The use of coagulation activation markers (soluble fibrin polymer, TpP™, prothrombin fragment 1.2, thrombin-antithrombin, and D-dimer) in the assessment of hypercoagulability in patients with inherited and acquired prothrombotic disorders

被引:15
作者
Arkel, YS [1 ]
Paidas, MJ [1 ]
Ku, DH [1 ]
机构
[1] NYU, Med Ctr, Dept Ob Gyn, Maternal & Fetal Med Div, New York, NY 10016 USA
关键词
activation markers; hypercoaguable disorders; TpP; factor V Leiden; prothrombin gene mutation; anticardiolipin antibodies/lupus inhibitor;
D O I
10.1097/00001721-200204000-00005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A total of 260 consecutive patients, referred for hypercoagulable assessment, was included in this study. Four coagulation activation markers were utilized to assess these patients [enzyme-linked immunosorbent assays for soluble fibrin polymer (TpP), prothrombin fragment 1.2, thrombin-antithrombin complex, and D-dimer]. The mean levels of the activation markers directly correlated with the number of hypercoagulable abnormalities. The percentage of patients with increased TpP levels for each group was lower than the other activation markers. The findings indicate that activation markers reflect the number of underlying thrombophilic abnormalities. Our data suggest that there is a utility in performing a panel of coagulation activation markers to assess the thrombotic risk. The measurement of soluble fibrin polymer may be more reflective of an impending vascular event. (C) 2002 Lippincott Williams Wilkins.
引用
收藏
页码:199 / 205
页数:7
相关论文
共 18 条
[11]  
KOELEMAN BPC, 1994, BLOOD, V84, P1031
[12]  
Manten B, 1996, THROMB HAEMOSTASIS, V76, P510
[13]   INHERITED PREDISPOSITION TO THROMBOSIS [J].
MILETICH, JP ;
PRESCOTT, SM ;
WHITE, R ;
MAJERUS, PW ;
BOVILL, EG .
CELL, 1993, 72 (04) :477-480
[14]   HEREDITARY-DEFICIENCY OF ANTITHROMBIN-III, PROTEIN-C AND PROTEIN-S - PREVALENCE IN PATIENTS WITH A HISTORY OF VENOUS THROMBOSIS AND CRITERIA FOR RATIONAL PATIENT SCREENING [J].
PABINGER, I ;
BRUCKER, S ;
KYRLE, PA ;
SCHNEIDER, B ;
KORNINGER, HC ;
NIESSNER, H ;
LECHNER, K .
BLOOD COAGULATION & FIBRINOLYSIS, 1992, 3 (05) :547-553
[15]   A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis [J].
Poort, SR ;
Rosendaal, FR ;
Reitsma, PH ;
Bertina, RM .
BLOOD, 1996, 88 (10) :3698-3703
[16]   Prothrombin fragment 1+2 and thrombin-antithrombin complex levels in patients with inherited APC resistance due to factor V Leiden mutation [J].
Simioni, P ;
Scarano, L ;
Gavasso, S ;
Sardella, C ;
Girolami, B ;
Scudeller, A ;
Girolami, A .
BRITISH JOURNAL OF HAEMATOLOGY, 1996, 92 (02) :435-441
[17]   Gene-gene and gene-environment interactions determine risk of thrombosis in families with inherited antithrombin deficiency [J].
van Boven, HH ;
Vandenbroucke, JP ;
Briët, E ;
Rosendaal, FR .
BLOOD, 1999, 94 (08) :2590-2594
[18]  
Zoller B, 1996, THROMB HAEMOSTASIS, V75, P270