Exploration of the potential association between GLP-1 receptor agonists and suicidal or self-injurious behaviors: a pharmacovigilance study based on the FDA Adverse Event Reporting System database.

FAERS database GLP-1RAs Obesity Pharmacovigilance Suicidal or self-injurious behaviors Type 2 diabetes

Journal

BMC medicine
ISSN: 1741-7015
Titre abrégé: BMC Med
Pays: England
ID NLM: 101190723

Informations de publication

Date de publication:
14 Feb 2024
Historique:
received: 18 08 2023
accepted: 25 01 2024
medline: 15 2 2024
pubmed: 15 2 2024
entrez: 14 2 2024
Statut: epublish

Résumé

Establishing whether there is a potential relationship between glucagon-like peptide 1 receptor agonists (GLP-1RAs) and suicidal or self-injurious behaviors (SSIBs) is crucial for public safety. This study investigated the potential association between GLP-1RAs and SSIBs by exploring the FDA Adverse Event Reporting System (FAERS) database. A disproportionality analysis was conducted using post-marketing data from the FAERS repository (2018 Q1 to 2022 Q4). SSIB cases associated with GLP-1RAs were identified and analyzed through disproportionality analysis using the information component. The parametric distribution with a goodness-of-fit test was employed to analyze the time-to-onset, and the Ω shrinkage was used to evaluate the potential effect of co-medication on the occurrence of SSIBs. In total, 204 cases of SSIBs associated with GLP-1RAs, including semaglutide, liraglutide, dulaglutide, exenatide, and albiglutide, were identified in the FAERS database. Time-of-onset analysis revealed no consistent mechanism for the latency of SSIBs in patients receiving GLP-1RAs. The disproportionality analysis did not indicate an association between GLP-1RAs and SSIBs. Co-medication analysis revealed 81 cases with antidepressants, antipsychotics, and benzodiazepines, which may be proxies of mental health comorbidities. We found no signal of disproportionate reporting of an association between GLP-1RA use and SSIBs. Clinicians need to maintain heightened vigilance on patients premedicated with neuropsychotropic drugs. This contributes to the greater acceptance of GLP-1RAs in patients with type 2 diabetes mellitus or obesity.

Sections du résumé

BACKGROUND BACKGROUND
Establishing whether there is a potential relationship between glucagon-like peptide 1 receptor agonists (GLP-1RAs) and suicidal or self-injurious behaviors (SSIBs) is crucial for public safety. This study investigated the potential association between GLP-1RAs and SSIBs by exploring the FDA Adverse Event Reporting System (FAERS) database.
METHODS METHODS
A disproportionality analysis was conducted using post-marketing data from the FAERS repository (2018 Q1 to 2022 Q4). SSIB cases associated with GLP-1RAs were identified and analyzed through disproportionality analysis using the information component. The parametric distribution with a goodness-of-fit test was employed to analyze the time-to-onset, and the Ω shrinkage was used to evaluate the potential effect of co-medication on the occurrence of SSIBs.
RESULTS RESULTS
In total, 204 cases of SSIBs associated with GLP-1RAs, including semaglutide, liraglutide, dulaglutide, exenatide, and albiglutide, were identified in the FAERS database. Time-of-onset analysis revealed no consistent mechanism for the latency of SSIBs in patients receiving GLP-1RAs. The disproportionality analysis did not indicate an association between GLP-1RAs and SSIBs. Co-medication analysis revealed 81 cases with antidepressants, antipsychotics, and benzodiazepines, which may be proxies of mental health comorbidities.
CONCLUSIONS CONCLUSIONS
We found no signal of disproportionate reporting of an association between GLP-1RA use and SSIBs. Clinicians need to maintain heightened vigilance on patients premedicated with neuropsychotropic drugs. This contributes to the greater acceptance of GLP-1RAs in patients with type 2 diabetes mellitus or obesity.

Identifiants

pubmed: 38355513
doi: 10.1186/s12916-024-03274-6
pii: 10.1186/s12916-024-03274-6
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

65

Informations de copyright

© 2024. The Author(s).

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Auteurs

Jianxing Zhou (J)

Department of Pharmacy, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.
School of Pharmacy, Fujian Medical University, Fuzhou, Fujian, China.

You Zheng (Y)

Department of Pharmacy, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.
School of Pharmacy, Fujian Medical University, Fuzhou, Fujian, China.

Baohua Xu (B)

Department of Pharmacy, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.
School of Pharmacy, Fujian Medical University, Fuzhou, Fujian, China.

Songjun Long (S)

School of Medical Imaging, Fujian Medical University, Fuzhou, Fujian, China.

Li-E Zhu (LE)

Department of Pharmacy, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.

Yunhui Liu (Y)

Department of Pharmacy, Fujian Medical University Union Hospital, Fuzhou, Fujian, China.

Chengliang Li (C)

Department of Respiratory, Shanghai Electric Power Hospital, Shanghai, China.

Yifan Zhang (Y)

Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.

Maobai Liu (M)

Department of Pharmacy, Fujian Medical University Union Hospital, Fuzhou, Fujian, China. liumb0591@fjmu.edu.cn.

Xuemei Wu (X)

Department of Pharmacy, Fujian Medical University Union Hospital, Fuzhou, Fujian, China. wuxuemei@fjmu.edu.cn.
School of Pharmacy, Fujian Medical University, Fuzhou, Fujian, China. wuxuemei@fjmu.edu.cn.

Classifications MeSH