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首页> 外文期刊>Kobe journal of medical sciences >Methylenetetrahydrofolate Reductase Gene Polymorphism and Ischemic Stroke: Sex Difference in Japanese.
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Methylenetetrahydrofolate Reductase Gene Polymorphism and Ischemic Stroke: Sex Difference in Japanese.

机译:亚甲基四氢叶酸还原酶基因多态性与缺血性中风:日语中的性别差异。

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Moderately elevated plasma homocysteine levels have been established as independent risk factors in vascular disease, including ischemic stroke. Recently, a common mutation (C677T) in the 5,10-methylenetetrahydrofolate reductase (MTHFR) gene reducing the activity of MTHFR and increasing homocysteine levels in plasma was reported. The C677T MTHFR mutation may be a risk factor for ischemic stroke, but the results of previous studies have been conflicting. One possible explanation is that the association with the MTHFR genotype may be different according to gender. To investigate the association for ischemic stroke, we conducted a case-control study of 77 hospital cases (49 men and 28 women) with ischemic stroke and 229 (120 men and 109 women) control subjects in Japanese. The prevalence of conventional vascular risk factors and MTHFR genotypes were determined in case and controls. After adjustment by multiple analysis in all there was no statistical significance in MTHFR genotypes. The conventional vascular risk factors such as diabetes mellitus (adjusted odds ratio [OR], 17.21), hypertension (adjusted OR, 4.67), smoking habit (adjusted OR, 4.70), and hyperlipidemia (adjusted OR, 2.73) were identified independently associated with ischemic stroke. With a separate sex analysis it was identified that the relationship of the MTHFR T/T gneotype was statisticaly significant in women (adjusted OR, 9.49; 95% CI, 1.75-51.47, P=0.0091). The relevance of the MTHFR T/T mutation appears to be restricted to women, suggesting a role of female hormones in the resistance to elevated homocysteine levels due to the MTHFR T/T mutation.
机译:血浆同型半胱氨酸水平的中度升高已被确定为包括缺血性中风在内的血管疾病的独立危险因素。最近,据报道5,10-亚甲基四氢叶酸还原酶(MTHFR)基因中的常见突变(C677T)降低了MTHFR的活性并增加了血浆中的高半胱氨酸水平。 C677T MTHFR突变可能是缺血性中风的危险因素,但先前的研究结果相互矛盾。一种可能的解释是,与MTHFR基因型相关的性别可能有所不同。为了调查与缺血性卒中的关系,我们进行了一项病例对照研究,研究了77例缺血性卒中的医院病例(49例男性和28例女性)和229例日语对照患者(120例男性和109例女性)。在病例和对照中确定了常规血管危险因素和MTHFR基因型的患病率。经过多重分析调整后,MTHFR基因型均无统计学意义。与糖尿病相关的常规血管危险因素(调整后的优势比[OR]为17.21),高血压(调整后的OR为4.67),吸烟习惯(调整后的OR为4.70)和高脂血症(调整后的OR为2.73)与以下因素独立相关:缺血性中风。通过单独的性别分析,发现MTHFR T / T基因型的关系在女性中具有统计学意义(校正OR,9.49; 95%CI,1.75-51.47,P = 0.0091)。 MTHFR T / T突变的相关性似乎仅限于女性,这表明女性荷尔蒙在由于MTHFR T / T突变而对高半胱氨酸水平产生抗性的作用。

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