GLP-1 receptor agonists and the path to sustainable obesity care

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dc.contributor.author Manne-Goehler, Jennifer
dc.contributor.author Teufel, Felix
dc.contributor.author Venter, Willem Daniel Francois
dc.date.accessioned 2024-11-12T05:52:04Z
dc.date.available 2024-11-12T05:52:04Z
dc.date.issued 2024-10
dc.description.abstract As of 2024, more than 1 billion people are estimated to be living with obesity worldwide. The glucagon-like peptide-1 receptor agonist (GLP-1RA) and closely related glucose-dependent insulinotropic polypeptide (GIP/GLP-1) dual agonist medication classes offer a promising strategy to treat obesity and prevent its downstream health complications. However, the optimal use of these medications is currently hindered by many unanswered questions, ranging from how best to select the optimal patients for treatment to their long-term effects to how to manage their costs. Among these is an increasingly urgent concern about the coverage and optimal treatment duration of GLP-1RAs at obesity dosing and evidence-based approaches to off-ramping, defined as the tapering or withdrawal of a GLP-1RA after this treatment period and its replacement by an alternative approach to weight maintenance. en_US
dc.description.department School of Health Systems and Public Health (SHSPH) en_US
dc.description.librarian hj2024 en_US
dc.description.sdg SDG-03:Good heatlh and well-being en_US
dc.description.sponsorship The National Institute of Diabetes and Digestive and Kidney Diseases; the Bill & Melinda Gates Foundation, South African Medical Research Council, National Institutes of Health, Unitaid, Foundation for Innovative New Diagnostics (FIND), Merck, and the Children’s Investment Fund Foundation (CIFF); previously receiving funding from US Agency for International Development; and receiving drug donations from ViiV Healthcare, Merck, Johnson & Johnson, and Gilead Sciences for investigator-led clinical studies to his institution; participating in commercial drug studies (including antiobesity medications) for Merck and Novo Nordisk; and receiving honoraria for educational talks and advisory board membership from Gilead Sciences, ViiV Healthcare, Mylan/Viatris, Merck, Adcock Ingram, Aspen, Abbott, Roche, Johnson & Johnson, Sanofi, Boehringer Ingelheim, Thermo Fisher Scientific, and Virology Education. en_US
dc.description.uri https://jamanetwork.com/journals/jamainternalmedicine/ en_US
dc.identifier.citation Manne-Goehler, J., Teufel, F. & Venter, W.D.F. GLP-1 Receptor Agonists and the Path to Sustainable Obesity Care. JAMA Intern Med. Published online October 14, 2024. doi: 10.1001/jamainternmed.2024.3579. en_US
dc.identifier.issn 2168-6106 (print)
dc.identifier.issn 2168-6114 (online)
dc.identifier.other 10.1001/jamainternmed.2024.3579
dc.identifier.uri http://hdl.handle.net/2263/99014
dc.language.iso en en_US
dc.publisher American Medical Association en_US
dc.rights © 2024 American Medical Association. All rights reserved. en_US
dc.subject Obesity en_US
dc.subject Glucagon-like peptide-1 receptor agonist (GLP-1RA) en_US
dc.subject Glucose-dependent insulinotropic polypeptide (GIP/GLP-1) en_US
dc.subject Health complications en_US
dc.subject SDG-03: Good health and well-being en_US
dc.subject Viewpoint en_US
dc.title GLP-1 receptor agonists and the path to sustainable obesity care en_US
dc.type Postprint Article en_US


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