Neuroscience Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, Iran.
Student Research Committee, School of Medicine, Kerman University of Medical Sciences, Kerman, Iran.
J Cell Biochem. 2019 Jun;120(6):9159-9171. doi: 10.1002/jcb.28191. Epub 2018 Dec 12.
The aim is to explore the treatment effect of coronary artery disease (CAD) and hypertension on plasma levels of renalase activity and also the possible association of renalase rs10887800 gene polymorphism with CAD and hypertension. A total of 286 patients who received coronary angiography were included in the study. Subjects were divided into four groups including (1) hypertensive with no CAD (H-Tens, n = 60); (2) CAD with hypertension (CAD + H-Tens, n = 71); (3) CAD with no hypertension (CAD, n = 61); and (4) nonhypertensive with no CAD as a control group (Con, n = 69). The plasma renalase activity was measured using the Amplex Red Monoamine Oxidase Assay Kit. Renalase rs10887800 single-nucleotide polymorphisms (SNPs) were genotyped by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Atorvastatin (P = 0.005), losartan (P < 0.001), and captopril (P = 0.001) were administered significantly more in case groups compared with the Con group. Significant higher and lower levels of renalase activity were observed in H-Tens and CAD patients compared with control subjects (P < 0.001 for both comparisons). Furthermore, no significant differences were obtained in the risk or protective effects of renalase rs10887800 SNP against hypertension and/or CAD in both recessive and dominant genetic models (P > 0.05). According to the findings of the present study, atorvastatin and losartan therapy assumes considerable significance in alleviating hypertension, but not CAD, by increasing the renalase activity. Furthermore, it was found that renalase rs10887800 is less likely a predisposing factor for susceptibility to hypertension and/or CAD in an Iranian southeast population.
目的是探讨冠状动脉疾病 (CAD) 和高血压对肾酶活性的治疗效果,以及肾酶 rs10887800 基因多态性与 CAD 和高血压的可能关联。共有 286 名接受冠状动脉造影的患者纳入本研究。受试者分为四组:(1) 高血压无 CAD (H-Tens,n=60);(2) CAD 合并高血压 (CAD+H-Tens,n=71);(3) CAD 无高血压 (CAD,n=61);和 (4) 非高血压无 CAD 作为对照组 (Con,n=69)。使用 Amplex Red 单胺氧化酶测定试剂盒测定血浆肾酶活性。采用聚合酶链反应-限制性片段长度多态性 (PCR-RFLP) 方法检测肾酶 rs10887800 单核苷酸多态性 (SNP)。阿托伐他汀 (P=0.005)、氯沙坦 (P<0.001) 和卡托普利 (P=0.001) 在病例组中的应用明显多于对照组。与对照组相比,H-Tens 和 CAD 患者的肾酶活性水平明显更高 (两者比较均 P<0.001)。此外,在隐性和显性遗传模型中,肾酶 rs10887800 SNP 对高血压和/或 CAD 的风险或保护作用均无显著差异 (P>0.05)。根据本研究的结果,阿托伐他汀和氯沙坦治疗通过增加肾酶活性对缓解高血压具有重要意义,但对 CAD 则不然。此外,在伊朗东南部人群中,肾酶 rs10887800 不太可能是高血压和/或 CAD 易感性的一个诱发因素。