Assessing the impact of evolocumab on thin-cap fibroatheroma and endothelial function in patients with very high-risk atherosclerotic cardiovascular disease: a study protocol for a randomized controlled trial.

IF 2.1 3区 医学 Q3 CARDIAC & CARDIOVASCULAR SYSTEMS Cardiovascular diagnosis and therapy Pub Date : 2024-12-31 Epub Date: 2024-12-19 DOI:10.21037/cdt-24-336
Bingyu Gao, Nan Nan, Mingduo Zhang, Jinfan Tian, Yanlong Ren, Yuguo Xue, Min Zhang, Xiantao Song, Changjiang Ge
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Abstract

Background: The prevalence of very high-risk atherosclerotic cardiovascular disease (ASCVD) is significant in China, with suboptimal rates of low-density lipoprotein cholesterol (LDL-C) compliance exacerbating plaque instability and causing a higher incidence of major adverse cardiac events (MACEs). Proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i) are effective in reducing LDL-C levels, increase the stability of vulnerable plaque, and influence the progression of atherosclerosis through multiple mechanisms as demonstrated in animal studies. However, there is currently a lack of in vivo evidence regarding the efficacy and safety of high-intensity statin therapy combined with PCSK9i in the secondary prevention of ASCVD in the Chinese population. This study aims to demonstrate the efficacy of high-intensity statins combined with PCSK9i on vulnerable plaques in very high-risk ASCVD patients through intravascular imaging and non-invasive endothelial function test.

Methods: This randomized, open-label, prospective clinical study involves 240 patients with very high-risk ASCVD who meet the criteria outlined in the 2023 Chinese lipid management guidelines. Patients recruitment will be processed in Beijing Anzhen Hospital from January 2021 to December 2024. Patients with thin-cap fibroatheroma (TCFA) detected by optical coherence tomography (OCT) are randomly assigned in a 1:1 ratio to the evolocumab group (evolocumab 140 mg every 2 weeks plus atorvastatin 40 mg nightly) or the standard treatment group (atorvastatin 40 mg nightly). The primary endpoint is the absolute change of the minimum fibrous cap thickness (FCT) at a median follow-up of 1 year. The secondary endpoints are other OCT metrics, assessment of MACE rates, alterations in serum lipid profiles and markers of inflammation, endothelial function, and adverse drug reactions. Logistic regression, analysis of covariance (ANCOVA), Kaplan-Meier curve survival analysis, and Cox regression will be used to investigate the relationship between variables and endpoints.

Discussion: The purpose of this study is to evaluate the efficacy of high-intensity statin therapy combined to PCSK9i for the secondary prevention of coronary artery disease in Chinese patients with very high-risk ASCVD. The results will provide evidence to optimize the management of this high-risk population.

Trial registration: This study was registered on chictr.org.cn (ChiCTR2000032570).

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评估evolocumab对高危动脉粥样硬化性心血管疾病患者薄帽纤维粥样硬化瘤和内皮功能的影响:一项随机对照试验的研究方案
背景:非常高危的动脉粥样硬化性心血管疾病(ASCVD)在中国的患病率非常高,低密度脂蛋白胆固醇(LDL-C)依从性的次优率加剧了斑块不稳定性,并导致主要不良心脏事件(mace)的发生率升高。动物研究表明,蛋白转化酶枯草杆菌素/ keexin 9型抑制剂(PCSK9i)可有效降低LDL-C水平,增加易损斑块的稳定性,并通过多种机制影响动脉粥样硬化的进展。然而,目前缺乏关于高强度他汀类药物联合PCSK9i在中国人群ASCVD二级预防中的有效性和安全性的体内证据。本研究旨在通过血管内成像和无创内皮功能测试,证明高强度他汀类药物联合PCSK9i对高危ASCVD患者易损斑块的疗效。方法:这项随机、开放标签、前瞻性临床研究纳入240例高危ASCVD患者,这些患者符合2023年中国脂质管理指南中概述的标准。2021年1月至2024年12月在北京安贞医院进行患者招募。通过光学相干断层扫描(OCT)检测到的薄帽纤维粥样瘤(TCFA)患者按1:1的比例随机分配到evolocumab组(evolocumab 140 mg每2周加阿托伐他汀40 mg每晚)或标准治疗组(阿托伐他汀40 mg每晚)。主要终点是最小纤维帽厚度(FCT)的绝对变化,中位随访1年。次要终点是其他OCT指标、MACE率评估、血脂谱改变和炎症标志物、内皮功能和药物不良反应。采用Logistic回归、协方差分析(ANCOVA)、Kaplan-Meier曲线生存分析、Cox回归等方法研究变量与终点之间的关系。讨论:本研究的目的是评价高强度他汀类药物联合PCSK9i对中国高危ASCVD患者冠状动脉疾病二级预防的疗效。研究结果将为优化这一高危人群的管理提供依据。试验注册:本研究已在chictr.org.cn注册(ChiCTR2000032570)。
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来源期刊
Cardiovascular diagnosis and therapy
Cardiovascular diagnosis and therapy Medicine-Cardiology and Cardiovascular Medicine
CiteScore
4.90
自引率
4.20%
发文量
45
期刊介绍: The journal ''Cardiovascular Diagnosis and Therapy'' (Print ISSN: 2223-3652; Online ISSN: 2223-3660) accepts basic and clinical science submissions related to Cardiovascular Medicine and Surgery. The mission of the journal is the rapid exchange of scientific information between clinicians and scientists worldwide. To reach this goal, the journal will focus on novel media, using a web-based, digital format in addition to traditional print-version. This includes on-line submission, review, publication, and distribution. The digital format will also allow submission of extensive supporting visual material, both images and video. The website www.thecdt.org will serve as the central hub and also allow posting of comments and on-line discussion. The web-site of the journal will be linked to a number of international web-sites (e.g. www.dxy.cn), which will significantly expand the distribution of its contents.
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