Genetic variants of cytochrome b-245, Alpha polypeptide gene and premature acute myocardial infarction risk in an Iranian population

Abstract

Background: Oxidative stress induced by superoxide anion plays critical roles in the pathogenesis of coronary artery disease (CAD) and hence acute myocardial infarction (AMI). The major source of superoxide production in vascular smooth muscle and endothelial cells is the NADPH oxidase complex. An essential component of this complex is p22phox, that is encoded by the cytochrome b-245, Alpha polypeptide (CYBA) gene. The aim of this study was to investigate the association of CYBA variants (rs1049255 and rs4673) and premature acute myocardial infarction risk in an Iranian population. Methods: The study population consisted of 158 patients under the age of 50 years, with a diagnosis of premature AMI, and 168 age-matched controls with normal coronary angiograms. Genotyping of the polymorphisms was performed by the polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP). Results: There was no association between the genotypes and allele frequencies of rs4673 polymorphism and premature acute myocardial infarction (P> 0.05). A significant statistical association was observed between the genotypes distribution of rs1049255 polymorphism and AMI risk (P= 0.037). Furthermore, the distribution of AA+ AG /G G genotypes was found to be statistically significant between the two groups (P= 0.011). Conclusions: Our findings indicated that rs1049255 but not rs4673 polymorphism is associated with premature AMI.

Keywords

• acute myocardial infarction
• p22phox
• polymorphism
• rs1049255
• rs4673