Role of rs10840293 and rs17087335 in patients with coronary artery disease in an Iranian population
DOI:
https://doi.org/10.22100/jkh.v15i2.2441Abstract
Introduction: Previous genome-wide association studies (GWASs) have shown an increased CAD risk associated with single nucleotide polymorphisms (SNPs) in SWAP70 (rs10840293) and Rest- NOA1 (rs17087335). This study aimed to investigate the relationship between rs10840293 and rs17087335 polymorphism with coronary artery disease in the Iranian population.
Methods: This study was a case-control study with the case-base sampling method for the control group. Genomic DNA was extracted from the peripheral blood collected from 150 patients with CAD and 150 healthy controls. Polymorphisms were genotyped by Taq-Man technology. SPSS software was used for statistical analysis.
Results: The genotype frequency distribution did not deviate significantly from the Hardy-Weinberg equilibrium (P>0.05). Allelic frequencies and genotype distributions of rs10840293 and rs17087335 did not show statistical significance between patients with POAG and control subjects (P<0.05).
Conclusion: To the best of our knowledge, this is the first report concerning the association between SWAP70 and Rest- NOA1 gene polymorphisms and CAD in an Iranian population. Our data suggest that rs1533428 and rs12994401 are unlikely major risk factors for CAD in an Iranian population.
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