Overall haemostasis potential assays performed in thrombophilic plasma: the effect of preactivating protein C and antithrombin

被引:8
作者
Andresen, MS
Iversen, N
Abildgaard, U [1 ]
机构
[1] Aker Univ Hosp, Dept Med, Haematol Res Lab, N-0514 Oslo, Norway
[2] Ullevaal Univ Hosp, Dept Med Genet, Oslo, Norway
关键词
thrombophilia; blood coagulation; thrombin; fibrin generation; protein S; laboratory method;
D O I
10.1016/S0049-3848(03)00067-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: The overall haemostatic potential (OHP) assay records fibrin polymerisation in plasma by areas under the opacity curve. The authors reported high area values in pregnancy, and still higher values in preeclampsia. We wanted to see if the assay detects thrombophilia, and particularly, if the area values were high in congenital combined protein S (PS) and the FV R506Q Leiden mutation, since low protein S and increased activated protein C (APC) resistance occur in pregnancy and preeclampsia. Materials and methods: The original overall haemostatic potential assay and our modified version with Protac and pentasaccharide to enhance inhibition by activation of protein C and by antithrombin (AT) were performed in plasma from 18 persons with thrombophilia. Seven had combined protein S deficiency and heterozygous FV Leiden mutation. Results: In the original assay, median area values in controls and thrombophilic plasma samples were similar. In the modified assay, area values tended to be lower in controls than in the thrombophilia group (P=0.035). The enhanced inhibition reduced area values more in control plasmas (median reduction 34.7%) than in thrombophilic plasmas (median reduction 2.2%) (P=0.0017). The responses to activation were also low in warfarin-treated patients with thrombophilia. Conclusions: High area values in pregnancy with the original assay are probably not caused by insufficient inhibition. The response to activation of protein C and antithrombin, as calculated by the difference between the original and a modified assay, was subnormal in thrombophilic plasma, but there was an overlap with the results in controls. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:323 / 328
页数:6
相关论文
共 15 条
  • [1] BEGUIN S, 1989, THROMB HAEMOSTASIS, V61, P397
  • [2] Bertina RM, 1997, CLIN CHEM, V43, P1678
  • [3] BREMME K, 1992, OBSTET GYNECOL, V80, P132
  • [4] THROMBIN REGULATION IN MOTHER AND FETUS DURING PREGNANCY
    DELORME, MA
    BURROWS, RF
    OFOSU, FA
    ANDREW, M
    [J]. SEMINARS IN THROMBOSIS AND HEMOSTASIS, 1992, 18 (01) : 81 - 90
  • [5] DUCHEMIN J, 1994, THROMB HAEMOSTASIS, V71, P331
  • [6] EXNER T, 1988, THROMB HAEMOSTASIS, V59, P40
  • [7] CHANGES IN PROTEIN-C AND PROTEIN-S LEVELS IN NORMAL-PREGNANCY
    FAUGHT, W
    GARNER, P
    JONES, G
    IVEY, B
    [J]. AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1995, 172 (01) : 147 - 150
  • [8] A laboratory method for determination of overall haemostatic potential in plasma.: I.: Method design and preliminary results
    He, S
    Bremme, K
    Blombäck, M
    [J]. THROMBOSIS RESEARCH, 1999, 96 (02) : 145 - 156
  • [9] A simple and rapid laboratory method for determination of haemostasis potential in plasma II.: Modifications for use in routine laboratories and research work
    He, S
    Antovic, A
    Blombäck, M
    [J]. THROMBOSIS RESEARCH, 2001, 103 (05) : 355 - 361
  • [10] Hemker HC, 2000, THROMB HAEMOSTASIS, V83, P589