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

Primary Purpose

Coronary Artery Disease Progression

Status
Recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Intensive lipid-lowering control
Moderate-intensity lipid-lowering control
Sponsored by
Chinese Academy of Medical Sciences, Fuwai Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Coronary Artery Disease Progression

Eligibility Criteria

40 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age 40-75 years
  2. Intermediate(and borderline) 10-year atherosclerotic cardiovascular disease (ASCVD) risk by using pooled cohort equations (PCE).
  3. Coronary CT angiography shows non-calcified plaque-dominated lesions in the main coronary vessels (>2mm diameter) with luminal stenosis <50%

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 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

Sites / Locations

  • Fuwai HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

intensive lipid-lowering group

moderate-intensity lipid-lowering group

Arm Description

Goal for LDL-C <1.8 mmol/L or ≥50% reduction from baseline.

Goal for LDL-C <2.6 mmol/L or 30%-50% reduction from baseline.

Outcomes

Primary Outcome Measures

Major Adverse Cardiovascular Events (MACE)
Composite of all-cause death, non-fatal MI, non-fatal stroke, any revascularization, and hospitalization for angina

Secondary Outcome Measures

Change in coronary total plaque volume(mm³) on CCTA
Total plaque volume(mm³) is defined as the sum of all plaque volumes for coronary arteries.
Change in coronary plaque burden(%) on CCTA
Plaque burden(%)=(plaque area/vessel area)×100%
Changes in coronary plaque compositions(mm³, %) on CCTA
Plaque compositions include lipid(<30 HU), fibrous(30-150HU), and calcified plaque(>350HU).
Changes in coronary high-risk plaque characteristics on CCTA
High-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 CT
CACS is a quantification of all coronary calcification by the scoring algorithm proposed by Agatston et al.

Full Information

First Posted
July 7, 2022
Last Updated
April 25, 2023
Sponsor
Chinese Academy of Medical Sciences, Fuwai Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05462262
Brief Title
Intensive Lipid-lowering for Plaque and Major Adverse Cardiovascular Events in Low to Intermediate 10-year ASCVD Risk Population
Acronym
ILLUMINATION
Official Title
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)
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 10, 2022 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese Academy of Medical Sciences, Fuwai Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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 (luminal stenosis<50%) 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(luminal stenosis<50%) 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. And 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 control group (goal for LDL-C <2.6 mmol/L or 30%-50% reduction from baseline).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease Progression

