Please use this identifier to cite or link to this item: https://doi.org/10.1212/WNL.0000000000000707
Title: Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12
Authors: Kilarski, L.L
Achterberg, S
Devan, W.J
Keywords: Article
brain hemorrhage
brain ischemia
cardioembolic stroke
cardiovascular risk
chromosome 10q
chromosome 12q
chromosome 7p
computer model
controlled study
coronary artery disease
diabetes mellitus
genetic association
genotype
human
hypercholesterolemia
hypertension
immunochip array
major clinical study
microarray analysis
risk factor
single nucleotide polymorphism
brain ischemia
chromosome 12
genetic association
genetic predisposition
genetics
meta analysis
risk
Stroke
Brain Ischemia
Cerebral Hemorrhage
Chromosomes, Human, Pair 12
Genetic Predisposition to Disease
Genome-Wide Association Study
Genotype
Humans
Polymorphism, Single Nucleotide
Risk
Stroke
Issue Date: 2014
Publisher: Lippincott, Williams & Wilkins
Citation: Kilarski, L.L, Achterberg, S, Devan, W.J (2014). Meta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12. Neurology 83 (8) : 678-685. ScholarBank@NUS Repository. https://doi.org/10.1212/WNL.0000000000000707
Rights: Attribution 4.0 International
Abstract: Results: In an overall analysis of 17,970 cases of ischemic stroke and 70,764 controls, we identified a novel association on chromosome 12q24 (rs10744777, odds ratio [OR] 1.10 [1.07-1.13], p 5 7.12 3 10-11) with ischemic stroke. The association was with all ischemic stroke rather than an individual stroke subtype, with similar effect sizes seen in different stroke subtypes. There was no association with intracerebral hemorrhage (OR 1.03 [0.90-1.17], p 5 0.695).Conclusion: Our results show, for the first time, a genetic risk locus associated with ischemic stroke as a whole, rather than in a subtype-specific manner. This finding was not associated with intracerebral hemorrhage.Methods: Using the Immunochip, we genotyped 3,420 ischemic stroke cases and 6,821 controls. After imputation we meta-analyzed the results with imputed GWAS data from 3,548 cases and 5,972 controls recruited from the ischemic stroke WTCCC2 study, and with summary statistics from a further 8,480 cases and 56,032 controls in the METASTROKE consortium. A final in silico "look-up" of 2 single nucleotide polymorphisms in 2,522 cases and 1,899 controls was performed. Associations were also examined in 1,088 cases with intracerebral hemorrhage and 1,102 controls.Objectives: To perform a genome-wide association study (GWAS) using the Immunochip array in 3,420 cases of ischemic stroke and 6,821 controls, followed by a meta-analysis with data from more than 14,000 additional ischemic stroke cases. © 2014 American Academy of Neurology.
Source Title: Neurology
URI: https://scholarbank.nus.edu.sg/handle/10635/183893
ISSN: 0028-3878
DOI: 10.1212/WNL.0000000000000707
Rights: Attribution 4.0 International
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