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.
Funding Information
  • Medical University of Silesia (KNW-1-014/N/4/0)

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