Wickremasinghe Dinushka, Peiris Hemantha, Chandrasena Lal Gotabhaya, Senaratne Vajira, Perera Rasika
Faculty of Medical Sciences, University of Sri Jayewardenepura, Nugegoda, Sri Lanka.
BMC Cardiovasc Disord. 2016 May 26;16:111. doi: 10.1186/s12872-016-0280-9.
Glutathione peroxidase-1 (GPX-1) activity was reported to be useful marker for monitoring cardiovascular disease. However, accurate assessment of coronary artery disease (CAD) using GPX-1 polymorphism is limited for South Asian population. Present study aim to assess GPX-1activity and GPX-1 polymorphismin patients with coronary artery disease (CAD) who were confirmed with coronary angiography findings and in apparently healthy subjects.
Case control study was carried out with 85 patients (58 males and 27 females) 40-60 years of age confirmed as having CAD on coronary angiography findings and 85 age and sex matched healthy volunteers as controls. Blood samples were analyzed for erythrocyte GPX-1 activity and GPX-1 polymorphism in both groups and the severity of CAD was assessed using coronary angiography scoring system based on vessel, stenosis and extent score.
Coronary angiography scores indicated that erythrocyteGPX-1 cutoff value of 23.9 U/gHb showed a high sensitivity and negative predictive value in ruling out major vessel disease. The GPX-1 Pro198Leu (CT) polymorphism was higher in patients with CAD (25.3 %) when compared to controls (10.7 %). Pro198Leu (CT) genotype showed a 2.84 fold risk for CAD [odds ratio 2.84 (95 % CI 1.15-6.98), p = 0.019].
Coronary angiography findings indicated that individuals possessing Pro198Leu (CT) polymorphism were found to be associated with low erythrocyte GPX-1 activity and increased susceptibility for CAD.
据报道,谷胱甘肽过氧化物酶-1(GPX-1)活性是监测心血管疾病的有用标志物。然而,对于南亚人群,利用GPX-1基因多态性准确评估冠状动脉疾病(CAD)存在局限性。本研究旨在评估经冠状动脉造影结果确诊的冠心病(CAD)患者以及明显健康受试者的GPX-1活性和GPX-1基因多态性。
进行病例对照研究,选取85例年龄在40 - 60岁之间、经冠状动脉造影结果确诊为CAD的患者(58例男性和27例女性),以及85例年龄和性别匹配的健康志愿者作为对照。对两组的血样进行红细胞GPX-1活性和GPX-1基因多态性分析,并使用基于血管、狭窄和范围评分的冠状动脉造影评分系统评估CAD的严重程度。
冠状动脉造影评分表明,红细胞GPX-1临界值为23.9 U/gHb时,在排除主要血管疾病方面具有较高的敏感性和阴性预测价值。与对照组(10.7%)相比,CAD患者中GPX-1 Pro198Leu(CT)基因多态性更高(25.3%)。Pro198Leu(CT)基因型患CAD的风险增加2.84倍[比值比2.84(95%可信区间1.15 - 6.98),p = 0.019]。
冠状动脉造影结果表明,具有Pro198Leu(CT)基因多态性的个体红细胞GPX-1活性较低,患CAD的易感性增加。