Novel Antiplatelet Agents in Cardiovascular Disease

被引:28
|
作者
Tscharre, Maximilian [1 ,2 ]
Michelson, Alan D. [3 ]
Gremmel, Thomas [1 ,2 ,4 ]
机构
[1] Landesklinikum Wiener Neustadt, Dept Internal Med Cardiol & Nephrol, Wiener Neustadt, Austria
[2] Karl Landsteiner Soc, Inst Vasc Med & Cardiac Electrophysiol, St Polten, Austria
[3] Harvard Med Sch, Dana Farber Boston Childrens Canc & Blood Disorde, Ctr Platelet Res Studies, Boston, MA 02115 USA
[4] Med Univ Vienna, Dept Internal Med 2, Waehringer Guertel 18-20, A-1090 Vienna, Austria
关键词
antiplatelet therapy; cardiovascular disease; targets; PROTEIN DISULFIDE-ISOMERASE; INDUCED PLATELET-AGGREGATION; P2Y(12) RECEPTOR ANTAGONIST; THROMBUS FORMATION; GLYCOPROTEIN-VI; PHOSPHOINOSITIDE; 3-KINASE; ARTERIAL THROMBOSIS; EX-VIVO; ACTIVATION; GPIIB/IIIA;
D O I
10.1177/1074248419899314
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Antiplatelet therapy reduces atherothrombotic risk and has therefore become a cornerstone in the treatment of cardiovascular disease. Aspirin, adenosine diphosphate P2Y(12) receptor antagonists, glycoprotein IIb/IIIa inhibitors, and the thrombin receptor blocker vorapaxar are effective antiplatelet agents but significantly increase the risk of bleeding. Moreover, atherothrombotic events still impair the prognosis of many patients with cardiovascular disease despite established antiplatelet therapy. Over the last years, advances in the understanding of thrombus formation and hemostasis led to the discovery of various new receptors and signaling pathways of platelet activation. As a consequence, many new antiplatelet agents with high antithrombotic efficacy and supposedly only moderate effects on regular hemostasis have been developed and yielded promising results in preclinical and early clinical studies. Although their long journey from animal studies to randomized clinical trials and finally administration in daily clinical routine has just begun, some of the new agents may in the future become meaningful additions to the pharmacological armamentarium in cardiovascular disease.
引用
收藏
页码:191 / 200
页数:10
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