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Impact of GLP-1 Receptor Agonists on Suicide Behavior: A Meta-Analysis Based on Randomized Controlled Trials
Jingqi Chen1, Qiufeng Zhang1, Qingping Wu1
1The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine), Hangzhou, China.
Background:
This meta-analysis aims to assess the association between exposure to glucagon-like peptide-1 receptor agonists (GLP-1 RAs) and the incidence of suicidal behavior in patients with type 2 diabetes mellitus (T2DM)/obesity.
Methods:
A comprehensive search of electronic databases, including PubMed, Web of Science, the Cochrane Library, and ClinicalTrials.gov, was conducted from the inception of the databases. The risk ratio (RR) and 95% confidence intervals (95% CI) were calculated.
Results:
This meta-analysis included data from 25 randomized controlled trials (RCTs). The results indicated no significant difference in the incidence of suicidal behavior between the GLP-1 RA exposure group and the control group (RR = 0.84, 95% CI: 0.54-1.32, p = 0.46, I2 = 0%). Subgroup analysis showed no significant differences in the incidence of suicidal behavior among participants with T2DM (RR = 0.74), obesity (RR = 1.07), adolescents (RR = 0.91), and adults (RR = 0.84). Additionally, no significant differences were observed between the two groups in any type of suicidal behavior, including suicidal ideation (RR = 1.04), suicide attempts (RR = 0.68), depression-related suicides (RR = 0.65), and completed suicides (RR = 1.06). There were also no significant differences between the groups for any type of GLP-1 RA, including dulaglutide (RR = 0.46), exenatide (RR = 0.98), semaglutide (RR = 0.82), lixisenatide (RR = 1.25), and liraglutide (RR = 0.92). No significant differences were observed between the exposure group and control group according to different comparators, including placebo (RR = 0.91) and others (RR = 1.08). All subgroup analyses showed p-values greater than 0.05 (two-sided tests) and I2 values of 0%.
Conclusion:
Our findings suggest that there is no significant association between GLP-1 RA exposure and suicidal behaviors in patients with T2DM or obesity.
Insights
Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) show no significant association with suicidal behavior in patients with type 2 diabetes mellitus (T2DM) or obesity. This meta-analysis of 25 RCTs found no increased risk across various subgroups and GLP-1 RA types.
Area of Science:
- Endocrinology
- Psychiatry
- Pharmacovigilance
Background:
- Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) are widely used for managing type 2 diabetes mellitus (T2DM) and obesity.
- Concerns have been raised regarding potential associations between GLP-1 RA use and suicidal behavior.
- Robust evidence is needed to clarify this risk.
Purpose of the Study:
- To conduct a meta-analysis assessing the association between GLP-1 RA exposure and suicidal behavior incidence.
- To evaluate this association in patient populations with T2DM and/or obesity.
Main Methods:
- A comprehensive literature search was performed across major electronic databases (PubMed, Web of Science, Cochrane Library, ClinicalTrials.gov).
- Data from 25 randomized controlled trials (RCTs) were included.
- Risk ratios (RR) and 95% confidence intervals (95% CI) were calculated to quantify the association.
Main Results:
- The overall meta-analysis revealed no significant difference in suicidal behavior incidence between GLP-1 RA and control groups (RR = 0.84, 95% CI: 0.54-1.32, p = 0.46).
- Subgroup analyses stratified by condition (T2DM, obesity), age (adolescents, adults), specific GLP-1 RAs, and comparator (placebo) also showed no significant associations.
- No significant differences were observed for specific types of suicidal behavior, including ideation, attempts, depression-related suicides, and completed suicides.
Conclusions:
- The findings suggest that GLP-1 RA use is not significantly associated with an increased risk of suicidal behavior in patients with T2DM or obesity.
- The results provide reassurance regarding the safety profile of GLP-1 RAs concerning suicidal behavior.
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