Acarturk Esmeray, Attila Gulen, Bozkurt Abdi, Akpinar Onur, Matyar Selcuk, Seydaoglu Gulsah
Cukurova University, School of Medicine, Department of Cardiology, 01330 Adana, Turkey.
J Biochem Mol Biol. 2005 Jul 31;38(4):486-90. doi: 10.5483/bmbrep.2005.38.4.486.
Genetic factors are important in the pathogenesis of coronary artery disease (CAD). Angiotensin converting enzyme (ACE) gene insertion(I)/deletion(D) polymorphism is one of the genetic factor found to be related with CAD. We investigated the association between I/D polymorphism of the ACE gene and the presence of CAD. Three hundred and seven patients (187 males and 120 females, aged between 35-80, mean 54.3 +/-9.8 years) who underwent diagnostic coronary angiography were included in the study. ACE I/D polymorphism was detected by polymerase chain reaction. Of the 307, 176 had CAD. The most frequently observed genotype in all subjects was ID (47.9 %). However, in patients with CAD the frequency of II genotype was lower whereas DD genotype was higher compared to the controls (p < 0.05). The number of D allele carrying subjects were also higher (p < 0.05) in CAD patients. The logistic regression analysis indicated that the ACE D allele is an independent risk factor (odds ratio = 1.48, 95 % CI = 1.01-2.18, p < 0.05). In conclusion, the I/D polymorphism of ACE gene (carrying D allele) is an independent risk factor for CAD in the studied Turkish population.
遗传因素在冠状动脉疾病(CAD)的发病机制中起着重要作用。血管紧张素转换酶(ACE)基因插入(I)/缺失(D)多态性是已发现的与CAD相关的遗传因素之一。我们研究了ACE基因的I/D多态性与CAD存在之间的关联。该研究纳入了307例接受诊断性冠状动脉造影的患者(187例男性和120例女性,年龄在35 - 80岁之间,平均54.3±9.8岁)。通过聚合酶链反应检测ACE I/D多态性。在这307例患者中,176例患有CAD。所有受试者中最常观察到的基因型是ID(47.9%)。然而,与对照组相比,CAD患者中II基因型的频率较低,而DD基因型的频率较高(p < 0.05)。CAD患者中携带D等位基因的受试者数量也较多(p < 0.05)。逻辑回归分析表明,ACE D等位基因是一个独立的危险因素(优势比 = 1.48,95%可信区间 = 1.01 - 2.18,p < 0.05)。总之,在本研究的土耳其人群中,ACE基因的I/D多态性(携带D等位基因)是CAD的一个独立危险因素。