Tarighi Shahriar, Najafi Mahdi, Hossein-Nezhad Arash, Ghaedi Hamid, Meshkani Reza, Moradi Nariman, Fadaei Reza, Kazerouni Faranak, Shanaki Mehrnoosh
Department of Medical Laboratory Sciences, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Department of Research, Tehran Heart Center, Tehran University of Medical Sciences, Tehran, Iran, Cardiac Outcome Research and Education (CORE), Universal Scientific Education and Research Network (USERN), Tehran, Iran.
J Med Biochem. 2017 Oct 28;36(4):349-357. doi: 10.1515/jomb-2017-0015. eCollection 2017 Oct.
Coronary Artery Disease (CAD) is one of the most widespread non-communicable diseases. Vitamin Dbinding protein (VDBP) and its genetic poly morphisms have been highlighted as the susceptible components for CAD. The aim of the present study was to examine the association of VDBP single nucleotide poly morphisms (SNPs) - rs7041 and rs4588 - with CAD susceptibility among the Iranian population.
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.
We found a significant association between GG genotype (rs7041) and CAD (p=0.02, OR=0.537 95% CI =0.306-0.944). Regarding rs4588 polymorphism, a significant difference was observed in which the CA genotype (p=0.00032, OR=2.578, 95% CI=1.579-4.208) and allele A (P=0.028, OR=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.
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.
冠状动脉疾病(CAD)是最普遍的非传染性疾病之一。维生素D结合蛋白(VDBP)及其基因多态性已被视为CAD的易感因素。本研究旨在探讨伊朗人群中VDBP单核苷酸多态性(SNP)- rs7041和rs4588与CAD易感性之间的关联。
采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法,对143例CAD男性患者和145例年龄、性别匹配的健康对照者进行- rs7041和rs4588多态性基因分型。采用微孔板比色酶免疫分析法检测血清25(OH)D水平。
我们发现GG基因型(rs7041)与CAD之间存在显著关联(p = 0.02,OR = 0.537,95%CI = 0.306 - 0.944)。关于rs4588多态性,观察到显著差异,CAD患者的CA基因型(p = 0.00032,OR = 2.578,95%CI = 1.579 - 4.208)和等位基因A(P = 0.028,OR = 1.491,95%CI = 1.043 - 2.132)显著高于对照组。尽管CAD患者的血清25(OH)D水平较低,但我们发现这些SNP与维生素D血清浓度之间无显著关联。
我们得出结论,VDBP多态性影响伊朗男性对CAD的易感性。因此,需要进一步研究以阐明VDBP表型及其血清水平与CAD之间的关联。