalmology. 2015;122(2):375-381.\n46. \u2191 Wells JA, Glassman AR, Ayala AR, et al. Aflibercept, bevacizumab, or ranibizumab\nfor diabetic macular edema. The New England journal of medicine.\n2015;372(13):1193-1203.\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n28/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\n47. \u2191 Bressler NM, Beaulieu WT, Glassman AR, et al. Persistent macular thickening\nfollowing intravitreous aflibercept, bevacizumab, or ranibizumab for centralinvolved diabetic macular edema with vision impairment: a secondary analysis of a\nrandomized clinical trial. JAMA ophthalmology. 2018;136(3):257-269.\n48. \u2191 Bressler SB, Ayala AR, Bressler NM, et al. Persistent macular thickening after\nranibizumab treatment for diabetic macular edema with vision impairment. JAMA\nophthalmology. 2016;134(3):278-285.\n49. \u2191 Papadopoulos N, Martin J, Ruan Q, et al. Binding and neutralization of vascular\nendothelial growth factor (VEGF) and related ligands by VEGF Trap, ranibizumab\nand bevacizumab. Angiogenesis. 2012;15(2):171-185.\n50. \u2191 Do DV, Nguyen QD, Vitti R, et al. Intravitreal aflibercept injection in diabetic\nmacular edema patients with and without prior anti\u2013vascular endothelial growth\nfactor treatment: outcomes from the phase 3 program. Ophthalmology.\n2016;123(4):850-857.\n51. \u2191 Ehrlich R, Dan I, Deitch I, et al. The effectiveness of intravitreal ranibizumab in\npatients with diabetic macular edema who have failed to respond to intravitreal\nbevacizumab. Ophthalmologica. 2016;235(3):133-136.\n52. \u2191 Hanhart J, Chowers I. Evaluation of the response to ranibizumab therapy\nfollowing bevacizumab treatment failure in eyes with diabetic macular edema. Case\nreports in ophthalmology. 2015;6(1):44-50.\n53. \u2191 Katz G, Moisseiev E, Goldenberg D, et al. Ranibizumab for persistent diabetic\nmacular edema after bevacizumab treatment. European journal of ophthalmology.\n2017;27(2):210-214.\n54. \u2191 Lee JH, Lee WK, Kim SE. Short-term outcomes of switching to ranibizumab\ntherapy for diabetic macular edema in patients with persistent fluid after\nbevacizumab therapy. Journal of Ocular Pharmacology and Therapeutics.\n2016;32(10):659-664.\n55. \u2191 Lim LS, Ng WY, Mathur R, et al. Conversion to aflibercept for diabetic macular\nedema unresponsive to ranibizumab or bevacizumab. Clinical Ophthalmology\n(Auckland, NZ). 2015;9:1715.\n56. \u2191 Rahimy E, Shahlaee A, Khan MA, et al. Conversion to aflibercept after prior antiVEGF therapy for persistent diabetic macular edema. American journal of\nophthalmology. 2016;164:118-127. e112.\n57. \u2191 Shah CP, Heier JS. Aflibercept for diabetic macular edema in eyes previously\ntreated with ranibizumab and/or bevacizumab may further improve macular\nthickness. Ophthalmic Surgery, Lasers and Imaging Retina. 2016;47(9):836-839.\n58. \u2191 Wood EH, Karth PA, Moshfeghi DM, et al. Short-term outcomes of aflibercept\ntherapy for diabetic macular edema in patients with incomplete response to\nranibizumab and/or bevacizumab. Ophthalmic Surgery, Lasers and Imaging\nRetina. 2015;46(9):950-954.\n59. \u2191 Ashraf M, Souka AA, ElKayal H. Short-term effects", "doc_id": "bb56e674-789c-4d95-bfba-6a720bc3727a", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "b3c5b93f-9d76-4b60-8a6a-22710c3f4e76", "node_info": {"start": 0, "end": 5840}}, "5349314647920839276": {"text": "\u2191 Ashraf M, Souka AA, ElKayal H. Short-term effects of early switching to\nranibizumab or aflibercept in diabetic macular edema cases with non-response to\nbevacizumab. Ophthalmic Surgery, Lasers and Imaging Retina. 2017;48(3):230236.\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n29/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\n60. \u2191 Bahrami B, Hong T, Zhu M, et al. Switching therapy from bevacizumab to\naflibercept for the management of persistent diabetic macular edema. Graefe's\nArchive for Clinical and Experimental Ophthalmology. 2017;255(6):1133-1140.\n61. \u2191 Klein KA, Cleary TS, Reichel E. Effect of intravitreal aflibercept on recalcitrant\ndiabetic macular edema. International journal of retina and vitreous. 2017;3(1):17.\n62. \u2191 Mira F, Paulo M, Henriques F, et al. Switch to aflibercept in diabetic macular\nedema patients unresponsive to previous anti-VEGF therapy. Journal of\nophthalmology. 2017;2017.\n63. \u2191 Fechter C, Frazier H, Marcus WB, et al. Ranibizumab 0.3 mg for persistent\ndiabetic macular edema after recent, frequent, and chronic bevacizumab: the\nROTATE trial. Ophthalmic Surgery, Lasers and Imaging Retina. 2016;47(11):1-18.\n64. \u2191 Ferris FL, Maguire MG, Glassman AR, et al. Evaluating effects of switching anti\u2013\nvascular endothelial growth factor drugs for age-related macular degeneration and\ndiabetic macular edema. JAMA ophthalmology. 2017;135(2):145-149.\n65. \u2191 Pieramici DJ, Wang P-w, Ding B, et al. Visual and anatomic outcomes in patients\nwith diabetic macular edema with limited initial anatomic response to ranibizumab\nin RIDE and RISE. Ophthalmology. 2016;123(6):1345-1350.\n66. \u2191 Jhaveri CD, Glassman AR, Ferris III FL, et al. Aflibercept Monotherapy or\nBevacizumab First for Diabetic Macular Edema. New England Journal of Medicine.\n2022;387(8):692-703.\n67. \u2191 Whitcup SM, Cidlowski JA, Csaky KG, et al. Pharmacology of corticosteroids for\ndiabetic macular edema. Investigative ophthalmology & visual science.\n2018;59(1):1-12.\n68. \u2191 Maturi RK, Glassman AR, Liu D, et al. Effect of adding dexamethasone to\ncontinued ranibizumab treatment in patients with persistent diabetic macular\nedema: a DRCR network phase 2 randomized clinical trial. JAMA ophthalmology.\n2018;136(1):29-38.\n69. \u2191 Ross EL, Hutton DW, Stein JD, et al. Cost-effectiveness of aflibercept,\nbevacizumab, and ranibizumab for diabetic macular edema treatment: analysis\nfrom the diabetic retinopathy clinical research network comparative effectiveness\ntrial. JAMA ophthalmology. 2016;134(8):888-896.\n70. \u2191 Michaelides M, Kaines A, Hamilton RD, et al. A prospective randomized trial of\nintravitreal bevacizumab or laser therapy in the management of diabetic macular\nedema (BOLT study): 12-month data: report 2. Ophthalmology. 2010;117(6):10781086. e1072.\n71. \u2191 Arevalo JF, Sanchez JG, Wu L, et al. Primary intravitreal bevacizumab for diffuse\ndiabetic macular edema: the Pan-American Collaborative Retina Study Group at 24\nmonths. Ophthalmology. 2009;116(8):1488-1497. e1481.\n72. \u2191 Krispel C, Rodrigues M, Xin X, et al. Ranibizumab in diabetic macular edema.\nWorld journal of diabetes. 2013;4(6):310.\n73. \u2191 Nguyen QD, Brown DM, Marcus DM, et al. Ranibizumab for diabetic macular\nedema: results from 2 phase III randomized trials: RISE and RIDE.\nOphthalmology. 2012;119(4):789-801.\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n30/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\n74. \u2191 Do DV, Nguyen QD, Boyer D, et al. One-year outcomes of the da Vinci Study of\nVEGF Trap-Eye in eyes with diabetic macular edema. Ophthalmology.\n2012;119(8):1658-1665.\n75. \u2191 David M. Brown, on behalf of the PHOTON study investigators. Intravitreal\nAflibercept Injection 8mg for DME: 48-Week Results From the Phase 2/3 PHOTON\nTrial. Presented at the American Academy of Ophthalmology 2022, September 30October 3, 2022. Website: https://investor.regeneron.com/static-files/da20405eb843-402e-855b-d824a15dec60. Accessed: November 29, 2022.\n76. \u2191 Sahni J, Patel SS, Dugel PU, et al. Simultaneous inhibition of angiopoietin-2 and\nvascular endothelial growth factor-A with faricimab in diabetic macular edema:\nBOULEVARD phase 2 randomized trial. Ophthalmology. 2019;126(8):1155-1170.\n77. \u2191 Wykoff CC, Abreu F, Adamis AP, et al. Efficacy, durability, and safety of\nintravitreal faricimab with extended dosing up to every 16 weeks in patients with\ndiabetic macular oedema (YOSEMITE and RHINE): two randomised, doublemasked, phase 3 trials. The Lancet. 2022.\n78. \u2191 Brown DM, Emanuelli A, Bandello F, et al. KESTREL and KITE: 52-week results\nfrom two Phase III pivotal trials of brolucizumab for diabetic macular edema.\nAmerican Journal of Ophthalmology. 2022.\n79. \u2191 Witkin AJ, Hahn P, Murray TG, et al. Occlusive retinal vasculitis following\nintravitreal brolucizumab. Journal of vitreoretinal diseases. 2020;4(4):269-279.\n80. \u2191 Baumal CR, Spaide RF, Vajzovic L, et al. Retinal vasculitis and intraocular\ninflammation after intravitreal injection of brolucizumab. Ophthalmology.\n2020;127(10):1345-1359.\n81. \u2191 Khanani AM, Zarbin MA, Barakat MR, et al. Safety outcomes of brolucizumab in\nneovascular age-related macular degeneration: results from the IRIS Registry and\nKomodo Healthcare Map. JAMA ophthalmology. 2021.\n82. \u2191 Enr\u00edquez AB, Baumal CR, Crane AM, et al. Early Experience With Brolucizumab\nTreatment of Neovascular Age-Related Macular Degeneration. JAMA\nophthalmology. 2021;139(4):441-448.\n83. \u2191 Network DRCR. A randomized trial comparing intravitreal triamcinolone\nacetonide and focal/grid photocoagulation for diabetic macular edema.\nOphthalmology. 2008;115(9):1447-1459. e1410.\n84. \u2191 Boyer DS, Yoon YH, Belfort Jr R, et al. Three-year, randomized, sham-controlled\ntrial of dexamethasone intravitreal implant in patients with diabetic macular\nedema. Ophthalmology. 2014;121(10):1904-1914.\n85. \u2191 Campochiaro PA, Brown DM, Pearson A, et al.", "doc_id": "5de3ff6b-e270-4906-92bb-665def70aa79", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "59e8d7b8-6ac1-4e8e-81da-ab14b6475a2c", "node_info": {"start": 0, "end": 5835}}, "6170659625372592210": {"text": "\u2191 Campochiaro PA, Brown DM, Pearson A, et al. Sustained delivery fluocinolone\nacetonide vitreous inserts provide benefit for at least 3 years in patients with\ndiabetic macular edema. Ophthalmology. 2012;119(10):2125-2132.\n86. \u2191 Campochiaro PA, Brown DM, Pearson A, et al. Long-term benefit of sustaineddelivery fluocinolone acetonide vitreous inserts for diabetic macular edema.\nOphthalmology. 2011;118(4):626-635. e622.\n87. \u2191 Elman MJ, Aiello LP, Beck RW, et al. Randomized trial evaluating ranibizumab\nplus prompt or deferred laser or triamcinolone plus prompt laser for diabetic\nmacular edema. Ophthalmology. 2010;117(6):1064-1077. e1035.\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n31/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\n88. \u2191 Brown DM, Ou WC, Wong TP, et al. Targeted retinal photocoagulation for\ndiabetic macular edema with peripheral retinal nonperfusion: three-year\nrandomized DAVE trial. Ophthalmology. 2018;125(5):683-690.\n89. \u2191 Muqit MM, Marcellino GR, Henson DB, et al. Optos\u2010guided pattern scan laser\n(Pascal)\u2010targeted retinal photocoagulation in proliferative diabetic retinopathy.\nActa ophthalmologica. 2013;91(3):251-258.\n90. \u2191 Reddy S, Hu A, Schwartz SD. Ultra wide field fluorescein angiography guided\ntargeted retinal photocoagulation (TRP). Paper presented at: Seminars in\nophthalmology, 2009.\n91. \u2191 Su\u00f1er IJ, Peden MC, Hammer ME, et al. RaScaL: a pilot study to assess the\nefficacy, durability, and safety of a single intervention with ranibizumab plus\nperipheral laser for diabetic macular edema associated with peripheral\nnonperfusion on ultrawide-field fluorescein angiography. Ophthalmologica.\n2015;233(2):89-95.\n92. \u2191 Takamura Y, Tomomatsu T, Matsumura T, et al. The effect of photocoagulation in\nischemic areas to prevent recurrence of diabetic macular edema after intravitreal\nbevacizumab injection. Investigative ophthalmology & visual science.\n2014;55(8):4741-4746.\n93. \u2191 Wessel MM, Nair N, Aaker GD, et al. Peripheral retinal ischaemia, as evaluated by\nultra-widefield fluorescein angiography, is associated with diabetic macular\noedema. British Journal of Ophthalmology. 2012;96(5):694-698.\n94. \u2191 Lee SS, Ghosn C, Yu Z, et al. Vitreous VEGF clearance is increased after\nvitrectomy. Investigative ophthalmology & visual science. 2010;51(4):2135-2138.\n95. \u2191 Simpson AR, Dowell NG, Jackson TL, et al. Measuring the effect of pars plana\nvitrectomy on vitreous oxygenation using magnetic resonance imaging.\nInvestigative ophthalmology & visual science. 2013;54(3):2028-2034.\n96. \u2191 Sivaprasad S, Ockrim Z, Massaoutis P, et al. Posterior hyaloid changes following\nintravitreal triamcinolone and macular laser for diffuse diabetic macular edema.\nRetina. 2008;28(10):1435-1442.\n97. \u2191 Stefansson E, Landers 3rd M, Wolbarsht M. Increased retinal oxygen supply\nfollowing pan-retinal photocoagulation and vitrectomy and lensectomy.\nTransactions of the American Ophthalmological Society. 1981;79:307.\n98. \u2191 Stefansson E, Landers 3rd M, Wolbarsht ML. Vitrectomy, lensectomy, and ocular\noxygenation. Retina (Philadelphia, Pa.). 1982;2(3):159-166.\n99. \u2191 Stefansson E, Novack R, Hatchell D. Vitrectomy prevents retinal hypoxia in\nbranch retinal vein occlusion. Investigative ophthalmology & visual science.\n1990;31(2):284-289.\n100. \u2191 Lee B, Litt M, Buchsbaum G. Rheology of the vitreous body. Part I: viscoelasticity\nof human vitreous. Biorheology. 1992;29(5-6):521-533.\n101. \u2191 Gandorfer A, Messmer EM, Ulbig MW, et al. Resolution of diabetic macular\nedema after surgical removal of the posterior hyaloid and the inner limiting\nmembrane. Retina (Philadelphia, Pa.). 2000;20(2):126-133.\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n32/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\n102. \u2191 Jackson TL, Nicod E, Angelis A, et al. Pars plana vitrectomy for diabetic macular\nedema: a systematic review, meta-analysis, and synthesis of safety literature.\nRetina. 2017;37(5):886-895.\n103. \u2191 Nakajima T, Roggia MF, Noda Y, et al. Effect of internal limiting membrane\npeeling during vitrectomy for diabetic macular edema: systematic review and metaanalysis. Retina. 2015;35(9):1719-1725.\n104. \u2191 Network DRCR. Vitrectomy outcomes in eyes with diabetic macular edema and\nvitreomacular traction. Ophthalmology. 2010;117(6):1087.\n105. \u2191 Bressler SB, Melia M, Glassman AR, et al. Ranibizumab plus prompt or deferred\nlaser for diabetic macular edema in eyes with vitrectomy prior to anti-vascular\nendothelial growth factor therapy. Retina (Philadelphia, Pa.). 2015;35(12):2516.\n106. \u2191 MASON III JO, White MF, Feist RM, et al. Incidence of acute onset\nendophthalmitis following intravitreal bevacizumab (Avastin) injection. Retina.\n2008;28(4):564-567.\n107. \u2191 Fintak DR, Shah GK, Blinder KJ, et al. Incidence of endophthalmitis related to\nintravitreal injection of bevacizumab and ranibizumab. Retina. 2008;28(10):13951399.\n108. \u2191 Diago T, McCANNEL CA, Bakri SJ, et al. Infectious endophthalmitis after\nintravitreal injection of antiangiogenic agents. Retina. 2009;29(5):601-605.\n109. \u2191 Tolentino M. Systemic and ocular safety of intravitreal anti-VEGF therapies for\nocular neovascular disease. Survey of ophthalmology. 2011;56(2):95-113.\n110. \u2191 Singerman LJ, Masonson H, Patel M, et al. Pegaptanib sodium for neovascular\nage-related macular degeneration: third-year safety results of the VEGF Inhibition\nStudy in Ocular Neovascularisation (VISION) trial. British Journal of\nOphthalmology. 2008;92(12):1606-1611.\n111. \u2191 Rosenfeld PJ, Brown DM, Heier JS, et al. Ranibizumab for neovascular agerelated macular degeneration. New England Journal of Medicine.\n2006;355(14):1419-1431.\n112. \u2191 Brown DM, Michels M, Kaiser PK, et al. Ranibizumab versus verteporfin\nphotodynamic therapy for neovascular age-related macular degeneration: two-year\nresults of the ANCHOR study. Ophthalmology. 2009;116(1):57-65.", "doc_id": "ea88e655-7581-45d6-ad22-5f82018aa759", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "4ba68cc5-2e23-405d-8d8f-06f040c0bec9", "node_info": {"start": 0, "end": 5832}}, "3802836866121863046": {"text": "the ANCHOR study. Ophthalmology. 2009;116(1):57-65. e55.\n113. \u2191 Martidis A, Duker JS, Greenberg PB, et al. Intravitreal triamcinolone for\nrefractory diabetic macular edema. Ophthalmology. 2002;109(5):920-927.\n114. \u2191 Network DRCR. Three-year follow-up of a randomized trial comparing focal/grid\nphotocoagulation and intravitreal triamcinolone for diabetic macular edema.\nArchives of ophthalmology. 2009;127(3):245-251.\n115. \u2191 Ladas ID, Karagiannis DA, Rouvas AA, et al. Safety of repeat intravitreal\ninjections of bevacizumab versus ranibizumab: our experience after 2,000\ninjections. Retina. 2009;29(3):313-318.\n116. \u2191 Bressler SB, Odia I, Maguire MG, et al. Factors associated with visual acuity and\ncentral subfield thickness changes when treating diabetic macular edema with anti\u2013\nvascular endothelial growth factor therapy: an exploratory analysis of the protocol T\nrandomized clinical trial. JAMA ophthalmology. 2019;137(4):382-389.\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n33/34\n\n\f1/4/23, 8:18 PM\n\nDiabetic Macular Edema - EyeWiki\n\n117. \u2191 Bressler SB, Qin H, Beck RW, et al. Factors associated with changes in visual\nacuity and central subfield thickness at 1 year after treatment for diabetic macular\nedema with ranibizumab. Archives of Ophthalmology. 2012;130(9):1153-1161.\n118. \u2191 Halim MS, Afridi R, Hasanreisoglu M, et al. Differences in the characteristics of\nsubjects achieving complete, partial, or no resolution of macular edema in the\nREAD-3 study. Graefe's Archive for Clinical and Experimental Ophthalmology.\n2021:1-8.\n119. \u2191 Chew EY, Klein ML, Ferris FL, et al. Association of elevated serum lipid levels\nwith retinal hard exudate in diabetic retinopathy: Early Treatment Diabetic\nRetinopathy Study (ETDRS) Report 22. Archives of ophthalmology.\n1996;114(9):1079-1084.\n120. \u2191 Matsunaga DR, Salabati M, Obeid A, et al. Outcomes of Eyes With Diabetic\nMacular Edema That Are Lost to Follow-up After Anti\u2013Vascular Endothelial\nGrowth Factor Therapy. American Journal of Ophthalmology. 2022;233:1-7.\n121. \u2191 Gao X, Obeid A, Aderman CM, et al. Loss to follow-up after intravitreal anti\u2013\nvascular endothelial growth factor injections in patients with diabetic macular\nedema. Ophthalmology Retina. 2019;3(3):230-236.