Antiinflammatory actions of glucagon-like peptide-1–based therapies beyond metabolic benefits
Therapies based on glucagon-like peptide-1 (GLP-1) reduce rates of cardiovascular and chronic kidney disease in people with type 2 diabetes and/or obesity, with ongoing clinical trials investigating their effects in people with metabolic liver disease, arthritis, and both substance use and neurodegenerative disorders. Acute and chronic activation of GLP-1 receptor signaling also reduces systemic and tissue inflammation in mice and humans, through weight loss-dependent and -independent mechanisms, actions that may contribute to the expanding spectrum of clinical benefits ascribed to GLP-1 medicines. In this Review, we highlight current understanding of the direct and indirect antiinflammatory effects and mechanisms of GLP-1 medicines in both preclinical and clinical studies, covering emerging concepts, clinical relevance, and areas of uncertainty that require further investigation.
Authors
- Chi Kin Wong (ORCID: https://orcid.org/0000-0003-4828-8413)
- Daniel J. Drucker
Institutions
- University of Toronto (CA)
- Lunenfeld-Tanenbaum Research Institute (CA)
- Sinai Health System (CA)
Publication Details
- Journal
- Journal of Clinical Investigation
- Published
- 2025-11-02
- DOI
- https://doi.org/10.1172/jci194751
- Citations
- 19
- Primary Topic
- Diabetes Treatment and Management
- Type
- article
- Field-Weighted Citation Impact
- 24.60
Funders
- Amgen
- Eli Lilly and Company
- Pfizer
- Diabetes Canada
- Novo Nordisk
- Canadian Institutes of Health Research
- Banting and Best Diabetes Centre, University of Toronto