Changes in lean body mass with glucagon‐like peptide‐1‐based therapies and mitigation strategies

Author:

Neeland Ian J.12ORCID,Linge Jennifer34,Birkenfeld Andreas L.5678ORCID

Affiliation:

1. Department of Medicine Case Western Reserve University School of Medicine Cleveland Ohio USA

2. Division of Cardiovascular Medicine University Hospitals Harrington Heart and Vascular Institute, University Hospitals Cleveland Medical Center Cleveland Ohio USA

3. AMRA Medical AB Linköping Sweden

4. Division of Diagnostics and Specialist Medicine, Department of Health, Medicine and Caring Sciences Linköping University Linköping Sweden

5. Institute for Diabetes Research and Metabolic Diseases (IDM) of the Helmholtz Center Munich at the Eberhard Karls University Tübingen Tübingen Germany

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

7. Department of Diabetology, Endocrinology, and Nephrology University Clinic Tübingen, Eberhard Karls University Tübingen Tübingen Germany

8. Department of Diabetes, Life Sciences & Medicine Cardiovascular Medicine & Sciences Kings College London London UK

Abstract

AbstractWeight loss induced by glucagon‐like peptide‐1 receptor agonists (GLP‐1RAs) and dual glucagon‐like peptide‐1 receptor (GLP‐1R)/glucose‐dependent insulinotropic polypeptide receptor agonists is coming closer to the magnitudes achieved with surgery. However, with greater weight loss there is concern about potential side effects on muscle quantity (mass), health and function. There is heterogeneity in the reported effects of GLP‐1‐based therapies on lean mass changes in clinical trials: in some studies, reductions in lean mass range between 40% and 60% as a proportion of total weight lost, while other studies show lean mass reductions of approximately 15% or less of total weight lost. There are several potential reasons underlying this heterogeneity, including population, drug‐specific/molecular, and comorbidity effects. Furthermore, changes in lean mass may not always reflect changes in muscle mass as the former measure includes not only muscle but also organs, bone, fluids, and water in fat tissue. Based on contemporary evidence with the addition of magnetic resonance imaging‐based studies, skeletal muscle changes with GLP‐1RA treatments appear to be adaptive: reductions in muscle volume seem to be commensurate with what is expected given ageing, disease status, and weight loss achieved, and the improvement in insulin sensitivity and muscle fat infiltration likely contributes to an adaptive process with improved muscle quality, lowering the probability for loss in strength and function. Nevertheless, factors such as older age and severity of disease may influence the selection of appropriate candidates for these therapies due to risk of sarcopenia. To further improve muscle health during weight loss, several pharmacological treatments to maintain or improve muscle mass designed in combination with GLP‐1‐based therapies are under development. Future research on GLP‐1‐based and other therapies designed for weight loss should focus on more accurate and meaningful assessments of muscle mass, composition, as well as function, mobility or strength, to better define their impact on muscle health for the substantial number of patients who will likely be taking these medications well into the future.

Publisher

Wiley

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