\n122. \u2191 Das A, McGuire PG, Rangasamy S. Diabetic macular edema: pathophysiology and\nnovel therapeutic targets. Ophthalmology. 2015;122(7):1375-1394.\n123. \u2191 Holekamp NM, Campochiaro PA, Chang MA, et al. Archway Randomized Phase 3\nTrial of the Port Delivery System with Ranibizumab for Neovascular Age-Related\nMacular Degeneration. Ophthalmology. 2021.\n\nhttps://eyewiki.aao.org/Diabetic_Macular_Edema\n\n34/34\n\n\f", "doc_id": "c72a8c6e-553d-4506-9ed6-f70d40ebbf69", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "e8d8df8d-6ed2-4895-bc17-66176085a013", "node_info": {"start": 0, "end": 2639}}, "5326439457053460692": {"text": "#!/usr/bin/env python3\n\n- Credits\n\t- Section Writer: [[Dr. Om J Lakhani]]  \n\t- Section Editor:  [[Dr. Om J Lakhani]] \n\t\n\n- Q. Give a broad outline of the terms NAFLD, NAFL, NASH\n\t- ![[CleanShot 2023-01-11 at 07.40.49@2x.png]]\n- Q. What is NAFLD?\n\t- (1) Evidence of hepatic steatosis (HS), either by imaging or histology\n\t- (2) lack of secondary causes of hepatic fat accumulation such as significant alcohol consumption, long-term use of a steatogenic medication, or monogenic hereditary disorders.\n\t- (3) no significant alcohol consumption (defined as ongoing or recent alcohol consumption of >21 drinks/week for men and >14 drinks/week for women)\n- Q. What is NASH?\n\t- NAFLD is subdivided into the nonalcoholic fatty liver (NAFL) and nonalcoholic steatohepatitis (NASH).\n\t- NAFL, hepatic steatosis is present without evidence of significant inflammation\n\t- NASH, hepatic steatosis is associated with hepatic inflammation that may be histologically indistinguishable from alcoholic steatohepatitis\n- Q. How do you differentiate NASH from NAFL?\n\t- Liver biopsy is the only method to differentiate  NAFL  from  NASH  #ClinicalPearl\n- Q. What is  MAFLD?\n\t- Metabolic dysfunction-associated fatty liver disease (MAFLD)\n\t-  Recently, based on insights gained from the past two decades, an international panel of experts from 22 countries has taken the initiative to propose a new name and definition for NAFLD in adult individuals - that is, metabolic dysfunction-associated fatty liver disease . \n\t- Idea is to make it a diagnosis of inclusion rather than the diagnosis of exclusion\n- Q. Give the direction in which the etiology for transplant is moving.\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2F8IFEsVedss.jpg?alt=media&token=9ac56e26-335e-489e-84c0-35b0bef6f2ad)\n- Applying Wilson and Junger criteria for nash/NAFLD screening\n- Q. The condition sought should be an important health problem. Is NAFLD an important health problem?\n\t- Yes\n\t- NASH is 2nd most common etiology for Liver transplant and will be number one soon.\n\t- Risk of Liver cancer is increased 2 folds in patients with NAFLD\n- Q. What is the prevalence of NAFLD in patients with type 2 diabetes?\n\t- Depending on the screening methodology used, as much as 65-70% of patients with Type 2 Diabetes have NAFLD\n- Q. There should be an accepted treatment for patients with recognized diseases. Can we prevent the progression of Fibrosis in patients with NASH?\n\t- Yes\n\t- Drugs like Pioglitazone, Empagliflozin, and Liraglutide have been shown to prevent the progression of fibrosis in NASH\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FTMqWVvioqU.png?alt=media&token=8d9537aa-f714-4404-b54c-5743300cbf59)\n\t- Weight loss is an effective option for preventing progress in patients with NASH.\n- Q. How do we screen for NAFLD/NASH?\n\t- 2/3rd of patients with NAFLD/NASH have normal liver enzymes\n\t\t- Typically ALT >AST\n\t\t- Newer Cut-offs are 30 in males and 19 in females\n\t- USG shows increased echogenicity\n\t- A meta-analysis found that the sensitivity and specificity for ultrasound were 85 and 94 percent, respectively, when using liver biopsy as the gold standard\n\t- The fatty liver index (FLI), is an algorithm based on waist circumference, body mass index (BMI), triglyceride, and gamma-glutamyl-transferase (GGT) used for recognizing fatty liver\n\t\t- Cutoff of 30 has a sensitivity of 87%\n\t\t- Cutoff of 60 has a specificity of 86%\n\t- Other tests like Transient elastography, MR spectroscopy, MR elastography, and liver biopsy are more useful for the assessment of fibrosis rather than mere screening\n- Q. Does the AST/ALT (SGOT/SGPT) ratio help in the diagnosis of NASH?\n\t- AST/ALT ratio in  NASH/NAFLD  is <1 (SGOT/SGPT)  while in Alcoholic liver disease, it is more than 2 \n- Q. Does the degree of ALT elevation correlate with the severity of the disease?\n\t- the degree of AST/ALT elevation does not correlate with the severity of the disease\n- Q What happens to the ALP levels?\n\t-  ALP  may be elevated 2-3 times the ULN\n- Q. What is the importance of serum ferritin levels in this disease?\n\t- Serum  ferritin  has an important role in  NASH/NAFLD  #ClinicalPearl  \n\t\t- Value >1.5 times the ULN is likely to be associated with greater progression of the liver disease \n- Q. What are the diagnostic criteria for MAFLD ?\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2F_mIEPhBkOn.png?alt=media&token=7288940f-c85b-4ec4-8331-e53271926637)\n- Q.  Do we have an early stage here?\n\t- Yes. NASH is an early precursor of Cirrhosis or End stage liver disease which is what we are trying to prevent.\n\t- There should be a suitable test or examination and the test should be acceptable to the population\n\t- Liver enzymes and ultrasound are acceptable tests for the population\n- Q. Upto what stage can the disease be reversed?\n\t- Upto the Fibrosis stage \n- Q. The natural history of the condition, including development from latent to declared disease, should be adequately understood. Do we understand the natural history of NAFLD/NASH?\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FrKUXI6R_Qo.png?alt=media&token=fdce4b36-1f4f-4377-ab25-b50c5a2a0a29)\n- Q. There should be an agreed policy on whom to treat as patients. What to do once NAFLD is recognized?\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FmGPk3GWK0I.png?alt=media&token=aa14aba6-2071-410b-b19d-be51eae4a626)\n- FIBROSIS BIOMARKERS AND SCORES\n- Q. Is screening for NAFLD cost-effective?\n\t- NAFLD is a reversible condition, particularly in the early stages.\n\t- Failing to detect the disease at an early stage can have detrimental clinical effects for some high-risk patients who are in danger of developing liver cirrhosis and related complications such as jaundice, ascites, variceal bleeding, hepatic encephalopathy, and", "doc_id": "2e3fa64f-bd7d-4f66-8d08-430d232419c2", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "3a7bf4e3-f715-4eea-b29b-c5a77b3fd148", "node_info": {"start": 0, "end": 6074}}, "2564095372138814618": {"text": "ascites, variceal bleeding, hepatic encephalopathy, and hepatocellular carcinoma.\n\t- NAFLD was considered cost-effective at a cost-effectiveness threshold of \u00a320,000 per QALY gained.\n\t- Fatty liver index is the most cost-effective screening test\n- Q. Give a broad outline of the treatment of  NASH/NAFLD.\n\t- Vaccination\n\t\t-  Hepatitis A \n\t\t-  Hepatitis B \n\t\t- Pneumococcal vaccine \n\t- Weight loss - 0.5-1 kg/week\n\t-  Biopsy proven NASH and fibrosis with stage \u22652 and not having diabetes - Vitamin E - 800 IU/day (C. EVION- 400 IU - twice a day)   \n\t- Diabetes patients\n\t\t-  Metformin \n\t\t-  Pioglitazone \n\t\t-  Liraglutide \n\t- If after weight loss - repeat ALT/AST after 3 months\n\t\t- if it has not come to normal - look for other causes \n- Q. Give some important notes on weight loss and  NASH/NAFLD.\n\t- Weight loss to be done to the tune of 0.5- 1 kg/week\n\t- weight loss can reverse all stages except  cirrhosis \n\t- Liver function test can be normal in 30% of patients with  NASH/NAFLD  #ClinicalPearl\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2F5HK92ZTJTn.jpg?alt=media&token=e82203f1-5ef8-4349-9c1f-b9c9935714e0)\n- Q. In which cases is Pharmacotherapy used?\n\t- Early \u00adstage NASH at high risk for disease progression (age > 50 years, metabolic syndrome, diabetes mellitus, or increased ALT)\n\t- Active NASH with high necroinflammatory activities\n\t- Progressive NASH (brid\u00adging fibrosis and cirrhosis)\n- Q. What is the main purpose of any medication used?\n\t- It should be able to prevent the fibrosis stage\n\t- This can be gauged by a reduction of the NAS score (NAFLD Activity score)\n- Q. Give an outline of various legacy drugs and their use in  NASH/NAFLD.\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FLRUI0aJdKw.png?alt=media&token=548bb470-d891-4879-bdcd-3ef3cb578b4c)\n- Q. Is  Saroglitazar approved in India for use in  NASH/NAFLD?\n\t- Yes\n- Q. What is the mechanism of action of  Saroglitazar?\n\t- Saroglitazar is a dual PPAR \u03b1 and \u03b3 agonist and through activation of these transcriptional factors PPAR \u03b1 & \u03b3 :\n\t\t- Reduces TG (predominantly through PPAR \u03b1 agonism)\n\t\t- Reduces Insulin resistance and controls blood sugar level (predominantly through PPAR \u03b3 agonism)\n- Q. How does  Saroglitazar compare with other drugs like OCA and UDCA?\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FNkXgs4MApu.25.43%402x.png?alt=media&token=552548c2-7104-4aed-b2b7-c271b9936702)\n- Q. Does  Saroglitazar reduce (NAFLD Activity score)?\n\t- Yes \n- Q. What is the role of  Semaglutide in  NASH/NAFLD?\n\t- This is from a trial published in the  NEJM \n\t\t- Nonalcoholic steatohepatitis (NASH) is a common disease that is associated with increased morbidity and mortality, but treatment options are limited. The efficacy and safety of the glucagon-like peptide-1 receptor agonist semaglutide in patients with NASH are not known\n\t\t-  This phase 2 trial involving patients with NASH showed that treatment with semaglutide resulted in a significantly higher percentage of patients with NASH resolution than placebo.  \n\t\t-  However, the trial did not show a significant between-group difference in the percentage of patients with an improvement in fibrosis stage  \n\t\t\n- Q. What is the most common cause of death in patients with  NASH/NAFLD?\n\t- The most common cause of death in patients with NASH/NAFLD is heart disease - need to screen and monitor for the same\n\t\n- Q. What is  MAFLD?\n\t- Metabolic dysfunction-associated fatty liver disease (MAFLD)\n\t- \"Nonalcoholic fatty liver disease (NAFLD) has become the most common cause of liver disease in many parts of the world, causing considerable liver-related (steatohepatitis, cirrhosis, liver failure, and hepatocellular carcinoma) and extra-hepatic morbidity and mortality (mainly cardiovascular disease, chronic kidney disease or certain types of extra-hepatic cancers). \n\t-  Recently, based on insights gained from the past two decades, an international panel of experts from 22 countries has taken the initiative to propose a new name and definition for NAFLD in adult individuals - that is, metabolic dysfunction-associated fatty liver disease . \n\t- This proposed change in nomenclature is not simply a semantic revision, but may facilitate improved diagnosis of this common liver disease for health promotion, case identification, patient awareness, ongoing clinical trials, and health services delivery\"\n\t- Until now the exclusion of other chronic liver diseases, including \u201cexcess\u201d alcohol intake, was necessary for the diagnosis of MAFLD. \n\t- As the pathogenic process leading to MAFLD is now better understood and is seen to originate from an underlying state of systemic metabolic dysfunction, MAFLD is perceived as a standalone disease that warrants a positive diagnosis, rather than a \u201cnone\u201d-disease rubric. \n\t- Moreover, the rising prevalence of MAFLD makes its coexistence with other chronic liver diseases quite possible, further negating a diagnosis based on the exclusion of concomitant diseases. \n\t-  It is therefore our belief that this disease needs to be defined by its own set of positive criteria, rather than by exclusion criteria. \n\t- > Idea is to make it a diagnosis of inclusion rather than the diagnosis of exclusion\n\t- \n- Q. What are the diagnostic criteria for MAFLD ?\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2F_mIEPhBkOn.png?alt=media&token=7288940f-c85b-4ec4-8331-e53271926637)\n\t\n- Q. What is  Hepatic hypothyroidism?\n\t- [Effects of Resmetirom on Noninvasive Endpoints in a 36\u2010Week Phase 2 Active Treatment Extension Study in Patients With NASH - PMC](https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8034581/)\n\t\t- Evidence suggests that NASH may be, in part, a condition of diminished liver thyroid hormone levels or hepatic hypothyroidism and that the incidence of clinical and subclinical hypothyroidism is higher in patients with NAFLD/NASH relative to age\u2010matched controls. Tag:  NASH/NAFLD;  NASH \n\t\t-", "doc_id": "d889124f-9288-4a77-8c53-1fd693a6b32c", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "464231f7-49d7-4988-aab7-92478d2a81c4", "node_info": {"start": 0, "end": 6138}}, "9202627592443874456": {"text": "controls. Tag:  NASH/NAFLD;  NASH \n\t\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2F-HsUN47vpJ.png?alt=media&token=264e7111-2a72-4496-a22e-dbf080986575)\n-  December 14th, 2022 - Updates from  ADA 2023 Guidelines \n- Q. What is the grading for hepatic fibrosis?\n\t- 1. F0- No fibrosis\n\t- 2. F1- Mild\n\t- 3. F2- Moderate\n\t- 4. F3- Severe\n\t- 5. F4- Cirrhosis\n- Q. Patients with type 2 diabetes generally have what level of fibrosis?\n\t- 20% of patients with type 2 diabetes have \u2265F2 level of fibrosis\n- Q. What is the link between  NAFLD  and  CKD?\n\t- Patients with NAFLD have an increased risk of developing CKD\n- Q. Should Type 1 diabetes patients be screened for  NAFLD?\n\t- The prevalence of NAFLD/NASH is lower in type 1 diabetes\n\t- Hence routine screening for type 1 diabetes is not recommended \n- Q. Which is the most effective screening tool for screening for  NASH/NAFLD  in patients with type 2 diabetes and prediabetes?\n\t-  FIB-4  score is the most effective screening tool for screening for patients \n- Q. Is it okay to screen patients having ALT >40?\n\t- No\n\t- Significant patients have \u2265F2 by the time they have ALT >40\n- Q. What are the ALT cut-off's given by the American college of Gastroenterology?\n\t- More than 29-33 male\n\t- More than 19-25 female \n- Q. What  FIB-4  score is suggestive of high risk?\n\t- <1.3- lower risk\n\t- 1.3-2.67- moderate risk\n\t- More than 2.67- high risk of fibrosis \n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FeIF0ukxfem.png?alt=media&token=6e83a99b-2982-44c0-86ec-aee23fd3ff39)\n- Q. What is the problem with  FIB-4  score?\n\t- 1. It has good specificity but low sensitivity \n\t\t- A lot of type 2 diabetes fall in intermediate-risk and hence may be missed out\n\t\t- hence a confirmation test is often required \n\t- 2. It is not recommended for pediatric patients\n\t- 3. It is less reliable for ages <35 years\n\t- 4. For ages > 65 years- a higher cutoff of 1.9-2.0 is suggested in place of 1.3 \n- Q. Which is a good confirmatory test?\n\t- Transient elastography \n- Q. What are the cut-off used in transient elastography?\n\t- <8.0 kPA- has good negative predictive value to rule out advanced fibrosis- \u2265 F3/F4 levels \n\t- More than 12 KPA - must be referred to a hepatologist\n- Q. Which test has good use in early fibrosis?\n\t- MR elastography \n- Q. Give the clinical care pathway for  NASH/NAFLD  as suggested by several guidelines.\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FsKpzo7jIfU.png?alt=media&token=791d6629-18de-4b01-89d7-06481a8a736f)\n\t- \n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2Fwk6kNg7mbf.png?alt=media&token=1ee2451a-b046-4dba-9b6d-88fca1a91aec)\n- Q. What type of diet has the best evidence for improving outcomes in NASH?\n\t-  Mediterranean diet \n- Q. Is obesity surgery helpful?\n\t- Yes\n\t- It is known to reduce all parameters in NASH including fibrosis\n- Q. Can obesity surgery lead to decompensation in patients with compensated cirrhosis?\n\t- The risk is no greater compared to other surgeries\n\t- However in patients already having decompensated cirrhosis, it is not recommended\n- Q.  Can  Pioglitazone reduce fibrosis in NASH?\n\t- Yes\n- Q. Does  GLP-1 receptor agonist  reduce fibrosis ?\n\t- It delays fibrosis as observed in two trials involving liver biopsies\n\t- The evidence is for liraglutide and semaglutide\n- Q. What about  SGLT2i?\n\t- It is known to reduce steatosis\n\t- But the impact on steatohepatitis and fibrosis is unknown \n- Q. Is currently any drug FDA-approved for NASH?\n\t- No\n- Q. What about Vitamin E?\n\t- Vitamin E is useful in non-diabetic patients with NASH\n\t- No clear evidence of benefit in patients with diabetes \n- Q. Summarize the treatment option for NASH based on the new guidelines.\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FV49qrD5Zsk.png?alt=media&token=56d78730-0e0c-4f35-ade2-0d54346eab11)\n\t\n\nSome notes from UptoDate \n\t- Most cases are diagnosed in the 40-the 50s \n\t- Some reports suggest that  NASH/NAFLD  may be more common after  cholecystectomy  (but not in patients having gallstones) #ClinicalPearl\n\t- AST/ALT ratio in  NASH/NAFLD  is <1 (SGOT/SGPT)  while in Alcoholic liver disease  it is more than 2 #ClinicalPearl  \n\t- the degree of AST/ALT elevation does not correlate with the severity of the disease #ClinicalPearl\n\t-  ALP  may be elevated 2-3 times the ULN\n\t- Serum  ferritin  has important role in  NASH/NAFLD  #ClinicalPearl  \n\t\t- Value >1.5 times the ULN is likely to be associated with greater progression of the liver disease \n\t- \n\t- Treatment of  NASH/NAFLD \n\t\t- Vaccination\n\t\t\t-  Hepatitis A \n\t\t\t-  Hepatitis B \n\t\t\t- Pneumococcal vaccine \n\t\t- Weight loss - 0.5-1 kg/week\n\t\t-  Biopsy proven NASH and fibrosis with stage \u22652 and not having diabetes - Vitamin E - 800 IU/day (C. EVION- 400 IU - twice a day)   \n\t\t- Diabetes patients\n\t\t\t-  Metformin \n\t\t\t-  Pioglitazone \n\t\t\t-  Liraglutide \n\t\t- If after weight loss - repeat ALT/AST after 3 months\n\t\t\t- if it has not come to normal - look for other causes\n\t\t\t-  ", "doc_id": "7b1839df-2a9e-4e6d-a885-6ca223e2fbeb", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "e3ae5adc-728e-47f0-9e18-c0788e666ac7", "node_info": {"start": 0, "end": 5246}}, "8061815979012457974": {"text": "#!