Literature DB >> 21148441

Genetic variant on chromosome 12p13 does not show association to ischemic stroke in 3 Swedish case-control studies.

Sandra Olsson1, Olle Melander, Katarina Jood, J Gustav Smith, Håkan Lövkvist, Marketa Sjögren, Gunnar Engström, Bo Norrving, Arne Lindgren, Christina Jern.   

Abstract

BACKGROUND AND
PURPOSE: in a genome-wide association study and subsequent case-control studies, the single-nucleotide polymorphism rs12425791 on chromosome 12p13 was reported to be associated with ischemic stroke, but this could not be validated in a recent well-powered study. We therefore investigated whether an association between ischemic stroke and rs12425791 could be detected in 3 different case-control studies from the southwest of Sweden.
METHODS: we examined 3606 patients with ischemic stroke and 2528 controls from 3 independent case-controls studies.
RESULTS: no significant association between ischemic stroke and the single-nucleotide polymorphism rs12425791 was detected in any of the 3 case-control samples or in the samples combined. The odds ratio for ischemic stroke for the minor allele in the combined sample was 1.02 (95% CI, 0.93 to 1.13).
CONCLUSIONS: the single-nucleotide polymorphism rs12425791 does not confer a substantial risk for ischemic stroke in our population. Our results support a recent large study including other European populations.

Entities:  

Mesh:

Year:  2010        PMID: 21148441     DOI: 10.1161/STROKEAHA.110.594010

Source DB:  PubMed          Journal:  Stroke        ISSN: 0039-2499            Impact factor:   7.914


  14 in total

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Journal:  Nat Genet       Date:  2012-02-05       Impact factor: 38.330

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