Please use this identifier to cite or link to this item: https://doi.org/10.1002/ana.24621
Title: Shared genetic contribution to ischemic stroke and Alzheimer's disease
Authors: Traylor, M
Adib-Samii, P
Harold, D
Keywords: Alzheimer disease
analysis
Article
brain ischemia
cerebrovascular accident
cholesterol transport
controlled study
genetic correlation
genetics
genome-wide association study
genotype
heredity
human
immune response
major clinical study
priority journal
risk
single nucleotide polymorphism
Issue Date: 2016
Publisher: John Wiley and Sons Inc.
Citation: Traylor, M, Adib-Samii, P, Harold, D (2016). Shared genetic contribution to ischemic stroke and Alzheimer's disease. Annals of Neurology 79 (5) : 739-747. ScholarBank@NUS Repository. https://doi.org/10.1002/ana.24621
Rights: Attribution 4.0 International
Abstract: Objective Increasing evidence suggests epidemiological and pathological links between Alzheimer's disease (AD) and ischemic stroke (IS). We investigated the evidence that shared genetic factors underpin the two diseases. Methods Using genome-wide association study (GWAS) data from METASTROKE + (15,916 IS cases and 68,826 controls) and the International Genomics of Alzheimer's Project (IGAP; 17,008 AD cases and 37,154 controls), we evaluated known associations with AD and IS. On the subset of data for which we could obtain compatible genotype-level data (4,610 IS cases, 1,281 AD cases, and 14,320 controls), we estimated the genome-wide genetic correlation (rG) between AD and IS, and the three subtypes (cardioembolic, small vessel, and large vessel), using genome-wide single-nucleotide polymorphism (SNP) data. We then performed a meta-analysis and pathway analysis in the combined AD and small vessel stroke data sets to identify the SNPs and molecular pathways through which disease risk may be conferred. Results We found evidence of a shared genetic contribution between AD and small vessel stroke (rG [standard error] = 0.37 [0.17]; p = 0.011). Conversely, there was no evidence to support shared genetic factors in AD and IS overall or with the other stroke subtypes. Of the known GWAS associations with IS or AD, none reached significance for association with the other trait (or stroke subtypes). A meta-analysis of AD IGAP and METASTROKE + small vessel stroke GWAS data highlighted a region (ATP5H/KCTD2/ICT1) associated with both diseases (p = 1.8 × 10-8). A pathway analysis identified four associated pathways involving cholesterol transport and immune response. Interpretation Our findings indicate shared genetic susceptibility to AD and small vessel stroke and highlight potential causal pathways and loci. Ann Neurol 2016;79:739-747 © 2016 The Authors. Annals of Neurology published by Wiley Periodicals, Inc. on behalf of American Neurological Association.
Source Title: Annals of Neurology
URI: https://scholarbank.nus.edu.sg/handle/10635/179578
ISSN: 0364-5134
DOI: 10.1002/ana.24621
Rights: Attribution 4.0 International
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