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Reducing Cardiovascular Disease Risk in Women Beyond Statin Therapy: New Insights 2020
Lori Mosca1, Ann Marie Navar2, Nanette Kass Wenger3
1Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center, New York, New York, USA.
Icosapent ethyl, an EPA-only omega-3 fatty acid, significantly reduced cardiovascular disease (CVD) events in high-risk patients. This CVD risk reduction was comparable between women and men, suggesting similar benefits for both sexes.
Area of Science:
- Cardiovascular Medicine
- Preventive Cardiology
- Pharmacology
Background:
- Managing residual cardiovascular disease (CVD) risk in statin-treated patients is crucial.
- Women face unique CVD risk factors and have historically been underrepresented in clinical trials.
- Triglyceride-lowering treatments show mixed results for CVD risk reduction, unlike LDL-cholesterol therapies.
Purpose of the Study:
- To review CVD in women and relevant prevention trials.
- To discuss the applicability of Reduction of Cardiovascular Events with Icosapent Ethyl-Intervention Trial (REDUCE-IT) results for statin-treated women.
- To highlight the potential of icosapent ethyl in managing CVD risk in women.
Main Methods:
- Review of prior cardiovascular disease prevention trials, focusing on women's representation.
- Analysis of recent clinical trial data, specifically the REDUCE-IT study.
- Examination of triglyceride-lowering treatments, including omega-3 fatty acids.
Main Results:
- The REDUCE-IT trial demonstrated significant CVD event reduction with icosapent ethyl plus statins (17.2% vs. 22.0%).
- Icosapent ethyl, an EPA-only omega-3 fatty acid, showed a hazard ratio of 0.75 (95% CI 0.68-0.83; p < 0.001).
- CVD risk reduction with icosapent ethyl was comparable between women and men (p for interaction = 0.33).
Conclusions:
- Icosapent ethyl is a novel therapy for CVD prevention in high-risk patients.
- Women appear to benefit similarly to men from icosapent ethyl treatment.
- Findings support the use of icosapent ethyl for managing residual CVD risk in statin-treated women.
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