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首页> 外文期刊>Thrombosis and Haemostasis: Journal of the International Society on Thrombosis and Haemostasis >A new T-287C polymorphism in the 5' regulatory region of the tissue factor pathway inhibitor gene. Association study of the T-287C and C-399T polymorphisms with coronary artery disease and plasma TFPI levels.
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A new T-287C polymorphism in the 5' regulatory region of the tissue factor pathway inhibitor gene. Association study of the T-287C and C-399T polymorphisms with coronary artery disease and plasma TFPI levels.

机译:组织因子途径抑制剂基因的5'调控区的新T-287C多态性。 T-287C和C-399T多态性与冠状动脉疾病和血浆TFPI水平的关联研究。

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摘要

Tissue factor pathway inhibitor (TFPI) is an important regulator of the extrinsic blood coagulation pathway. We screened the untranslated 5' region of the TFPI gene for polymorphisms and investigated their possible involvement in arterial thrombosis. The allele frequencies of a new polymorphism, located 287 base pairs upstream of the transcription start site (T-287C), and that of the previously described C-399T polymorphism, were similar in cases and controls. In controls, the -287C allele was associated with significantly higher levels of total TFPI antigen, arguing for an effect of this polymorphism on TFPI gene expression. In controls, the C-399T polymorphism did not alter TFPI levels. In the cases, however, decreased total and post-heparin free TFPI levels and increased F1+2 levels were significantly associated with the -399T allele. These findings suggest that the T-287C and C-399T polymorphisms are not associated with an increased risk of coronary heart disease, a result which should be confirmed by a larger study. However, their influence on outcome, or a link with subtypes of acute coronary syndromes, cannot be excluded.
机译:组织因子途径抑制剂(TFPI)是外在凝血途径的重要调节剂。我们筛选了TFPI基因的未翻译的5'区域的多态性,并调查了它们可能参与动脉血栓形成。在病例和对照中,位于转录起始位点(T-287C)上游287个碱基对的新多态性的等位基因频率与先前描述的C-399T多态性的等位基因频率相似。在对照中,-287C等位基因与总TFPI抗原的显着较高水平相关,认为该多态性对TFPI基因表达有影响。在对照中,C-399T多态性没有改变TFPI水平。但是,在这种情况下,-399T等位基因显着降低了肝素总量和肝素释放后的TFPI水平,并增加了F1 + 2水平。这些发现表明,T-287C和C-399T多态性与冠心病风险增加无关,这一结果应通过更大的研究予以证实。但是,不能排除它们对预后的影响或与急性冠脉综合征亚型的联系。

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