Author/Authors :
Piryaei، Mohammad Mohammad نويسنده Department of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran. Piryaei, Mohammad Mohammad , Ghaderian ، Sayyed Mohammad Hossein نويسنده Department of Medical Genetics, Faculty of Medicine, Shahid Beheshti University of Medical Sciences & Health Services,Tehran, Iran Ghaderian , Sayyed Mohammad Hossein , Vakili، Hossein نويسنده , , Zaimkohan، Hooshang نويسنده Department of Medical Genetics, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran , , Mohammadi Ghahhari، Nastaran نويسنده Department of Biochemistry, Pasteur Institute of Iran, Tehran, Iran , , Mafi Golchin، Maryam نويسنده Department of Genetics and Anatomy, Babol University of Medical Sciences, Babol, Iran ,
Abstract :
Although genetic variants that affect susceptibility to coronary artery disease (CAD) have been greatly known, a
number of these single nucleotide polymorphisms (SNPs) remain to be analyzed in populations with different
ethnicities. CAD is influenced by numerous genetic, environmental, and lifestyle factors, and is an important
reason for mortality around the globe. In this study, a novel SNP (rs6725887) in the WD Repeat Protein 12
(WDR12) gene was selected to be examined in Iranian patients with CAD. Ninety eigth healthy controls and one
hundred and one CAD patients were enrolled from Iranian population, and their clinical data were collected for
further comparisons. After DNA extraction from each sample, genotypes were characterized by Taq Man probe
real- time PCR assay. Statistical analyses were performed to evaluate genotype and allele frequencies and
compared the values with clinical variables. Body mass index, blood pressure, fasting blood sugar, LDL, HDL,
cholesterol, and triglyceride significantly differed in CAD and control groups. Genotype and allele frequencies
of rs6725887 in CAD patients and controls showed no significant association in the distribution. However,
clinical parameters of CAD patients like HDL, LDL, FBS, TG, DBP and SBP had significantly (P < 0.05) higher
levels compared to control group. The rs6725887 polymorphism is unlikely to play a key role in CAD risk in our
population. Further additional samples are required for better appreciation of the influence of WDR12 SNP on
CAD occurrence.