Gao Bingyu, Nan Nan, Zhang Mingduo, Tian Jinfan, Ren Yanlong, Xue Yuguo, Zhang Min, Song Xiantao, Ge Changjiang
Department of Cardiology, Beijing An Zhen Hospital, Capital Medical University, Beijing Institute of Heart, Lung and Blood Vessel Diseases, Beijing Engineering Research Center of Cardiovascular Wisdom Diagnosis and Treatment, Beijing, China.
Cardiovasc Diagn Ther. 2024 Dec 31;14(6):1236-1246. doi: 10.21037/cdt-24-336. Epub 2024 Dec 19.
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 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.
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.
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.
This study was registered on chictr.org.cn (ChiCTR2000032570).
在中国,极高风险的动脉粥样硬化性心血管疾病(ASCVD)患病率颇高,低密度脂蛋白胆固醇(LDL-C)达标率欠佳,这加剧了斑块不稳定,导致主要不良心脏事件(MACE)发生率更高。前蛋白转化酶枯草溶菌素/kexin 9型抑制剂(PCSK9i)在降低LDL-C水平方面有效,可增加易损斑块的稳定性,并通过动物研究中所证实的多种机制影响动脉粥样硬化的进展。然而,目前在中国人群中,关于高强度他汀类药物治疗联合PCSK9i在ASCVD二级预防中的疗效和安全性缺乏证据。本研究旨在通过血管内成像和非侵入性内皮功能测试,证明高强度他汀类药物联合PCSK9i对极高风险ASCVD患者易损斑块的疗效。
本随机、开放标签、前瞻性临床研究纳入240例符合2023年中国血脂管理指南标准的极高风险ASCVD患者。患者招募将于2021年1月至2024年12月在北京安贞医院进行。通过光学相干断层扫描(OCT)检测到薄帽纤维粥样斑块(TCFA)的患者按1:1比例随机分配至依洛尤单抗组(每2周皮下注射依洛尤单抗140mg,每晚口服阿托伐他汀40mg)或标准治疗组(每晚口服阿托伐他汀40mg)。主要终点是在中位随访1年时最小纤维帽厚度(FCT)的绝对变化。次要终点包括其他OCT指标、MACE发生率评估、血脂谱和炎症标志物变化、内皮功能以及药物不良反应。将采用逻辑回归、协方差分析(ANCOVA)、Kaplan-Meier曲线生存分析和Cox回归来研究变量与终点之间的关系。
本研究的目的是评估高强度他汀类药物联合PCSK9i在中国极高风险ASCVD患者冠状动脉疾病二级预防中的疗效。研究结果将为优化这一高危人群的管理提供依据。
本研究已在中国临床试验注册中心(www.chictr.org.cn)注册(注册号:ChiCTR2000032570)。