Association between glucagon‐like peptide‐1 receptor agonists and risk of suicidality: A comprehensive analysis of the global pharmacovigilance database

Author:

Kim Tae Hyeon12,Lee Kyeongmin23,Park Seoyoung24,Cho Hanseul12,Park Jaeyu23,Jo Hyesu23,Son Yejun24,Kim Soeun24,Kang Jiseung56,Smith Lee7,Rahmati Masoud8910,Fond Guillaume8,Boyer Laurent8,Pizzol Damiano1112,Lee Hayeon2,Rhee Sang Youl123413ORCID,Hwang Jiyoung2,Sang Hyunji213,Yon Dong Keon123414ORCID

Affiliation:

1. Department of Medicine Kyung Hee University College of Medicine Seoul South Korea

2. Centre for Digital Health, Medical Science Research Institute, Kyung Hee University Medical Centre Kyung Hee University College of Medicine Seoul South Korea

3. Department of Regulatory Science Kyung Hee University Seoul South Korea

4. Department of Precision Medicine Kyung Hee University College of Medicine Seoul South Korea

5. Division of Sleep Medicine Harvard Medical School Boston Massachusetts USA

6. Department of Anaesthesia, Critical Care and Pain Medicine Massachusetts General Hospital Boston Massachusetts USA

7. Centre for Health, Performance and Wellbeing Anglia Ruskin University Cambridge UK

8. CEReSS‐Health Service Research and Quality of Life Centre, Assistance Publique‐Hôpitaux de Marseille Aix‐Marseille University Marseille France

9. Department of Physical Education and Sport Sciences, Faculty of Literature and Human Sciences Lorestan University Khoramabad Iran

10. Department of Physical Education and Sport Sciences, Faculty of Literature and Humanities Vali‐E‐Asr University of Rafsanjan Rafsanjan Iran

11. Health Unit Eni Maputo Mozambique

12. Health Unit, Eni San Donato Milanese Italy

13. Department of Endocrinology and Metabolism Kyung Hee University College of Medicine Seoul South Korea

14. Department of Paediatrics, Kyung Hee University Medical Centre Kyung Hee University College of Medicine Seoul South Korea

Abstract

AbstractAimTo evaluate the potential association between suicidality and glucagon‐like peptide‐1 receptor agonists (GLP‐1RAs), as well as other medications used for obesity and diabetes, using comprehensive global data.Materials and MethodsThis study utilized the World Health Organization's pharmacovigilance database, encompassing adverse drug reaction reports from 1967 to 2023, from 170 countries (total reports, N = 131 255 418). We present the reported odds ratios (RORs) with 95% confidence intervals (CIs) and information component (IC) with IC025 regarding the association between GLP‐1RA use and suicidality.ResultsAlthough reports of GLP‐1RA‐associated suicidality increased gradually from 2005 to 2023 (n = 332), no evidence of an association was observed (ROR 0.15 [95% CI 0.13 to 0.16]; IC −2.77 [IC025 −2.95]). The lack of evidence of an association persisted regardless of whether GLP‐1RAs were used for diabetes treatment (ROR 0.13 [95% CI 0.11 to 0.14]; IC −2.95 [IC025 −3.14]) or obesity treatment (ROR 0.44 [95% CI 0.34 to 0.58]; IC −1.16 [IC025 −1.62]). However, an association was found between suicidality and other diabetes medications excluding GLP‐1RAs (ROR 1.13 [95% CI 1.10 to 1.15]; IC 0.17 [IC025 0.13]). Similarly, the potential association with suicidality was observed in medications used to treat obesity excluding GLP‐1RAs (ROR 1.08 [95% CI 1.01 to 1.14]; IC 0.10 [IC025 0.01]).ConclusionsThe suspected association between GLP‐1RA use and suicidality, as raised by the European Medicines Agency, was not found in our global analysis. This indicates that the sporadic reports of GLP‐1RA‐associated suicidality are likely influenced by factors such as comorbidities present in the GLP‐1RA user population.

Funder

National Research Foundation of Korea

Publisher

Wiley

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