Anticoagulant action of melagatran, the active form of the oral direct thrombin inhibitor ximetagatran, in umbilical cord and adult plasma: an in vitro examination

被引:10
作者
Koestenberger, M
Gallistl, S
Cvirn, G
Baier, K
Leschnik, B
Muntean, W
机构
[1] Graz Univ, Dept Pediat, A-8036 Graz, Austria
[2] Karl Franzens Univ, Dept Pediat, Ludwig Boltzmann Res Inst Pediat Hemostasis & Thr, Graz, Austria
[3] Karl Franzens Univ Graz, Inst Med Chem, Dept Pediat, Graz, Austria
[4] Karl Franzens Univ Graz, Pregl Lab, Dept Pediat, Graz, Austria
关键词
melagatran; oral direct thrombin inhibitor; ximetagatran; umbilical cord plasma; adult plasma;
D O I
10.1016/j.thromres.2004.07.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: This study was performed to compare the anticoagulant activity of melagatran, the active form of the oral direct thrombin inhibitor ximelagatran, in umbilical cord plasma with that in adult plasma. In contrast with the most frequently administered anticoagulants, the heparins, melagatran acts independently of antithrombin (AT). As a consequence, administration of melagatran is of special interest in neonates, who have physiologically low levels of AT. Materials and methods: Plasma samples were activated under high (as used in standard clotting assays) and low (more comparable with the physiological milieu) coagulant challenge. In the absence of melagatran, adult plasma clotted significantly faster than umbilical cord plasma under high coagulant challenge. Conversely, under low coagulant challenge, clotting of adult plasma was significantly delayed compared with umbilical cord plasma. For both high and tow coagulant challenges, clotting times increased and prothrombin fragment 1.2 and thrombin-antithrombin (TAT) formation decreased with melagatran in a concentration-dependent fashion in umbilical cord and adult plasma. With increasing melagatran concentrations, the quotient between prothrombin fragment 1.2 and TAT formation increased in adult and umbilical cord plasma under both high and tow coagulant challenges. Results and conclusions: Our in vitro results cannot be directly extrapolated to clinical efficacy, but assessing the degree of inhibition of thrombin generation may be a useful surrogate for selecting effective doses of ximetagatran for in vivo studies in neonates with thromboembolic complications. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:135 / 142
页数:8
相关论文
共 30 条
[1]  
ANDREW M, 1990, THROMB HAEMOSTASIS, V63, P27
[2]  
ANDREW M, 1994, THROMB HAEMOSTASIS, V72, P836
[3]   DEVELOPMENT OF THE HUMAN COAGULATION SYSTEM IN THE FULL-TERM INFANT [J].
ANDREW, M ;
PAES, B ;
MILNER, R ;
JOHNSTON, M ;
MITCHELL, L ;
TOLLEFSEN, DM ;
POWERS, P .
BLOOD, 1987, 70 (01) :165-172
[4]  
ANDREW M, 1990, AM J PEDIAT HEMATOL, V12, P95
[5]   Normal thrombin generation [J].
Butenas, S ;
van't Veer, C ;
Mann, KG .
BLOOD, 1999, 94 (07) :2169-2178
[6]  
Chan AKC, 2002, THROMB HAEMOSTASIS, V87, P606
[7]   Elevated thrombin-forming capacity of tissue factor-activated cord compared with adult plasma [J].
Cvirn, G ;
Gallistl, S ;
Rehak, T ;
Jürgens, G ;
Muntean, W .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2003, 1 (08) :1785-1790
[8]   Low tissue factor pathway inhibitor (TFPI) together with low antithrombin allows sufficient thrombin generation in neonates [J].
Cvirn, G ;
Gallistl, S ;
Leschnik, B ;
Muntean, W .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2003, 1 (02) :263-268
[9]   Effects of antithrombin and protein C on thrombin generation in newborn and adult plasma [J].
Cvirn, G ;
Gallistl, S ;
Muntean, W .
THROMBOSIS RESEARCH, 1999, 93 (04) :183-190
[10]   THE COAGULATION CASCADE - INITIATION, MAINTENANCE, AND REGULATION [J].
DAVIE, EW ;
FUJIKAWA, K ;
KISIEL, W .
BIOCHEMISTRY, 1991, 30 (43) :10363-10370