STEMI患者全身炎症反应基因标记物基因型多态性分布

E. Sid, O. Soloviov
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引用次数: 0

摘要

心血管疾病的不断增加是现代医学面临的重要问题之一。现阶段的一个紧迫问题是治疗急性冠心病患者,因为血管意外是心血管疾病死亡的主要原因。近年来,越来越多的研究确定了遗传标记在预测包括急性心肌梗死在内的各种心血管疾病不良病程中的作用。测定STEMI患者全身炎症反应基因标记物的分布。纳入研究的标准是:46 - 75岁的男性和女性患者;绝经后妇女,1年以上;在发病前12小时内存在STEMI;患者参与研究的知情同意。使用Express DNA blood Kit (Litech)从全血白细胞中分离DNA。在提取DNA的过程中,按照试剂盒说明书中的建议进行。采用Rotor-Gene 6000热循环仪实时聚合酶链反应检测c反应蛋白基因G-3014>A、肿瘤坏死因子-α G-308>A、白细胞介素-10 G-1082>A的SNP多态性。引物结构采用标准SNP-express-PB试剂盒(Litech)引物结构。结果表明,与Hardy-Weinberg分布相比,STEMI患者c反应蛋白基因G-3014> a多态性基因型的纯合子比例(GG)增加,杂合子比例(GA)减少。STEMI患者肿瘤坏死因子-α基因G-308>A多态性与Hardy-Weinberg平衡存在显著差异,纯合子(GG)比例增加,杂合子(GA)和纯合子(AA)比例减少。与Hardy-Weinberg分布相比,STEMI患者白细胞介素-10基因G-1082>A多态性的分布表现为纯合子(GG)比例增加,杂合子(GA)比例减少。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Distribution of genotypes polymorphisms of genes markers of systemic inflammatory response among patients with STEMI
One of the important problems of modern medicine is the continuous increase of cardiovascular disease. An urgent problem at the present stage is the treatment of patients with acute forms of coronary heart disease, since vascular accidents are the leading causative factors of mortality from cardiovascular disease. Recently, an increasing number of studies have determined the role of genetic markers for predicting the adverse course of various cardiovascular diseases, including acute myocardial infarction. The distribution of genes markers of systemic inflammatory responses was determined in patients with STEMI. There are riteria for inclusion in the study: male and female patients from 46 to 75 years old; for postmenopausal women, more than 1 year; the presence of STEMI in the first 12 hours of the onset of the disease; informed consent of the patient to participate in the study. DNA was isolated from leukocytes from whole blood using the Express DNA Blood Kit (Litech). In the process of DNA extraction, the recommendations given in the kit instructions were followed. SNP polymorphisms of C-reactive protein genes were determined G-3014>A, tumor necrosis factor-α G-308>A, interleukin-10 G-1082>A by real-time polymerase chain reaction using a Rotor-Gene 6000 thermocycler (Corbett Research, Australia). The structure of the primers from the standard SNP-express-PB sets (Litech) was used. It was determined, that in patients with STEMI, an increase in the proportion of homozygotes (GG) and a decrease in heterozygotes (GA) of the genotypes of the G-3014>A polymorphism of the C-reactive protein gene are determined in comparison with the Hardy–Weinberg distribution. Polymorphism G-308>A of the tumor necrosis factor-α gene among patients with STEMI had a significant discrepancy with Hardy–Weinberg equilibrium, with an increase in the proportion of homozygotes (GG) and a decrease in heterozygotes (GA) and homozygotes (AA). The distribution of G-1082>A polymorphism of the interleukin-10 gene was characterized by an increase in the proportion of homozygotes (GG) and a decrease in heterozygotes (GA) in patients with STEMI compared to the Hardy–Weinberg distribution.
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