/usr/bin/env python3\n\n- Credits\n\t- Section Writer: [[Dr. Om J Lakhani]]  \n\t- Section Editor:  [[Dr. Om J Lakhani]] \n\t\n\n- Q. Give a broad outline of the terms NAFLD, NAFL, NASH\n\t- ![[CleanShot 2023-01-11 at 07.40.49@2x.png]]\n- Q. What is NAFLD?\n\t- (1) Evidence of hepatic steatosis (HS), either by imaging or histology\n\t- (2) lack of secondary causes of hepatic fat accumulation such as significant alcohol consumption, long-term use of a steatogenic medication, or monogenic hereditary disorders.\n\t- (3) no significant alcohol consumption (defined as ongoing or recent alcohol consumption of >21 drinks/week for men and >14 drinks/week for women)\n- Q. What is NASH?\n\t- NAFLD is subdivided into the nonalcoholic fatty liver (NAFL) and nonalcoholic steatohepatitis (NASH).\n\t- NAFL, hepatic steatosis is present without evidence of significant inflammation\n\t- NASH, hepatic steatosis is associated with hepatic inflammation that may be histologically indistinguishable from alcoholic steatohepatitis\n- Q. How do you differentiate NASH from NAFL?\n\t- Liver biopsy is the only method to differentiate  NAFL  from  NASH  #ClinicalPearl\n- Q. What is  MAFLD?\n\t- Metabolic dysfunction-associated fatty liver disease (MAFLD)\n\t-  Recently, based on insights gained from the past two decades, an international panel of experts from 22 countries has taken the initiative to propose a new name and definition for NAFLD in adult individuals - that is, metabolic dysfunction-associated fatty liver disease . \n\t- Idea is to make it a diagnosis of inclusion rather than the diagnosis of exclusion\n- Q. Give the direction in which the etiology for transplant is moving.\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2F8IFEsVedss.jpg?alt=media&token=9ac56e26-335e-489e-84c0-35b0bef6f2ad)\n- Applying Wilson and Junger criteria for nash/NAFLD screening\n- Q. The condition sought should be an important health problem. Is NAFLD an important health problem?\n\t- Yes\n\t- NASH is 2nd most common etiology for Liver transplant and will be number one soon.\n\t- Risk of Liver cancer is increased 2 folds in patients with NAFLD\n- Q. What is the prevalence of NAFLD in patients with type 2 diabetes?\n\t- Depending on the screening methodology used, as much as 65-70% of patients with Type 2 Diabetes have NAFLD\n- Q. There should be an accepted treatment for patients with recognized diseases. Can we prevent the progression of Fibrosis in patients with NASH?\n\t- Yes\n\t- Drugs like Pioglitazone, Empagliflozin, and Liraglutide have been shown to prevent the progression of fibrosis in NASH\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FTMqWVvioqU.png?alt=media&token=8d9537aa-f714-4404-b54c-5743300cbf59)\n\t- Weight loss is an effective option for preventing progress in patients with NASH.\n- Q. How do we screen for NAFLD/NASH?\n\t- 2/3rd of patients with NAFLD/NASH have normal liver enzymes\n\t\t- Typically ALT >AST\n\t\t- Newer Cut-offs are 30 in males and 19 in females\n\t- USG shows increased echogenicity\n\t- A meta-analysis found that the sensitivity and specificity for ultrasound were 85 and 94 percent, respectively, when using liver biopsy as the gold standard\n\t- The fatty liver index (FLI), is an algorithm based on waist circumference, body mass index (BMI), triglyceride, and gamma-glutamyl-transferase (GGT) used for recognizing fatty liver\n\t\t- Cutoff of 30 has a sensitivity of 87%\n\t\t- Cutoff of 60 has a specificity of 86%\n\t- Other tests like Transient elastography, MR spectroscopy, MR elastography, and liver biopsy are more useful for the assessment of fibrosis rather than mere screening\n- Q. Does the AST/ALT (SGOT/SGPT) ratio help in the diagnosis of NASH?\n\t- AST/ALT ratio in  NASH/NAFLD  is <1 (SGOT/SGPT)  while in Alcoholic liver disease, it is more than 2 \n- Q. Does the degree of ALT elevation correlate with the severity of the disease?\n\t- the degree of AST/ALT elevation does not correlate with the severity of the disease\n- Q What happens to the ALP levels?\n\t-  ALP  may be elevated 2-3 times the ULN\n- Q. What is the importance of serum ferritin levels in this disease?\n\t- Serum  ferritin  has an important role in  NASH/NAFLD  #ClinicalPearl  \n\t\t- Value >1.5 times the ULN is likely to be associated with greater progression of the liver disease \n- Q. What are the diagnostic criteria for MAFLD ?\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2F_mIEPhBkOn.png?alt=media&token=7288940f-c85b-4ec4-8331-e53271926637)\n- Q.  Do we have an early stage here?\n\t- Yes. NASH is an early precursor of Cirrhosis or End stage liver disease which is what we are trying to prevent.\n\t- There should be a suitable test or examination and the test should be acceptable to the population\n\t- Liver enzymes and ultrasound are acceptable tests for the population\n- Q. Upto what stage can the disease be reversed?\n\t- Upto the Fibrosis stage \n- Q. The natural history of the condition, including development from latent to declared disease, should be adequately understood. Do we understand the natural history of NAFLD/NASH?\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FrKUXI6R_Qo.png?alt=media&token=fdce4b36-1f4f-4377-ab25-b50c5a2a0a29)\n- Q. There should be an agreed policy on whom to treat as patients. What to do once NAFLD is recognized?\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FmGPk3GWK0I.png?alt=media&token=aa14aba6-2071-410b-b19d-be51eae4a626)\n- FIBROSIS BIOMARKERS AND SCORES\n- Q. Is screening for NAFLD cost-effective?\n\t- NAFLD is a reversible condition, particularly in the early stages.\n\t- Failing to detect the disease at an early stage can have detrimental clinical effects for some high-risk patients who are in danger of developing liver cirrhosis and related complications such as jaundice, ascites, variceal bleeding, hepatic encephalopathy, and", "doc_id": "574e0878-0f1f-48fa-9596-f3d7adf3417a", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "9f45c9d1-f6eb-49c6-8d03-acb231763170", "node_info": {"start": 0, "end": 6074}}, "8898691990590731229": {"text": "ascites, variceal bleeding, hepatic encephalopathy, and hepatocellular carcinoma.\n\t- NAFLD was considered cost-effective at a cost-effectiveness threshold of \u00a320,000 per QALY gained.\n\t- Fatty liver index is the most cost-effective screening test\n- Q. Give a broad outline of the treatment of  NASH/NAFLD.\n\t- Vaccination\n\t\t-  Hepatitis A \n\t\t-  Hepatitis B \n\t\t- Pneumococcal vaccine \n\t- Weight loss - 0.5-1 kg/week\n\t-  Biopsy proven NASH and fibrosis with stage \u22652 and not having diabetes - Vitamin E - 800 IU/day (C. EVION- 400 IU - twice a day)   \n\t- Diabetes patients\n\t\t-  Metformin \n\t\t-  Pioglitazone \n\t\t-  Liraglutide \n\t- If after weight loss - repeat ALT/AST after 3 months\n\t\t- if it has not come to normal - look for other causes \n- Q. Give some important notes on weight loss and  NASH/NAFLD.\n\t- Weight loss to be done to the tune of 0.5- 1 kg/week\n\t- weight loss can reverse all stages except  cirrhosis \n\t- Liver function test can be normal in 30% of patients with  NASH/NAFLD  #ClinicalPearl\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2F5HK92ZTJTn.jpg?alt=media&token=e82203f1-5ef8-4349-9c1f-b9c9935714e0)\n- Q. In which cases is Pharmacotherapy used?\n\t- Early \u00adstage NASH at high risk for disease progression (age > 50 years, metabolic syndrome, diabetes mellitus, or increased ALT)\n\t- Active NASH with high necroinflammatory activities\n\t- Progressive NASH (brid\u00adging fibrosis and cirrhosis)\n- Q. What is the main purpose of any medication used?\n\t- It should be able to prevent the fibrosis stage\n\t- This can be gauged by a reduction of the NAS score (NAFLD Activity score)\n- Q. Give an outline of various legacy drugs and their use in  NASH/NAFLD.\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FLRUI0aJdKw.png?alt=media&token=548bb470-d891-4879-bdcd-3ef3cb578b4c)\n- Q. Is  Saroglitazar approved in India for use in  NASH/NAFLD?\n\t- Yes\n- Q. What is the mechanism of action of  Saroglitazar?\n\t- Saroglitazar is a dual PPAR \u03b1 and \u03b3 agonist and through activation of these transcriptional factors PPAR \u03b1 & \u03b3 :\n\t\t- Reduces TG (predominantly through PPAR \u03b1 agonism)\n\t\t- Reduces Insulin resistance and controls blood sugar level (predominantly through PPAR \u03b3 agonism)\n- Q. How does  Saroglitazar compare with other drugs like OCA and UDCA?\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FNkXgs4MApu.25.43%402x.png?alt=media&token=552548c2-7104-4aed-b2b7-c271b9936702)\n- Q. Does  Saroglitazar reduce (NAFLD Activity score)?\n\t- Yes \n- Q. What is the role of  Semaglutide in  NASH/NAFLD?\n\t- This is from a trial published in the  NEJM \n\t\t- Nonalcoholic steatohepatitis (NASH) is a common disease that is associated with increased morbidity and mortality, but treatment options are limited. The efficacy and safety of the glucagon-like peptide-1 receptor agonist semaglutide in patients with NASH are not known\n\t\t-  This phase 2 trial involving patients with NASH showed that treatment with semaglutide resulted in a significantly higher percentage of patients with NASH resolution than placebo.  \n\t\t-  However, the trial did not show a significant between-group difference in the percentage of patients with an improvement in fibrosis stage  \n\t\t\n- Q. What is the most common cause of death in patients with  NASH/NAFLD?\n\t- The most common cause of death in patients with NASH/NAFLD is heart disease - need to screen and monitor for the same\n\t\n- Q. What is  MAFLD?\n\t- Metabolic dysfunction-associated fatty liver disease (MAFLD)\n\t- \"Nonalcoholic fatty liver disease (NAFLD) has become the most common cause of liver disease in many parts of the world, causing considerable liver-related (steatohepatitis, cirrhosis, liver failure, and hepatocellular carcinoma) and extra-hepatic morbidity and mortality (mainly cardiovascular disease, chronic kidney disease or certain types of extra-hepatic cancers). \n\t-  Recently, based on insights gained from the past two decades, an international panel of experts from 22 countries has taken the initiative to propose a new name and definition for NAFLD in adult individuals - that is, metabolic dysfunction-associated fatty liver disease . \n\t- This proposed change in nomenclature is not simply a semantic revision, but may facilitate improved diagnosis of this common liver disease for health promotion, case identification, patient awareness, ongoing clinical trials, and health services delivery\"\n\t- Until now the exclusion of other chronic liver diseases, including \u201cexcess\u201d alcohol intake, was necessary for the diagnosis of MAFLD. \n\t- As the pathogenic process leading to MAFLD is now better understood and is seen to originate from an underlying state of systemic metabolic dysfunction, MAFLD is perceived as a standalone disease that warrants a positive diagnosis, rather than a \u201cnone\u201d-disease rubric. \n\t- Moreover, the rising prevalence of MAFLD makes its coexistence with other chronic liver diseases quite possible, further negating a diagnosis based on the exclusion of concomitant diseases. \n\t-  It is therefore our belief that this disease needs to be defined by its own set of positive criteria, rather than by exclusion criteria. \n\t- > Idea is to make it a diagnosis of inclusion rather than the diagnosis of exclusion\n\t- \n- Q. What are the diagnostic criteria for MAFLD ?\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2F_mIEPhBkOn.png?alt=media&token=7288940f-c85b-4ec4-8331-e53271926637)\n\t\n- Q. What is  Hepatic hypothyroidism?\n\t- [Effects of Resmetirom on Noninvasive Endpoints in a 36\u2010Week Phase 2 Active Treatment Extension Study in Patients With NASH - PMC](https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8034581/)\n\t\t- Evidence suggests that NASH may be, in part, a condition of diminished liver thyroid hormone levels or hepatic hypothyroidism and that the incidence of clinical and subclinical hypothyroidism is higher in patients with NAFLD/NASH relative to age\u2010matched controls. Tag:  NASH/NAFLD;  NASH \n\t\t-", "doc_id": "30d5c78c-128d-481c-84a8-fc3af5b36bc7", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "b86e7dc2-bc3c-402a-aa15-21a381e43ce4", "node_info": {"start": 0, "end": 6138}}, "6082735417801160857": {"text": "controls. Tag:  NASH/NAFLD;  NASH \n\t\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2F-HsUN47vpJ.png?alt=media&token=264e7111-2a72-4496-a22e-dbf080986575)\n-  December 14th, 2022 - Updates from  ADA 2023 Guidelines \n- Q. What is the grading for hepatic fibrosis?\n\t- 1. F0- No fibrosis\n\t- 2. F1- Mild\n\t- 3. F2- Moderate\n\t- 4. F3- Severe\n\t- 5. F4- Cirrhosis\n- Q. Patients with type 2 diabetes generally have what level of fibrosis?\n\t- 20% of patients with type 2 diabetes have \u2265F2 level of fibrosis\n- Q. What is the link between  NAFLD  and  CKD?\n\t- Patients with NAFLD have an increased risk of developing CKD\n- Q. Should Type 1 diabetes patients be screened for  NAFLD?\n\t- The prevalence of NAFLD/NASH is lower in type 1 diabetes\n\t- Hence routine screening for type 1 diabetes is not recommended \n- Q. Which is the most effective screening tool for screening for  NASH/NAFLD  in patients with type 2 diabetes and prediabetes?\n\t-  FIB-4  score is the most effective screening tool for screening for patients \n- Q. Is it okay to screen patients having ALT >40?\n\t- No\n\t- Significant patients have \u2265F2 by the time they have ALT >40\n- Q. What are the ALT cut-off's given by the American college of Gastroenterology?\n\t- More than 29-33 male\n\t- More than 19-25 female \n- Q. What  FIB-4  score is suggestive of high risk?\n\t- <1.3- lower risk\n\t- 1.3-2.67- moderate risk\n\t- More than 2.67- high risk of fibrosis \n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FeIF0ukxfem.png?alt=media&token=6e83a99b-2982-44c0-86ec-aee23fd3ff39)\n- Q. What is the problem with  FIB-4  score?\n\t- 1. It has good specificity but low sensitivity \n\t\t- A lot of type 2 diabetes fall in intermediate-risk and hence may be missed out\n\t\t- hence a confirmation test is often required \n\t- 2. It is not recommended for pediatric patients\n\t- 3. It is less reliable for ages <35 years\n\t- 4. For ages > 65 years- a higher cutoff of 1.9-2.0 is suggested in place of 1.3 \n- Q. Which is a good confirmatory test?\n\t- Transient elastography \n- Q. What are the cut-off used in transient elastography?\n\t- <8.0 kPA- has good negative predictive value to rule out advanced fibrosis- \u2265 F3/F4 levels \n\t- More than 12 KPA - must be referred to a hepatologist\n- Q. Which test has good use in early fibrosis?\n\t- MR elastography \n- Q. Give the clinical care pathway for  NASH/NAFLD  as suggested by several guidelines.\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FsKpzo7jIfU.png?alt=media&token=791d6629-18de-4b01-89d7-06481a8a736f)\n\t- \n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2Fwk6kNg7mbf.png?alt=media&token=1ee2451a-b046-4dba-9b6d-88fca1a91aec)\n- Q. What type of diet has the best evidence for improving outcomes in NASH?\n\t-  Mediterranean diet \n- Q. Is obesity surgery helpful?\n\t- Yes\n\t- It is known to reduce all parameters in NASH including fibrosis\n- Q. Can obesity surgery lead to decompensation in patients with compensated cirrhosis?\n\t- The risk is no greater compared to other surgeries\n\t- However in patients already having decompensated cirrhosis, it is not recommended\n- Q.  Can  Pioglitazone reduce fibrosis in NASH?\n\t- Yes\n- Q. Does  GLP-1 receptor agonist  reduce fibrosis ?\n\t- It delays fibrosis as observed in two trials involving liver biopsies\n\t- The evidence is for liraglutide and semaglutide\n- Q. What about  SGLT2i?\n\t- It is known to reduce steatosis\n\t- But the impact on steatohepatitis and fibrosis is unknown \n- Q. Is currently any drug FDA-approved for NASH?\n\t- No\n- Q. What about Vitamin E?\n\t- Vitamin E is useful in non-diabetic patients with NASH\n\t- No clear evidence of benefit in patients with diabetes \n- Q. Summarize the treatment option for NASH based on the new guidelines.\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FV49qrD5Zsk.png?alt=media&token=56d78730-0e0c-4f35-ade2-0d54346eab11)\n\t\n\nSome notes from UptoDate \n\t- Most cases are diagnosed in the 40-the 50s \n\t- Some reports suggest that  NASH/NAFLD  may be more common after  cholecystectomy  (but not in patients having gallstones) #ClinicalPearl\n\t- AST/ALT ratio in  NASH/NAFLD  is <1 (SGOT/SGPT)  while in Alcoholic liver disease  it is more than 2 #ClinicalPearl  \n\t- the degree of AST/ALT elevation does not correlate with the severity of the disease #ClinicalPearl\n\t-  ALP  may be elevated 2-3 times the ULN\n\t- Serum  ferritin  has important role in  NASH/NAFLD  #ClinicalPearl  \n\t\t- Value >1.5 times the ULN is likely to be associated with greater progression of the liver disease \n\t- \n\t- Treatment of  NASH/NAFLD \n\t\t- Vaccination\n\t\t\t-  Hepatitis A \n\t\t\t-  Hepatitis B \n\t\t\t- Pneumococcal vaccine \n\t\t- Weight loss - 0.5-1 kg/week\n\t\t-  Biopsy proven NASH and fibrosis with stage \u22652 and not having diabetes - Vitamin E - 800 IU/day (C. EVION- 400 IU - twice a day)   \n\t\t- Diabetes patients\n\t\t\t-  Metformin \n\t\t\t-  Pioglitazone \n\t\t\t-  Liraglutide \n\t\t- If after weight loss - repeat ALT/AST after 3 months\n\t\t\t- if it has not come to normal - look for other causes\n\t\t\t-  ", "doc_id": "17c8c7eb-265d-41e8-9ce8-fb3732447d7f", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "d2647d5f-92e0-4a18-b5fc-647917574b21", "node_info": {"start": 0, "end": 5246}}, "1673236348063257803": {"text": "#!