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Haplotypes Encompassing the KIAA0391 and PSMA6 Gene Cluster Confer a Genetic Link for Myocardial Infarction and Coronary Artery Disease
Author(s) -
Alsmadi Osama,
Muiya Paul,
Khalak Hanif,
AlSaud Haya,
Meyer Brian F.,
AlMohanna Futwan,
Alshahid Maie,
Dzimiri Nduna
Publication year - 2009
Publication title -
annals of human genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.537
H-Index - 77
eISSN - 1469-1809
pISSN - 0003-4800
DOI - 10.1111/j.1469-1809.2009.00534.x
Subject(s) - myocardial infarction , haplotype , coronary artery disease , cardiology , medicine , cluster (spacecraft) , genetics , gene , biology , allele , computer science , computer network
Summary The role of the KIAA0391 and PSMA6 genes in predisposing individuals to disease is still not fully understood. We evaluated by molecular beacon‐based genotyping assays the roles of five single nucleotide polymorphisms (SNPs) in the chromosomal region 14q13.2 harbouring the KIAA0391 and PSMA6 gene cluster in coronary artery disease (CAD) in the Saudi population. Two of the studied SNPs rs8008319 (denoted as 1) and rs7157492 (2), reside in the KIAA0391 locus, two others rs1048990 (3) and rs12878391 (4) are components of the PSMA6 , while rs4981283 (5) resides downstream of both genes. In a study involving 1071 patients and 929 controls, none of the studied SNPs showed significant association with CAD. In contrast, two haplotypes consisting of 1A‐2G‐3C‐4A‐5A [O.R.(95% C.I.) = 1.49(0.95–2.35); p = 0.022] and 1A‐2G‐3G‐4A‐5A [2.24(0.84–5.98); p = 0.031] conferred risk for both CAD and myocardial infarction (MI) in a five‐SNP locus model, while another comprising 1A‐2G‐3C‐4A‐5G [2.24(0.84–5.98); p = 0.079] showed a borderline association. One haplotype consisting of 1T‐2G‐3C‐4G‐5A [0.79(0.59–1.05); p = 0.015] exhibited protective properties and another, 1T‐2G‐3C‐4A‐5G [0.20(0.03–139); p = 0.073], showed a similar but weaker trend. Our study identified haplotypes in the chromosomal region encompassing the KIAA0391 and PSMA6 genes as a possible genetic link between CAD and MI. These results also suggest that haplotypes may be more informative than individual SNPs in identifying risk factors for disease.