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rctstrongn = 8179

Cardiovascular Risk Reduction with Icosapent Ethyl for Hypertriglyceridemia

Bhatt DL, Steg PG, Miller M, Brinton EA, Jacobson TA, Ketchum SB, Doyle RT, Juliano RA, Jiao L, Granowitz C, REDUCE-IT Investigators · 2019 · New England Journal of Medicine

DOI: 10.1056/NEJMoa1812792View source ↗

Among patients with elevated triglyceride levels despite the use of statins, the risk of major adverse cardiovascular events was significantly lower with icosapent ethyl than with placebo.

Summary

The REDUCE-IT trial randomized 8,179 statin-treated adults with elevated triglycerides and either established cardiovascular disease or diabetes plus risk factors to receive 2 grams of icosapent ethyl twice daily (a purified prescription-grade EPA preparation, total daily dose 4 grams) or matching placebo. After a median follow-up of 4.9 years, the icosapent ethyl arm experienced a 25% relative reduction in the primary composite endpoint of major adverse cardiovascular events (cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, coronary revascularization, or unstable angina) compared with placebo. Reductions were observed across multiple individual endpoint components, including cardiovascular death. The trial reignited debate over high-dose omega-3 cardiovascular prevention after several earlier mixed-result trials and stands as the largest, longest, and methodologically strongest RCT supporting a cardiovascular benefit from a specific EPA preparation.

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Not medical advice. This page summarizes primary research. It is not a substitute for consultation with a qualified clinician. See safety for exclusion criteria.