/usr/bin/env python3\n\nG PROTEIN COUPLED RECEPTORS \n\n\n\nQ. What is signal transduction ? \n\nIt is a process by which peptide hormone sends a signal inside the cell to effect a certain function \n\nQ. Describe with flow chart the signal tranduction process ? \n\nHormone  binds to cell surface receptor \uf0e0 activate effector \uf0e0 carries out specific function \n\nQ. What are GPCR ? \n\nMost peptide hormones act via receptors which have G protein \nHence they are known as GPCR \n\nQ. What are G proteins ? \n\nThey are proteins which initiate the signal transduction process \n\nQ. Which are subunits of G protein ? \n\nIt has 3 subunits- alpha, beta and gamma \n\nQ. What is Gs and Gi ? \n\nGs  G protein that activates adenyl cyclase\nGi \uf0e0 G protein that inhibits Adenyl cyclase \n\nQ. What are the three classes of GPCR ? \n\n\nQ. Which are the various effector systems for GPCR ? \n\ncAMP\ncGMP\nIP3 / DAG\nCa channel\nK channel \n\nQ. What are the process of Signal termination ? \n\nDesensitization\nInternalization\nTagging with Beta arrestin \n\nQ. What is desensitization? \n\nIt is done by protein kinases A and C\nThey phosphorylate the receptor and prevent the ligand from binding to the receptor \n\nQ. What is internalization ? \n\nThe hormone and receptor are internalized by the cell\nHence further hormone binding is prevented \n\nQ. What is the role of beta arrestin  ? \n\nBinds with GPCR from cytoplasmic side and tags it for internalization \nClinical significance \n\nQ. Describe the clinical significance of GPCR ? \n\nVarious diseases are seen with loss of function or gain of function mutation in GPCR \nMcCune Albright is a disease where there is increase production of Gs alpha leading to continous activation of adeny cyclase and production of cAMP\nSimilar in Pseudohypoparathyroidism  - there is lack of Gs alpha leading to lack of cAMP production despite binding of hormone to receptor \n\nQ. Name some diseases associated with Loss of function mutation in GPCR? \n\nAVP2- Familial nephrogenic diabetes insipidus\nGnRH receptor, Kiss1 Receptor- hypo hypo\nMC2R- familial glucocorticoid deficiceincy  type 1\nMC4R- obesity\nPTH receptor- bloomstead\u2019s chondroplsia\nCaSR- FHH\nLH receptor- Leydig cell hypoplasia  \n\nQ. name some diseases associated with Gain of function mutation in GPCR  ? \n\nGermline\nKISS1R- Precocious puberty\nFSH Receptor- Ovarian hyperstimulation syndrome\nTSH receptor- Nonautoimmune familial hyperthyroidism\nCaSR- Autosomal dominant hypocalcemia\nPTH- Jansen\u2019s metaphysial chondroplasia\nAVP2- SIADH type\nSomatic\nTSH receptor- Toxic adenoma\nLH receptor- Leydig cell adenoma \n\n\nQ. Enlist some drugs acting on GPCR ? \n\nD2 receptor\nAgonist- Levodopa\nAntagonist \u2013 Haloperidol\nBeta 1 receptor \u2013 antagonist \u2013 beta blockers\nBeta 2 receptor \u2013 agonist- terbutaline etc\nAlpha 1 receptor- antagonist- prazosin , tamsulosin\nAT II receptor antagonist- Losartan \n5 HT2 \u2013\nAntagonist- clozapine \u2013 depressin\nAgonist- lorcaserin \u2013 obesity \n+ \n\nQ. Describe the action of hormone via GPCR and cAMP pathway ?  \n\n3rd Gen NB 4 , Point 299 \n\nQ. Which hormones act via cAMP pathway  ?\n\nPituitary \nACTH\nFSH/LH\nTSH\nADH (v2 receptor)\nOthers\nGlucagon\nPTH\nBeta 1 and beta 2 receptor \n\n\nQ. Which hormones act via cGMP ? \n\nNitric oxide \nANP\n\n\nQ. Describe the IP3 /DAG pathway ? \n\n3rd Gen NB 4 , Point 300 \n\nQ. Which hormones act via IP3/DAG system ?  \n\nHypothalamic hormones\nGnRH\nGHRH\nTRH\nADH (V1 receptor)\nOxytocin\nOthers\n1. Alpha 1 receptor \nPearl \nPituitary hormones- cAMP pathway\nHypothalamic hormones- IP3/DAG pathway \n", "doc_id": "13a516e8-8e4e-44c3-9027-b9d4faca8bde", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "4b066a76-1e66-4aac-8074-bead2a86f89f", "node_info": {"start": 0, "end": 3466}}, "7834724997186347148": {"text": "C H A P T E R 61\n\nDiabetic retinopathy and other ocular complications\nGavin S. Tan1 and Tien Yin Wong2\n1 Vitreo-Retinal Service, Singapore National Eye Centre; Singapore Eye Research Institute, Duke-NUS Graduate Medical School, Singapore\n2\n\nSingapore Eye Research Institute, Singapore National Eye Centre, Department of Ophthalmology, National University of Singapore & National University Hospital; Duke NUS\nGraduate Medical School, Singapore\n\nKey points\n\u2022 Diabetic retinopathy affects one third of persons with diabetes and\nis the most common cause of reversible visual loss in working adults.\n\u2022 About 10% of persons with diabetes will have vision-threatening\nretinopathy, including diabetic macular edema.\n\u2022 The presence of diabetic retinopathy is associated with an increased\nrisk of other diabetic complications such as nephropathy and cardiovascular diseases.\n\u2022 Chronic exposure to hyperglycemia and other causal factors (e.g.\nhypertension) is believed to initiate a cascade of biochemical and\nphysiologic changes that ultimately lead to microvascular damage\nand retinal dysfunction.\n\u2022 Optimal management of the modifiable risk factors blood glucose,\nblood pressure, and blood lipids is key to preventing development\nand progression of retinopathy.\n\u2022 Regular dilated eye examinations are effective in detecting and\ntreating asymptomatic vision-threatening diabetic retinopathy.\nPersons with T1DM should have a complete dilated retinal\nexamination within 5 years from the onset of diabetes. Persons\nwith T2DM should have a complete dilated retinal examination\nat the time of diagnosis, Subsequent examination and referral for\ntreatment should be determined by the presence and severity of\nretinopathy.\n\u2022 Laser photocoagulation can prevent visual loss in proliferative\nretinopathy and diabetic macular edema. Intraocular administration of vascular endothelial growth factor inhibitors have been\nestablished as useful new treatment modalities in diabetic macular\nedema. Surgical intervention by vitrectomy may occasionally be\nindicated in advanced proliferative disease.\n\nIntroduction\nDiabetic retinopathy (DR) is a clinically well-defined, specific\nmicrovascular complication of diabetes, which is likely to\n\ndevelop to some degree in nearly all patients with diabetes\nmellitus over time. Although diabetes affects the eye in multiple\nways (e.g. increases the risk of cataract and retinal vascular\nocclusions) [1], DR is the most common and specific ocular complication, being the leading cause of visual loss in\nworking-aged adults in the developed world [2]. Of the 366\nmillion persons with diabetes worldwide [3], one third will\nhave diabetic retinopathy, of which a third is likely to have\nvision-threatening retinopathy, which includes severe or proliferative retinopathy and diabetic macular edema [4]. Diabetic\nretinopathy is reported to cause visual impairment in 10\u201320%\nof persons with diabetes [4\u20139]. Although DR blindness appears\nto have fallen in the developed world [6\u20138], the rapidly increasing number of persons with diabetes worldwide, especially in\ndeveloping countries [10\u201312] where access to optimal medical\ncare may be limited, has led to a continuing increase in the\nglobal burden of this disease [11,13\u201315].\nDiabetic retinopathy is characterized by changes and lesions\nin the retinal vasculature including hemorrhages, microaneurysms, arteriolar and venular dilatation. These have a\nprogressive nature eventually leading to areas of retinal nonperfusion, increased vasopermeability with retinal edema and\nexudates, and pathologic proliferative of intraocular blood\nvessels resulting in hemorrhage, tractional retinal detachment\nor neovascular glaucoma, all of which contribute to visual\nimpairment and blindness. Apart from its effects on vision, the\npresence of DR also signifies a greater risk of life-threatening\nsystemic vascular complications [16].\nRecent epidemiologic, genetic, and experimental studies have\nfurthered our understanding of the pathophysiology underlying\nDR. In addition, over the last 5 years, there have been several\nlarge-phase clinical trials that have provided contemporary\ndata regarding evidence-based treatment strategies for DR,\nincluding systemic management and ocular treatment using\n\nInternational Textbook of Diabetes Mellitus, Fourth Edition. Edited by Ralph A. DeFronzo, Ele Ferrannini, Paul Zimmet, and K. George M. M. Alberti.\n\u00a9 2015 John Wiley & Sons, Ltd. Published 2015 by John Wiley & Sons, Ltd.\n\n889\n\n\f890\n\nChapter 61\n\nantivascular endothelial growth factor (VEGF) agents. These\nhave provided paradigm shifts in management of DR and\ndiabetic macular edema.\n\nPrevalence of diabetic retinopathy\nThe epidemiology of DR is well described in the literature. In\nmany countries, DR is the most frequent cause of preventable\nblindness in working-aged adults [17]. In a major meta-analysis,\nYau et al. described the global prevalence of DR based on 35\nstudies across the world with a total of 22,896 patients with\ndiabetes and estimated the prevalence of any retinopathy to be\n34.6% with 10.2% having vision-threatening retinopathy [4].\nIn the United States, a pooled analysis of data from different\nstudies reported a prevalence rate of 40% for any retinopathy and\n8% for vision-threatening retinopathy in T2DMs and 86% (42%\nfor vision-threatening retinopathy) in T1DM [18,19].\nSimilarly high prevalence estimates have been reported in\nother countries (Figure 61.1) [20]. Amongst white Caucasian\npopulations, there have been studies in the UK, Europe, and\nAustralia [21\u201325]. Data from western Scotland showed the\nprevalence of any DR to be 26.7% [26]. Studies from Danish\npopulations have shown an overall prevalence of retinopathy of\n77% in men and 74% in women with T1DM [27]. Variations in\nthe prevalence of retinopathy may be due in part to differences in\npopulation selection and in methods for assessing retinopathy.\n\nIn Australia, three large population-based studies assessed\nDR from a standardized grading of fundus photographs. The\nMelbourne Visual Impairment Project reported a retinopathy\nprevalence of 29.1% among persons aged 40 years or older\nwith self-reported diabetes [28]. The Blue Mountains Eye Study\nfound a similar retinopathy prevalence of 32.4% among older\npersons aged 49 years and above with known or newly diagnosed diabetes [29], with signs of proliferative disease in 1.6%\nand macular edema in 5.5%. The Australian Diabetes Obesity\nand Lifestyle (AusDiab) study examined 11,247 adults aged\n25 years or older from 42 randomly selected urban and rural\ncommunities [30]. Overall, 25% of participants with known\ndiabetes were found to have retinopathy, including 2% with\nproliferative retinopathy. As in other studies, the prevalence of\nretinopathy was strongly related to the duration of diabetes,\nwith a prevalence of 9.2% among those with a duration of less\nthan 5 years, 23% for durations between 5 and 9 years, 33% for\ndurations between 10 and 19 years, and 57% for those with a\nduration of 20 or more years.\nIn many Asian countries, the prevalence of diabetes has\nincreased substantially over the past few decades [15,31\u201334],\nand there is concern about a potential diabetes epidemic in\nAsia [35]. In Singapore, for example, serial population surveys\nin 1975, 1985, and 1992 showed increasing prevalence rates of\ndiabetes of 2%, 4.7%, and 8.6%, respectively, in the population\nbetween the ages of 15 and 69 years [33,34]. There are now\nincreasing data on the epidemiology of diabetic retinopathy\n\nVision threatening diabetic retinopathy\n\nAll diabetic retinopathy\n\n60\n\n50\n\nPrevalence", "doc_id": "1dc9080f-3a74-4eb8-bcfc-a113b9878204", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "1c3e677e-22e6-402d-add5-02458a62585b", "node_info": {"start": 0, "end": 7574}}, "6169038610544347281": {"text": "diabetic retinopathy\n\n60\n\n50\n\nPrevalence (%)\n\n40\n\n30\n\n20\n\n10\n\nU\n\nW\n\nG\n\nlo\n\nba\n\nlp\n\nre\nv\n\nal\n\nen\n\nce\n\nES (2\n0\nKA DR 12\n)\nD\n(\nPr\noy S S 198\n4\nec\nA\n)\nto\n(\nVE 200\n9)\nH R(\nan\n20\nda\n01\nLA n (2 )\nLE 00\n9\nS\nBe (2 )\nU\n0\n04\nKA ijin\nD g (2 )\nBe S\n0\nav WE 08\ner\n(2 )\nD\nAM 009\n)\n(1\nSi\n99\nm\nes\n2)\nBl\n(2\nue M\nM ES 008\nou A\n)\nnt (20\nai\n0\nns\n6)\nSi (19\n9\nBa nd\n8\nrb i (2 )\n0\na\n12\nd\nM\nel os\n)\nbo\n(1\n99\nur\nn\n9\nAu e\n)\nsD (20\n00\nia\nb\n)\nSN (2\nD 008\n)\nC R(\nU\nR 200\nES\n9)\n(2\n00\n5)\n\n0\n\nFigure 61.1 Prevalence of diabetic retinopathy in various studies.\n\n\fDiabetic retinopathy and other ocular complications\n\nin Asians [36\u201338]. In China, the Beijing Eye Study and the\nHandan Eye Study examined the prevalence of DR in urban\nand rural Chinese persons, respectively [36,38,39]. In the\nBeijing Eye Study, the prevalence of DR detected on the\nfundus photographs was 37.1%, with macular edema present\nin 5.2%, clinically significant macular edema in 2.6%, and\nvision-threatening retinopathy in 5.2%. Diabetic retinopathy\nwas associated with rural region, longer duration of diabetes,\ndiabetic medications use, and lower education status. The\nHandan eye study in a rural region in China shows that\ndiabetic retinopathy is common, with prevalence rates of 43%\nfor any retinopathy, 5.2% for macular edema, and 6.3% for\nvision-threatening retinopathy [36]. Like in other studies, the\nprevalence of retinopathy was strongly related to duration\nof disease. These estimates are higher than those reported in\nanother study in Beijing amongst mostly urban Chinese residents [39], suggesting the need to target preventative efforts in\nrural areas of China. Based on these data, there are an estimated\n9.2 million Chinese persons living in rural areas with DR, of\nwhom 1.2 million have vision-threatening retinopathy [36].\nThere is thus a pressing need for appropriate screening and\nmanagement of diabetes and its complications in rural China.\nThe Singapore Malay Eye Study [37] reported on DR in Asian\nMalays, the third largest ethnic group in Asia. The overall\nprevalence of any retinopathy was 35.0%, macular edema 5.7%,\nand vision-threatening retinopathy 9.0%. Independent risk factors for any retinopathy were longer diabetes duration, higher\nhemoglobin A1c, hypertension, and higher pulse pressure.\nVision-threatening retinopathy additionally was associated\nwith previous stroke, cardiovascular disease, and chronic\nkidney disease.\nIn Indians, the Aravind Eye Disease Survey in southern India\nreported a retinopathy prevalence of 27% in a population aged\n50 years or older with self-reported diabetes [40], similar to\nthe 22% prevalence reported from another population-based\nstudy in an urban population in Hyderabad, India [41]. The\nSingapore Indian Eye Study examining an urban population of\nethnic Indians aged 40 and older, found a prevalence of 30.4%\nfor any retinopathy, 7.2% for macular edema, and 7.1% for\nvision-threatening retinopathy. The independent risk factors\nfor any retinopathy were younger age, longer diabetes duration,\nhigher hemoglobin A1c, higher systolic blood pressure, lower\ndiastolic blood pressure, previous stroke, and insulin treatment [42]. Thus, these population data suggest that diabetic\nretinopathy is common in Asian populations with diabetes, who\nshare similar risk factors to White populations, suggesting that\ncontrol of these risk factors may reduce both the prevalence and\nimpact of retinopathy.\n\nIncidence and progression of diabetic\nretinopathy\nThere are fewer data on the incidence and natural history of\ndiabetic retinopathy. In the Wisconsin Epidemiologic Study\n\n891\n\nof Diabetic Retinopathy (WESDR), the 4-year incidence\nof retinopathy was 40% [43,44], the 10-year incidence of\nretinopathy was 60\u201370% [45], and the 10-year incidence\nof macular edema was 15\u201325% [46]. There are few other\nlong-term population-based incidence data using objective\nmeasures to detect retinopathy to compare with these findings\n[47\u201354]. In the United Kingdom Prospective Diabetes Study\n(UKPDS), a multicenter randomized clinical trial, the 6-year\nincidence of retinopathy was 41% [53]. The Liverpool Diabetic\nEye Study reported an annual incidence of sight-threatening\nretinopathy of 0.3% in the first year, rising to 1.8% in the fifth\nyear [54].\n\nTime trends in the epidemiology of diabetic\nretinopathy\nThere have been some suggestions that over the past 30 years,\nbetter recognition and management of retinopathy risk factors\nand the institution of structured retinopathy screening programs\nhave led to a decline in both the prevalence and incidence of\nmoderate to severe microvascular diabetic complications.\nStudies conducted in contemporary populations have\nsuggested this to be the case. For example, data from both\nthe UKPDS [53] and the Liverpool Diabetic Eye Study [54]\nshow lower incidence rates for retinopathy, particularly sightthreatening retinopathy, than was reported previously in the\nWESDR and studies in the early 1980s [55]. A recent study\nassessed the age at which retinopathy was first diagnosed in\na sample of patients with T1DM and showed that the median\ndiabetes duration until the first occurrence of retinopathy was\n16.6 years [56], which is longer than reported in previous\nstudies. The meta-analysis review showed that estimates of\nretinopathy prevalence were about 10\u201320% lower in the seven\nlater studies as compared to the initial WESDR prevalence [18].\nThe WESDR follow-up study showed that from 1980 to 2007,\nthe estimated annual incidence of proliferative DR decreased by\n77% and vision impairment decreased by 57% among persons\nwith T1DM [6].\nThese data suggest that improvements in diabetes management and improved levels of metabolic and blood pressure\ncontrol may have had a positive impact in reducing the\nprevalence and incidence of retinopathy in Western countries. Nevertheless, it is uncertain whether this declining\ntrend will continue, with expectedly increasing number,\nduration, and lifespan of people with diabetes [57]. These\ntrends however, may not apply to Asian populations. In the\nHandan Eye Study [36], the prevalence of retinopathy was\n43.1%, higher than those reported in contemporary studies in\nWhites (ranging from 15.3% to 29.0%), Blacks (27.7\u201336.7%),\nand in Asian Indians (17.6%). In fact, the Handan Eye\nStudy suggests that the prevalence of retinopathy in rural\nChinese populations is more similar to rates seen in the initial\nWESDR.