γ-谷氨酰羧化酶基因rs2592551多态性与缺血性动脉粥样硬化血栓性卒中的相关性分析。

Ye I Dubovyk, V Yu Harbuzova, O A Obukhova, A V Ataman
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引用次数: 0

摘要

对170例缺血性动脉粥样硬化性血栓性脑卒中患者和124例无急性脑血管疾病(对照组)的γ-谷氨酰羧化酶基因rs2592551多态性检测结果进行了评价。结果显示,rs2592551多态性与乌克兰人群缺血性卒中相关。T/T基因型患者发生本病的风险高于主要c等位基因携带者(优势比(OR) = 3.117;95%置信区间(CI) = 1.016-9.566;P = 0.047)。根据动脉粥样硬化的某些危险因素将患者分成亚组,在女性和非吸烟者中也建立了类似的关联。同时,与C/C和T/T基因型相比,女性杂合子基因型(C/T)对缺血性脑卒中的发展具有显著的保护作用(OR = 0.460;95% ci 0.213-0.994;P = 0.048)。即使在调整了年龄、体重指数、吸烟和高血压等因素后,这些结果仍然具有统计学意义。
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[ANALYSIS OF γ-GLUTAMYL CARBOXYLASE GENE rs2592551 POLYMORPHISM ASSOCIATION WITH ISCHEMIC ATHEROTHROMBOTIC STROKE].

The results of γ-glutamyl carboxylase gene rs2592551 polymorphism determining in 170 patients with ischemic atherothrombotic stroke and 124 subjects without acute cerebrovascular disease (control group) have been evaluated. Obtained results revealed that rs2592551 polymorphism was related to ischemic stroke in Ukrainian population. The risk for this disease in patients with T/T genotype was higher than in major C-allele carriers (odds ratio (OR) = 3.117; 95% confidence interval (CI) = 1.016-9.566; P = 0.047). After dividing patients into subgroups, formed by the presence of certain risk factors for atherosclerosis, similar association has been established for women and non-smokers. At the same time, the heterozygous genotype (C/T) in females had significantly protective effect against ischemic stroke development when compared to C/C and T/T genotypes (OR = 0.460; 95% CI 0.213-0.994; P = 0.048). Statistical significance of these results persisted even after adjustment for age, body mass index, smoking and hypertension.

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