Increased plasma levels of tissue factor pathway inhibitor-activated factor X complex in patients with disseminated intravascular coagulation

被引:1
作者
Okugawa, Y
Wada, H
Noda, T
Sakakura, M
Nakasaki, T
Watanabe, R
Deguchi, H
Gabazza, EC
Mori, Y
Nishikawa, M
Deguchi, K
Nobori, T
Shiku, H
机构
[1] Mie Univ, Sch Med, Dept Internal Med 2, Tsu, Mie 514, Japan
[2] Mie Univ, Sch Med, Dept Clin Lab, Tsu, Mie 514, Japan
[3] Mie Univ, Sch Med, Dept Internal Med 3, Tsu, Mie 514, Japan
[4] Mie Red Cross Blood Ctr, Tsu, Mie, Japan
关键词
TFPI-Xa complex; TF; TFPI; pre-DIC; DIC;
D O I
10.1002/1096-8652(200011)65:3<210::AID-AJH6>3.0.CO;2-P
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Plasma levels of tissue factor pathway inhibitor (TFPI)-activated factor Xa (FXa) complex were measured in patients with disseminated intravascular coagulation (DIC), pre-DIG, and DIG. Plasma levels of plasmin-plasmin inhibitor complex (PPIC), D-dimer, and soluble fibrin monomer (SFM) were significantly higher in patients with DIG than in those with pre-DIG or non-DIG; the levels of these hemostatic markers were significantly higher in patients with pre-DIG than in those with non-DIG. Plasma levels of thrombin-antithrombin complex (TAT) were significantly higher in patients with DIG or pre-DIG than in those with non-DIG. Plasma levels of tissue factor (TF), total TFPI, free TFPI, and TFPI-Xa complex were significantly higher in patients with DIG than in those with non-DIC. Plasma levels of TFPI-Xa complex were significantly increased in patients with pre-DIG as compared to those with non-DIG; however, plasma free TFPI levels were significantly decreased in patients with pre-DIG as compared to those with non-DIG. These findings suggest that free TFPI might be consumed in the pre-DIG state, thereby confirming the activation of the extrinsic pathway. Plasma levels of TFPI-Xa complex were significantly correlated with TF, free TFPI, and total TFPI. Increased plasma TFPI-Xa complex levels might be useful for the diagnosis of DIG or pre-DIG, particularly that occurring by activation of the extrinsic pathway of blood coagulation. (C) 2000 Wiley-Liss, Inc.
引用
收藏
页码:210 / 214
页数:5
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