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Intensive Lipid-lowering for Plaque and Major Adverse Cardiovascular Events in Low to Intermediate 10-year ASCVD Risk Population

Effects of Intensive Lipid-lowering on Coronary Atherosclerotic Plaque Phenotype and Major Adverse Cardiovascular Events in Adults With Low to Intermediate 10-year ASCVD Risk: a Prospective, Randomized, Open-label, Blinded Endpoint Analysis(PROBE)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05462262
Acronym
ILLUMINATION
Enrollment
2900
Registered
2022-07-18
Start date
2022-10-10
Completion date
2029-08-01
Last updated
2026-07-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coronary Artery Disease Progression

Brief summary

Current guidelines recommend moderate-intensity lipid-lowering therapy (goal for LDL-C \<2.6 mmol/L or 30%-50% reduction from baseline) for patients with intermediate 10-year ASCVD risk. In these patients, early coronary atherosclerotic plaques detected by coronary CT angiography are common, but further interventions are lacking. This study aims to analyze whether intensive lipid-lowering therapy (goal for LDL-C \<1.8 mmol/L or ≥50% reduction from baseline) could delay the progression of coronary atherosclerotic lesions and reduce the adverse cardiovascular events in these target patients.

Detailed description

Both American (2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease) and European (2019 ESC/EAS Guidelines for the management of dyslipidemias) guidelines currently recommended moderate-intensity lipid-lowering (goal for LDL-C \<2.6 mmol/L or 30%-50% reduction from baseline) for primary prevention in the population at intermediate (or borderline) 10-year ASCVD risk, but the residual risk in this group of the population remains to be explored, especially in a subset with only nonobstructive atherosclerotic plaques detected by CCTA, for whom further risk stratification and precise interventions for primary prevention are lacking. CCTA could show accurate images of patients' early coronary atherosclerotic lesions and provides a wealth of image-based anatomical and functional information including plaque burden (total plaque volume, calcification score, segment involvement score, etc.), plaque composition, high-risk plaque characteristics, luminal stenosis, and CT-FFR. With this complete imaging information on CCTA, there is an urgent need to investigate primary prevention strategies and the evidence-based rationale for performing precise risk stratification in low to intermediate-risk populations with nonobstructive coronary atherosclerotic lesions using CCTA. A prospective, randomized, open-label, blinded endpoint analysis (PROBE) will be conducted in the population at clinical low to intermediate 10-year ASCVD risk with nonobstructive coronary atherosclerotic lesions, predominantly non-calcified plaques detected by CCTA. The purpose of this study is to demonstrate that intensive lipid-lowering could slow down plaque progression and reduce the incidence of MACE in the target population, which provides an evidence-based rationale for further risk re-stratification. Enrolled people will be randomized into the intervention group (goal for LDL-C \<1.8 mmol/L or ≥50% reduction from baseline) and the control group (goal for LDL-C \<2.6 mmol/L or 30%-50% reduction from baseline).

Interventions

DRUGIntensive lipid-lowering control

The initial recommended therapy is 10-20mg atorvastatin plus Ezetimibe, and the type and dosage of drugs can be adjusted according to the situation.

DRUGModerate-intensity lipid-lowering control

The initial recommended therapy is 10-20mg atorvastatin, and the type and dosage of drugs can be adjusted according to the situation.

Sponsors

Chinese Academy of Medical Sciences, Fuwai Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Masking description

blinded endpoint

Eligibility

Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Age 40-75 years 2. Low to Intermediate 10-year atherosclerotic cardiovascular disease (ASCVD) risk using pooled cohort equations (PCE). 3. Coronary CT angiography shows atherosclerotic plaque in the main coronary vessels (\>2mm diameter) with luminal stenosis \<70%

Exclusion criteria

1. Combination with serious cardiovascular diseases, including 1. Heart failure (ejection fraction \<30%) 2. Arrhythmias (persistent atrial flutter/atrial fibrillation, second-degree or third-degree atrioventricular block) 3. Hemodynamically important valvular disease 4. Hemodynamically important congenital heart disease 5. Stroke 2. Myocardial infarction, coronary revascularization, or severe/unstable angina before or within 1 month of screening 3. Active liver disease or hepatic dysfunction (defined as alanine aminotransferase or aspartate aminotransferase\> 3 times the upper limit of normal) 4. Unexplained creatine phosphokinase\> 6 times the upper limit of normal 5. Nephrotic syndrome 6. Diabetes mellitus 7. Uncontrollable hypertension 8. Uncontrollable hypothyroidism 9. Hypersensitivity to statins 10. Any planned surgical procedure for the treatment of atherosclerosis 11. Gastrointestinal diseases affecting drug absorption or history of gastrointestinal surgery 12. Survival-limiting diseases 13. Concurrent long-term immunosuppressive therapy 14. Participation in another clinical trial concurrently or within 30 days before screening 15. Pregnant or breastfeeding 16. Other unsuitable situations deemed by physicians

Design outcomes

Primary

MeasureTime frameDescription
Major Adverse Cardiovascular Events (MACE)Within 3 years after the enrollmentComposite of all-cause death, non-fatal MI, non-fatal stroke, any revascularization, and hospitalization for angina

Secondary

MeasureTime frameDescription
Change in coronary total plaque volume(mm³) on CCTAWithin 3 years after the enrollmentTotal plaque volume(mm³) is defined as the sum of all plaque volumes for coronary arteries.
Change in coronary plaque burden(%) on CCTAWithin 3 years after the enrollmentPlaque burden(%)=(plaque area/vessel area)×100%
Changes in coronary plaque compositions(mm³, %) on CCTAWithin 3 years after the enrollmentPlaque compositions include lipid(\<30 HU), fibrous(30-150HU), and calcified plaque(\>350HU).
Changes in coronary high-risk plaque characteristics on CCTAWithin 3 years after the enrollmentHigh-risk plaque characteristics are defined as positive remodeling(remodeling index, \>1.1), low CT attenuation (mean CT number \<30 HU), spotty calcification(punctate calcium within a plaque measuring less than 3 mm in all dimensions), or napkin-ring sign (a ringlike peripheral higher attenuation with central low CT attenuation).
Change in coronary artery calcium score (CACS) on CTWithin 3 years after the enrollmentCACS is a quantification of all coronary calcification by the scoring algorithm proposed by Agatston et al.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 21, 2026