TheCYBAGene⁎49A>G Polymorphism (rs7195830) Is Associated with Hypertension in Patients with Coronary Artery Disease

Adult Male 0301 basic medicine Heterozygote Genotype Oligonucleotides NADPH Oxidases Coronary Artery Disease Sequence Analysis, DNA Middle Aged Coronary Vessels Lipids Polymorphism, Single Nucleotide 03 medical and health sciences Risk Factors Case-Control Studies Hypertension Odds Ratio Humans Female Hypertrophy, Left Ventricular Alleles Research Article
DOI: 10.1155/2016/1539671 Publication Date: 2016-05-24T21:15:10Z
ABSTRACT
Purpose. Single nucleotide polymorphisms of theCYBAgene may modify the risk of coronary artery disease (CAD). The aim of the present study was to investigate whether the⁎49A>G (rs7195830) polymorphism is associated with CAD.Materials and Methods.CYBAgene⁎49A>G polymorphism was determined in 481 subjects: 242 patients with premature CAD and 239 age and sex matched controls using the fluorescently labeled allele-specific oligonucleotides method.Results. The frequency of the⁎49G allele carrier state was significantly higher in patients than in controls (84.8% versus 76.6%, resp.,P=0.020), as well as the frequency of the⁎49G allele (62.2% versus 54.0%,P=0.009). Both factors were associated with CAD in the analyzed population (OR = 1.70, 95% CI: 1.04–2.76 for GG+AG versus AA and OR = 1.40, 95% CI: 1.08–1.83 for⁎49G versus  ⁎49A). Carrier state of the⁎49G allele was a stronger and independent risk factor for CAD among women (OR = 4.35, 95% CI: 1.50–13.20,P=0.002), as well as the⁎49G allele (OR = 2.25, 95% CI: 1.34–3.77,P=0.001). The⁎49G allele carrier state was also associated with left ventricular hypertrophy in patients with coronary artery disease (P=0.015).Conclusion. TheCYBAgene⁎49A>G polymorphism modifies the risk of coronary artery disease.
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