The role of incretin receptor agonists in the treatment of obesity

Author:

Forst Thomas1ORCID,De Block Christophe2ORCID,Del Prato Stefano3ORCID,Armani Sara1ORCID,Frias Juan4ORCID,Lautenbach Anne5ORCID,Ludvik Bernhard6ORCID,Marinez Marina1,Mathieu Chantal7ORCID,Müller Timo D.8910ORCID,Schnell Oliver11ORCID

Affiliation:

1. CRS Clinical Research Services GmbH Mannheim Germany

2. Antwerp University Hospital and University of Antwerp Antwerp Belgium

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

4. Biomea Fusion Redwood City California USA

5. University Medical‐Center Hamburg‐Eppendorf Hamburg Germany

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

7. Department of Endocrinology KU Leuven Leuven Belgium

8. Institute for Diabetes and Obesity, Helmholtz Diabetes Center, Helmholtz Munich Neuherberg Germany

9. German Center for Diabetes Research (DZD) Neuherberg Germany

10. Walther‐Straub Institute of Pharmacology and Toxicology Ludwig‐Maximilians‐Universität München (LMU) Munich Germany

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

Abstract

AbstractIntrodroductionObesity 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.MethodsThe objective of this narrative review was to summarize the available data on approved and emerging incretin‐based agents for the treatment of obesity.ResultsIn 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.ConclusionsMany 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.

Publisher

Wiley

Reference151 articles.

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