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Hyperhomocysteinemia and Methylenetetrahydrofolate Reductase C677T Polymorphism in Cerebral Veno-sinus Thrombosis

机译:高同型半胱氨酸血症和亚甲基四氢叶酸还原酶C677T基因多态性与脑静脉窦血栓形成。

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There is limited data on the role of hyperhomocysteinemia as a risk factor for cerebral veno-sinus thrombosis (CVT) in Indians. We examined the association between plasma homocysteine (Hcy), methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism, and CVT in 185 patients with aseptic CVT (puerperal 80 and nonpuerperal 105) and 248 healthy controls (puerperal 67 and nonpuerperal 181). Fasting Hcy was higher in patients compared to controls (20.25 ± 5.97 vs 9.81 ± 5.19 μmol/L, P MTHFR 677TT compared to 677CT and 677CC genotypes (34.44 ± 32.8 vs 25.81 ± 33.3 vs 18.50 ± 23.7 μmol/L, respectively, P MTHFR 677TT was insignificant (OR: 1.91, 95% CI: 0.53-7.06). We conclude that hyperhomocysteinemia is a risk marker for Indian patients with aseptic CVT. MTHFR 677TT genotype is not linked with CVT but is a determinant of plasma Hcy.
机译:关于高同型半胱氨酸血症作为印度人脑静脉窦血栓形成(CVT)危险因素的作用的数据有限。我们检查了185例无菌CVT(产褥期80和非产褥期105)和248名健康对照(产褥期67和非产褥期181)的血浆同型半胱氨酸(Hcy),亚甲基四氢叶酸还原酶(MTHFR)C677T多态性和CVT之间的关系。患者的空腹Hcy比对照组高(20.25±5.97 vs 9.81±5.19μmol/ L,P MTHFR 677TT与677CT和677CC基因型(34.44±32.8 vs 25.81±33.3 vs 18.50±23.7μmol/ L,P MTHFR 677TT无关紧要(OR:1.91,95%CI:0.53-7.06)我们得出结论,高同型半胱氨酸血症是印度人无菌CVT的危险标志物,MTHFR 677TT基因型与CVT无关,而是血浆Hcy的决定因素。

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