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Dulaglutide and neurodegeneration biomarkers: REWIND post hoc analysis.

Alzheimers Dement · 2026

Last updated 2026-05-28

In a study of 7,368 people, those taking dulaglutide did not show overall changes in brain-related biomarkers or cognitive decline compared to placebo. However, participants with high levels of a biomarker called NfL (56 pg/mL or more) saw a 27.4% reduction in NfL after 2 years with dulaglutide, compared to a 14.2% reduction with placebo. Additionally, those with high levels of another biomarker, p-tau217 (25 pg/mL or more), had a 22% lower risk of cognitive decline with dulaglutide.

AI summary of the abstract below.

JournalAlzheimers Dement, 2026
Citations0
Molecules dulaglutide
Conditions studied Alzheimers

Abstract

INTRODUCTION: This post hoc analysis of the Researching Cardiovascular Events with a Weekly Incretin in Diabetes (REWIND) trial examined associations between dulaglutide, Alzheimer's disease and related dementia (ADRD) biomarkers, and substantive cognitive impairment (SCI). METHODS: Participants (dulaglutide, n = 3741; placebo, n = 3627) completed cognitive tests and provided blood samples at baseline and 2 years, with additional cognitive tests at 5-year and final visits. Analysis of covariance and Cox models tested associations between dulaglutide, SCI, and plasma neurofilament light chain (NfL), phosphorylated tau217 (p-tau217), and glial fibrillary acidic protein (GFAP) biomarkers. RESULTS: Dulaglutide-associated changes in biomarkers or SCI were nonsignificant overall. Participants with NfL ≥56 pg/mL had a dulaglutide-associated 2-year reduction in NfL (-27.4% vs -14.2%; p = 0.003). Participants with p-tau217 ≥25 pg/mL had a dulaglutide-associated SCI reduction (hazard ratio = 0.78; p = 0.0064). DISCUSSION: Dulaglutide reduced NfL and SCI in participants with select elevated plasma ADRD biomarkers, with limited 2-year effects on p-tau217 and GFAP. Future studies with longer follow-up should explore incretin-related cognitive changes. CLINICAL TRIAL REGISTRATION INFORMATION: NCT01394952, registered July 15, 2011.

Verbatim abstract via PubMed 41988866 ↗

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