Koopman M M W, Büller H R
Department of Vascular Medicine, Academic Medical Centre, Amsterdam, The Netherlands. m.m.koopman.uva.nl
J Intern Med. 2003 Oct;254(4):335-42. doi: 10.1046/j.1365-2796.2003.01226.x.
Inhibition of activated coagulation factor X (FXa) is an attractive target for antithrombotic treatment strategies, because of the central position of FXa in the coagulation cascade. Most of the now available anticoagulant drugs have inhibitory effects not only on FXa, but also on thrombin. With the development of pentasaccharides, a new class of antithrombotic agents has emerged that acts by specific inhibition of FXa and lacks activity against FIIa. Fondaparinux, the first synthetic short-acting pentasaccharide, has been evaluated, in a large phase II and III clinical programme concerning prophylaxis and treatment of venous thromboembolism and also in phase II studies in patients with acute coronary syndromes. Idraparinux, the long-acting pentasaccharide, has been studied in a dose-finding study in patients with established deep-vein thrombosis and phase III studies are now planned in patients with venous thromboembolism and in patients with atrial fibrillation.
抑制活化凝血因子X(FXa)是抗血栓治疗策略的一个有吸引力的靶点,因为FXa在凝血级联反应中处于核心地位。目前大多数可用的抗凝药物不仅对FXa有抑制作用,而且对凝血酶也有抑制作用。随着戊糖的发展,一类新的抗血栓药物出现了,其作用机制是特异性抑制FXa且对凝血因子IIa(FIIa)无活性。磺达肝癸钠是首个合成的短效戊糖,已在一项关于静脉血栓栓塞症预防和治疗的大型II期和III期临床研究项目中进行了评估,并且也在急性冠脉综合征患者中进行了II期研究。依达肝素是长效戊糖,已在已确诊的深静脉血栓形成患者中进行了剂量探索研究,目前计划在静脉血栓栓塞症患者和房颤患者中开展III期研究。