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Association of GLP-1 Receptor Agonists with Intentional Self-Harm in Patients with Type 2 Diabetes: A Sentinel Distributed Database Study

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    The U.S. Food and Drug Administration (FDA) investigated the potential risk of suicidal ideation and behaviors for glucagon-like peptide 1 receptor agonists (GLP-1 RAs) on learning of post-marketing reports of suicidal ideation and behaviors in patients taking GLP-1 RAs. This study assessed a potential association with intentional self-harm comparing GLP-1 RAs to other antidiabetic products.

    We conducted an active-comparator, new-user cohort study—using FDA’s Sentinel System—with data from October 1, 2015, to September 30, 2023. The study included health plan members ≥18 years old diagnosed with type 2 diabetes, newly initiated GLP-1 RAs (n=1,161,983), sodium-glucose cotransporter-2 inhibitors (SGLT-2is, n=1,081,155), or dipeptidyl peptidase-4 inhibitors (DPP-4is, n=1,396,382), and continuously enrolled in a health plan with medical and drug coverage for ≥183 days. The main outcome was intentional self-harm. We estimated hazard ratios (HR) and 95% confidence intervals (CI) for intentional self-harm events and used inverse probability of treatment weighting of propensity scores to control for confounding.

    Author(s)

    Aida Kuzucan, Van Tran, Jamal T. Jones, Sarah K. Dutcher, Meg Her, Maria E. Kempner, Joo-Yeon Lee, Andrew Mosholder, Katherine E. Round, Sengwee Toh, Jennifer G. Lyons

    Corresponding Author

    Jamal T. Jones; U.S. Food and Drug Administration, Silver Spring, Maryland, USA

    Email: Jamal.Jones@fda.hhs.gov