\n\n\f892\n\nChapter 61\n\nTable 61.1 Risk factors for diabetic retinopathy\n\nModifiable risk factors\n\nNon-modifiable risk factors\n\nHyperglycemia\nHypertension\nDyslipidemia\nCataract surgery\nObesity\u2217\nSmoking\u2217\nAlcohol consumption\u2217\n\nAge\nDiabetes duration\nEthnicity (Hispanic, South Asian)\nGenetic predisposition\nPuberty\nPregnancy\nNephropathy\n\n\u2217 Risk factors with inconsistent evidence.\n\nRisk factors\nThere are several important risk factors", "doc_id": "d5839317-68cc-41e2-b403-40f149b30aff", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "4bd74581-4b35-4fbb-b4b7-1bf3d096c709", "node_info": {"start": 0, "end": 6812}}, "6696820208936123683": {"text": "inconsistent evidence.\n\nRisk factors\nThere are several important risk factors for diabetic retinopathy\n(Table 61.1).\nHyperglycemia, hypertension, and dyslipidemia\nThe three major modifiable risk factors, including hyperglycemia, hypertension, and dyslipidemia are discussed in\ngreater detail in the section on systemic management of diabetic\nretinopathy. Briefly, reducing glycated hemoglobin levels by 1%\nthrough intensive glycemic control reduced the risk of DR by\n15\u201340% [58], progression to vision-threatening retinopathy by\n25% [59], need for laser photocoagulation by 25\u201330%, and risk\nof legal blindness by 16% [60]. Controlling hypertension with a\n10 mmHg decrease in systolic blood pressure reduces the risk of\nDR progression by 34%, visual loss by 37%, and need for laser\nphotocoagulation by 35% [61]. Epidemiologic studies have not\nfound a consistent association between serum lipid levels and\nDR. However, studies have found that fibrates may be protective\nagainst DR progression [62,63].\nDuration of diabetes\nEpidemiologic studies have shown that the prevalence of\ndiabetic retinopathy in persons with diabetes increases with\nthe duration of disease. The WESDR study reported that after\n20 years of diabetes, nearly 99% of T1DM patients and 60% of\nT2DM patients had developed DR [64,65]. Age of onset also\nplays an important role as DR rarely develops in children under\n10 years of age irrespective of duration of disease.\nRace\nRacial/ethnic differences in the prevalence of diabetic retinopathy have been a major focus of recent research. Population-based\nstudies suggest that the prevalence and severity of DR are higher\nin African Americans, Hispanics, and South Asians than in\nWhites, which is not fully explained by differences in the distribution of retinopathy risk factors [20,66\u201368]. For example,\nthe UK Asian Diabetes Study showed that after controlling\nfor retinopathy risk factors, South Asians were more likely\nto have diabetic retinopathy than Whites [20], a finding also\nsupported by a recent large clinical trial [69]. Nevertheless, it is\n\nuncertain whether these apparent ethnic variations represent\nsubpopulation differences associated with medical care, or\nvariability in genetic predisposition to microvascular damage.\nGenetic factors\nThere is evidence to support a genetic component for diabetic\nretinopathy [70,71]. Familial aggregation studies and clinical\ntrials including the Diabetes Control and Complications Trial\n(DCCT) have demonstrated a heritable tendency for DR independent of shared risk factors [72]. Studies of other populations\nreported similar heritability for severe DR not fully explained by\nlifestyle or environmental factors [70]. A recent meta-analysis\nidentified several genes (e.g. aldose reductase gene) associated\nwith DR [71].\nGender\nIn women, pregnancy and puberty are risk factors for diabetic\nretinopathy in T1DM [73\u201375]. In the WESDR, diabetes\nduration after menarche, a marker of puberty onset, was\nassociated with a 30% excess risk of retinopathy compared to\ndiabetes duration before menarche [73]. Pregnancy is similarly\nassociated with progression of diabetic retinopathy and risk of\nvision-threatening retinopathy both in T1 and T2DM [76\u201378].\nPlanned dilated retinal examination should be offered for\npatients with T1DM after puberty and for all pregnant women\nwith pre-existing diabetes.\nCataract surgery\nIn patients with diabetes, cataract surgery has been reported\nto exacerbate the development and progression of diabetic\nretinopathy. Macular edema after cataract surgery is also a\nmajor cause of vision loss in diabetic patients, especially in\nthose with pre-existing DR. Considerations for the management\nof the diabetic subjects with a cataract are discussed in the\nsection on ocular management of retinopathy.\n\nRelationship with other complications\nPrevious epidemiologic studies have also shown that diabetic\nretinopathy is associated with many other systemic and lifestyle\nfactors, including nephropathy [79], obesity [80], alcohol consumption [81], smoking [82], as well as hematological markers of anemia [83], inflammation, and endothelial dysfunction\n[84,85]. However, some of these findings have been inconsistent,\nand the precise role of such factors in the pathogenesis of DR is\nnot well defined.\nDiabetic retinopathy reflects widespread end-organ microcirculatory damage and findings from epidemiologic studies\nsuggest that DR predicts an excess risk of systemic vascular\ncomplications [16]. The presence of retinopathy, even in its\nmildest form, may double or triple the risk of coronary heart\ndisease, heart failure and stroke, independent of other vascular\n\n\fDiabetic retinopathy and other ocular complications\n\nrisk factors [86\u201388]. These findings suggest the need for closer\ncardiovascular monitoring and follow-up for patients with\nDR [16].\n\nPathogenesis\nChronic exposure to hyperglycemia and other risk factors (e.g.\nhypertension) is believed to trigger a cascade of biochemical and\nphysiologic changes that results in the microvascular damage\nand retinal dysfunction manifest in diabetic retinopathy (see\nChapter 68).\nBiochemical changes\nHyperglycemia is considered the key initiator of the cascade\nof retinal changes associated with diabetic retinopathy. Several\nbiochemical mechanisms are thought to be associated with\nthe pathogenesis of retinopathy through effects on cellular\nmetabolism, signaling, and growth factors [17,89]. Implicated\npathways include the accumulation of sorbitol and advanced\nglycation end-products, oxidative stress, protein kinase C activation, inflammation, and upregulation of the renin-angiotensin\nsystem and vascular endothelial growth factor (VEGF). Recognition of the potential roles for each of these processes has led\nto the development of new therapeutic agents, several of which\nhave been or are currently being tested in clinical trials.\nProtein kinase C is a key mediator in intracellular signal\ntransduction and is involved in diabetic microvascular complications [90]. Hyperglycemia increases activation of retinal\ncellular protein kinase C, leading to increased expression of\nmatrix proteins and vasoactive mediators, with adverse structural (pericyte apoptosis [91], basement membrane thickening)\nand functional (increased retinal vascular permeability and\nretinal blood flow) retinal vascular changes.\nHyperglycemia increases glucose flux through the polyol\npathway, via which aldose reductase converts glucose into intracellular sorbitol, which may induce osmotic damage to retinal\nendothelial cells and pericytes. Aldose reductase gene had the\nlargest number of polymorphisms associated with DR [92].\nOxidative stress is also a key process where hyperglycemia\nincreases production of reactive-oxygen species, leading to\nactivation of protein kinase C, formation of advanced glycation\nend-products, activation of the polyol pathway and VEGF\nproduction.\nProlonged exposure to hyperglycemia induces nonenzymatic\nglycation of proteins to form advanced glycation end-products\n(AGEs), which may contribute to retinal perictye loss, microaneurysm formation, and vascular endothelial damage. AGEs\nmediate their effects on the microvasculature through interaction with the receptors for AGEs (RAGE). Modulation of RAGE\nmay be a possible future means of therapeutic intervention for\nDR [93].\nThe intraocular renin-angiotensin system has been found to\nbe upregulated in diabetes, and angiotensin II may stimulate\n\n893\n\nexpression of VEGF and other growth factors in retinal vascular\nendothelial cells and promote cell growth, proliferation, and the\ndeposition of extrecellular matrix proteins.\nVEGF is a key mediator in the retinal vasculature changes\ninvolved in the development and progression of DR [94].\nIncreased levels of VEGF have been shown in the ocular\nfluids of diabetic patients [95]. In response", "doc_id": "602e776f-9287-40a3-b79a-9d823eed66c2", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "cbc827b3-67ad-4e15-a5ae-e49cf5cb8a4b", "node_info": {"start": 0, "end": 7839}}, "4930479436725890519": {"text": "have been shown in the ocular\nfluids of diabetic patients [95]. In response to hypoxia, retinal\nendothelial cells, pericytes and pigment epithelial cells express\nVEGF, stimulating angiogenesis which results in neovascularization and increasing capillary permeability resulting in\nmacula edema.\nRecent work has identified new VEGF-independent pathways\nfor DR [96,97]. Among these, erythropoietin has been shown to\nbe a potent ischemia-induced angiogenic factor in proliferative\nretinopathy which acts independently of VEGF [98,99]. Inhibition of erythropoietin is remarkably effective in suppressing retinal neovascularization in animal models [98,100]. In the retina,\nerythropoietin is also expressed in response to stimuli other than\nischemia [101], and it has been suggested that it may serve to\nprotect the neural retina at the early stage of DR [102,103]. Therapeutic inhibition of erythropoietin as a treatment approach for\nDR must be balanced by its potential adverse effects on photoreceptor survival [96].\nProteomic analyses have identified other VEGF-independent\npathways in DR. The vitreous level of extracellular carbonic\nanhydrase was markedly elevated in eyes with DR [104].\nInhibiting carbonic anhydrase activity has been demonstrated\nto reduce retinal vascular permeability in animal models [104].\nHowever, it remains undetermined whether topical carbonic\nanhydrase inhibitors, which are commonly used to lower\nintraocular pressure in patients with glaucoma, could reduce\nthe risk of DR [105].\nInflammation has been shown to play a critical role in\nthe pathogenesis of DR [106\u2013108]. An array of inflammatory mediators are upregulated in diabetes in response to\nhyperglycemia and other stresses (e.g. dyslipidemia) which\ntrigger pro-inflammatory responses that may cause abnormal\nleukocyte\u2013endothelial interactions and retinal microvascular\ndamage. There is little evidence for a strong association between\nmarkers of systemic inflammation and risk of DR suggesting\nthat this it is likely to be a local phenomenon [85,109].\nFinally, there are new insights into retinal physiology that\nsuggest the concept that DR cannot be attributed as purely a\nmanifestation of microvascular damage. Neuroretinal compromise may occur early in the course of DR, and can precede the\nonset of microvascular changes [106]. It has been proposed that\ndiabetes may reduce insulin receptor signaling in the retina,\nleading to neurodegeneration [106]. Experimental studies\nsuggest that diabetes adversely affects the entire neurosensory\nretina, with accelerated neuronal apoptosis, and activation or\naltered metabolism of neuroretinal supporting cells [106]. These\nfindings suggest that DR could be similar to peripheral diabetic\nneuropathy, but involving the retinal parenchyma. While the\n\n\f894\n\nChapter 61\n\ncomplex relationship between the neural and vascular elements\nof retinopathy pathogenesis remains to be elucidated [106],\nunderstanding how diabetes affects the neural retina may\nultimately lead to the development of neuroprotective agents as\nnew potential disease modifiers [110].\nRetinal vascular changes\nDiabetes and diabetic retinopathy is associated with structural\nand functional changes in the retinal vasculature [111]. Quantitative assessment of the retinal vasculature with computer-based\nretinal image analysis has been used to study these changes in\ngreater detail.\nIncreased retinal arteriolar caliber is found to be associated\nwith the development of retinopathy in both T1 and T2DM\n[112\u2013114]. Dilation of retinal arterioles may be an early indicator of microvascular dysfunction [115], implying impaired\narteriolar autoregulation [114,115]. Based on the laws of Starling\nand Laplace, retinal arteriolar dilatation has been postulated\nto increase retinal capillary pressure, leading to capillary\nwall dilatation (microaneurysms), leakage (edema and hard\nexudates), and rupture (hemorrhages) [114]. Increased retinal\nvenular caliber is independently associated with the progression\nof DR [116\u2013120], and predicts the risk of proliferative retinopathy [116]. Proposed mechanisms underlying this association\nare likely to be multifactorial (e.g. retinal hypoxia, inflammation, endothelial dysfunction) [121\u2013124]. Collectively, these\nfindings suggest that retinal arteriolar dilatation may be an early\nsubclinical marker of microvascular dysfunction preceding the\ndevelopment of nonproliferative DR, whereas retinal venular\ndilatation may be a marker of progression to more severe or\nproliferative retinopathy.\nFractal analysis has been used to evaluate the overall geometry\nof the retinal vascular network in diabetes [125]. A recent study\nshowed that retinal fractal dimension, a measure of the density\nof the vascular branching pattern, is associated with early\nretinopathy in T1DM [126]. Furthermore, research investigating new dynamic retinal vascular changes has demonstrated\nthat eyes with DR have reduced retinal vasodilation after\nflicker-light stimulation, a measure of endothelial dysfunction\n[127,128]. These imaging techniques may offer new means of\nassessing DR risk.\n\nClinical features and assessment\nDiabetic retinopathy is defined clinically as the presence of\ntypical retinal microvascular changes in an individual with diabetes mellitus. As the disease progresses, maculopathy (macular\nedema and ischemia) and neovascularization of the retina (vitreous hemorrhage, retinal detachment) and iris (neovascular glaucoma) leads to vision loss. The aim of clinical assessment is to\ndetect these serious ocular manifestations, and in their absence,\nto assess the risk of progression to vision-threatening disease.\nDirect ophthalmoscopy enables adequate assessment of DR\nsigns, but this is enhanced by slit-lamp biomicroscopy with a\n\ncondensing lens and indirect ophthalmoscopy. Severe DR may\nbe present without symptomatic visual impairment, therefore\nvisual acuity assessment while important, can be misleading.\nExamination of the peripheral fundus is critical, particularly\nin patients with T1DM, to avoid missing the presence of\nperipheral retinal ischemia and neovascularization. Referral\nof patients with sight-threatening retinopathy to a specialist\nin ophthalmology for properly and timely treatment is key\nto reducing the risk of visual impairment. For patients with\nnewly diagnosed DR, a comprehensive systemic examination\nby physicians is also advisable [16].\nThe classic retinal microvascular signs of nonproliferative\nDR include microaneurysms, hemorrhages, hard exudates\n(lipid deposits), cotton-wool spots (accumulations of axoplasmic debris within adjacent bundles of ganglion cell axons)\n[129], venous dilation and beading, and intraretinal microvascular abnormalities (i.e., dilated pre-existing capillaries)\n(Figure 61.2(a,b)). Standard clinical classifications of DR are\nshown in Table 61.2 [130]. This classification aims to identify\nstages of retinopathy that may present a significant threat to\nvisual acuity or confer a high risk for progression to those\nstages, which in turn guides follow-up duration and necessity\nfor intervention.\nThe appearance of retinal neovascularization is a critical change in the progression of diabetic retinopathy\n(Figure 61.2(c,d)). The clinical features of proliferative retinopathy may vary from a few fine new blood vessels appearing\non the retina or optic disc to an increase in the size, number,\nand extent of these new vessels. This may be asymptomatic\nin the early stages but predicts that the eye is at significant\nrisk of severe visual loss. Eyes have high risk of proliferative\nDR when there are new vessels of about one fourth disc area\non or within one disc diameter; or new", "doc_id": "b356c010-dd9e-4059-8006-5a74c9c9522c", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "6c4df072-ac22-4b2f-a7ca-43759f3a8f35", "node_info": {"start": 0, "end": 7660}}, "7700062768632820780": {"text": "new vessels of about one fourth disc area\non or within one disc diameter; or new vessels at the optic\ndisc associated with vitreous hemorrhage; or new vessels away\nfrom the disc which are greater than half disc area in size and\nassociated with vitreous hemorrhage. These eyes have a 1-year\ncumulative rate of severe visual loss, defined as visual acuity\nless than 5/200 of 10% and a 3- and 5-year risk of 35% and\n50%, respectively. Advanced proliferative disease is marked by\nfibrovascular proliferation, and visual loss may occur suddenly\ndue to vitreous hemorrhage from new vessels, or tractional\nretinal detachment from progressive fibrosis or may be subacute\ndue to macular ischemia and neovascular glaucoma.\nDiabetic macular edema is an important sign that is assessed\nseparately from the stages of retinopathy (Figure 61.2(f)), as\nit can run an independent course. Macular edema is a major\ncause of visual impairment in persons with diabetes and results\nfrom the abnormal collection of extracellular fluid in the retina,\nobserved clinically as the presence of hard exudates and retinal\nthickening in the macula. Since not all maculopathy results\nin visual impairment, the ETDRS study proposed a new term\n\u201cclinically significant macular edema\u201d (CSME), which is defined\nas retinal thickening that involves or threatens the center of\nthe macular, the specific definition of which is elaborated in\nTable 61.2.