组织因子及组织因子通路抑制剂多态性对稳定型冠状动脉疾病凝血酶生成的影响。

Pathophysiology of Haemostasis and Thrombosis Pub Date : 2010-01-01 Epub Date: 2011-05-10 DOI:10.1159/000327491
Trine B Opstad, Alf-Aage R Pettersen, Vibeke Bratseth, Harald Arnesen, Ingebjørg Seljeflot
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引用次数: 6

摘要

在稳定性冠心病患者(n = 1,001)中,我们研究了组织因子(TF)和TF途径抑制剂(TFPI)多态性对体内凝血酶生成的影响,通过凝血酶原片段(F) 1和2来测量,以及通过校准的自动血栓图谱测定来测量体外凝血酶生成的潜力。此外,循环中TF和TFPI水平与凝血酶生成的不同参数相关。TF 5466和TFPI -399多态性与体内凝血酶生成较高相关,后者也与体外凝血酶生成滞后时间延长相关(p < 0.05)。TF -1812 TT和TF -603 GG基因型在繁殖期凝血酶峰值较低,凝血酶平均净激活率降低(p≤0.05),TFPI -33 TC基因型凝血酶延迟时间延长(p < 0.05),达到峰值的时间延长(p = 0.06)。观察到TFPI水平,凝血酶原片段1和2以及校准的自动血栓图参数之间的强相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The influence of tissue factor and tissue factor pathway inhibitor polymorphisms on thrombin generation in stable coronary artery disease.

In patients with stable coronary heart disease (n = 1,001) we investigated the influence of tissue factor (TF) and TF pathway inhibitor (TFPI) polymorphisms on thrombin generation in vivo, measured by prothrombin fragment (F) 1 and 2, and the potential to generate thrombin ex vivo, measured by the calibrated automated thrombogram assay. Additionally, circulating levels of TF and TFPI were correlated to the different parameters of thrombin generation. The TF 5466 and TFPI -399 polymorphisms associated with higher thrombin generation in vivo, the latter also with a prolonged lag time of the thrombin generation ex vivo(p < 0.05 for all).The TF -1812 TT and the TF -603 GG genotypes were associated with lower peak thrombin and a decreased average net rate of thrombin activation during the propagation phases (p ≤ 0.05), and the TFPI -33 TC genotype with prolonged lag time (p < 0.05) and additionally time to peak (p = 0.06). Strong correlations between TFPI levels, prothrombin fragment 1 and 2 as well as calibrated automated thrombogram parameters were observed.

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