Association between two common polymorphisms of vitamin D binding protein and the risk of coronary artery disease: A case-control study

Abstract

Background: Coronary Artery Disease (CAD) is one of the most widespread non-communicable diseases. Vitamin Dbinding protein (VDBP) and its genetic polymorphisms have been highlighted as the susceptible components for CAD. The aim of the present study was to examine the association of VDBP single nucleotide polymorphisms (SNPs) - rs7041 and rs4588 - with CAD susceptibility among the Iranian population. Methods: A total of 143 men with CAD and 145 healthy age-sex matched controls underwent genotyping for the - rs7041 and rs4588 polymorphisms using the polymerase chain reaction restriction fragment length polymorphism (PCR-RFLP) method. Serum level of 25(OH)D was assayed using microplate colorimetric enzyme immunoassay. Results: We found a significant association between GG genotype (rs7041) and CAD (p= 0.02, O R= 0.537 95% CI = 0.306-0.944). Regarding rs4588 polymorphism, a significant difference was observed in which the CA genotype (p = 0.00032, O R= 2.578, 95% CI = 1.5 7 9 -4 .2 0 8 ) and allele A (P = 0.028, O R= 1.491, 95% CI = 1 .043-2.132) were significantly higher in CAD patients compared to controls. In spite of lower serum levels of 25(OH)D in CAD patients, we found no significant association between these SNPs and Vitamin D serum concentrations. Conclusions: We concluded that VDBP polymorphisms affect the susceptibility to CAD in Iranian men. Therefore, further studies are required to clarify the association of VDBP phenotypes and its serum levels with CAD.

Keywords

• coronary artery disease
• polymorphism
• vitamin d-binding protein
• 25(oh )d