Evidence map›Paper›PMID 41850718›Full record

ArticleBMJ open diabetes research & care2026

Association of GLP-1 receptor agonists with intentional self-harm in patients with type 2 diabetes: a Sentinel Distributed Database study.

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 and 1 more

Abstract read
In one paragraph

Article in BMJ open diabetes research & care, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Aida KuzucanFormerly at U.S. Food and Drug Administration, Silver Spring, Maryland, USA.
Van TranU.S. Food and Drug Administration, Silver Spring, Maryland, USA.
Jamal T JonesU.S. Food and Drug Administration, Silver Spring, Maryland, USA Jamal.Jones@fda.hhs.gov.ORCID http://orcid.org/0000-0002-2709-0806
Sarah K DutcherU.S. Food and Drug Administration, Silver Spring, Maryland, USA.
Meg HerHarvard Pilgrim Health Care Institute LLC, Boston, Massachusetts, USA.
Maria E KempnerHarvard Pilgrim Health Care Institute LLC, Boston, Massachusetts, USA.
Joo-Yeon LeeU.S. Food and Drug Administration, Silver Spring, Maryland, USA.
Andrew MosholderFormerly at U.S. Food and Drug Administration, Silver Spring, Maryland, USA.ORCID http://orcid.org/0000-0001-7821-8067
Katherine E RoundHarvard Pilgrim Health Care Institute LLC, Boston, Massachusetts, USA.
Sengwee TohHarvard Medical School, Boston, Massachusetts, USA.
Jennifer G LyonsHarvard Medical School, Boston, Massachusetts, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe 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. RESEARCH DESIGN AND

methodsWe 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.

resultsThe comparator groups had a mean age that was slightly above 60 years and similar percentages of males and females. Adjusted incidence rates of intentional self-harm per 1000 person-years were 1.13 for GLP-1 RAs, 1.22 for SGLT-2is, and 1.37 for DPP-4is. Adjusted HRs indicated no increased risk of intentional self-harm comparing GLP-1 RAs to SGLT-2is (HR 0.93; 95% CI 0.81 to 1.08) or DPP-4is (HR 0.94; 95% CI 0.82 to 1.07). Subgroup analyses by comorbid obesity and diabetes, psychiatric history, prior intentional self-harm, age, and sex yielded similar results.

conclusionsThe use of GLP-1 RAs did not show increased risk of intentional self-harm compared with SGLT-2is or DPP-4is, which provides some reassurance regarding the safety of GLP-1 RA use in patients with type 2 diabetes.

Indexed as

Diabetes Mellitus, Type 2Glucagon-Like Peptide-1 Receptor AgonistsHypoglycemic AgentsSelf-Injurious BehaviorAdultAgedDatabases, FactualDipeptidyl-Peptidase IV InhibitorsFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisSodium-Glucose Transporter 2 InhibitorsUnited StatesDipeptidyl-Peptidase IV InhibitorsGlucagon-Like Peptide-1 Receptor AgonistsHypoglycemic AgentsSodium-Glucose Transporter 2 InhibitorsDiabetes Mellitus, Type 2EpidemiologyGlucagon-Like Peptide 1Pharmacoepidemiology

Identifiers

PMID41850718
PMCPMC13007165

What Socratic holds

Textmetadata
LicenceCC BY-NC
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.