Evidence map›Paper›PMID 42812740›Full record

ArticleNeurology. Genetics2026

Genetic Insights Into Protective Effects of GLP-1 Receptor Agonists on Stroke and Alzheimer Disease Across Ancestries.

Ilana Caro-Châtelier, Muralidharan Sargurupremraj, Chengran Yang, Callistus Akinleye, David-Alexandre Trégouët, Rufus Olusola Akinyemi, Daichi Shigemizu, Motunrayo Coker, Joshua O Akinyemi, Hemant K Tiwari and 13 more

Abstract read
In one paragraph

Article in Neurology. Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

23 authors.

Ilana Caro-ChâtelierBordeaux Population Health Research Center, Inserm, UMR U1219, Université de Bordeaux, France.ORCID https://orcid.org/0000-0003-3075-4682
Muralidharan SargurupremrajGlenn Biggs Institute for Alzheimer's and Neurodegenerative Diseases, University of Texas Health Sciences Center, San Antonio.ORCID https://orcid.org/0000-0003-1684-3750
Chengran YangDepartment of Psychiatry, Washington University School of Medicine, St. Louis, MO.ORCID https://orcid.org/0000-0003-4577-5590
Callistus AkinleyeOsun State University, Osogbo, Nigeria.ORCID https://orcid.org/0000-0003-3778-3638
David-Alexandre TrégouëtBordeaux Population Health Research Center, Inserm, UMR U1219, Université de Bordeaux, France.ORCID https://orcid.org/0000-0001-9084-7800
Rufus Olusola AkinyemiCenter for Genomic and Precision Medicine, University of Ibadan, Nigeria.ORCID https://orcid.org/0000-0001-5286-428X
Daichi ShigemizuMedical Genome Center, Research Institute, National Center for Geriatrics and Gerontology, Obu, Japan.ORCID https://orcid.org/0000-0002-4412-0552
Motunrayo CokerInstitute for Advanced Medical Research and Training, College of Medicine, University of Ibadan, Nigeria.ORCID https://orcid.org/0000-0003-4445-914X
Joshua O AkinyemiCenter for Genomic and Precision Medicine, University of Ibadan, Nigeria.ORCID https://orcid.org/0000-0002-0675-2110
Hemant K TiwariUniversity of Alabama at Birmingham.ORCID https://orcid.org/0000-0003-4016-1856
Daniel I ChasmanDivision of Preventive Medicine, Brigham and Women's Hospital, Boston, MA.ORCID https://orcid.org/0000-0003-3357-0862
Bruce OvbiageleUCSF Weill Institute for Neurosciences, School of Medicine, University of California San Francisco.ORCID https://orcid.org/0000-0002-9958-0644
Hugues ChabriatCentre Neurovasculaire Translationnel-CERVCO and Département de Neurologie, Hopital Lariboisiere, APHP, Université Paris-Cité and Brain Institute, Paris, France.ORCID https://orcid.org/0000-0001-8436-6074
Vincent MooserVictor Phillip Dahdaleh Institute of Genomic Medicine, McGill Genome Centre, McGill University Montréal, Québec, Canada.ORCID https://orcid.org/0000-0002-8632-0448
Thierry CouffinhalUniv. Bordeaux, INSERM, Biologie des maladies Cardiovasculaires, U1034, Pessac, France.ORCID https://orcid.org/0000-0002-9217-2533
Aniket MishraBordeaux Population Health Research Center, Inserm, UMR U1219, Université de Bordeaux, France.ORCID https://orcid.org/0000-0002-8141-1543
Carlos CruchagaDepartment of Psychiatry, Washington University School of Medicine, St. Louis, MO.ORCID https://orcid.org/0000-0002-0276-2899
Christiane ReitzGertrude H. Sergievsky Center, Taub Institute for Research on Alzheimer's Disease and the Aging Brain, Departments of Neurology and Epidemiology, Columbia University, New York, NY.
Brian KunkleThe John P. Hussman Institute for Human Genomics, University of Miami, FL.ORCID https://orcid.org/0000-0002-9515-5157
Yoichiro KamataniGraduate School of Frontier Sciences, The University of Tokyo, Japan.ORCID https://orcid.org/0000-0001-8748-5597
Mayowa Ojo OwolabiCenter for Genomic and Precision Medicine, University of Ibadan, Nigeria.ORCID https://orcid.org/0000-0003-1146-3070
Kamel MohammediUniv. Bordeaux, INSERM, Biologie des maladies Cardiovasculaires, U1034, Pessac, France.ORCID https://orcid.org/0000-0001-6139-1197
Stéphanie DebetteBordeaux Population Health Research Center, Inserm, UMR U1219, Université de Bordeaux, France.ORCID https://orcid.org/0000-0001-8675-7968

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Objectives: Stroke and dementia are leading causes of death and disability worldwide, requiring enhanced preventive strategies. Glucagon-like peptide-1 receptor agonists (GLP-1RA), widely used for type 2 diabetes (T2D) and obesity, have demonstrated pleiotropic effects, including cardiovascular benefits, with mounting evidence also suggesting potential beneficial effects on brain health. The objective of this study was to investigate the genetically proxied effect of GLP-1RA on stroke, Alzheimer disease (AD), and related endophenotypes, in a cross-ancestry setting. Methods: We conducted a 2-sample Mendelian randomization (MR) study using both a locus-based and a protein quantitative trait loci (pQTL)-based approach. The study leveraged summary statistics from large-scale genome-wide association studies (GWAS). These GWAS comprised participants of European, East-Asian, and African ancestry with and without T2D, stroke, and AD, and with measurements of fasting glucose, glycated hemoglobin, stroke, and AD endophenotypes. Sample size ranged from 3,026 to 1,812,017 individuals. Genetically proxied GLP-1RA exposure was instrumented using independent T2D-associated variants ( Results: In Europeans, locus-based MR indicated significant protective associations of GLP-1RA with any stroke and ischemic stroke ( Discussion: GLP-1RAs may confer protective effects against stroke (especially ischemic and cardioembolic) and AD risk, across ancestries. These findings warrant further investigation in experimental models and clinical trials to confirm benefits on brain health and understand underlying mechanisms.

Identifiers

PMID42812740
PMCPMC13621555

What Socratic 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 Socratic graph.