Effect of PCSK9 Inhibitors on Coronary Atherosclerotic Plaques Derived From Optical Coherence Tomography in Patients With Premature Coronary Artery Disease: a Randomized Controlled Trial
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
- 入组人数
- 396
- 试验地点
- 1
- 主要终点
- Calcification
研究概览
简要总结
The presence of coronary atherosclerotic vulnerable plaque significantly impacts the clinical outcomes of patients diagnosed with coronary artery disease (CAD). However, the influence of PCSK9 inhibitors on stabilizing coronary atherosclerotic plaques in individuals with early-onset CAD, evaluated through optical coherence tomography (OCT), remains inadequately understood. Moreover, there is a notable absence of relevant randomized controlled trials investigating this phenomenon. This current study represents a single-center, randomized, controlled, open-label trial conducted among Asian patients with early-onset CAD. Its principal objective was to explore the effects of PCSK9 inhibitors on coronary atherosclerotic plaque morphology as assessed by OCT.
详细描述
Following initial percutaneous coronary intervention (PCI) for culprit lesions in patients with early-onset coronary artery disease (CAD) and ≥2 additional lesions meeting baseline lipid criteria, optical coherence tomography (OCT) was employed to evaluate non-culprit lesion sites for detailed characterization of plaque features including calcification, fibrosis, fibrolipid deposition, necrosis, minimum fibrous cap thickness (mFCT), and maximum lipid arc (MLA). Subsequently, patients were randomized in a 1:1 ratio to receive either intensive statin therapy alone or a combination of PCSK9 inhibitor with moderate-intensity statin therapy, using a random number allocation method. After 1 year of treatment and follow-up, OCT reassessment of non-culprit vessel critical lesions was conducted, documenting plaque characteristics such as calcification, fibrosis, fibrolipid content, necrosis, as well as stability parameters like mFCT and MLA at lesion sites. OCT findings were compared longitudinally within each treatment group and between groups receiving PCSK9 inhibitor combined with statin therapy versus intensive statin therapy alone. Baseline clinical profiles, biochemical markers, imaging findings, and incidence of adverse cardiovascular events during the follow-up period were also meticulously recorded for all enrolled early-onset CAD patients.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 65 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Men aged 18-55 years and women aged 18-65 years;
- •CAD patients with coronary angiographically confirmed lesions in ≥2 vessels; at least one vessel was critically diseased (50-70% stenosis level);
- •LDL-C >3.4 mmol/L without regular statin therapy or LDL-C >1.8 mmol/L after 4 weeks of statin lipid-lowering therapy.
排除标准
- •Known allergies or contraindications to PCSK9 inhibitors and/or statin therapy;
- •Prior use of PCSK9 inhibitors;
- •Prior history of hemorrhagic stroke;
- •Prior coronary artery bypass grafting or coronary intervention;
- •Inability to perform OCT imaging or unclear imaging;
- •Severe renal insufficiency (creatinine clearance < 30 mL/min);
- •Severe hepatic dysfunction;
- •Baseline triglycerides > 5.6 mmol/L;
- •Pregnant or lactating women;
- •Life expectancy not exceeding 1 year;
- •In the judgment of the investigator, unsuitable for this study for any reason.
研究组 & 干预措施
PCSK9 inhibitor group
PCSK9 Inhibitors Combined with Moderate-Intensity Statin Therapy
干预措施: PCSK9 inhibitor (Drug)
Intensive statin group
Intensive statin therapy
干预措施: Statin (Drug)
结局指标
主要结局
Calcification
时间窗: Immediate and 1 year after PCI
calcification
Fibrosis
时间窗: Immediate and 1 year after PCI
fibrosis
Fibrolipid deposition
时间窗: Immediate and 1 year after PCI
fibrolipid deposition
Necrosis
时间窗: Immediate and 1 year after PCI
necrosis
MLA
时间窗: Immediate and 1 year after PCI
maximum lipid arc
mFCT
时间窗: Immediate and 1 year after PCI
minimum fibrous cap thickness
次要结局
未报告次要终点
研究者
Zhenyan Fu, PHD
Principle Investigator
First Affiliated Hospital of Xinjiang Medical University
