[N5, n10 -亚甲基四氢叶酸还原酶基因C(677)—>T多态性对多种危险因素人群缺血性卒中发展的影响分析]。

V. Harbuzova, O. V. Polonikov, D. O. Stroi, O. Matlai, Iu O Ataman, V. A. Sukharieva, O. Ataman
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引用次数: 1

摘要

本文报道了170例缺血性动脉粥样硬化性血栓性卒中(IATS)患者和124例健康人(对照组)的mthfr基因C(677)- >T (rs1801133)多态性检测结果。结果表明,IATS患者主纯合子(CC)、杂合子(CT)和次纯合子(TT)的频率分别为52.4、35.9、11.8%(对照组分别为46.0、48.4、5.6%,χ 2检验P = 0.044)。TT纯合子发生IATS的几率高于主c等位基因(CT + CC)携带者(OR = 2.3, CI = 0.911 ~ 5.449, P = 0.049)。在乌克兰人口的代表中,MTHFR基因C(677)- >t多态性基因型的频率与IATS的风险之间存在关系。这种联系表现在男性患者、血压正常的人以及没有吸烟习惯的人身上。患者的性别、体重指数、血压和吸烟会影响所研究的多态性与脑卒中相关的水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Analysis of the effect of N5, N10-methylenetetrahydrofolate reductase gene C(677)-->T polymorphism on the ischemic stroke development in persons with various risk factors].
The results ofMTHFR gene C(677)-->T (rs1801133) polymorphism determined in 170 patients with ischemic atherothrombotic stroke (IATS) and 124 healthy subjects (control group) are presented in the paper. It has been shown that in patients with IATS, the frequencies of main homozygotes (CC), heterozygotes (CT) and minor homozygotes (TT) are 52.4, 35.9, 11.8% (in control--46.0, 48.4, 5.6%, P = 0.044 by chi2-test). TT homozygotes have a greater chance of developing IATS than carriers of main C-allele (CT + CC) (OR = 2.3, CI = 0.911-5.449, P = 0.049). In the representatives of the Ukrainian population there is a relationship between the frequency of MTHFR gene C(677)-->T polymorphism genotypes and the risk of IATS. This connection is manifested in male patients, in persons with normal blood pressure, and in people who do not have the habit of smoking. The sex of the patients, body mass index, blood pressure and smoking affect the level of the studied polymorphism association with stroke.
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