Glucagon-like peptide 1 (GLP-1) receptor agonists as a protective factor for incident depression in patients with diabetes mellitus: A systematic review

杜拉鲁肽 医学 胰高血糖素样肽1受体 神经保护 心理信息 艾塞那肽 糖尿病 内科学 萧条(经济学) 兴奋剂 抗抑郁药 药理学 内分泌学 生物信息学 受体 2型糖尿病 梅德林 生物 海马体 经济 宏观经济学 生物化学
作者
Daniel Cooper,Ranuk Ramachandra,Felicia Ceban,Joshua D. Di Vincenzo,Taeho Greg Rhee,Rodrigo B. Mansur,Kayla M. Teopiz,Hartej Gill,Roger Ho,Bing Cao,Leanna M.W. Lui,Muhammad Youshay Jawad,Juliet Arsenault,Gia Han Le,Diluk Ramachandra,Ziji Guo,Roger S. McIntyre
出处
期刊:Journal of Psychiatric Research [Elsevier BV]
卷期号:164: 80-89 被引量:24
标识
DOI:10.1016/j.jpsychires.2023.05.041
摘要

Glucagon-like peptide 1 (GLP-1) receptor agonists are widely used for glycemic control in patients with diabetes mellitus (DM) and are primarily indicated for type 2 diabetes mellitus (T2DM). GLP-1 receptor agonists have also been shown to have neuroprotective and antidepressant properties. Replicated evidence suggests that individuals with DM are significantly more likely to develop depression. Herein, we aim to investigate whether GLP-1 receptor agonists can be used prophylactically on patients with DM to lower the risk of incident depression. We conducted a systematic search for English-language articles published on the PubMed/MEDLINE, Scopus, Embase, APA, PsycInfo, Ovid and Google Scholar databases from inception to June 6, 2022. Four retrospective observational studies were identified that evaluated the neuroprotective effects of GLP-1 receptor agonists on incident depression in patients with DM. We found mixed results with regards to lowering the risk of incident depression, with two studies demonstrating a significant reduction in risk and two studies showing no such effect. A single study found that dulaglutide may lower susceptibility to depression. Our results were limited by high interstudy heterogeneity, paucity of literature, and lack of controlled trials. While we did not find evidence of GLP-1 receptor agonists significantly lowering risk of incident depression in patients with DM, promising neuroprotective data presented in two of the included papers, specifically on dulaglutide where information is scarce, provide the impetus for further investigation. Future research should focus on better elucidating the neuroprotective potential of different classes and doses of GLP-1 receptor agonists using controlled trials.
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