Vorapaxar, a Protease-Activated Receptor-1 Antagonist, a Double-Edged Sword!

Bharti Bhandari, Bharati Mehta
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引用次数: 7

Abstract

Acute coronary syndrome (ACS) constitutes a group of pathophysiological entities resulting from reduced blood flow in the coronary arteries leading to decreased or improper functioning or death of heart muscle. Such patients are usually prescribed combination antiplatelet drug therapy, containing acetylsalicylic acid (aspirin) and an adenosine diphosphate receptor inhibitor to prevent recurrence of ischemic events. The combination prophylactic therapy to certain extend has been successful in preventing secondary complications including ischemic/thrombotic events in these patients. However, research is still on for newer advances in anti-thrombotic therapy that can further prevent secondary complications of Acute Coronary Syndrome. Vorapaxar is a newer drug recommended along with aspirin or clopidogril for prevention of recurrence of cardiac events. Vorapaxar, a thrombin receptor antagonist acts by reversible inhibition of the protease-activated receptor-1 (PAR-1). PAR-1 is expressed on platelets, and it inhibits platelet aggregation, both thrombin-induced and thrombin receptor agonist peptide (TRAP)-induced. Various trials world -wide have documented its efficacy as an anti-platelet agent for preventing recurrent cardiovascular ischemic events but at the expense of increased bleeding complications including intracranial haemorrhage (ICH), when compared to standard therapy alone. For the same reason, vorapaxar is contraindicated in patients with prior stroke, transient ischemic attack and ICH. U.S. Food and Drug Administration (FDA) approved vorapaxar in May 2014 as an antiplatelet agent along with standard anti-platelet therapy for the reduction of recurring thrombotic cardiovascular events in patients with a history of myocardial infarction or with peripheral arterial disease. Vorapaxar is developed and marketed by Merck Sharp Dohme and is available by the brand name 'Zontivity' as 2.5 mg oral tablet equivalent to 2.08 mg of vorapaxar sulfate. There are two patents protecting this drug.

蛋白酶激活受体-1拮抗剂Vorapaxar是一把双刃剑!
急性冠状动脉综合征(Acute冠脉综合征,ACS)是由冠状动脉血流减少导致心肌功能下降或不正常或死亡而引起的一组病理生理实体。这类患者通常给予联合抗血小板药物治疗,包括乙酰水杨酸(阿司匹林)和二磷酸腺苷受体抑制剂,以防止缺血事件复发。联合预防治疗在一定程度上成功地预防了这些患者的继发性并发症,包括缺血/血栓事件。然而,研究仍在寻找抗血栓治疗的新进展,以进一步预防急性冠状动脉综合征的继发性并发症。Vorapaxar是一种较新的药物,与阿司匹林或氯吡格雷一起推荐用于预防心脏事件的复发。Vorapaxar是一种凝血酶受体拮抗剂,通过可逆抑制蛋白酶激活受体-1 (PAR-1)起作用。PAR-1在血小板上表达,它抑制凝血酶诱导和凝血酶受体激动肽(TRAP)诱导的血小板聚集。世界各地的各种试验都证明了其作为抗血小板药物预防复发性心血管缺血事件的有效性,但与单独标准治疗相比,其代价是出血并发症增加,包括颅内出血(ICH)。出于同样的原因,有卒中、短暂性脑缺血发作和脑出血史的患者禁用沃拉帕沙。美国食品和药物管理局(FDA)于2014年5月批准vorapaxar作为抗血小板药物,与标准抗血小板治疗一起用于减少有心肌梗死史或外周动脉疾病患者复发性血栓性心血管事件。Vorapaxar由Merck Sharp Dohme开发和销售,其品牌名为“Zontivity”,为2.5毫克口服片剂,相当于2.08毫克硫酸Vorapaxar。这种药有两项专利保护。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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