Moradi Nariman, Fadaei Reza, Ahmadi Reza, Mohammad Milad Hajimirza, Shahmohamadnejad Serveh, Tavakoli-Yaraki Masoumeh, Aghajani Hassan, Fallah Soudabeh
Department of Biochemistry, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Department of Clinical Biochemistry, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Gene. 2017 Sep 10;628:295-300. doi: 10.1016/j.gene.2017.07.060. Epub 2017 Jul 21.
Data concerning the association of serum levels of vitamin D and metalloproteinases and vitamin D receptor gene polymorphism with coronary artery disease (CAD) is not fully demonstrated. The present study aimed to evaluate the association of vitamin D receptor gene polymorphism, serum levels of 25(OH) vitamin D and metalloproteinase-9 (MMP-9) with CAD.
104 patients with CAD and 69 Non-CAD subjects were included in current study. Vitamin D receptor genotypes were determined by PCR-RFLP method. The 25(OH) vitamin D and MMP-9 were determined by ELISA assay.
There was a significant reduction of vitamin D in CAD patients (P=0.001). The metalloproteinase 9 levels of CAD patient was increased significantly compared with controls (P=0.001). A significant reverse correlation also was found between MMP-9 concentration and 25(OH) vitamin D levels of patients (r=-0.28, P<0.001). In addition, we identified that VDR gene FokI polymorphism was significantly associated with CAD. Furthermore, MMP-9 levels of CAD patients with ff genotype of FokI polymorphism was higher significantly than patients with FF and Ff genotypes. It has been also found that MMP-9 levels of CAD patients with ff genotype of FokI polymorphism was higher significantly than patients with FF and Ff genotypes.
Our results indicated that 25(OH) vitamin D, MMP-9 levels and VDR gene FokI polymorphisms play a critical role in the development and progression of CAD and may contribute to susceptibility to CAD in Iranian populations.
关于血清维生素D水平、金属蛋白酶与维生素D受体基因多态性和冠状动脉疾病(CAD)之间关联的数据尚未完全阐明。本研究旨在评估维生素D受体基因多态性、血清25(OH)维生素D水平和金属蛋白酶-9(MMP-9)与CAD的关联。
本研究纳入了104例CAD患者和69例非CAD受试者。通过PCR-RFLP方法确定维生素D受体基因型。采用ELISA法测定25(OH)维生素D和MMP-9。
CAD患者的维生素D水平显著降低(P=0.001)。与对照组相比,CAD患者的金属蛋白酶9水平显著升高(P=0.001)。患者的MMP-9浓度与25(OH)维生素D水平之间也存在显著的负相关(r=-0.28,P<0.001)。此外,我们发现VDR基因FokI多态性与CAD显著相关。此外,FokI多态性ff基因型的CAD患者的MMP-9水平显著高于FF和Ff基因型的患者。还发现FokI多态性ff基因型的CAD患者的MMP-9水平显著高于FF和Ff基因型的患者。
我们的结果表明,25(OH)维生素D、MMP-9水平和VDR基因FokI多态性在CAD的发生和发展中起关键作用,可能导致伊朗人群对CAD的易感性。