Laurence Aoun , Shaza Almardini , Fares Saliba , Fadi Haddadin , Omar Mourad , Jennifer Jdaidani , Zeina Morcos , Ibrahim Al Saidi , Elie Bou Sanayeh , Saliba Saliba , Michel Almardini , Julie Zaidan
{"title":"GLP-1 受体激动剂:治疗暴食症(暴食症和贪食症)的新型药物疗法?系统综述","authors":"Laurence Aoun , Shaza Almardini , Fares Saliba , Fadi Haddadin , Omar Mourad , Jennifer Jdaidani , Zeina Morcos , Ibrahim Al Saidi , Elie Bou Sanayeh , Saliba Saliba , Michel Almardini , Julie Zaidan","doi":"10.1016/j.jcte.2024.100333","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><p>Systematically review evidence on using GLP-1RAs for reducing BEB in BED and BN.</p></div><div><h3>Methods</h3><p>Comprehensive literature search (PubMed and Google Scholar) conducted for studies evaluating GLP-1Ras for BEB. Extracted data on study characteristics, efficacy, and safety.</p></div><div><h3>Results</h3><p>Studies show that GLP-1RAs (liraglutide and dulaglutide) reduce BE frequency and comorbidities in addition to favorable psychiatric side effect profile compared to current options. However, large-scale, blinded placebo-controlled trials are lacking.</p></div><div><h3>Conclusion</h3><p>Early findings suggest promising effects of GLP-1RAs on BEB. However, rigorous clinical trials are needed to firmly establish efficacy, dosing, safety, and comparative effectiveness before considering GLP-1RAs a viable novel approach.</p></div>","PeriodicalId":46328,"journal":{"name":"Journal of Clinical and Translational Endocrinology","volume":"35 ","pages":"Article 100333"},"PeriodicalIF":4.2000,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214623724000048/pdfft?md5=c4acfc67aff009fa931f433ff8458828&pid=1-s2.0-S2214623724000048-main.pdf","citationCount":"0","resultStr":"{\"title\":\"GLP-1 receptor agonists: A novel pharmacotherapy for binge eating (Binge eating disorder and bulimia nervosa)? A systematic review\",\"authors\":\"Laurence Aoun , Shaza Almardini , Fares Saliba , Fadi Haddadin , Omar Mourad , Jennifer Jdaidani , Zeina Morcos , Ibrahim Al Saidi , Elie Bou Sanayeh , Saliba Saliba , Michel Almardini , Julie Zaidan\",\"doi\":\"10.1016/j.jcte.2024.100333\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><p>Systematically review evidence on using GLP-1RAs for reducing BEB in BED and BN.</p></div><div><h3>Methods</h3><p>Comprehensive literature search (PubMed and Google Scholar) conducted for studies evaluating GLP-1Ras for BEB. Extracted data on study characteristics, efficacy, and safety.</p></div><div><h3>Results</h3><p>Studies show that GLP-1RAs (liraglutide and dulaglutide) reduce BE frequency and comorbidities in addition to favorable psychiatric side effect profile compared to current options. However, large-scale, blinded placebo-controlled trials are lacking.</p></div><div><h3>Conclusion</h3><p>Early findings suggest promising effects of GLP-1RAs on BEB. However, rigorous clinical trials are needed to firmly establish efficacy, dosing, safety, and comparative effectiveness before considering GLP-1RAs a viable novel approach.</p></div>\",\"PeriodicalId\":46328,\"journal\":{\"name\":\"Journal of Clinical and Translational Endocrinology\",\"volume\":\"35 \",\"pages\":\"Article 100333\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2024-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2214623724000048/pdfft?md5=c4acfc67aff009fa931f433ff8458828&pid=1-s2.0-S2214623724000048-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Clinical and Translational Endocrinology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2214623724000048\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENDOCRINOLOGY & METABOLISM\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical and Translational Endocrinology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214623724000048","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
GLP-1 receptor agonists: A novel pharmacotherapy for binge eating (Binge eating disorder and bulimia nervosa)? A systematic review
Objective
Systematically review evidence on using GLP-1RAs for reducing BEB in BED and BN.
Methods
Comprehensive literature search (PubMed and Google Scholar) conducted for studies evaluating GLP-1Ras for BEB. Extracted data on study characteristics, efficacy, and safety.
Results
Studies show that GLP-1RAs (liraglutide and dulaglutide) reduce BE frequency and comorbidities in addition to favorable psychiatric side effect profile compared to current options. However, large-scale, blinded placebo-controlled trials are lacking.
Conclusion
Early findings suggest promising effects of GLP-1RAs on BEB. However, rigorous clinical trials are needed to firmly establish efficacy, dosing, safety, and comparative effectiveness before considering GLP-1RAs a viable novel approach.