Polygenic Risk-based Detection of Subclinical Coronary Atherosclerosis and Intervention With Statin and Colchicine

Coronary Artery Disease Clinical Trial

— PROACT 2  

Official title:

Polygenic Risk-based Detection of Subclinical Coronary Atherosclerosis and Intervention With Statin and Colchicine

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05850091
• Other study ID #: 2023P000945
• Status: Recruiting
• Phase: Phase 4
• Start date: December 7, 2023
• Est. completion date: July 2027

Study information

• Verified date: May 2024
• Source: Massachusetts General Hospital
• Contact: Fangzhou Cheng
• Phone: (617)-643-4842
• Email: proact[@]mgb.org
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The goal of this double-blind randomized controlled trial is to determine how treatment with high intensity statin, low-dose colchicine, and their combination modulates progression and composition of coronary atherosclerosis in individuals with high polygenic risk for coronary artery disease.

Description:

The main question PROACT 2 aims to answer is whether and how single or dual targeting of cholesterol-lowering and inflammation modulates coronary plaque in individuals with high polygenic risk and subclinical coronary atherosclerosis.

This is a double-blind randomized controlled trial of 200 individuals with high polygenic risk for coronary artery disease and subclinical plaque on coronary computed tomography angiography. Participants will be randomized into four equal treatment groups: group A receiving a placebo daily, group B receiving rosuvastatin 20mg daily, group C receiving colchicine 0.6mg daily, and group D receiving both rosuvastatin 20mg daily and colchicine 0.6mg daily. The primary outcome is change in total non-calcified plaque volume on coronary computed tomography angiography from baseline to one year. Multiple secondary plaque imaging and biomarker outcomes will be explored in this pilot mechanistic trial.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 200
• Est. completion date: July 2027
• Est. primary completion date: July 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: 40 Years to 75 Years

Eligibility

Inclusion Criteria:

• Males and females between 40 and 75 years of age capable and willing to provide informed consent

• Participant has high CAD PRS as defined on a clinical test

• Participant with subclinical atherosclerosis defined as plaque visible on CCTA and causing <70% luminal stenosis

Exclusion Criteria:

• Participant with a history of cardiovascular disease, defined by a diagnosis of coronary artery disease, peripheral artery disease, or cerebrovascular disease

• Participant with a history of Liver disease (cirrhosis, active hepatitis, or severe hepatic disease) or any of the following recent lab results and determined to be non-transient: alanine aminotransferase greater than 3 times the upper limit of normal or total bilirubin greater than 2 times the upper limit of normal (unless due to Gilbert syndrome)

• Participant with estimated glomerular filtration rate <60 mL/min/1.73 m2 or creatinine greater than 2 times the upper limit of normal

• Patient with history of an allergic reaction or significant sensitivity to iodinated contrast, colchicine, or statins

• Patient currently taking LDL cholesterol lowering or anti- inflammatory medications including colchicine

• Participants requiring regular drugs known to be potent CY2P inhibitors (eg. ketoconazole, clarithromycin)

• Female patient who is pregnant, or breast-feeding or is considering becoming pregnant during the study

• Participant with BMI = 40 kg/m2

• Participant unable to provide informed consent

• Participant unable to hold breath for 10 seconds

Related Conditions & MeSH terms

• Atherosclerosis
• Coronary Artery Disease
• Myocardial Ischemia

Intervention

Drug:
• Rosuvastatin
Pharmacotherapy for reduction in LDL cholesterol level
• Colchicine
Pharmacotherapy for inflammation inhibition
• Placebo
Capsule with sugar pill that mimics active study drugs

Locations

Country	Name	City	State
United States	Massachusetts General Hospital	Boston	Massachusetts

Sponsors (2)

Lead Sponsor	Collaborator
Massachusetts General Hospital	National Heart, Lung, and Blood Institute (NHLBI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in total non-calcified plaque volume from baseline to one year	The primary outcome of this study is the change in total non-calcified plaque volume between the two groups from baseline to one year. This outcome will be measured using coronary computed tomography angiography (CCTA) and reported in cubic millimeters (mm³). The comparison of the changes in non-calcified plaque volume will help assess the effectiveness of the intervention on plaque progression and composition.	1 year
Secondary	Change in total plaque volumes from baseline to one year	The change in the following plaque volumes will be compared between the two groups from baseline to one year: total plaque volume, total calcified plaque volume, and total low attenuation plaque volume. These volumes will be analyzed individually and reported in cubic millimeters (mm³).	1 year
Secondary	Change in maximal luminal stenosis from baseline to one year	The change in maximal luminal stenosis will be compared between the two groups from baseline to one year, reported as a percentage (%).	1 year
Secondary	Change in calcium score from baseline to one year	The change in calcium score will be compared between the two groups from baseline to one year, reported in Agatston units.	1 year
Secondary	Change in number of high-risk features from baseline to one year	The change in the number of high-risk features will be compared between the two groups from baseline to one year, reported as a count (number of features).	1 year
Secondary	Change in fat attenuation index from baseline to one year	The change in fat attenuation index will be compared between the two groups from baseline to one year, reported in Hounsfield units (HU).	1 year
Secondary	Progression in non-calcified plaque volume from baseline to one year	The proportion of participants who had progression in non-calcified plaque volume from baseline to one year (%)	1 year
Secondary	Change in low-density lipoprotein cholesterol (LDL-C) from baseline to one year	The change in low-density lipoprotein cholesterol (LDL-C) will be compared between the two groups from baseline to one year, reported in milligrams per deciliter (mg/dL).	1 year
Secondary	Change in C-reactive protein (CRP) from baseline to one year	The change in C-reactive protein (CRP) will be compared between the two groups from baseline to one year, reported in milligrams per liter (mg/L).	1 year
Secondary	Change in Interleukin-6 and Interleukin-1 beta (IL-1ß) from baseline to one year	The change in Interleukin-6 (IL-6) and Interleukin-1 beta (IL-1ß) will be compared between the two groups from baseline to one year. Both biomarkers will be analyzed individually and reported in picograms per milliliter (pg/mL).	1 year