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The Effect of MTHFR Gene C677t Polymorphism on the Diagnosis of St-Elevation Myocardial Infarction

机译:MTHFR基因C677T多态性对ST升高心肌梗死诊断的影响

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Diverse studies have attempted to identify the association between Methylenetetrahydrofolate Reductase (MTHFR) gene C677T polymorphism and myocardial infarction (MI) which finally remain inconclusive. We aimed to investigate the possible associations between C677T polymorphism and ST-elevationmyocardial infarction(STEMI). Studywas conducted by considering case-control as 78 patients with STEMI and 77 other participants with no cardiovascular disease (CVD), ages 30 and higher. A polymerase chain reaction-restriction fragment length polymorphism assay (PCR-RFLP) was performed to determine the C677T polymorphism in all participants. Moreover, a questionnaire was used to assess the demographic and clinical characteristics of all participants. This study showed no significant relationship between MTHFR gene C677T polymorphism and STEMI. However, a highly signi?cant association was also evidenced in between this typeof mutationand hypertension. The resultsofthis study showed no significant relationship between MTHFR gene C677T mutation and MI risk. But the MTHFR gene C677T mutation polymorphism showed a significant relationship withhypertension.
机译:不同的研究已经试图鉴定甲基四氢呋喃酸盐还原酶(MTHFR)基因C677T多态性和心肌梗塞(MI)之间的关联,其最终保持不确定。我们旨在研究C677T多态性和ST-exivationMyeachard梗死(Stemi)之间的可能关联。通过考虑案例控制的学习和78名患者的STEMI和77名没有心血管疾病(CVD),年龄较高和更高的患者进行。进行聚合酶链反应限制片段长度多态性测定(PCR-RFLP)以确定所有参与者中的C677T多态性。此外,调查问卷用于评估所有参与者的人口统计和临床特征。该研究表明MTHFR基因C677T多态性和STEMI之间没有显着的关系。然而,这种类型的蛋白质和高血压之间也可以在高度符号中证明具有高度标志性的。结果表明MTHFR基因C677T突变与MI风险之间没有显着的关系。但MTHFR基因C677T突变多态性显示出与高效的显着关系。

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