Cleaved protein S (PS), total PS, free PS, and activated protein C cofactor activity as risk factors for venous thromboembolism

被引:10
作者
Borgel, D [1 ]
Reny, JL
Fischelis, D
Gandrille, S
Emmerich, J
Fiessinger, JN
Aiach, M
机构
[1] Hop Europeen Georges Pompidou, Serv Hematol Biol A, APHP, F-75908 Paris 15, France
[2] Hop Europeen Georges Pompidou, Serv Malad Vasc, APHP, Paris, France
[3] Univ Paris 05, UFR Pharm, INSERM 428, F-75270 Paris, France
关键词
D O I
10.1373/49.4.575
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: Although hereditary protein S (PS) deficiency is clearly associated with venous thromboembolism (VTE), the importance of low PS concentrations as a risk factor for VTE in other patients is still a matter of debate. To clarify this issue, we designed a case-control study to evaluate the role of different molecular forms of plasma PS. Methods: We quantified plasma cleaved, total, and free PS and activated protein C (APC) cofactor activity in 87 VTE patients and 174 controls matched for age, sex, and hormonal treatment. Free PS was measured by ELISA or by enzyme-linked ligand sorbent assay (ELSA). Cleaved and total PS were measured by ELISA. Results: In controls, the mean (SD) concentration of circulating cleaved PS was 39 (14) nmol/L, corresponding to 10% (3.5%) of total PS. Concentrations of cleaved PS and total PS were not significantly different in patients with VTE compared with controls. However, in our population, low free PS measured by ELISA or ELSA, as well as APC cofactor activity values were significantly associated with VTE with odds ratios (95% confidence intervals) of 2.9 (1.3-6.3), 2.5 (1.1-75.6), and 2.9 (1.3-6.4), respectively, in multivariate analyses. Conclusion: Phenotypic low PS detected by APC cofactor activity assay or by an assay specific for free PS should be considered a risk factor,for VTE. (C) 2003 American Association for Clinical Chemistry.
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页码:575 / 580
页数:6
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