CIRCULATING THROMBOMODULIN AS A NOVEL ENDOTHELIAL-CELL MARKER - COMPARISON OF ITS BEHAVIOR WITH VONWILLEBRAND-FACTOR AND TISSUE-TYPE PLASMINOGEN-ACTIVATOR

被引:107
作者
TAKAHASHI, H
ITO, S
HANANO, M
WADA, K
NIWANO, H
SEKI, Y
SHIBATA, A
机构
[1] First Department of Internal Medicine, Niigata University School of Medicine, Niigata
关键词
THROMBOMODULIN; ENDOTHELIAL CELL INJURY; VONWILLEBRAND FACTOR; TISSUE-TYPE PLASMINOGEN ACTIVATOR;
D O I
10.1002/ajh.2830410107
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Circulating thrombomodulin is a novel endothelial cell marker, which may reflect the endothelial injury. Plasma levels of thrombomodulin were quantitated by an enzyme-linked immunosorbent assay (ELISA) in patients with hematological malignancies, liver disease, diabetes mellitus, collagen disease, thrombotic disease, and disseminated intravascular coagulation (DIC), and the thrombomodulin values were compared with those of von Willebrand factor antigen (vWf:Ag) and tissue-type plasminogen activator (t-PA) which are released from stimulated or damaged endothelial cells. The mean plasma concentrations of thrombomodulin in these disease states were elevated as compared with healthy subjects. A relatively high mean thrombomodulin level was observed in DIC, liver disease, and collagen disease. Abnormally high thrombomodulin values (> normal mean value + 3 SD) were found in 32.3% of patients with hematological malignancies, 57.7% of patients with liver disease, 39.3% of patients with diabetes mellitus, 30.0% of patients with collagen disease, 23.1% of patients with thrombotic disease, and 69.0% of patients with DIC. Plasma concentrations of both vWf:Ag and t-PA were also elevated in these patients. On the whole, the plasma thrombomodulin concentration was positively correlated with vWf:Ag (r = 0.441, P < 0.001) and t-PA (r = 0.398, P < 0.001). These findings indicate that the elevation of plasma thrombomodulin is frequently seen in a variety of diseases and circulating thrombomodulin is possibly useful for evaluating the endothelial damage in selected disease states.
引用
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页码:32 / 39
页数:8
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