心肌梗死后血栓活性升高:一项2年随访研究。

Haemostasis Pub Date : 1998-11-01 DOI:10.1159/000022446
V Martínez-Sales, V Vila, E Réganon, M A Goberna, F Ferrando, M A Palencia, J Aznar
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引用次数: 26

摘要

本研究研究了心肌梗死(MI)患者服用阿司匹林(200 mg/天)2年后血栓形成活动的演变。在7、30、60、90、120、150、180、360和720天收集10例患者的血浆样本。在所有样品中,我们测量了纤维蛋白原(Fg)、高分子量Fg (HMW-Fg)、纤维蛋白肽A (FPA)、凝血酶原片段1+2 (F1+2)、β -血栓球蛋白(β - tg)、血管性血友病因子(vWF)、组织因子(TF)和TF途径抑制剂(TFPI)。与正常组相比,患者在研究开始时血浆Fg、HMW-Fg、FPA、F1+2、β - tg和vWF水平显著升高。95%置信区间为Fg 277 ~ 333 mg/dl, HMW-Fg 200 ~ 244 mg/dl, FPA 5.3 ~ 16.5 ng/ml, F1+2 1.4 ~ 1.8 nmol/l, β - tg 110 ~ 118 IU/ml, vWF 139 ~ 195%。在第30天,Fg和HMW-Fg恢复到正常水平,而FPA和F1+2水平在整个研究过程中持续升高。在120天和150天,β - tg和vWF分别恢复到正常水平。凝血酶生成和活性的增加表明心肌梗死后2年仍处于持续高凝状态。在研究的2年期间,血浆中TF和TFPI水平与正常值相比没有统计学上的显著变化。总之,这些结果表明心肌梗死后这些患者凝血酶的持续产生和活性以及细胞活化。
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Elevated thrombotic activity after myocardial infarction: A 2-year follow-up study.

This study examines the evolution of the thrombotic activity in patients with myocardial infarction (MI) treated with aspirin (200 mg/day) for 2 years after MI. Plasma samples of 10 patients were collected at 7, 30, 60, 90, 120, 150, 180, 360 and 720 days. In all the samples we measured fibrinogen (Fg), high molecular weight Fg (HMW-Fg), fibrinopeptide A (FPA), prothrombin fragment 1+2 (F1+2), beta-thromboglobulin (beta-TG), von Willebrand factor (vWF), tissue factor (TF) and TF pathway inhibitor (TFPI). The plasma Fg, HMW-Fg, FPA, F1+2, beta-TG and vWF levels were significantly elevated in the patients at the beginning of the study as compared to the normal group. The 95% confidence intervals were Fg 277-333 mg/dl, HMW-Fg 200-244 mg/dl, FPA 5.3-16.5 ng/ml, F1+2 1.4-1.8 nmol/l, beta-TG 110-118 IU/ml and vWF 139-195%. At thirty days Fg and HMW-Fg returned to normal levels, whereas the increase in FPA and F1+2 levels persisted throughout the study. At 120 and 150 days, respectively, beta-TG and vWF returned to normal levels. The increase in thrombin generation and activity pointed to a persistent hypercoagulable state 2 years after MI. Plasma levels of TF and TFPI showed no statistically significant variations with respect to the normal values over the 2-year period studied. In conclusion, these results suggest a persistent generation and activity of thrombin and cellular activation in these patients after MI.

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