慢性肾衰竭患者凝血酶生成增加。

A Sagripanti, V Cozza, U Baicchi, M Camici, A Cupisti, G Barsotti
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引用次数: 21

摘要

血浆凝血酶原片段1 + 2 (F1 + 2)的浓度被认为是特异性检测潜伏性高凝的一个非常敏感的参数。为了评估慢性尿毒症相关的高凝程度,我们用ELISA法检测了51例重度或终末期慢性肾功能衰竭患者血浆中的F1 + 2(男性35例,女性16例,年龄22-81岁):24例饮食治疗,15例联合饮食和每周一次血液透析,12例定期维持血液透析;健康受试者33例作为对照组。饮食组血浆F1 + 2显著升高;在每周一次血液透析组中进一步增加,在维持性血液透析组中更显着增加。在饮食治疗的患者中,血浆F1 + 2与血清肌酐呈正相关。在维持性血液透析患者中,F1 + 2血浆水平在单次血液透析过程中未发现升高。7例患者在饮食治疗中使用低分子肝素,导致血浆F1 + 2水平显著下降,这表明F1 + 2水平升高表明体内凝血酶生成加速,而不是肾脏分解代谢受损。凝血激活的增强似乎与残余肾功能的减少有关,即与肾功能衰竭的严重程度有关,并可能导致尿毒症患者血管事件的风险增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Increased thrombin generation in patients with chronic renal failure.

The plasma concentration of prothrombin fragment 1 + 2 (F1 + 2) is considered a very sensitive parameter for specific detection of latent hypercoagulability. To evaluate the degree of hypercoagulation associated with chronic uremia, we measured F1 + 2 by ELISA in the plasma of 51 patients with severe or end-stage chronic renal failure (35 males, 16 females, aged 22-81 years): 24 on dietary treatment 15 on combined dietary and once a week hemodialysis, and 12 on regular maintenance hemodialysis; 33 healthy subjects served as a control group. Plasma F1 + 2 showed a significant elevation in the group on dietary treatment; it was further increased in the group on once a week hemodialysis, and even more markedly increased in the group on maintenance hemodialysis. In patients on dietary treatment a positive correlation was found between plasma F1 + 2 and serum creatinine. In patients on maintenance hemodialysis, no increase in the F1 + 2 plasma level was found during the course of a single hemodialysis session. Low molecular weight heparin, administered to 7 patients on dietary treatment, caused a marked drop in the F1 + 2 plasma level, providing evidence that the elevation in F1 + 2 indicates an accelerated in vivo thrombin generation rather than impaired renal catabolism. The enhanced coagulation activation appears to be related to the reduction of residual renal function, i.e., to the severity of renal failure, and may contribute to the increased risk of vascular events in uremic patients.

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