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Rationale and design of REDUCE-IT: Reduction of Cardiovascular Events with Icosapent Ethyl-Intervention Trial
Deepak L Bhatt1, Ph Gabriel Steg2,3, Eliot A Brinton4
1Brigham and Women's Hospital Heart & Vascular Center and Harvard Medical School, Boston, Massachusetts.
Insights
High-dose icosapent ethyl (EPA) shows promise in reducing cardiovascular events for high-risk patients on statins. This study investigated its efficacy in preventing ischemic events beyond standard triglyceride-lowering therapy.
Area of Science:
- Cardiology
- Pharmacology
- Clinical Trials
Background:
- Residual cardiovascular risk persists in patients treated with statins.
- Elevated triglycerides are an independent risk factor for cardiovascular events.
- Previous studies have not confirmed added benefit of lipid-targeted therapies beyond LDL-C reduction.
Purpose of the Study:
- To evaluate if icosapent ethyl reduces ischemic events in statin-treated patients with high triglycerides.
- To assess the efficacy of highly purified eicosapentaenoic acid (EPA) in a high-risk population.
- To determine the cardiovascular outcome benefits of triglyceride lowering with icosapent ethyl.
Main Methods:
- The Reduction of Cardiovascular Events with Icosapent Ethyl-Intervention Trial (REDUCE-IT) is a phase 3b, randomized, double-blind, placebo-controlled trial.
- Approximately 8000 patients with elevated triglycerides and cardiovascular risk factors were randomized.
- Patients received either icosapent ethyl or placebo, in addition to stable statin therapy.
Main Results:
- The primary endpoint is a composite of cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, coronary revascularization, or unstable angina.
- The key secondary endpoint includes cardiovascular death, nonfatal myocardial infarction, or nonfatal stroke.
- The trial is event-driven, continuing until approximately 1612 primary efficacy endpoint events occur.
Conclusions:
- This trial aims to provide definitive evidence on the role of icosapent ethyl in managing residual cardiovascular risk.
- Findings will clarify the benefit of triglyceride reduction beyond LDL-C lowering in high-risk patients.
- The study will contribute significant data on the pleiotropic effects of omega-3 fatty acids in cardiovascular disease prevention.
Abstract:
Residual cardiovascular risk persists despite statins, yet outcome studies of lipid-targeted therapies beyond low-density lipoprotein cholesterol (LDL-C) have not demonstrated added benefit. Triglyceride elevation is an independent risk factor for cardiovascular events. High-dose eicosapentaenoic acid (EPA) reduces triglyceride-rich lipoproteins without raising LDL-C. Omega-3s have postulated pleiotropic cardioprotective benefits beyond triglyceride-lowering. To date, no large, multinational, randomized clinical trial has proved that lowering triglycerides on top of statin therapy improves cardiovascular outcomes. The Reduction of Cardiovascular Events with Icosapent Ethyl-Intervention Trial (REDUCE-IT; NCT01492361) is a phase 3b randomized, double-blinded, placebo-controlled trial of icosapent ethyl, a highly purified ethyl ester of EPA, vs placebo. The main objective is to evaluate whether treatment with icosapent ethyl reduces ischemic events in statin-treated patients with high triglycerides at elevated cardiovascular risk. REDUCE-IT enrolled men or women age ≥45 years with established cardiovascular disease or age ≥50 years with diabetes mellitus and 1 additional risk factor. Randomization required fasting triglycerides ≥150 mg/dL and <500 mg/dL and LDL-C >40 mg/dL and ≤100 mg/dL with stable statin (± ezetimibe) ≥4 weeks prior to qualifying measurements. The primary endpoint is a composite of cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, coronary revascularization, or unstable angina. The key secondary endpoint is the composite of cardiovascular death, nonfatal myocardial infarction, or nonfatal stroke. Several secondary, tertiary, and exploratory endpoints will be assessed. Approximately 8000 patients have been randomized at approximately 470 centers worldwide. Follow-up will continue in this event-driven trial until approximately 1612 adjudicated primary-efficacy endpoint events have occurred.
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