Overview
The primary objective was to evaluate the effect of PCSK9 inhibitors in addition to the background lipid-modifying therapy (LMT), compared with placebo plus background LMT in terms of clinical outcomes in patients with coronary CT angiography (CCTA)-detected high-risk plaques.
Description
CCTA is an accurate, noninvasive alternative to invasive coronary angiography. CCTA can provide detailed information about the characteristics of coronary artery plaques, such as their composition, morphology, and distribution. Various CCTA-detected plaque characteristics indicative of plaque quantity and quality have been identified as high-risk features independently predicting clinical events, including the presence of positive remodeling, low attenuation plaque, spotty calcification, and napkin ring sign. Currently, the treatment for CCTA-detected high-risk plaque has been receiving increasing interest. The current study aimed to prove the efficacy of PCSK9 inhibitors in addition to the background LMT, as compared with placebo plus background LMT in patients with CCTA-detected high-risk plaques.
Hypothesis: PCSK9 inhibitors in addition to background LMT will show a superior event rate, compared with placebo plus background LMT, in terms of major adverse cardiac and cerebrovascular events (MACCEs) at 24 months after the last patient's randomization in patients with high-risk coronary plaques assessed by CT Angiography.
Eligibility
Inclusion Criteria:
- Subject must be ≥ 18 years.
- Patients with at least one target lesion meet CCTA-detected plaque features of the
- following
-
- Degree of stenosis ≥ 50%
- At least 2 of the following high-risk plaque features:
- Low-attenuation plaque ii. Positive remodeling iii. Napkin-ring sign iv. Spotty calcium
- The target lesion is located at the proximal or mid segment of left anterior
descending artery, left circumflex artery or right coronary artery.
- Subject is able to confirm his/her understanding of the risks, benefits, and treatment alternatives of receiving study-related treatment. He/she or his/her legally authorized representative provides written informed consent prior to any study-related procedure.
Exclusion Criteria:
- Target lesions underwent or planned to revascularization.
- Patients with acute coronary syndrome.
- New York Heart Association class III or IV, or last known left ventricular ejection fraction < 30%.
- Uncontrolled or recurrent ventricular tachycardia.
- Homozygous familial hypercholesterolemia.
- Active liver disease or hepatic dysfunction.
- Failed CCTA plaque analysis.
- Non-cardiac co-morbid conditions with life expectancy < 2 years.
- Pregnant and/or lactating women.
- Known hypersensitivity or contraindication to statin or PCSK9 inhibitors.