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The risk of depression, anxiety, and suicidal behavior in patients with obesity on glucagon like peptide-1 receptor agonist therapy.

Sci Rep · 2024

Last updated 2026-05-28

A study of 162,253 patients with obesity compared those taking GLP-1 drugs like Liraglutide and Semaglutide to those not taking them. It found that patients on GLP-1 drugs had nearly double the risk of developing psychiatric disorders, including a 195% higher risk of major depression, a 108% higher risk of anxiety, and a 106% higher risk of suicidal behavior.

AI summary of the abstract below.

JournalSci Rep, 2024
Citations89
Relative citation ratio21.29
NIH percentile99
Molecules
Conditions studied Obesity, Depression, Anxiety

Abstract

This large community-based cohort study investigates the impact of glucagon-like peptide-1 receptor agonists (GLP-1 RAs), specifically Liraglutide and Semaglutide, on the risk of developing psychiatric conditions such as depression, anxiety, and suicidal behaviors in patients with obesity. Utilizing post-marketing data, this research compares patients prescribed GLP-1 RAs (cases) with those not taking these medications (controls). The analysis spanned data from January 1, 2015, to December 31, 2023. To minimize selection bias, we employed 1:1 propensity score matching to account for demographic factors such as age, sex, race, and comorbidities. After matching, the study included 162,253 case and control patients. This study showed a significant association between GLP-1 RA treatment and an 98% increased risk of any psychiatric disorders. Notably, patients on GLP-1 RAs exhibited a 195% higher risk of major depression, a 108% increased risk for anxiety, and a 106% elevated risk for suicidal behavior. These findings underscore the critical need for physicians to thoroughly assess patient history before prescribing GLP-1 RAs and highlight the urgent requirement for further prospective clinical trials to fully understand the implications of GLP-1 RA use on mental health in the obese patient population.

Verbatim abstract via PubMed 39424950 ↗