\n\n\fDiabetic retinopathy and other ocular complications\n\n(a)\n\n(b)\n\n(c)\n\n(d)\n\n(e)\n\n(f)\n\n895\n\nFigure 61.2 (a) Mild nonproliferative diabetic retinopathy (b) severe nonproliferative diabetic retinopathy (c) proliferative diabetic retinopathy (d) new\n\nvessels at disc (e) proliferative diabetic retinopathy with fibrovascular proliferation (f) clinically significant macular edema.\n\nInvestigations\nAdvances in ophthalmic imaging have resulted in these modalities playing important roles in the screening, diagnosis, and\nmonitoring of diabetic retinopathy.\nRetinal photography serves as a useful screening tool for\nDR, especially where access to ophthalmologists is limited.\nStudies have shown that retinal photography interpreted by\ntrained readers has high sensitivity (61\u201390%) and specificity\n\n(85\u201397%) [131], and may guide appropriate ophthalmic referral [132]. There is recent evidence to suggest that automated\ncomputer grading systems may be effective in DR screening\nthereby reducing the workload of manual grading [133].\nFluorescein angiography is an established modality used\nin clinical evaluation of DR. Microaneurysms and increased\ncapillary permeability are the earliest detectable changes. Focal\nareas of capillary nonperfusion represent retinal ischemia while\nenlargement of the foveal avascular zone identifies macular\n\n\fNo retinal abnormalities\nMicroaneurysms only\n\nMore than just microaneurysms but less than\nsevere NPDR\n\nAny of the following:\n1 More than 20 intraretinal hemorrhages in\neach of four quadrants\n2 Definite venous beading in two or more\nquadrants\n3 Prominent IRMA in one or more quadrants\nand no signs of proliferative retinopathy.\nNeovascularization of optic disc (NVD) or\nelsewhere (NVE), preretinal hemorrhage, or\nvitreous hemorrhage.\n\nAny apparent retinal thickening or hard\nexudates in posterior pole.\nSome retinal thickening or hard exudates in\nthe posterior pole but distant from the center\nof the macula.\nRetinal thickening or hard exudates\napproaching the center of the macula but not\ninvolving the center.\nRetinal thickening or hard exudates involving\nthe center of the macula.\n\nNo retinopathy\n\nMild nonproliferative diabetic\nretinopathy (NPDR)\n\nModerate NPDR\n\nSevere NPDR\n\nProliferative diabetic\nretinopathy (PDR)\n\nDiabetic macular edema (DME)\n\nMild DME\n\nSevere DME\n\nModerate DME\n\nDefining features\n\nInternational Clinical\nDiabetic Retinopathy\nDisease severity scale [130]\n\nTable 61.2 Classification of diabetic retinopathy\n\nClinical significant macular edema\n\nMacular edema\n\nHigh-risk PDR\n\nMild PDR\nModerate PDR\n\nSevere NPDR\n\nModerately severe NPDR\n\nModerate NPDR\n\nMild nonproliferative diabetic\nretinopathy (NPDR)\n\nNo retinopathy\n\nETDRS scale [18,224]\n\nRetinal thickening at or within 500 \u03bcm of the center of the macula, or\nHard exudate at or within 500 \u03bcm of the center of the macula with\nassociated thickening of the adjacent retina, or\nA zone or zones of retinal thickening one disc diameter or larger, any\npart of which is within one disc diameter of the center of the macula.\n\nAny retinal thickening or hard exudates in posterior pole.\n\nFibrous proliferation on the optic disc or elsewhere or visible NVEs.\nNVE \u22651/2 disc area, or\nvisible NVD, or\nVitreous or preretinal hemorrhage and NVE < 1/2 disc area.\nNVD \u22651/4\u20131/3 disc area, or\nNVD < 1/4 disc area and vitreous or preretinal hemorrhage, or\nNVE \u22651/2 disc area and vitreous or preretinal hemorrhage, or\nVitreous or preretinal hemorrhage. obscuring \u22651 disc area\n\nMicroaneurysms and hemorrhages severe in 4\u20135 fields, or\nVenous beading definite in 2 fields, or\nIRMA moderate in 1 field.\n\nMicroaneurysm and hemorrhages moderate in 4 fields or severe in\n1 field or IRMA\nTwo out of three moderate characteristics and or one of the\nfollowing: microaneurysms and hemorrhages severe in 2 or 3 fields,\nIRMA present in 4\u20135 fields or venous beading in 1 field\n\nMicroaneurysms only, or\nVenous loops in 1 field; retinal hemorrhages present; hard exudates or\nsoft exudates in 1 field\n\nNo retinal abnormalities\n\nDefining features (based on 7 \u00d7 30\u2218 field stereo photographs)\n\n896\nChapter 61\n\n\fDiabetic retinopathy and other ocular complications\n\nischemia. Retinal neovascularization presents as dye leakage\ninto the vitreous. Diabetic macular edema has two main\nangiographic patterns: focal (from leaking microaneurysms),\nand diffuse (generalized breakdown of blood\u2013retinal barrier).\nOptical coherence tomography (OCT) has become an increasingly important imaging modality. It generates cross-sectional\nimages of ocular structures by measuring the echo-time\ndelay and intensity of reflected light, offering high-resolution,\nthree-dimensional or cross-sectional images that closely\napproximate the histologic appearance of the retina [134]. OCT\nallows accurate and reproducible measurements of the retinal\nthickness, critical for monitoring progression and treatment\nresponse for diabetic macular edema. It is a more accurate\nand objective method of diagnosing macular edema than\nclinical examination, and has become an established clinical\ntrial endpoint for treatment in diabetic macular edema. It is\nalso useful to detect structural changes (e.g. vitreomacular\ntraction or epiretinal membranes) that may indicate a need for\nsurgical intervention. There is also a suggestion that it may be\nuseful in screening for diabetic macular edema compared with\nnonstereoscopic retinal photography [135].\n\nRecommended timing and frequency\nof screening for diabetic retinopathy\nRegular", "doc_id": "9eaf7bfb-7a0c-4d73-8363-7812e5317055", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "cb1903e0-a5ea-42d7-972a-f102efbc3af8", "node_info": {"start": 0, "end": 6865}}, "5163912367925872599": {"text": "timing and frequency\nof screening for diabetic retinopathy\nRegular dilated eye examinations can detect asymptomatic\nvision-threatening diabetic retinopathy effectively. In the\nWESDR, 14% of people with T1DM and 33% of those with\nT2DM developed DR within 5 years of the diagnosis of diabetes. Almost all the retinopathy cases in T1DM were mild,\ncompared with the older participants with T2DM where 2%\n\n897\n\nhad proliferative retinopathy and 3% had clinically significant\nmacular edema [46,136,137]. This suggests that DR screening\nshould be performed at diagnosis and either yearly or second\nyearly thereafter in persons with T2DM. In persons with T1DM,\nbaseline examinations could be extended to 5 years after diagnosis. The Liverpool Diabetic Eye Study, reporting retinopathy\nincidence in a large cohort of people with T2DM, suggests\nthat a 3-year screening interval could be safe for patients\nwithout any evidence of retinopathy, though in patients with\nany sign of retinopathy, yearly or more frequent examination\nis recommended [138]. The most reliable and cost-effective\nmeans of screening for DR is with mydriatic digital retinal\nphotography [139] and this has been implemented successfully\nin many countries resulting in cost-effective reduction of visual\nimpairment [131,140]. Telemedicine-based digital retinal imaging may provide more cost-effective and efficacious screening\nfor DR in diabetic patients.\nGuidelines for screening and management at differing\nseverity of DR are elaborated in Table 61.3. In practice, the\ntiming and frequency of eye examinations in people with\ndiabetes are often individualized. Examination at least annually\nis recommended for high-risk patients (e.g. those with longer\nduration of diabetes, poor systemic risk factor control), even in\nthe absence of retinopathy [58]. In patients with pre-pubertal\ndiabetes, it may be appropriate to begin retinopathy screening\nat puberty [73\u201375]. In pregnant women with nongestational\ndiabetes, a comprehensive eye examination may be warranted\nduring the first trimester, with follow-up throughout the\npregnancy in presence of retinopathy [141]. Regular eye\nexaminations also exert positive psychosocial effects on the\ncare of patients with diabetes (e.g. education about risk factors,\ncompliance) [17].\n\nTable 61.3 Management and follow-up recommendations for diabetic retinopathy\n\nRetinopathy severity [130]\n\nNo retinopathy\n\nClinical implications\n\nManagement\n\nFrequency of\nexamination\n\n\u2013\n\n\u2013\n\n1\u20132 yearly\n\nMild nonproliferative diabetic\nretinopathy (NPDR)\n\n5% (within 1 year) and 14% (within 3 years)\nprogress to PDR\n\nOptimize medical therapy of glucose, blood\npressure and lipids.\n\nAnnually\n\nModerate NPDR\n\n5\u201326% (within 1 year) and 30\u201348% (within\n3 years) progress to PDR.\n1.2\u20138.1% progress to high-risk PDR [225]\n\nRefer to ophthalmologist.\nOptimize medical therapy of glucose, blood\npressure and lipids\n\n3\u20136 monthly\n\nSevere NPDR\n\n52% (within 1 year) and 71% (within 3 years)\nprogress to PDR.\n14.6\u201345.0% progress to high-risk PDR\n\nConsider panretinal photocoagulation for\npatients with type 2 diabetes\n\n3\u20134 monthly\n\nProliferative diabetic\nretinopathy (PDR)\n\nRisk of severe visual loss\n\nIndication for panretinal photocoagulation\n\u2013 Urgent if high-risk PDR present\n\nVariable\n\nDiabetic macular edema (DME)\n\nMay occur at any stage of DR\n\nClinically significant macular\nedema\n\nNeed intervention to prevent visual loss\n\nIndication for macular laser.\nConsider intravitreal anti-VEGF therapy if\ncenter involving macula edema with vision loss\ndue to DME.\n\nVariable\n\nVariable\n\n\f898\n\nChapter 61\n\nSystemic treatment of diabetic retinopathy\nThe most effective treatment for diabetic retinopathy is prevention and this involves the optimization of systemic risk factors.\nSeveral important studies in recent years have made a significant\ncontribution in addressing the concerns regarding systemic\noptimization including the target glycemic and blood pressure\nlevels for effective prevention of retinopathy development and\nprogression, the efficacy of various hypoglycemic and blood\npressure-lowering agents, and the role of lipid-lowering agents.\n1 Glycemic control Hyperglycemia is the key initiator in the\npathogenesis and development of diabetic retinopathy. The\nDCCT and the United Kingdom Prospective Diabetes Study\n(UKPDS) are the key studies providing definitive evidence\nthat tighter control of glycemia (HbA1c 7%) reduces the risk\nof development and progression of DR in both T1 and T2DM\n[60,142,143]. There is evidence of a small risk of initial worsening of retinopathy at the onset of therapy, but the long-term\nbenefits outweigh this risk [144]. Each percent reduction in\nHbA1c (e.g. from 9% to 8%) lowers the risk of retinopathy\nby 30\u201340% and the effect is long-lasting even if subsequent\nmetabolic control deteriorates later in life, an effect termed\n\u201cmetabolic memory\u201d [145]. In keeping with these findings, a\nrecent meta-analysis shows a graded relationship between the\nlevel of glycemia and frequency of retinopathy signs [146].\nThere is recent evidence to show that there is a limit to\nthe benefit of further lowering of glycemic levels in persons\nwith diabetes. The Action in Diabetes and Vascular Disease (ADVANCE) trial [147], demonstrated that aggressive\nglycemic control (HbA1c <6.5%) did not significantly impact\non retinopathy development or progression in T2DM [147].\nThe Action to Control Cardiovascular Risk in Diabetes\n(ACCORD) trial showed that while intensive therapy for\nglycemic control did reduce macrovascular and microvascular\nevents and progression of DR, it was also associated with\nincreased episodes of severe hypoglycemia and increased\nmortality [148], although the cause of unexpected excess\ndeaths remains unclear [149]. This suggests that in older\npatients and in those with established cardiovascular disease,\nperhaps glycemic targets should be less strict.\nThe Veterans Affairs Diabetes Trial (VADT) also recently\nreported that after 5-years follow-up, intensive glycemic control\n(HbA1c 6.9%; comparable to the DCCT and UKPDS) did not\nyield any significant benefit on the retinopathy outcomes [150].\nWhile these findings contrast with those from the UKPDS, they\ncould be related to the population in the VADT having more\nmales (97%), shorter length of follow-up, and later initiation\nof therapy. Although it was not statistically significant, the rate\nof retinopathy progression in the VADT was modestly lower in\nthe intervention group than in the control group (17% vs. 22%;\np = 0.07), so that a delayed benefit of intensive glycemic control,\nas found in previous studies [151,152], cannot be excluded.\nRecent analysis from the UKPDS and DCCT trials have\nsuggested that the protective effect of intensified blood glucose\n\ncontrol, especially early in disease, has a sustained effect over\ntime. This \u201cmetabolic memory\u201d effect persists even if glycemic\ncontrol is less intensive later in the course of disease. In the\nDCCT, follow-up analysis showed that 4 years after the end of\nthe trial, 17.8% of patients who were originally randomized to\nintensified glycemic control had progression in DR compared\nwith 48.9% of those randomized to the conventional group;\nand at 10 years progression was found in 35.8% compared with\n60.6% [145]. In the UKPDS, at 10 years follow-up, although\nthe between group differences in glycated", "doc_id": "a70a3d47-1732-4a98-b722-02d022aa455d", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "5a723a75-5fef-4091-a14c-6976c24a002f", "node_info": {"start": 0, "end": 7333}}, "7981076277951461203": {"text": "at 10 years follow-up, although\nthe between group differences in glycated hemoglobin levels\nwere lost after the first years, in the intensively treated group,\nthe relative risk reduction persisted at 24% for microvascular\ndisease compared with the less intensive group [153].\n2 Blood pressure control Epidemiologic studies and clinical\ntrials found that hypertension is a major modifiable risk factor\nfor diabetic retinopathy [58]. Hypertension leads to increased\nretinal blood flow and mechanical damage and stretching of\nvascular endothelial cells, stimulating the release of VEGF\nwhich contributes to progression of DR [154,155]. Each\n10 mmHg increase in systolic blood pressure is associated with\nan approximately 10% excess risk of early DR and a 15% excess\nrisk of proliferative retinopathy [156,157]. In the UKPDS,\ntighter blood pressure control reduced the risks of retinopathy\nprogression by about one third, visual loss by half, and need\nfor laser treatment by one third in people with T2DM [61,155].\nHowever, these benefits are not sustainable without ongoing\nand long-term maintenance of blood pressure control [158].\nClinical trials have shown that renin-angiotensin system\ninhibitors may reduce the incidence and progression of DR\nbeyond their blood pressure-lowering effects compared with\nother antihypertensive drugs. The EURODIAB Controlled\nTrial of Lisinopril in Insulin-Dependent Diabetes Mellitus\n(EUCLID) showed that lisinopril reduced the risk of retinopathy progression by 50% and proliferative retinopathy by\n80% [159]. The EUCLID, however, was limited by treatment\narm differences in baseline glycemia and by its short (2-year)\nfollow-up. The Diabetic Retinopathy Candesartan Trials\n(DIRECT) and the Renin-Angiotensin System Study (RASS)\nsupported these findings. In the DIRECT trials, candesartan\nreduced the risk of retinopathy development by 18% to 35%\nin T1DM, and increased regression of retinopathy by 34%\nin T2DM [160\u2013162]. In the RASS, enalapril and losartan\nreduced the risk of retinopathy progression by 65% and 70%,\nrespectively, in T1DM, independent of the changes in blood\npressure over the period of the trial [163].\nIn the 10-year post trial monitoring of patients from the\nUKPDS, difference in blood pressure between the tight and less\ntight blood pressure control regimens disappears within 2 years\nafter termination of the trial. In contrast to the sustained benefit of early glucose control, the risk reductions found during\nthe trial for microvascular disease were no longer significant\nduring the follow-up. This suggests that good blood pressure\ncontrol must be continued if the benefit of reduced incidence\nand progression of retinopathy is to be maintained [158].\n\n\fDiabetic retinopathy and other ocular complications\n\n3 Lipid-lowering therapy Observational studies support a role\nfor dyslipidemia in the pathogenesis of diabetic retinopathy [58]. The DCCT showed that the severity of retinopathy\nwas associated with increasing triglycerides and lower levels\nof HDL-cholesterol [164]. A high total to HDL-cholesterol\nratio and elevated LDL-cholesterol were also associated with\nthe development of clinically significant macular edema [165].\nThe Fenofibrate Intervention and Event Lowering in Diabetes\n(FIELD) trial showed that fenofibrate, a lipid-modifying agent,\nreduced the need for laser treatment of vision-threatening DR\nby 31% in patients with T2DM over 5 years [62]. The ACCORD\nstudy reported a 40% reduction in the odds of having progression of retinopathy over 4 years afforded by fenofibrate\ncombined with simvastatin compared with simvastatin alone,\nfurther supporting the efficacy of fenofibrate [63,166]. Interestingly, this finding did not appear to be secondary to changes\nin the traditional serum lipid profile [167]. Experimental\nstudies have suggested a number of possible mechanisms for\nthe action of fenofibrate which involve lipid and nonlipid\npathways, including upregulation of apo A-I, antiapoptotic\nactivity, oxidative stress, inflammation, protective effects\non blood\u2013retinal barrier breakdown, and neuroprotective\neffect [168,169]. These results suggest that fenofibrate may be\nbeneficial in the early stages of DR.