Department of Clinical Biochemistry, Faculty of Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran.
Department of Biochemistry and Genetics, School of Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran.
BMC Cardiovasc Disord. 2019 Aug 1;19(1):184. doi: 10.1186/s12872-019-1158-4.
It has been indicated that Angiotensin-Converting Enzyme Insertion/Deletion (ACE I/D) polymorphism (rs4646994) could be regarded as a genetic factor that raises the risk of CAD through its impact on the activity of Angiotensin-Converting Enzyme (ACE) and angiotensin II level. The present study seeks to examine the relationship between ACE I/D polymorphism with the risk of atherosclerosis. Moreover, its potential effects on ACE activity and oxLDL level are investigated.
In this study, 145 healthy individuals and 154 patients (143 males and 156 females) were selected among the subjects referred to Shahid Madani Hospital. Atherosclerosis was determined in all subjects with gold standard angiography. Blood samples were collected, used to isolate white blood cells (WBC) and serum separation. The DNA was extracted and the polymorphism was determined by polymerase chain reaction (PCR). The enzyme activity was measured using high-performance liquid chromatography (HPLC).
This study indicated that patients with atherosclerosis had higher levels of oxidized Low-Density Lipoprotein (oxLDL) and ACE activity (P < 0.05) as compared to controls. Although we found a significant association between ACE I/D polymorphism genotype and the allele with atherosclerosis in the male group, there were no association when the entire patient group was compared to the entire control group.
Our study revealed the ACE I/D polymorphism of the ACE gene may not be an independent risk factor in the development of atherosclerosis and evaluation of ACE activity level is more important in evaluating the risk of disease. The researchers found no relation between ACE I/D polymorphism and atherosclerosis and also between types of genotype, ACE activity, and OxLDL level.
血管紧张素转换酶插入/缺失(ACE I/D)多态性(rs4646994)可被视为一种遗传因素,通过影响血管紧张素转换酶(ACE)的活性和血管紧张素 II 水平,增加 CAD 的发病风险。本研究旨在探讨 ACE I/D 多态性与动脉粥样硬化风险的关系。此外,还研究了其对 ACE 活性和氧化低密度脂蛋白(oxLDL)水平的潜在影响。
本研究选取沙希德·马丹尼医院就诊的 145 名健康个体和 154 名患者(143 名男性和 156 名女性)作为研究对象。所有受试者均采用金标准血管造影术确定动脉粥样硬化。采集血样,用于分离白细胞(WBC)和血清分离。提取 DNA,采用聚合酶链反应(PCR)确定多态性。采用高效液相色谱法(HPLC)测定酶活性。
本研究表明,与对照组相比,动脉粥样硬化患者的氧化型低密度脂蛋白(oxLDL)和 ACE 活性更高(P<0.05)。虽然我们发现 ACE I/D 多态性基因型与男性组动脉粥样硬化之间存在显著相关性,但将整个患者组与整个对照组进行比较时,无相关性。
本研究表明 ACE 基因的 ACE I/D 多态性可能不是动脉粥样硬化发生的独立危险因素,评估 ACE 活性水平在评估疾病风险方面更为重要。研究人员未发现 ACE I/D 多态性与动脉粥样硬化以及不同基因型、ACE 活性和 OxLDL 水平之间存在关系。