Comparative dementia risk with GLP1 receptor agonists, SGLT2 inhibitors, or DPP4 inhibitors: a population-based cohort study
We aim to investigate comparative dementia risk associated with glucagon-like peptide-1 receptor agonists (GLP1-RAs), sodium-glucose cotransporter-2 inhibitors (SGLT2i), and dipeptidyl peptidase-4 inhibitors (DPP4i) in adults aged ≥ 60 years with type 2 diabetes. This target trial emulation cohort study used primary care electronic health records from the UK Clinical Practice Research Datalink. Initiators of GLP1-RAs, SGLT2i, or DPP4i aged ≥ 60 years with type 2 diabetes and without cognitive impairment were compared pairwise in three separate analyses. After propensity scores overlap weighting, 13,965 pairs of GLP1-RA versus DPP4i initiators (cohort entry: 2006–2022; mean age: 66.9 years), 25,533 pairs of SGLT2i versus DPP4i initiators (cohort entry: 2013–2022; mean age: 69.0 years), and 14,214 pairs of GLP1-RA versus SGLT2i initiators (cohort entry: 2013–2022; mean age: 67.9 years) were analyzed. The primary outcome was incident all-cause dementia. The primary analysis was an intention-to-treat analysis. A secondary as-treated analysis for continuous use was performed. In the intention-to-treat analysis, dementia risk was not different between GLP1-RA and DPP4i initiators (hazard ratio [HR] 0.95, 95% confidence interval [CI] 0.87–1.04; rates: 6.29 versus 6.64 per 1000 person-years; mean follow-up: 6.54 years); however, continuous GLP1-RA versus DPP4i use was associated with a 21% lower risk (HR 0.79, 95% CI 0.64–0.97; rates: 3.64 versus 4.82; mean follow-up: 2.71 years). SGLT2i versus DPP4i initiation was associated with a 14% lower dementia risk in the intention-to-treat analysis (HR 0.86, 95% CI 0.79–0.94; rates: 4.83 versus 5.60; mean follow-up: 4.91 years), and the as-treated analysis showed greater risk reduction (HR 0.70, 95% CI 0.60–0.82; rates: 3.82 versus 5.46; mean follow-up: 2.43 years). Dementia risk was comparable between GLP1-RA versus SGLT2i in both intention-to-treat (HR 0.98, 95% CI 0.87–1.11; rates: 4.85 versus 4.95; mean follow-up: 5.09 years) and as-treated (HR 1.07, 95% CI 0.85–1.36; rates: 3.71 versus 3.56; mean follow-up: 2.40 years) analyses. In people with type 2 diabetes aged ≥ 60 years, SGLT2i are associated with reduced dementia risk, but dementia risk reduction associated with the GLP1-RAs studied is less certain.
Authors
- Wajd Alkabbani (ORCID: https://orcid.org/0000-0002-7030-0442)
- Colleen J. Maxwell (ORCID: https://orcid.org/0000-0002-7988-2899)
- Che-Yuan Wu
- Jodi D. Edwards (ORCID: https://orcid.org/0000-0002-9275-4787)
- Moira K. Kapral (ORCID: https://orcid.org/0000-0002-3444-9928)
- Baiju R. Shah (ORCID: https://orcid.org/0000-0003-3598-3628)
- Walter Swardfager (ORCID: https://orcid.org/0000-0002-0030-8908)
Institutions
- Sunnybrook Health Science Centre (CA)
- University Health Network (CA)
- University of Waterloo (CA)
- University of Ottawa (CA)
- University of Toronto (CA)
- Toronto Rehabilitation Institute (CA)
- Toronto General Hospital (CA)
- Canada Research Chairs (CA)
- Ontario Brain Institute (CA)
- Sunnybrook Research Institute
Publication Details
- Journal
- Alzheimer s Research & Therapy
- Published
- 2025-12-20
- DOI
- https://doi.org/10.1186/s13195-025-01929-x
- Citations
- 1
- Primary Topic
- Diabetes Treatment and Management
- Type
- article
- Field-Weighted Citation Impact
- 1.29
Funders
- Alzheimer's Drug Discovery Foundation
- Canada Research Chairs
- University of Toronto
- Novo Nordisk
- Ministry of Colleges and Universities
- Canadian Institutes of Health Research
- Temerty Faculty of Medicine, University of Toronto