Literature DB >> 17975119

Association of gene variants with incident myocardial infarction in the Cardiovascular Health Study.

Dov Shiffman1, Ellen S O'Meara, Lance A Bare, Charles M Rowland, Judy Z Louie, Andre R Arellano, Thomas Lumley, Kenneth Rice, Olga Iakoubova, May M Luke, Bradford A Young, Mary J Malloy, John P Kane, Stephen G Ellis, Russell P Tracy, James J Devlin, Bruce M Psaty.   

Abstract

OBJECTIVE: We asked whether single nucleotide polymorphisms (SNPs) that had been nominally associated with cardiovascular disease in antecedent studies were also associated with cardiovascular disease in a population-based prospective study of 4522 individuals aged 65 or older. METHODS AND
RESULTS: Based on antecedent studies, we prespecified a risk allele and an inheritance model for each of 74 SNPs. We then tested the association of these SNPs with myocardial infarction (MI) in the Cardiovascular Health Study (CHS). The prespecified risk alleles of 8 SNPs were nominally associated (1-sided P<0.05) with increased risk of MI in White CHS participants. The false discovery rate for these 8 was 0.43, suggesting that about 4 of these 8 are likely to be true positives. The 4 of these 8 SNPs that had the strongest evidence for association with cardiovascular disease before testing in CHS (association in 3 antecedent studies) were in KIF6 (CHS HR=1.29; 90%CI 1.1 to 1.52), VAMP8 (HR=1.2; 90%CI 1.02 to 1.41), TAS2R50 (HR=1.13; 90%CI 1 to 1.27), and LPA (HR=1.62; 90%CI 1.09 to 2.42).
CONCLUSIONS: Although most of the SNPs investigated were not associated with MI in CHS, evidence from this investigation combined with previous studies suggests that 4 of these SNPs are likely associated with MI.

Entities:  

Mesh:

Year:  2007        PMID: 17975119      PMCID: PMC2636623          DOI: 10.1161/ATVBAHA.107.153981

Source DB:  PubMed          Journal:  Arterioscler Thromb Vasc Biol        ISSN: 1079-5642            Impact factor:   8.311


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