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

Sci Rep. 2024 Oct 18;14(1):24433. doi: 10.1038/s41598-024-75965-2.

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.

Keywords: Anxiety; Depression; GLP-1 RA; Obesity; Suicidal behavior.

MeSH terms

  • Adult
  • Aged
  • Anxiety* / epidemiology
  • Cohort Studies
  • Depression* / drug therapy
  • Depression* / epidemiology
  • Female
  • Glucagon-Like Peptide-1 Receptor Agonists*
  • Glucagon-Like Peptides / adverse effects
  • Glucagon-Like Peptides / therapeutic use
  • Humans
  • Hypoglycemic Agents / adverse effects
  • Hypoglycemic Agents / therapeutic use
  • Liraglutide* / therapeutic use
  • Male
  • Middle Aged
  • Obesity* / epidemiology
  • Risk Factors

Substances

  • Liraglutide
  • semaglutide
  • Glucagon-Like Peptides
  • Hypoglycemic Agents
  • Glucagon-Like Peptide-1 Receptor Agonists