Effect of Evolocumab on Coronary Plaque Phenotype and Burden in Statin-Treated Patients Following Myocardial Infarction

Evolocumab公司 医学 心脏病学 阿利罗库单抗 心肌梗塞 内科学 PCSK9 血管内超声 安慰剂 他汀类 纤维帽 耐受性 可欣 动脉粥样硬化 胃肠病学 胆固醇 泌尿科 载脂蛋白B 脂蛋白 病理 不利影响 载脂蛋白A1 替代医学 低密度脂蛋白受体
作者
Stephen J. Nicholls,Yu Kataoka,Steven E. Nissen,Francesco Prati,Stephan Windecker,Rishi Puri,Thomas Hucko,Daniel Aradi,Jean‐Paul R. Herrman,Renicus S. Hermanides,Bei Wang,Huei Wang,Julie Butters,Giuseppe Di Giovanni,Stephen Jones,Gianluca Pompili,Peter J. Psaltis
出处
期刊:Jacc-cardiovascular Imaging [Elsevier BV]
卷期号:15 (7): 1308-1321 被引量:421
标识
DOI:10.1016/j.jcmg.2022.03.002
摘要

The proprotein convertase subtilisin kexin type-9 inhibitor evolocumab produced coronary atheroma regression in statin-treated patients.The purpose of this study was to determine the effect of evolocumab on optical coherence tomography (OCT) measures of plaque composition.Patients with a non-ST-segment elevation myocardial infarction were treated with monthly evolocumab 420 mg (n = 80) or placebo (n = 81) for 52 weeks. Patients underwent serial OCT and intravascular ultrasound imaging within a matched arterial segment of a nonculprit vessel. The primary analysis determined the change in the minimum fibrous cap thickness and maximum lipid arc throughout the imaged arterial segment. Additional analyses determined changes in OCT features in lipid-rich plaque regions and plaque burden. Safety and tolerability were evaluated.Among treated patients (age 60.5 ± 9.6 years; 28.6% women; low-density lipoprotein cholesterol [LDL-C], 141.3 ± 33.1 mg/dL), 135 had evaluable imaging at follow-up. The evolocumab group achieved lower LDL-C levels (28.1 vs 87.2 mg/dL; P < 0.001). The evolocumab group demonstrated a greater increase in minimum fibrous cap thickness (+42.7 vs +21.5 μm; P = 0.015) and decrease in maximum lipid arc (-57.5o vs. -31.4o; P = 0.04) and macrophage index (-3.17 vs -1.45 mm; P = 0.04) throughout the arterial segment. Similar benefits of evolocumab were observed in lipid-rich plaque regions. Greater regression of percent atheroma volume was observed with evolocumab compared with placebo (-2.29% ± 0.47% vs -0.61% ± 0.46%; P = 0.009). The groups did not differ regarding changes in microchannels or calcium.The combination of statin and evolocumab after a non-ST-segment elevation myocardial infarction produces favorable changes in coronary atherosclerosis consistent with stabilization and regression. This demonstrates a potential mechanism for the improved clinical outcomes observed achieving very low LDL-C levels following an acute coronary syndrome. (Imaging of Coronary Plaques in Participants Treated With Evolocumab; NCT03570697).
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刘海英完成签到 ,获得积分10
1秒前
3秒前
4秒前
小马甲应助lll采纳,获得10
5秒前
5秒前
6秒前
7秒前
7秒前
JC325T发布了新的文献求助20
8秒前
123发布了新的文献求助10
9秒前
周济完成签到 ,获得积分10
9秒前
杭向彤鸭完成签到,获得积分10
10秒前
www发布了新的文献求助10
10秒前
evelynnni完成签到,获得积分10
10秒前
11秒前
所所应助狂野的幻翠采纳,获得10
12秒前
421发布了新的文献求助10
13秒前
我是老大应助林苏采纳,获得10
14秒前
16秒前
17秒前
桐桐应助忧郁柜子采纳,获得10
18秒前
万事遂意完成签到,获得积分10
20秒前
Lurant完成签到,获得积分10
22秒前
英吉利25发布了新的文献求助10
22秒前
SciGPT应助Lunar611采纳,获得10
22秒前
22秒前
卡斯优完成签到,获得积分20
23秒前
23秒前
SHANSHAN完成签到 ,获得积分10
26秒前
26秒前
AWYF完成签到,获得积分10
26秒前
Xlx发布了新的文献求助10
27秒前
兴奋的白桃完成签到,获得积分10
27秒前
彭十八完成签到,获得积分10
28秒前
西洲长风发布了新的文献求助10
29秒前
共享精神应助忧心的康采纳,获得10
31秒前
烟花应助一碗淘米水采纳,获得10
33秒前
今后应助421采纳,获得10
33秒前
OnlyHarbour完成签到,获得积分10
33秒前
兔子完成签到,获得积分10
33秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Developing Genetic Editing Tools for Lysobacter 2000
卤化钙钛矿人工突触的研究 2000
Моделирование процессов самоорганизации в кристаллообразующих системах 1000
History of U.S. Space Surveillance and Satellite Cataloging 1000
Adhesion Science: Principles & Practice 800
Signals, Systems, and Signal Processing 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6521455
求助须知:如何正确求助?哪些是违规求助? 8314730
关于积分的说明 17786544
捐赠科研通 5623742
什么是DOI,文献DOI怎么找? 2927686
邀请新用户注册赠送积分活动 1904426
关于科研通互助平台的介绍 1764631