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[Anti-platelets without a bleeding risk: novel targets and strategies].

机译:[没有出血风险的抗血小板:新的靶标和策略]。

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摘要

Anti-platelet agents such as aspirin, clopidogrel and antagonists of integrin αIIbβ3 allowed to efficiently reduce morbidity and mortality associated with arterial thrombosis. A major limit of these drugs is that they increase the risk of bleeding. During the last few years, several innovative anti-thrombotic strategies with a potentially low bleeding risk were proposed. These approaches target the collagen receptor glycoprotein (GP) VI, the GPIb/von Willebrand factor axis, the thrombin receptor PAR-1, the activated form of integrin αIIbβ3 or the ADP receptor P2Y1. While an antagonist of PAR-1 was recently marketed, the clinical proofs of the efficiency and safety of the other agents remain to be established. This review evaluates these new anti-platelet approaches toward safer anti-thrombotic therapies.
机译:抗血小板药,例如阿司匹林,氯吡格雷和整联蛋白αIIbβ3拮抗剂,可有效降低与动脉血栓形成有关的发病率和死亡率。这些药物的主要限制是它们会增加出血的风险。在过去的几年中,提出了一些具有潜在的低出血风险的创新抗血栓形成策略。这些方法靶向胶原蛋白受体糖蛋白(GP)VI,GPIb / von Willebrand因子轴,凝血酶受体PAR-1,整联蛋白αIIbβ3的活化形式或ADP受体P2Y1。尽管最近已经销售了PAR-1拮抗剂,但其他药物的有效性和安全性的临床证据仍有待建立。这篇综述评估了这些新的抗血小板方法,以实现更安全的抗血栓形成疗法。

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