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Rationale and design of REDUCE‐IT: Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial
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 ac...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wiley Periodicals, Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396348/ https://www.ncbi.nlm.nih.gov/pubmed/28294373 http://dx.doi.org/10.1002/clc.22692 |
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author | Bhatt, Deepak L. Steg, Ph. Gabriel Brinton, Eliot A. Jacobson, Terry A. Miller, Michael Tardif, Jean‐Claude Ketchum, Steven B. Doyle, Ralph T. Murphy, Sabina A. Soni, Paresh N. Braeckman, Rene A. Juliano, Rebecca A. Ballantyne, Christie M. |
author_facet | Bhatt, Deepak L. Steg, Ph. Gabriel Brinton, Eliot A. Jacobson, Terry A. Miller, Michael Tardif, Jean‐Claude Ketchum, Steven B. Doyle, Ralph T. Murphy, Sabina A. Soni, Paresh N. Braeckman, Rene A. Juliano, Rebecca A. Ballantyne, Christie M. |
author_sort | Bhatt, Deepak L. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5396348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Wiley Periodicals, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53963482017-04-25 Rationale and design of REDUCE‐IT: Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial Bhatt, Deepak L. Steg, Ph. Gabriel Brinton, Eliot A. Jacobson, Terry A. Miller, Michael Tardif, Jean‐Claude Ketchum, Steven B. Doyle, Ralph T. Murphy, Sabina A. Soni, Paresh N. Braeckman, Rene A. Juliano, Rebecca A. Ballantyne, Christie M. Clin Cardiol Trial Designs 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. Wiley Periodicals, Inc. 2017-03-15 /pmc/articles/PMC5396348/ /pubmed/28294373 http://dx.doi.org/10.1002/clc.22692 Text en © 2017 The Authors. Clinical Cardiology published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Trial Designs Bhatt, Deepak L. Steg, Ph. Gabriel Brinton, Eliot A. Jacobson, Terry A. Miller, Michael Tardif, Jean‐Claude Ketchum, Steven B. Doyle, Ralph T. Murphy, Sabina A. Soni, Paresh N. Braeckman, Rene A. Juliano, Rebecca A. Ballantyne, Christie M. Rationale and design of REDUCE‐IT: Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial |
title | Rationale and design of REDUCE‐IT: Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial |
title_full | Rationale and design of REDUCE‐IT: Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial |
title_fullStr | Rationale and design of REDUCE‐IT: Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial |
title_full_unstemmed | Rationale and design of REDUCE‐IT: Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial |
title_short | Rationale and design of REDUCE‐IT: Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial |
title_sort | rationale and design of reduce‐it: reduction of cardiovascular events with icosapent ethyl–intervention trial |
topic | Trial Designs |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396348/ https://www.ncbi.nlm.nih.gov/pubmed/28294373 http://dx.doi.org/10.1002/clc.22692 |
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