GLP-1 receptor agonists for the treatment of alcohol use disorder.
J Clin Invest · 2025
Last updated 2026-05-28A study found that GLP-1 receptor agonists (like semaglutide), but not another diabetes drug class called DPP-4 inhibitors, were linked to reduced alcohol consumption in humans. The same effect was observed in animal tests, where GLP-1 drugs lowered alcohol intake, while DPP-4 drugs did not.
AI summary of the abstract below.
| Journal | J Clin Invest, 2025 |
|---|---|
| Citations | 5 |
| Relative citation ratio | 2.27 |
| Molecules | — |
| Conditions studied | Alcohol Use Disorder |
Abstract
Glucagon-like peptide-1 receptor agonists (GLP-1RAs), such as semaglutide, are widely used in the treatment of metabolic disorders, including type 2 diabetes (T2D) and obesity. These medications primarily function by enhancing insulin secretion; however, emerging evidence suggests that the effects extend beyond metabolic regulation. In this issue of the JCI, Farokhnia et al. evaluated the effects of GLP-1RAs alongside another T2D treatment, dipeptidyl peptidase-4 inhibitors (DPP-4Is), on alcohol consumption in humans and preclinical models. In humans, GLP1-RAs, but not DPP-4Is, were associated with reductions in alcohol consumption. Similarly, DPP-4 inhibition had no effect on alcohol intake in rodents. These findings invite further exploration of the mechanisms by which GLP-1RAs reduce alcohol consumption and redefine our pharmacotherapy approach to alcohol use disorder (AUD) by opening the possibility for application as an early harm-reduction tool.
Verbatim abstract via PubMed 40309769 ↗