阿利罗库单抗
医学
替卡格雷
普拉格雷
P2Y12
内科学
他汀类
PCSK9
临床终点
四分位间距
安慰剂
经皮冠状动脉介入治疗
心肌梗塞
心脏病学
随机对照试验
载脂蛋白B
胆固醇
病理
脂蛋白
替代医学
载脂蛋白A1
低密度脂蛋白受体
作者
Yasushi Ueki,Jonas Häner,Sylvain Losdat,Giuseppe Gargiulo,Hiroki Shibutani,Sarah Bär,Tatsuhiko Otsuka,Raminta Kavaliauskaite,Vera Mitter,Fabrice Temperli,David Spirk,Stefan Stortecky,George C.M. Siontis,Marco Valgimigli,Stephan Windecker,Clemens Gutmann,Konstantinos C. Koskinas,Manuel Mayr,Lorenz Räber
出处
期刊:Thrombosis and Haemostasis
[Georg Thieme Verlag KG]
日期:2023-08-18
卷期号:124 (06): 517-527
被引量:4
摘要
The effect of the PCSK9 (proprotein convertase subtilisin/kexin type 9) inhibitor alirocumab on platelet aggregation among patients with acute myocardial infarction (AMI) remains unknown. We aimed to explore the effect of alirocumab added to high-intensity statin therapy on P2Y12 reaction unit (PRU) among AMI patients receiving dual antiplatelet therapy (DAPT) with a potent P2Y12 inhibitor (ticagrelor or prasugrel). In addition, we assessed circulating platelet-derived noncoding RNAs (microRNAs and YRNAs).
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