Arslan Serdal, Berkan Öcal, Bayyurt Burcu, Beton Osman, Şahin Ni L Özbi Lüm, Aydemir Eylem Itır
Department of Medical Biology, Faculty of Medicine, Cumhuriyet University, 58140 Sivas, Turkey.
Department of Cardiovascular Surgery, Heart Center, Cumhuriyet University, 58140 Sivas, Turkey.
Biomed Rep. 2017 Dec;7(6):547-552. doi: 10.3892/br.2017.995. Epub 2017 Oct 3.
Myeloperoxidase (MPO) is an oxidative hemoprotein compound expressed in polymorphonuclear leukocytes that contributes to inflammatory responses. Coronary artery disease (CAD), as the most prevalent form of heart disease, is considered to originate from an interaction between genetic and environmental factors. In the present study, the potential associations between and - polymorphisms with CAD were investigated in a Turkish population using a polymerase chain reaction-based restriction fragment length polymorphism (RFLP) assay technique. To the best of our knowledge, the study was the first to examine the association of and - with patient survival rate in a Turkish population. The study population consisted of 201 patients with CAD and 201 healthy controls. The results indicated that there was a significant association of the genotype of with the case population (P=0.048). Meanwhile, in the patients with CAD, the frequency distributions of the allele (P=0.006) and genotype (P=0.001) were significantly increased compared with the allele and genotype, respectively, in CAD patients. Additionally, compared with the genotype, the frequency distribution of was significantly increased in the patient group regarding smoking status (P=0.001) and the presence of hypercholesterolemia (P=0.028). However, survival analysis did not detect an effect of either polymorphism on the survival rate of the CAD patients (P>0.05). Therefore, the genotype may be a significant risk factor for the development of CAD.
髓过氧化物酶(MPO)是一种在多形核白细胞中表达的氧化血红素蛋白化合物,它参与炎症反应。冠状动脉疾病(CAD)作为最常见的心脏病形式,被认为源于遗传和环境因素之间的相互作用。在本研究中,使用基于聚合酶链反应的限制性片段长度多态性(RFLP)分析技术,在土耳其人群中研究了[具体基因]和[具体基因]多态性与CAD之间的潜在关联。据我们所知,该研究是首次在土耳其人群中研究[具体基因]和[具体基因]与患者生存率的关联。研究人群包括201例CAD患者和201名健康对照。结果表明,[具体基因]的[具体基因型]与病例组存在显著关联(P = 0.048)。同时,在CAD患者中,[具体基因]的[具体等位基因]频率分布(P = 0.006)和[具体基因型]频率分布(P = 0.001)分别与CAD患者中的[另一个等位基因]和[另一个基因型]相比显著增加。此外,与[另一个基因型]相比,在患者组中,关于吸烟状况(P = 0.001)和高胆固醇血症的存在(P = 0.028),[具体基因型]的频率分布显著增加。然而,生存分析未检测到任何一种多态性对CAD患者生存率的影响(P>0.05)。因此,[具体基因型]可能是CAD发生的一个重要危险因素。