The role of incretin receptor agonists in the treatment of obesity.

dual co‐agonists incretins obesity semaglutide tirzepatide

Journal

Diabetes, obesity & metabolism
ISSN: 1463-1326
Titre abrégé: Diabetes Obes Metab
Pays: England
ID NLM: 100883645

Informations de publication

Date de publication:
29 Jul 2024
Historique:
revised: 28 06 2024
received: 03 05 2024
accepted: 29 06 2024
medline: 29 7 2024
pubmed: 29 7 2024
entrez: 29 7 2024
Statut: aheadofprint

Résumé

Obesity and its associated metabolic conditions have become a significant global health problem in recent years, with many people living with obesity fulfilling criteria for pharmacological treatment. The development of the glucagon-like peptide-1 receptor agonists for chronic weight management has triggered new interest in the incretins and other hormones as targets for obesity, and investigations into dual and triple co-agonists. The objective of this narrative review was to summarize the available data on approved and emerging incretin-based agents for the treatment of obesity. In clinical trials of currently available agents in people with overweight or obesity, weight loss of between 6% and 21% of baseline body weight has been observed, with between 23% and 94% of participants achieving 10% or higher weight loss, depending on the study and the agent used. Favourable outcomes have also been seen with regard to cardiovascular risk and outcomes, diabetes prevention, metabolic dysfunction-associated steatotic liver disease/steatohepatitis and prevention of weight regain after metabolic surgery. Limitations associated with these agents include high costs, the potential for weight regain once treatment is stopped, the potential loss of lean body mass and gastrointestinal adverse events; potential issues with respect to gallbladder and biliary diseases require further investigation. Many dual and triple co-agonists are still in development, and more data are needed to assess the efficacy, safety and tolerability of these emerging therapies versus the established incretin-based therapies; however, data are promising, and further results are eagerly awaited.

Identifiants

pubmed: 39072877
doi: 10.1111/dom.15796
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Clinical Research Services, Grenadiesrstrasse 1, 68167 Mannheim, Germany

Informations de copyright

© 2024 The Author(s). Diabetes, Obesity and Metabolism published by John Wiley & Sons Ltd.

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Auteurs

Thomas Forst (T)

CRS Clinical Research Services GmbH, Mannheim, Germany.

Christophe De Block (C)

Antwerp University Hospital and University of Antwerp, Antwerp, Belgium.

Stefano Del Prato (S)

Interdisciplinary Research Center "Health Science," Sant'Anna School of Advanced Studies, Pisa, Italy.

Sara Armani (S)

CRS Clinical Research Services GmbH, Mannheim, Germany.

Juan Frias (J)

Biomea Fusion, Redwood City, California, USA.

Anne Lautenbach (A)

University Medical-Center Hamburg-Eppendorf, Hamburg, Germany.

Bernhard Ludvik (B)

Landstrasse Clinic and Karl Landsteiner Institute for Obesity and Metabolic Disorders, Vienna, Austria.

Marina Marinez (M)

CRS Clinical Research Services GmbH, Mannheim, Germany.

Chantal Mathieu (C)

Department of Endocrinology, KU Leuven, Leuven, Belgium.

Timo D Müller (TD)

Institute for Diabetes and Obesity, Helmholtz Diabetes Center, Helmholtz Munich, Neuherberg, Germany.
German Center for Diabetes Research (DZD), Neuherberg, Germany.
Walther-Straub Institute of Pharmacology and Toxicology, Ludwig-Maximilians-Universität München (LMU), Munich, Germany.

Oliver Schnell (O)

Forschergruppe Diabetes e.V. at the Helmholtz Center Munich, Munich, Germany.

Classifications MeSH