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
blinded endpoint
Allocation
Randomized
Enrollment
2900 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
intensive lipid-lowering group
Arm Type
Experimental
Arm Description
Goal for LDL-C <1.8 mmol/L or ≥50% reduction from baseline.
Arm Title
moderate-intensity lipid-lowering group
Arm Type
Active Comparator
Arm Description
Goal for LDL-C <2.6 mmol/L or 30%-50% reduction from baseline.
Intervention Type
Drug
Intervention Name(s)
Intensive lipid-lowering control
Other Intervention Name(s)
Lower goal for reducing LDL-C
Intervention Description
The initial recommended therapy is 10-20mg atorvastatin plus Ezetimibe, and the type and dosage of drugs can be adjusted according to the situation.
Intervention Type
Drug
Intervention Name(s)
Moderate-intensity lipid-lowering control
Other Intervention Name(s)
Standard goal for reducing LDL-C
Intervention Description
The initial recommended therapy is 10-20mg atorvastatin, and the type and dosage of drugs can be adjusted according to the situation.
Primary Outcome Measure Information:
Title
Major Adverse Cardiovascular Events (MACE)
Description
Composite of all-cause death, non-fatal MI, non-fatal stroke, any revascularization, and hospitalization for angina
Time Frame
Within 3 years after the enrollment
Secondary Outcome Measure Information:
Title
Change in coronary total plaque volume(mm³) on CCTA
Description
Total plaque volume(mm³) is defined as the sum of all plaque volumes for coronary arteries.
Time Frame
Within 3 years after the enrollment
Title
Change in coronary plaque burden(%) on CCTA
Description
Plaque burden(%)=(plaque area/vessel area)×100%
Time Frame
Within 3 years after the enrollment
Title
Changes in coronary plaque compositions(mm³, %) on CCTA
Description
Plaque compositions include lipid(<30 HU), fibrous(30-150HU), and calcified plaque(>350HU).
Time Frame
Within 3 years after the enrollment
Title
Changes in coronary high-risk plaque characteristics on CCTA
Description
High-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).
Time Frame
Within 3 years after the enrollment
Title
Change in coronary artery calcium score (CACS) on CT
Description
CACS is a quantification of all coronary calcification by the scoring algorithm proposed by Agatston et al.
Time Frame
Within 3 years after the enrollment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 40-75 years Low to Intermediate 10-year atherosclerotic cardiovascular disease (ASCVD) risk by using pooled cohort equations (PCE). Coronary CT angiography shows atherosclerotic plaque in the main coronary vessels (>2mm diameter) with luminal stenosis <50% Exclusion Criteria: Combination with serious cardiovascular diseases, including Heart failure (ejection fraction <30%) Arrhythmias (persistent atrial flutter/atrial fibrillation, second-degree or third-degree atrioventricular block) Hemodynamically important valvular disease Hemodynamically important congenital heart disease Stroke Myocardial infarction, coronary revascularization, or severe/unstable angina before or within 1 month of screening Active liver disease or hepatic dysfunction (defined as alanine aminotransferase or aspartate aminotransferase> 3 times the upper limit of normal) Unexplained creatine phosphokinase> 6 times the upper limit of normal Nephrotic syndrome Diabetes mellitus Uncontrollable hypertension Uncontrollable hypothyroidism Hypersensitivity to statins Any planned surgical procedure for the treatment of atherosclerosis Gastrointestinal diseases affecting drug absorption or history of gastrointestinal surgery Survival-limiting diseases Concurrent long-term immunosuppressive therapy Participation in another clinical trial concurrently or within 30 days before screening Pregnant or breastfeeding Other unsuitable situations deemed by physicians
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Bin Lu, MD
Phone
13911285857
Email
blu@vip.sina.com
Facility Information:
Facility Name
Fuwai Hospital
City
Beijing
State/Province
Beijing
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bin Lu, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31504418
Citation
Mach F, Baigent C, Catapano AL, Koskinas KC, Casula M, Badimon L, Chapman MJ, De Backer GG, Delgado V, Ference BA, Graham IM, Halliday A, Landmesser U, Mihaylova B, Pedersen TR, Riccardi G, Richter DJ, Sabatine MS, Taskinen MR, Tokgozoglu L, Wiklund O; ESC Scientific Document Group. 2019 ESC/EAS Guidelines for the management of dyslipidaemias: lipid modification to reduce cardiovascular risk. Eur Heart J. 2020 Jan 1;41(1):111-188. doi: 10.1093/eurheartj/ehz455. No abstract available. Erratum In: Eur Heart J. 2020 Nov 21;41(44):4255.
Results Reference
background
PubMed Identifier
30879355
Citation
Arnett DK, Blumenthal RS, Albert MA, Buroker AB, Goldberger ZD, Hahn EJ, Himmelfarb CD, Khera A, Lloyd-Jones D, McEvoy JW, Michos ED, Miedema MD, Munoz D, Smith SC Jr, Virani SS, Williams KA Sr, Yeboah J, Ziaeian B. 2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Circulation. 2019 Sep 10;140(11):e596-e646. doi: 10.1161/CIR.0000000000000678. Epub 2019 Mar 17. No abstract available. Erratum In: Circulation. 2019 Sep 10;140(11):e649-e650. Circulation. 2020 Jan 28;141(4):e60. Circulation. 2020 Apr 21;141(16):e774.
Results Reference
background
PubMed Identifier
30586774
Citation
Grundy SM, Stone NJ, Bailey AL, Beam C, Birtcher KK, Blumenthal RS, Braun LT, de Ferranti S, Faiella-Tommasino J, Forman DE, Goldberg R, Heidenreich PA, Hlatky MA, Jones DW, Lloyd-Jones D, Lopez-Pajares N, Ndumele CE, Orringer CE, Peralta CA, Saseen JJ, Smith SC Jr, Sperling L, Virani SS, Yeboah J. 2018 AHA/ACC/AACVPR/AAPA/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA Guideline on the Management of Blood Cholesterol: A Report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines. Circulation. 2019 Jun 18;139(25):e1082-e1143. doi: 10.1161/CIR.0000000000000625. Epub 2018 Nov 10. Erratum In: Circulation. 2019 Jun 18;139(25):e1182-e1186. Circulation. 2023 Aug 15;148(7):e5.
Results Reference
background
Links:
URL
https://www.cvdrisk.com.cn/ASCVD/Eval
Description
China-PAR 10-year ASCVD risk model

Learn more about this trial

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

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