Effects of the oral direct thrombin inhibitor ximelagatran on P-selectin expression and thrombin generation in atrial fibrillation

被引:17
作者
Wolzt, M
Boström, SL
Svensson, M
Wåhlander, K
Grind, M
Sarich, TC
机构
[1] AstraZeneca LP, Wilmington, DE 19850 USA
[2] Univ Vienna, Dept Clin Pharmacol, Vienna, Austria
[3] AstraZeneca R&D, Molndal, Sweden
[4] Sahlgrens Univ Hosp, Dept Clin Chem & Transfus Med, S-41345 Gothenburg, Sweden
[5] AstraZeneca R&D Charnwood, Loughborough, Leics, England
关键词
ximelagatran; melagatran; P-selectin; endogenous thrombin potential; atrial fibrillation;
D O I
10.1159/000073849
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This study investigated the pharmacodynamic effects of the oral direct thrombin inhibitor ximelagatran on platelet activation and thrombin generation in patients with nonvalvular atrial fibrillation. Using an open, group-matched study design, the effects of ximelagatran ( 36 mg twice daily for 5 days) were studied in 12 patients with permanent nonvalvular atrial fibrillation and in 12 healthy controls. After ximelagatran for 5 days, elevated platelet P- selectin expression in atrial fibrillation patients was lowered to that during coumarin treatment or in controls but had no effect in control subjects. Using the endogenous thrombin potential as a marker, ximelagatran decreased and delayed thrombin generation in both groups. In conclusion, direct thrombin inhibition with ximelagatran reduced elevated platelet P- selectin expression and inhibited thrombin generation. Copyright (C) 2003 S. Karger AG, Basel.
引用
收藏
页码:68 / 74
页数:7
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