Evidence map›Paper›PMID 41123870›Full record

ArticleDrug safety2026

Incretin-Based Drugs and the Risk of Dementia Among Patients with Type 2 Diabetes.

Yun-Han Wang, Kyle Johnson, Sarah Beradid, Hui Yin, Oriana H Y Yu, Samy Suissa, Laurent Azoulay, Christel Renoux

Abstract read
PubMed Publisher
In one paragraph

Article in Drug safety, 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

8 authors.

Yun-Han WangDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Canada.
Kyle JohnsonDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Canada.
Sarah BeradidCentre for Clinical Epidemiology, Lady Davis Institute for Medical Research, Jewish General Hospital, 3755 Côte Sainte Catherine H 416.1, Montreal, QC, H3T 1E2, Canada.
Hui YinCentre for Clinical Epidemiology, Lady Davis Institute for Medical Research, Jewish General Hospital, 3755 Côte Sainte Catherine H 416.1, Montreal, QC, H3T 1E2, Canada.
Oriana H Y YuCentre for Clinical Epidemiology, Lady Davis Institute for Medical Research, Jewish General Hospital, 3755 Côte Sainte Catherine H 416.1, Montreal, QC, H3T 1E2, Canada.
Samy SuissaDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Canada.
Laurent AzoulayDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Canada.
Christel RenouxDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Canada. christel.renoux@mcgill.ca.ORCID http://orcid.org/0000-0002-4691-9579

Funding

CIHR PJT-180357
6 · The paper itself

Abstract

backgroundIncretin-based drugs, namely glucagon-like peptide 1 receptor agonists (GLP-1 RAs) and dipeptidyl peptidase 4 (DPP-4) inhibitors, may have neuroprotective effects. Thus, we assessed whether these drugs are associated with a decreased risk of dementia among patients with type 2 diabetes.

methodsUsing the Clinical Practice Research Datalink from the UK, we formed two new user cohorts of patients at least 50 years of age with type 2 diabetes starting incretin-based drugs or sulfonylureas between 2007 and 2021. Hazard ratios (HRs) and 95% confidence intervals (CIs) for dementia were estimated separately for GLP-1 RAs and DPP-4 inhibitors using Cox proportional hazards models with propensity score fine-stratification weighting and inverse probability of censoring weights.

resultsAmong 275,144 initiators of DPP-4 inhibitors or sulfonylureas, followed for 750,846 person-years, DPP-4 inhibitors were associated with a reduced dementia risk compared with sulfonylureas (4.4 vs. 5.7 events per 1000 person-years; HR 0.77, 95% CI 0.71-0.85). HRs decreased with increasing cumulative duration of use and dose. Similar associations were observed across dementia subtypes and individual DPP-4 inhibitors molecules. Among 181,215 initiators of GLP-1 RAs or sulfonylureas, followed for 530,415 person-years, GLP-1 RAs were associated with a similar reduction in dementia risk compared with sulfonylureas, although with high uncertainty (2.3 vs. 3.1 events per 1000 person-years; HR 0.74, 95% CI 0.46-1.18). The magnitude of the association increased with cumulative duration of use and dose but with high uncertainty.

conclusionsIn this population-based study, DPP-4 inhibitors, and possibly GLP-1 RAs, were associated with a reduced dementia risk compared with sulfonylureas.

Indexed as

DementiaDiabetes Mellitus, Type 2Dipeptidyl-Peptidase IV InhibitorsHypoglycemic AgentsIncretinsAgedCohort StudiesFemaleGlucagon-Like Peptide-1 Receptor AgonistsHumansMaleMiddle AgedSulfonylurea CompoundsUnited KingdomDipeptidyl-Peptidase IV InhibitorsGlucagon-Like Peptide-1 Receptor AgonistsHypoglycemic AgentsIncretinsSulfonylurea Compounds

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.