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Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke.

Citation
Keene, K. L., et al. “Genome-Wide Association Study Meta-Analysis Of Stroke In 22 000 Individuals Of African Descent Identifies Novel Associations With Stroke.”. Stroke, pp. 2454-2463.
Center UCSD-UCLA
Author Keith L Keene, Hyacinth I Hyacinth, Joshua C Bis, Steven J Kittner, Braxton D Mitchell, Yu-Ching Cheng, Guillaume Paré, Michael Chong, Martin O'Donnell, James F Meschia, Wei-Min Chen, Michele M Sale, Stephen S Rich, Mike A Nalls, Alan B Zonderman, Michele K Evans, James G Wilson, Adolfo Correa, Hugh S Markus, Matthew Traylor, Cathryn M Lewis, Cara L Carty, Alexander Reiner, Jeff Haessler, Carl D Langefeld, Rebecca Gottesman, Thomas H Mosley, Daniel Woo, Kristine Yaffe, Yongmei Liu, William T Longstreth, Bruce M Psaty, Charles Kooperberg, Leslie A Lange, Ralph Sacco, Tatjana Rundek, Jin-Moo Lee, Carlos Cruchaga, Karen L Furie, Donna K Arnett, Oscar R Benavente, Raji P Grewal, Leema Reddy Peddareddygari, Martin Dichgans, Rainer Malik, Bradford B Worrall, Myriam Fornage, and METASTROKE Consortia COMPASS SiGN
Keywords brain ischemia, coronary artery disease, genome-wide association study, META-ANALYSIS, phenotype, risk factors
Abstract

BACKGROUND AND PURPOSE: Stroke is a complex disease with multiple genetic and environmental risk factors. Blacks endure a nearly 2-fold greater risk of stroke and are 2× to 3× more likely to die from stroke than European Americans.

METHODS: The COMPASS (Consortium of Minority Population Genome-Wide Association Studies of Stroke) has conducted a genome-wide association meta-analysis of stroke in >22 000 individuals of African ancestry (3734 cases, 18 317 controls) from 13 cohorts.

RESULTS: In meta-analyses, we identified one single nucleotide polymorphism (rs55931441) near the gene that reached genome-wide significance (=4.62×10) and an additional 29 variants with suggestive evidence of association (<1×10), representing 24 unique loci. For validation, a look-up analysis for a 100 kb region flanking the COMPASS single nucleotide polymorphism was performed in SiGN (Stroke Genetics Network) Europeans, SiGN Hispanics, and METASTROKE (Europeans). Using a stringent Bonferroni correction value of 2.08×10 (0.05/24 unique loci), we were able to validate associations at the locus in both SiGN (=8.18×10) and METASTROKE (=1.72×10) European populations. Overall, 16 of 24 loci showed evidence for validation across multiple populations. Previous studies have reported associations between variants in the gene and lipids, C-reactive protein, and risk of coronary artery disease and stroke. Suggestive associations with variants in the and genes represent potential novel ischemic stroke loci.

CONCLUSIONS: These findings represent the most thorough investigation of genetic determinants of stroke in individuals of African descent, to date.

Year of Publication
2020
Journal
Stroke
Volume
51
Issue
8
Number of Pages
2454-2463
Date Published
12/2020
ISSN Number
1524-4628
DOI
10.1161/STROKEAHA.120.029123
Alternate Journal
Stroke
PMID
32693751
PMCID
PMC7387190
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