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首页> 外文期刊>European journal of neurology: the official journal of the European Federation of Neurological Societies >Association of acute ischemic stroke with the MTHFR C677T polymorphism but not with NOS3 gene polymorphisms in a Singapore population.
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Association of acute ischemic stroke with the MTHFR C677T polymorphism but not with NOS3 gene polymorphisms in a Singapore population.

机译:在新加坡人群中,急性缺血性卒中与MTHFR C677T多态性相关,而与NOS3基因多态性无关。

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Background and purpose: The association of polymorphisms in the nitric oxide synthase 3 (NOS3) gene (T-786C, variable number tandem repeats 4A/B/C, and G894T) and in the methylenetetrahydrofolate reductase (MTHFR) gene (C677T) with acute ischemic stroke have been reported. Methods: First-time onset acute ischemic stroke patients (n = 120) and controls (n = 207) with no past history of stroke were compared. Allele specific gene amplification and restriction fragment length polymorphism (RFLP) analysis were used to determine the genotype and allelic frequencies in both groups. Plasma homocysteine (Hcy) and nitrite levels were measured. Results: No significant association of NOS3 polymorphisms with ischemic stroke was noted. The TT genotype of the MTHFR C677T polymorphism was significantly associated with ischemic stroke (P = 0.004). Elevated plasma Hcy levels were also significantly associated with ischemic stroke (P = 0.001). Conclusions: The TT genotype of C677T polymorphism in the MTHFR gene contributes to genetic susceptibility of acute ischemic stroke in a Singapore population.
机译:背景与目的:一氧化氮合酶3(NOS3)基因(T-786C,可变数目的串联重复序列4A / B / C和G894T)和亚甲基四氢叶酸还原酶(MTHFR)基因(C677T)的多态性与急性缺血性中风已有报道。方法:比较没有首次卒中史的首次发病的急性缺血性卒中患者(n = 120)和对照组(n = 207)。等位基因特异性基因扩增和限制性片段长度多态性(RFLP)分析用于确定两组的基因型和等位基因频率。测量血浆同型半胱氨酸(Hcy)和亚硝酸盐水平。结果:未发现NOS3多态性与缺血性卒中有显着相关性。 MTHFR C677T多态性的TT基因型与缺血性卒中显着相关(P = 0.004)。血浆Hcy水平升高也与缺血性卒中显着相关(P = 0.001)。结论:MTHFR基因中C677T多态性的TT基因型有助于新加坡人群急性缺血性卒中的遗传易感性。

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