Glucagon-like peptide-1 receptor agonists (GLP-1 RAs) and suicidality: A replication study using reports to the World Health Organization pharmacovigilance database (VigiBase®).

IF 4.9 2区 医学 Q1 CLINICAL NEUROLOGY
Journal of affective disorders Pub Date : 2025-01-15 Epub Date: 2024-10-19 DOI:10.1016/j.jad.2024.10.062
Roger S McIntyre, Rodrigo B Mansur, Joshua D Rosenblat, Taeho Greg Rhee, Bing Cao, Kayla M Teopiz, Sabrina Wong, Gia Han Le, Roger Ho, Angela T H Kwan
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引用次数: 0

Abstract

Introduction: Reports of suicidality associated with glucagon-like peptide 1 receptor agonists (GLP-1 RAs) have been reported to the European Medicines Agency (EMA) and the United States Food and Drug Administration (FDA). We previously reported an increased reporting odds ratio (ROR) of some measures of suicidality with semaglutide and liraglutide using the FDA Adverse Event Reporting System (FAERS). Notwithstanding the increased ROR, causality between GLP-1 RAs exposure and any aspect of suicidality is not established.

Research design and methods: The analysis herein aims to extend a previous analysis of the FAERS by evaluating the ROR for suicidality reported to the World Health Organization (WHO) Pharmacovigilance Database (VigiBase). We aimed to characterize the ROR of suicidality associated with GLP-1 RAs, as extrapolated from spontaneous reports. As per our previous report, the ROR was considered significant when the lower limit of the 95 % confidence (CI) was >1.0.

Results: We searched VigiBase reports from inception to January 2024. The RORs for suicidal ideation were significantly increased for semaglutide (5.82), liraglutide (4.03) and tirzepatide (2.25). For "depression/suicidal", the ROR was significantly increased for semaglutide (14.74) and liraglutide (5.86); and for suicidal behaviour, the ROR was significantly increased for semaglutide (6.52) and liraglutide (3.90). However, for suicide attempts, the ROR was significantly decreased for semaglutide (0.11), dulaglutide (0.075), exenatide (0.047) and liraglutide (0.15). For completed suicide, the ROR was also significantly decreased for semaglutide (0.01), dulaglutide (0.003), exenatide (0.002) and liraglutide (0.008).

Conclusion: Unlike our previous report with FAERS, a mixed pattern of ROR emerged in the WHO VigiBase with respect to suicidality and exposure to select GLP-RAs. Causation between GLP-1 RA exposure and suicidality (either increased or decreased) cannot be ascertained from ROR data.

胰高血糖素样肽-1受体激动剂(GLP-1 RAs)与自杀:一项利用世界卫生组织药物警戒数据库(VigiBase®)报告进行的重复研究。
导言:欧洲药品管理局(EMA)和美国食品和药物管理局(FDA)都收到过与胰高血糖素样肽1激动剂(GLP-1 RA)相关的自杀报告。我们以前曾报告过,使用 FDA 不良事件报告系统 (FAERS),服用塞马鲁肽和利拉鲁肽后,某些自杀行为的报告几率比 (ROR) 有所增加。尽管ROR有所增加,但GLP-1 RAs暴露与自杀的任何方面之间的因果关系尚未确定:本文的分析旨在通过评估向世界卫生组织(WHO)药物警戒数据库(VigiBase)报告的自杀率,扩展之前对食品药品管理局不良事件报告系统(FAERS)的分析。我们的目的是从自发报告中推断出与 GLP-1 RAs 相关的自杀率。根据我们之前的报告,当 95% 置信度 (CI) 的下限大于 1.0 时,ROR 被认为是显著的:我们检索了 VigiBase 从开始到 2024 年 1 月的报告。在 "自杀意念 "方面,semaglutide(5.82)、liraglutide(4.03)和tirzepatide(2.25)的ROR显著增加。在 "抑郁/自杀 "方面,塞马鲁肽(14.74)和利拉鲁肽(5.86)的ROR显著增加;在自杀行为方面,塞马鲁肽(6.52)和利拉鲁肽(3.90)的ROR显著增加。然而,在自杀未遂方面,塞马鲁肽(0.11)、度拉鲁肽(0.075)、艾塞那肽(0.047)和利拉鲁肽(0.15)的ROR明显下降。结论:与我们之前关于FAERS的报告不同的是,我们的研究结果表明,semaglutide(0.01)、dulaglutide(0.003)、exenatide(0.002)和liraglutide(0.008)的ROR显著降低:与我们之前关于FAERS的报告不同,在自杀和暴露于特定GLP-RA方面出现了混合的ROR模式。ROR数据无法确定GLP-1 RA暴露与自杀率(增加或减少)之间的因果关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of affective disorders
Journal of affective disorders 医学-精神病学
CiteScore
10.90
自引率
6.10%
发文量
1319
审稿时长
9.3 weeks
期刊介绍: The Journal of Affective Disorders publishes papers concerned with affective disorders in the widest sense: depression, mania, mood spectrum, emotions and personality, anxiety and stress. It is interdisciplinary and aims to bring together different approaches for a diverse readership. Top quality papers will be accepted dealing with any aspect of affective disorders, including neuroimaging, cognitive neurosciences, genetics, molecular biology, experimental and clinical neurosciences, pharmacology, neuroimmunoendocrinology, intervention and treatment trials.
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