\n4 Multifactorial intervention The Steno-2 study investigated\nthe effect of intensive multifactorial intervention, with tight\nglucose regulation and the use of renin-angiotensin system\nblockers, aspirin, and lipid-lowering agents, in patients with\nT2DM and microalbuminuria [170]. The Steno-2 study\nencompassed treatment goals similar to those recommended\nin the American Diabetes Association guidelines. It showed\nthat after 8 years of intensified, target-driven intervention\nthat aimed to control multiple vascular risk factors the risk of\nretinopathy was reduced by 58% [170]. The differences in the\nlevels of risk factors between the controlled and intervention\ngroups were no longer significant 5 years later; however, the\nbeneficial effects on retinopathy were sustained [170]. This is\nin keeping with the \u201cmetabolic memory\u201d findings seen in the\nDCCT [145], and UKPDS [153] reinforcing the importance of\nearly and strict implementation of multifactorial interventions\nto prevent the development and progression of DR.\n5 Emerging medical treatments Understanding the biochemical pathways in the pathogenesis of diabetic retinopathy,\nvarious novel systemic therapies are being developed. Protein\nkinase C is a key mediator resulting in increased retinal\nneovascularization and vascular permeability. Ruboxistaurin,\na well-tolerated selective protein kinase C inhibitor, has been\nshown in initial trials to reduce the risk of progression and need\nfor laser treatment for diabetic macular edema [171\u2013174], and\ncould reduce visual impairment from long-standing macular\nedema [175]. However, additional trials are needed to verify\nthese findings. Diabetes results in accumulation of AGE in the\nretina and the DCCT showed that AGE levels from skin biopsy\nmay predict retinopathy progression [176,177]. A clinical\n\n899\n\ntrial in T1DM suggests that patients treated with Pimagedine,\nan aminoguanidine that inhibits the formation of AGE, has\nbeen shown in a clinical trial involving T1DM to reduce the\nlikelihood of retinopathy progression [178].\n\nOcular therapy\nLaser photocoagulation has long been established as the gold\nstandard for ophthalmic therapy for vision-threatening diabetic\nretinopathy. Timely and appropriate laser treatment is effective\nin preventing visual loss but has significant ocular side effects\nsince photocoagulation is ultimately a destructive procedure.\nFurthermore, reversal of visual loss is uncommon even with\nadequate treatment. Recently, new and more effective therapeutic strategies aimed at improving vision have been developed\n(see Table 61.4).\nLaser photocoagulation\nLaser therapies for diabetic retinopathy are panretinal photocoagulation (PRP) for proliferative retinopathy and macular\n(focal/grid) laser photocoagulation for diabetic macular edema.\nIn PRP, the laser burns are placed over the entire retina sparing the central macula in order to promote regression and\narrest progression of retinal neovascularization, possibly by\nreducing ischemia-driven VEGF production [95]. The Diabetic\nRetinopathy Study (DRS) and the Early Treatment Diabetic\nRetinopathy Study (ETDRS), two landmark clinical trials in\nthe management of DR, established PRP as the primary treatment for proliferative retinopathy and severe nonproliferative\nretinopathy.\nIn the DRS, PRP reduced the risk of severe visual loss (visual\nacuity \u22645/200) by 50% over 5 years in more than 1758 patients\nwith proliferative disease [179]. In the ETDRS of 3711 patients\nwith less severe DR,", "doc_id": "31bd21ea-aa10-4d91-aa3e-53200b925fec", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "beb33758-24b1-4569-89a9-bc59efe5d07a", "node_info": {"start": 0, "end": 7677}}, "213475912161956304": {"text": "[179]. In the ETDRS of 3711 patients\nwith less severe DR, early PRP reduced the risk of progression to\nhigh-risk proliferative retinopathy by 50% [180]. The DRS and\nETDRS findings have been further reinforced by subsequent\nclinical trials [58]. The adverse effects of PRP include difficulty\nwith light\u2013dark adaptation (25%), a small decrease in visual\nacuity (10%), and peripheral visual loss (5%), which may impair\nnight vision and affect driving [58]. Other adverse effects\ninclude changes in color vision and worsening of macular\nedema [58]. Both DRS and ETDRS indicate that less severe\nstages of DR may not benefit from laser treatment, especially\ngiven the risk of adverse effects.\nIn the ETDRS, macular laser reduced the risk of moderate visual loss from clinically significant macular edema by\n50% [181]. The Diabetic Retinopathy Clinical Research Network\n(DRCRnet) showed that about 30% of patients treated with\nmacular laser gained better vision (\u226510 letters) over a 2-year\nperiod [182]. As these studies included a mixture of patients\nwith focal or diffuse macular edema, the relative efficacy of\nlaser treatment for specific patterns of macular edema remains\nundetermined.\n\n\f900\n\nChapter 61\n\nTable 61.4 Summary of treatments for diabetic retinopathy\n\nIntervention\n\nRecommendation\n\nEvidence\n\nDiabetic macular edema (DME)\nFocal laser\n\nFocal laser therapy is recommended in eyes with CSME and has long-term visual acuity benefits.\nTreatment should be considered to DME threatening the center of the macula.\n\nA, I\n\nIntravitreal anti-VEGF agents\n\nIntravitreal anti-VEGF therapy is effective as primary treatment for most cases of DME and is\nsuperior in the short term to laser treatment for visual acuity again. It is recommended for center\ninvolving DME with loss of vision secondary to DME.\n\nA, I\n\nIntravitreal steroids\n\nIntravitreal steroids are not effective as primary treatment for most cases of DME, but may have a\nrole in diffuse DME unresponsive to focal laser.\n\nA, II\n\nVitrectomy\n\nVitrectomy may have a role in selected cases of diffuse severe DME unresponsive to focal laser,\nespecially in the presence of vitreomacular traction.\n\nB, III\n\nMedical therapies\n\nThere is currently insufficient evidence to recommend the routine use of PKC inhibitors and other\ntreatments.\n\nC, III\n\nPRP is recommended in cases with proliferative DR. Treatment should be promptly institutes if\nhigh-risk features are present.\n\nA, I\n\nPRP is recommended in severe nonproliferative DR if any difficulty or delay in follow-up is\nanticipated or there are associated risk factors or signs of progression, especially in patients with\ntype 2 diabetes.\n\nA, II\n\nEarly vitrectomy is recommended within 3 months in patients with type 1 diabetes with\nsevere vitreous hemorrhage and significant DR. Type 2 diabetics benefit from vitrectomy for\npersistent vitreous hemorrhage, although the benefit of early vitrectomy is less.\nVitrectomy should be considered in eyes with severe PDR not responsive to extensive\nPRP, associated with traction involving the macula, or both.\n\nB, II\n\nDiabetic retinopathy (DR)\nPanretinal photocoagulation (PRP)\n\nVitrectomy\n\nIntraocular antivascular endothelial growth\nfactor (VEGF) agents\nVEGF is a potent mediator for abnormal retinal vessel growth\nand leakage, making it an important therapeutic target in\ndiabetic retinopathy [94]. Intraocular VEGF levels correlate\nclosely with hypoxia and active neovascularization, and its levels\ndecline after successful laser photocoagulation [95]. In addition,\ninhibitors of VEGF activity ameliorate ischemia-induced retinal\nneovascularization in animal models [94,96]. These findings all\nsupport the theory that anti-VEGF agents could arrest, or even\nreverse, proliferative retinopathy and macular edema.\nSeveral agents have been evaluated in clinical trials of\nanti-VEGF therapy. These agents are delivered by injection\ndirectly into the vitreous of the eye (intravitreal injection),\nthus theoretically maximizing local efficacy and minimizing\nsystemic adverse effects. The two most widely used anti-VEGF\nagents are ranibizumab, a humanized, monoclonal VEGF\nantibody fragment and bevacizumab, a humanized monoclonal\nantibody to VEGF. Newer agents are being developed including\nafibercept, a soluble decoy receptor fusion protein that binds\nVEGF. Most trials have demonstrated benefits with the use\nof intravitreal anti-VEGF agents, either alone or combined\nwith laser or intravitreal corticosteroids, for both diabetic\nmacular edema (DME) and proliferative retinopathy or as an\nadjunctive therapy for vitrectomy. The RISE and RIDE trial, two\n\nphase 3 randomized trials assessing ranibizumab for diabetic\nmacular edema found that a significantly greater proportion of\npatients receiving either 0.3 mg or 0.5 mg ranibizumab (33.6%\nto 45.7%) gained 15 letters or more in best corrected visual\nacuity compared with sham injection (12.3 to 18.1%) at 2 years,\ndemonstrating a rapid and sustained improvement in vision\nwith reduced risk of further vision loss and improved macular\nedema from ranibizumab with low rates of ocular and nonocular harm [183]. The RESTORE trial reported a 12-month\nvisual acuity improvement of 6.1 letters in patients treated with\nranibizumab plus sham laser and 5.9 letters in ranibizumab\ncombined with laser therapy compared with 0.8 letters in laser\nplus sham injection [184]. The Diabetic Retinopathy Clinical\nResearch Network (DRCRnet) demonstrated that patients\ntreated with ranibizumab plus prompt laser or deferred laser\nhad significantly better visual outcomes (9 +/\u2212 12 letter gain)\nat 1 year compared with those treated with sham injections\nplus prompt laser (3 +/\u2212 13 letter gain), and this difference\nwas maintained at 3-year follow-up [185,186]. The FDA has\napproved monthly 0.3 mg ranibizumab intravitreal injections\nfor DME. An expert panel recommended that ranibizumab\nwas indicated in the treatment of DME when both center\ninvolvement and significant visual loss (20/40 or worse) due\nto DME were present [187]. The off-label use of bevacizumab\nin DME is common due to its lower cost. The DRCRnet group\n\n\fDiabetic retinopathy and other ocular complications\n\nexamined the use of bevacizumab for DME in a phase 2 clinical\ntrial and found that subjects who received bevacizumab alone\nhad greater visual improvement compared with laser alone.\nThe combination of bevacizumab with laser had no short-term\nbenefit compared with bevacizumab alone [188]. The BOLT\nstudy compared bevacizumab with laser in DME patients with\nvisual acuity of 20/40 to 20/320 and found at 2 years that the\nbevacizumab arm had a median gain of 9 letters compare with a\n2.5 letter gain in the laser arm [189]. A recent systematic review\nexamining the relative clinical effectiveness of ranibizumab\nand bevacizumab in DME found no statistically significant\ndifference in the improvement in best corrected visual acuity\n(BCVA) of more than two lines, the mean change in best\ncorrected visual acuity or the mean change in central macular\nthickness between the two drugs [190]. The role of combination\ntherapy with both anti-VEGF injections and laser remains to\nbe defined. In the", "doc_id": "1c5b9eea-db2e-4318-a7a2-38f286084db0", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "1b31d1b8-d8df-44fc-be7d-647707405c28", "node_info": {"start": 0, "end": 7135}}, "2048946003246905004": {"text": "both anti-VEGF injections and laser remains to\nbe defined. In the current trials, no additional benefit has been\nshown with adding laser to ranibizumab. The RESTORE and\nDRCRnet trials may suggest that combination therapy may have\ninferior visual acuity outcomes compared with ranibizumab\ninjection alone. The DA VINCI study, a phase 2 clinical trial\nof Afibercept in eyes with center-involved DME, found that\nvarious regimens of afibercept at 52 weeks resulted in a 9\u201313\nletters gain in BCVA compared with a 1.3 letter loss of BCVA\nin eyes treated with laser. This benefit was also seen in the\ngroup given 8 weekly treatments after 3 initial doses suggesting\nthat less frequent treatments may be required given the longer\nhalf-life of Afibercept [191].\nOcular and systemic safety of intraocular\nanti-VEGF therapy\nAlthough anti-VEGF therapy has promising clinical application\nin the management of diabetic retinopathy, its long-term safety\nin patients with diabetes has not yet been established [94].\nLocal adverse effects of intravitreal anti-VEGF therapy include\ncataract formation, retinal detachment, vitreous hemorrhage,\ninfection, and potential loss of neural retinal cells [94].\nAlthough injected intravitreally, significant levels of antiVEGF agents injected may pass into the systemic circulation\n[94,192]. Thus, systemic inhibition of angiogenesis is a potential\nrisk, which could compromise critical vascular responses to\nischemic events in patients with diabetes. Other unwanted\nsystemic side effects may include hypertension, proteinuria,\nand impaired wound healing [94], which are also of relevant\nconcern for patients with diabetes. Prolonged systemic exposure\nto anti-VEGF agents, due to the lengthy half-life of some agents\nand the need for repeated administration, may be associated\nwith higher risks of systemic vascular complications, such as\nstroke and nonocular (e.g. gastric, renal) hemorrhage [192,193].\nAlthough clinical trials on the use of intravitreal anti-VEGF\ntherapy for treatment of age-related macular degeneration\ngenerally show low (0.6\u20131.2%) incidence of stroke [194],\npatients with DR may be at higher risk due to pre-existing\ndiabetes-related vascular disease [16]. A systematic review of\n\n901\n\nstudies examining the use of anti-VEGF therapy in DME found\nno consistent increase in adverse events with either ranibizumab\nor bevacizumab although these trials were underpowered to\ndetect differences in adverse events [190]. Meta-analysis of\ncombined data from all ranibizumab trials of patients receiving\nmonthly injections showed that the incidence of cerebrovascular accidents was 2.2% in the ranibizumab-treated subjects\nversus 0.7% in sham-treated subjects (p = 0.045) [195]. It\nhas been suggested that ranibizumab may have a lower risk\nadverse effects compared to bevacizumab due to its shorter\nsystemic half-life. The comparison in the age-related macular\ndegeneration treatment trials found that the proportion of\nserious systemic adverse events was higher with bevacizumab\nthan with ranibizumab (24.1% vs. 19.0%; RR = 1.29; 95%\nCI 1.01\u20131.66) [196]. A safety review and meta-analysis of\nbevacizumab and ranibizumab found that the proportion of\npatients with serious infections and gastrointestinal disorders\nwas higher with bevacizumab than with ranibizumab (RR = 1.3;\n95% CI 1.0\u20131.7), although arterial thromboembolic events were\nequally distributed among the groups [197]. Thus, treatment\nof DR with these agents must involve both clinicians and\npatients recognizing and assessing the potential risks and\nbenefits.\nIntraocular steroids\nInflammation has been shown to play an important role in\nthe pathogenesis of diabetic retinopathy [106]. Although\nintraocular administration of corticosteroids has been widely\nused to treat diabetic macular edema [182,198,199], there has\nbeen ongoing debate regarding its use due to the potential\nside effects. A systematic review of seven randomized clinical trials involving 632 eyes with diabetic macular edema\nsuggests that eyes treated with intravitreal triamcinolone, a\nlong-acting corticosteroid, had modest improvement in visual\nacuity [198].\nThe DRCRnet conducted a multicenter randomized clinical\ntrial in the US that compared intravitreal triamcinolone with\nmacular laser for treating diabetic macular edema [182]. Eyes\ntreated with intravitreal triamcinolone demonstrated a better\ntreatment response compared with eyes treated with laser at\n4 months. However, this difference disappeared after 1 year\nand by 2 years, eyes treated with laser had significantly better\nvision than eyes treated with intravitreal triamcinolone. These\nfindings remained unchanged after 3 years of follow-up [200].\nIntravitreal triamcinolone was also found to be frequently\nassociated with significant ocular adverse effects, including\nsecondary raised intraocular pressure and cataract progression\n[182,200].\nThe DRCRnet did not address the role of intravitreal triamcinolone in eyes that do not respond well to laser (diffuse or\nrefractory diabetic macular edema). A recent systematic review\nreported that while intravitreal triamcinolone improves vision\nin eyes with refractory diabetic macular edema in the short term\n(3 months), the benefits are not long-lasting [199]. Nevertheless,\n\n\f902\n\nChapter 61\n\nintravitreal triamcinolone may have a role as an adjunctive therapy to laser [201].\nA trial on sustained release steroid implants showed some\nefficacy in improving visual acuity in eyes with DME [198].\nLong-acting dexamethasone implants have shown improvement in vision for DME in vitrectomized eyes and for patients\nwith persistent DME. The adverse effects may be less frequent\nthan seen with triamcinolone but there were still a significant\nnumber of eyes developing raised intraocular pressure requiring\nmedical treatment [202]. Sustained delivery of fluocinolone\nacetonide vitreous inserts has also been shown to provide sustained improvement in visual acuity in patients with persistent\nDME for up 3 years compared with sham injections, although\nthere was an increased incidence of cataract in phakic patients\nand glaucoma requiring incisional surgery in the fluocinolone\nimplant groups [203].\nSurgical intervention\nVitrectomy is the surgical treatment for blinding complications\nof advanced retinopathy including persistent vitreous hemorrhage, tractional retinal detachment, and persistent macular\nedema with vitreous traction. It can reduce the risk of retinal\nneovascularization and macular edema but conversely may\nincite harm by increasing the risk of iris neovascularization and\ncataract formation [204].\nThe Diabetic Retinopathy Vitrectomy Study (DRVS) was the\nlargest randomized clinical trial that evaluated the indications\nand timing of vitrectomy for the management of advanced\nproliferative retinopathy [205,206]. In the DRVS, patients\nwith T1DM with severe vitreous hemorrhage were more likely\nto achieve desirable visual outcome (visual acuity 20/40) if\nearly vitrectomy was performed (within 1 to 6 months), as\ncompared to late vitrectomy (at 1 year). However, this benefit\nwas not observed in patients with T2DM. This could have been\nrelated to more frequent macular ischemia in patients with\nT2DM. Although data from the DRVS are still valuable for\nclinical guidance, the threshold for performing vitrectomy has\nlowered in recent years due to advances in vitreoretinal surgery,\nincluding smaller gauge", "doc_id": "55e695b9-4ad8-4813-8fe1-cf323f60291c", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "d9311b33-2ba4-4634-b709-8cac96e621c5", "node_info": {"start": 0, "end": 7401}}, "3981769359824014436": {"text": "due to advances in vitreoretinal surgery,\nincluding smaller gauge instruments and the ability to apply\nretinal laser during surgery [58].