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改善急性冠状动脉综合征患者心血管结局的新兴治疗选择:聚焦洛索匹明。

Emerging treatment options to improve cardiovascular outcomes in patients with acute coronary syndrome: focus on losmapimod.

作者信息

Kragholm Kristian, Newby Laura Kristin, Melloni Chiara

机构信息

Duke Clinical Research Institute, Duke University Medical Center, Durham, NC, USA.

出版信息

Drug Des Devel Ther. 2015 Aug 5;9:4279-86. doi: 10.2147/DDDT.S69546. eCollection 2015.

Abstract

Each year, despite optimal use of recommended acute and secondary prevention therapies, 4%-5% of patients with acute coronary syndrome (ACS) experience relapse of ACS or other cardiovascular events including stroke, heart failure, or sudden cardiac death after the index ACS. The sudden atherosclerotic plaque rupture leading to an ACS event is often accompanied by inflammation, which is thought to be a key pathogenic pathway to these excess cardiovascular events. Losmapimod is a novel, oral p38 mitogen-activated protein kinase (MAPK) inhibitor that targets MAPKs activated in macrophages, myocardium, and endothelial cells that occur as a part of global coronary vascular inflammation following plaque rupture. This review aims to 1) discuss the pathophysiological pathways through which p38 MAPKs may play key roles in initiation and progression of inflammatory disease and how losmapimod is thought to counteract these p38 MAPKs, and 2) to describe the efficacy and safety data for losmapimod obtained from preclinical studies and randomized controlled trials that support the hypothesis that it has promise as a treatment for patients with ACS.

摘要

尽管每年都对急性冠脉综合征(ACS)患者优化使用推荐的急性和二级预防疗法,但仍有4%-5%的ACS患者在首次发生ACS后出现ACS复发或其他心血管事件,包括中风、心力衰竭或心源性猝死。导致ACS事件的动脉粥样硬化斑块突然破裂通常伴有炎症,炎症被认为是这些额外心血管事件的关键致病途径。洛索匹莫德是一种新型口服p38丝裂原活化蛋白激酶(MAPK)抑制剂,其靶向在巨噬细胞、心肌和内皮细胞中被激活的MAPK,这些细胞在斑块破裂后作为整体冠状动脉血管炎症的一部分而出现。本综述旨在:1)讨论p38 MAPK可能在炎症性疾病的发生和发展中发挥关键作用的病理生理途径,以及洛索匹莫德被认为如何对抗这些p38 MAPK;2)描述从临床前研究和随机对照试验中获得的关于洛索匹莫德的疗效和安全性数据,这些数据支持其有望作为ACS患者治疗药物的假设。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/36aa/4532348/0d3e3d66e2b0/dddt-9-4279Fig1.jpg

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