Please use this identifier to cite or link to this item: https://doi.org/10.1212/WNL.0000000000000707
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dc.titleMeta-analysis in more than 17,900 cases of ischemic stroke reveals a novel association at 12q24.12
dc.contributor.authorKilarski, L.L
dc.contributor.authorAchterberg, S
dc.contributor.authorDevan, W.J
dc.date.accessioned2020-11-23T08:56:50Z
dc.date.available2020-11-23T08:56:50Z
dc.date.issued2014
dc.identifier.citationKilarski, 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
dc.identifier.issn0028-3878
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/183893
dc.description.abstractResults: 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.
dc.publisherLippincott, Williams & Wilkins
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectArticle
dc.subjectbrain hemorrhage
dc.subjectbrain ischemia
dc.subjectcardioembolic stroke
dc.subjectcardiovascular risk
dc.subjectchromosome 10q
dc.subjectchromosome 12q
dc.subjectchromosome 7p
dc.subjectcomputer model
dc.subjectcontrolled study
dc.subjectcoronary artery disease
dc.subjectdiabetes mellitus
dc.subjectgenetic association
dc.subjectgenotype
dc.subjecthuman
dc.subjecthypercholesterolemia
dc.subjecthypertension
dc.subjectimmunochip array
dc.subjectmajor clinical study
dc.subjectmicroarray analysis
dc.subjectrisk factor
dc.subjectsingle nucleotide polymorphism
dc.subjectbrain ischemia
dc.subjectchromosome 12
dc.subjectgenetic association
dc.subjectgenetic predisposition
dc.subjectgenetics
dc.subjectmeta analysis
dc.subjectrisk
dc.subjectStroke
dc.subjectBrain Ischemia
dc.subjectCerebral Hemorrhage
dc.subjectChromosomes, Human, Pair 12
dc.subjectGenetic Predisposition to Disease
dc.subjectGenome-Wide Association Study
dc.subjectGenotype
dc.subjectHumans
dc.subjectPolymorphism, Single Nucleotide
dc.subjectRisk
dc.subjectStroke
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.1212/WNL.0000000000000707
dc.description.sourcetitleNeurology
dc.description.volume83
dc.description.issue8
dc.description.page678-685
dc.published.statepublished
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