\nVitrectomy has also been suggested for diabetic macular\nedema refractory to laser therapy, particularly if there is\nevidence of macular traction (e.g. vitreomacular traction,\nepiretinal membrane, tractional retinal detachment close to the\nmacula) [204]. A few trials have demonstrated some benefits\nof vitrectomy combined with peeling of the internal limiting\nmembrane, the innermost layer of the retina, for diffuse or\nrefractory diabetic macular edema [58].\nCataract surgery\nPeople with diabetes have a higher risk of developing cataract\nrequiring surgery [1]. However, cataract surgery may exacerbate\nmacular edema [207], and retinopathy progression [208,209].\n\nThus, laser treatment for patients with DR prior to or promptly\nafter cataract surgery may be useful. Clinical trials also suggest\nthat intravitreal anti-VEGF agents during cataract surgery may\nbe an effective adjunctive therapy to optimize visual outcome\nafter surgery in selected cases [210,211].\n\nOther ocular complications\nDiabetic retinopathy may be the major cause of visual loss in diabetic patients; however, diabetes is also associated with a range\nof ocular disease which can also cause visual impairment and\nmorbidity.\nCataract\nMultiple studies have shown the association between cataracts\nand diabetes [212,213]. The prevalence of cataract is increased\nin persons with diabetes and the risk of cataract increases\nwith longer duration of diabetes and poorer metabolic control.\nDeposition of advanced glycation end-products in the lens has\nbeen postulated as one possible mechanism for diabetic cataract.\nCataract is a major cause of visual impairment in persons with\ndiabetes. Although the overall outcome with cataract surgery\nis excellent, persons with diabetes have poorer visual outcomes\ncompared with nondiabetic subjects after cataract surgery\nespecially in eyes with pre-existing macular edema or proliferative DR [1]. Studies have also suggested that individuals with\ndiabetes are at greater risk of postoperative endophthalmitis, a\nsevere potentially blinding intraocular infection [214].\nRefractive error\nDiabetic subjects can present with fluctuating refractive error.\nThis is due to accumulation of sorbitol in the lens as a result\nof hyperglycemia and increased aldose reductase activity. This\nresults in lens swelling with change in refractive error which may\nfluctuate with improved glycemic control [215].\nOptic disc\nAnterior ischemic optic neuropathy (AION) is an ischemic\nvascular condition involving the optic nerve head which\npresents with acute, monocular, painless visual loss with optic\ndisc swelling. Diabetic microvascular disease is postulated to\ncontribute to the ischemia and up to 25% of patients with AION\nhave a history of diabetes [216].\nDiabetic papillopathy presents with mild visual loss and optic\nnerve swelling which should be distinguished from other causes\nof disc swelling such as papilledema and malignant hypertension. Diabetic papillopathy is a risk factor for progression of DR\nand may precede the development of AION [1].\nOcular motility disorders\nDiabetes can cause mononeuropathies involving the third,\nfourth, or sixth cranial nerves, and is responsible for 25\u201330% of\n\n\f", "doc_id": "ad89a6b7-c13a-47f6-b0f5-21722774c681", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "41bbb4a8-f66f-42af-9cf3-0eacf4e66cfd", "node_info": {"start": 0, "end": 3332}}, "308619061275110203": {"text": "#!/usr/bin/env python3\n\n- Credits\n\t- Section Writer: Dr. Om J Lakhani\n\t- Section Editor: Dr. Om J Lakhani\n\t\n> Download the new \"Notes in Endocrinology\" App\n> Apple iOS- https://shrtm.nu/H45n\n> Android - https://shrtm.nu/SyBG\n\n- Q. At what stage does macular edema occur in diabetes?\n\t- Macular edema can occur at any stage\n- Q. What is  Diabetic macular edema  ?\n\t- Diabetic macular edema (DME) is the accumulation of excess fluid in the extracellular space within the retina in the macular area, typically in the inner nuclear, outer plexiform, Henle\u2019s fiber layer, and subretinal space.\n- Q. What is the pathophysiology of  Diabetic macular edema  ?\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2F9-BPuKACLv.png?alt=media&token=741f89c6-4274-486e-81bf-6d2a3360baa2)\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FzhTiwLevCy.png?alt=media&token=0764bd49-a782-44d9-bef6-33d762db68dd)\n- Q. What are the clinical features of  Diabetic macular edema ?\n\t-  Diabetic macular edema  involving the fovea can cause blurred vision and metamorphopsia (a syndrome in which the shape of objects appears distorted)\n\t- This can eventually lead to moderate to severe visual loss \n\t- However in some patients it can be asymptomatic\n- Q. What are the two most important clinical signs of macular edema?\n\t- 1. Hard exudates\n\t- 2. Retinal thickening\n- Q. What exactly are   Hard exudates  ?\n\t- Hard exudates are lipoprotein residues of serous leakage from damaged vessels, seen as biomarkers for diabetic macular edema (DME). They are typically seen in various patterns, including circinate rings and focal aggregations of exudates\n- Q. What are the various patterns of retinal thickening in diabetic macular edema?\n\t- The various patterns of retinal thickening in diabetic macular edema (DME) include focal leakage from microaneurysms or capillaries, diffuse poorly demarcated areas of capillary leakage, disorganization of the retinal inner layers (DRIL), external limiting membrane (ELM) and ellipsoid zone (EZ) disruption, and vitreomacular interface abnormalities (VMIA) such as vitreomacular adhesion (VMA), vitreomacular traction (VMT), and the epiretinal membrane (ERM)\n- Q. What is the difference in terms of treatment of focal leakage versus diffuse capillary leakage in  Diabetic macular edema ?\n\t- The treatment of focal leakage in diabetic macular edema involves laser photocoagulation, which involves burning the affected area to reduce the leakage. \n\t- The treatment of diffuse capillary leakage involves pan-retinal photocoagulation, which involves burning the peripheral retina to reduce the leakage\n- Q. What are the risk factors for  Diabetic macular edema ?\n\t- 1. High HbA1c\n\t- 2. Hypertension\n\t- 3. Dyslipidemia\n\t- 4. Impaired renal function\n\t- 5. use of  Pioglitazone  and other thiazolidinediones\n- Q. Apart from the usual, what other treatment can be given to prevent  Diabetic macular edema  from developing?\n\t- In patients with  NPDR (Non-proliferative diabetic retinopathy) - the use of Anti-VEGF injections is known to prevent the development of  Diabetic macular edema \n- Q. How is macular edema visualized?\n\t- Fluorescein angiography\n\t- Optical coherence tomography- OCT\n\t- Fundus with stereoscopic vision\n- Q. What is the definition of CSME?\n\t- Retinal thickening within 500 microns from the fovea\n\t- Hard exudate within 500 microns from the fovea\n\t- Retinal thicking of 1500 microns area within 1 disc diameter from the fovea\n- Q. What is the name of this criteria?\n\t- Modified Airlie house criteria\n- Q. What is Wilkinson\u2019s classification of DME?\n\t- Mild- exudates near posterior pole but far from the macula\n\t- Moderate- approaching the macula\n\t- Severe \u2013 involving the macula\n- Q. What is the use of Fluorescein angiography?\n\t- Fluorescein angiography confirms the diagnosis of ME\n\t- It also defines the area of ischemia which guides laser therapy\n- Q. What does the thickness mapping in OCT designate?\n\t- Thick areas designate capillary leakage\n\t- It correlates with loss of visual acuity\n- \n- **Role of  Optical Coherence Tomography (OCT)  in  Diabetic macular edema **\n- Q.  What is OCT?\n\t- It is a non-invasive test that gives a cross-section of the retina\n- Q. What technology does it use?\n\t- It uses a concept called interferometry to create a cross-section of retina of 10-15 microns in size\n- Q. What is the main use of this?\n\t- The main use of OCT is to see macular lesions in the retina\n\t- Macula is better to the image compared to the periphery of the retina\n- Q. Which are the conditions for which OCT is used?\n\t- Macular hole\n\t- Macular pucker/epiretinal membrane\n\t- Vitreomacular traction\n\t- Macular edema and exudates\n\t- Detachments of the neurosensory retina\n\t- Detachments of the retinal pigment epithelium (e.g. central serous retinopathy or age-related macular degeneration)\n\t- Retinoschisis\n\t- Pachychoroid\n\t- Choroidal tumors\n- Q. Where is it gaining popularity?\n\t- OCT is gaining popularity in the evaluation of optic nerve disorders\n- Q. What is the main disadvantage of OCT?\n\t- OCT uses light instead of sound which is used in ultrasound\n\t- Hence the media needs to be clear for proper OCT imaging\n\t- So it cannot be used if the patient has a cataract\n- Q. What are the layers of the retina seen on the OCT?\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2Fz5lEappxzK.png?alt=media&token=5ecb7329-541c-4795-9278-24e848d5dcea)\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FnGuxgV9Dhb.png?alt=media&token=73e2d4d9-6e40-441a-b1ba-03f1e3c5855b)\n- Q. What does the following OCT show?\n\t-", "doc_id": "c4d84b25-3c14-4f41-8563-bf26abf7a878", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "71d04a7d-ea90-4f35-964b-55af3a16fbb1", "node_info": {"start": 0, "end": 5789}}, "7250525322904209556": {"text": "Q. What does the following OCT show?\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FI7HBzO-Ozy.png?alt=media&token=85e24814-7fe5-4da2-a808-25af193a6094)\n\t- This is an image of a classic  Diabetic macular edema \n\t- There is cystoid intraretinal fluid collection in the outer plexiform layer of the retina\n- Q. What is the use of OCT in  glaucoma ?\n\t- OCT is very useful for the assessment of optic nerve for glaucoma\n\t- It measures the nerve fiber layer thickness and cup-to-disc ratio\n\t- it compares this to normal personal data\n\t- This helps to track the optic nerve edema\n- Q. What is the difference between the terms Cystoid macular edema,  Diabetic macular edema , and  Clinically significant macular edema ?\n\t- Cystoid macular edema refers to macular edema due to any cause\n\t-  Diabetic macular edema  refers to CME due to Diabetes\n\t-  Clinically significant macular edema  refers to macular edema due to diabetes which fulfills the ETDRS criteria\n- Q. What is the ETDRS criteria for  Clinically significant macular edema  ?\n\t- Retinal thickening within 500 um of the fovea\n\t- Hard exudates within 500 um of the fovea with associated retinal thickening\n\t- Retina thickening greater than 1 disc area which is located within 1 disc diameter of the fovea\n- Q. Do the OCT measurements correlate with vision in patients with  Diabetic macular edema ?\n\t- There is a correlation but it is generally poor to modest\n\t- Studies have shown that eyes with disorganization of the retinal inner layers (DRIL) have a worse baseline and final visual acuity despite anti-VEGF injections and that the resolution of DRIL has resulted in better visual outcomes\n- Q. What is the center involving DME and non-center involving DME based on OCT?\n\t- Center Involving DME: Diabetic Macular Edema (DME) that involves the central subfield zone (1 mm in diameter) as seen on OCT. This type of DME is associated with worse baseline and final visual acuity and is characterized by focal leakage from microaneurysms or capillaries. It is also associated with a lower rate of complete resolution of DME, with 40% of eyes still showing persistent DME after two years of treatment.\n\t- Non-Center Involving DME: Diabetic Macular Edema (DME) that does not involve the central subfield zone (1 mm in diameter) as seen on OCT. This type of DME is associated with disorganization of the retinal inner layers (DRIL), external limiting membrane (ELM) and ellipsoid zone (EZ) disruption, and vitreomacular interface abnormalities (VMIA)\n- Q. What is DRIL?\n\t- DRIL stands for Disorganization of the Retinal Inner Layers. It is an OCT biomarker for DME and is identified on OCT when there is disruption of the demarcating interface lines between the ganglion cell-inner plexiform complex (GCL-IPL), inner nuclear layer (INL), outer plexiform layer (OPL), and outer nuclear layer (ONL). \n\t- Eyes with DRIL have a worse baseline and final visual acuity despite anti-Vascular Endothelial Growth Factor (VEGF) injections and have almost eight times greater risk for poor visual recovery.\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FxcvSknn64e.png?alt=media&token=d11381f3-90cc-4079-9605-4c0b22bc3625)\n- Q. What is the role of Fluorescein angiography in  Diabetic macular edema ?\n\t- Fluorescein angiography is a diagnostic imaging technique used to assess the blood vessels in the retina. \n\t- It can be used to detect and diagnose diabetic macular edema by identifying areas of leakage and abnormal blood vessel growth. \n\t- It can also be used to monitor the progression of the disease and the effectiveness of treatments.\n\t- it is mainly used at present to guide laser therapy\n\t- Its application is gradually reducing with the advent of the use of OCT \n- Q. Tell me more about Fluorescein angiography.\n\t- Fluorescein angiography is a diagnostic imaging technique used to detect and monitor diabetic retinopathy. \n\t- It involves injecting a fluorescent dye into the bloodstream, which is then absorbed by the retinal blood vessels. \n\t- The dye is then illuminated with a special light source, allowing the blood vessels to be visualized and any abnormalities to be identified. \n\t- This technique can be used to detect early signs of diabetic retinopathy, such as microaneurysms, and to monitor the progression of the disease.\n\t- ![](https://firebasestorage.googleapis.com/v0/b/firescript-577a2.appspot.com/o/imgs%2Fapp%2FMedical_learning%2FS5ZOG3J5In.png?alt=media&token=2a0d63f3-8b09-46fc-a175-c482f26cc9d3)\n- **Management of Diabetic macular edema**\n- Q. What is the first line therapy for  Diabetic macular edema ?\n\t- Anti-VEGF agents are the first line therapy for  Diabetic macular edema \n- Q. Which are the various anti-VEGF agents used in  Diabetic macular edema ?\n\t- The various anti-VEGF agents used in Diabetic macular edema include bevacizumab, ranibizumab, and the Port Delivery System with Ranibizumab.\n- Q. What is the DRCR retina network algorithm for Anti-VEGF therapy in  DME?\n\t- The DRCR Retina Network anti-VEGF treatment algorithm recommends six monthly injections, unless the visual acuity is 20/20 or better and the central subfield thickness is <320\u03bcm for men or <305\u03bcm for women on the Heidelberg Spectralis, in which case treatment may be withheld starting the fourth month. \n\t- If there is evidence of stability over the previous two or more visits, further treatment may be withheld.\n- Q. What is the advantage of Aflibercept over other anti-VEGF agents?\n\t- The advantage of Aflibercept over other anti-VEGF agents is that it has a longer half-life, which may require less frequent treatments. Additionally, it has been shown to result in a 9-13 letter gain in BCVA compared with a 1.3 letter loss of BCVA in eyes treated with laser\n- Q. What is the role of intravitreal steroids DME?\n\t- The role of intravitreal steroids in DME is to improve vision and decrease retinal thickness, as there is an inflammatory component to DME. Steroids have powerful anti-edematous and anti-inflammatory effects as they decrease several pro-inflammatory mediators (IL-6, IL-8, TNF-\u03b1, MCP-1, ICAM-1, VEGF, etc.). However, long-term results have not shown the maintenance of these effects.\n- Q. What is the role of laser photocoagulation in DME?\n\t- Laser photocoagulation is a treatment option for diabetic macular edema (DME). It is used to reduce the amount of fluid in the macula, which can help improve vision. \n\t- Laser photocoagulation can be used as a primary treatment for DME or as an adjunct to anti-VEGF therapy. \n\t- It is most effective when used in combination with anti-VEGF therapy, as it can help reduce", "doc_id": "dee644af-63d0-4c96-804b-29b6e2b09890", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "e5d71b5a-dc95-4707-ac8c-f485c1b0136b", "node_info": {"start": 0, "end": 6720}}, "3159958672870783788": {"text": "effective when used in combination with anti-VEGF therapy, as it can help reduce the number of injections needed. \n\t- Laser photocoagulation can also be used to treat persistent DME that does not respond to anti-VEGF therapy.\n- Q. What kind of laser is used for Focal and diffuse CSME?\n\t- Focal laser and grid laser are used as an adjuvant for Focal and diffuse CSME respectively\n- Q. What is the role of surgery for DME?\n\t- Surgery is not typically recommended as a first-line treatment for diabetic macular edema (DME). \n\t- However, in cases where medical therapy and pharmacotherapy have not been successful in resolving the DME, vitrectomy surgery may be considered. \n\t- Vitrectomy surgery involves removing the vitreous gel from the eye and peeling away the epiretinal membrane, which can help to reduce macular edema and improve vision.\n\t\n\n", "doc_id": "62d8d832-ddfa-4da1-a734-5216631c9e0c", "embedding": null, "extra_info": null, "index": 0, "child_indices": [], "ref_doc_id": "6f8ece36-5ecb-4dda-b4be-6aa7058d5641", "node_info": {"start": 0, "end": 846}}}, "id_map": {"d08d4fd4-df27-4861-b98f-2475ea12cb86": 3738475026862369325, "307f5592-3736-40e9-a413-210d920531c4": 5409451774554091213, "5d3ec436-0c2d-4c36-ad48-8e6ddc6d4728": 4392219367997839596, "369c98cb-40ee-4ac4-9e1d-3c80d6399481": 2232762506725266668, "0300187f-e8cc-4451-8e48-3a207b9ac7e8": 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