Division of Cardiology, Department of Medicine, Duke University School of Medicine, Durham, NC, USA.
Duke Clinical Research Institute, 300 W Morgan St, Durham, NC, 27710, USA.
Curr Cardiol Rep. 2023 Nov;25(11):1601-1609. doi: 10.1007/s11886-023-01972-w. Epub 2023 Oct 9.
There has been much debate surrounding the use of omega-3 fatty acids, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), for cardiovascular (CV) risk reduction.
Recent trials of EPA and DHA have offered conflicting evidence. Some demonstrate reduction in CV risk using EPA alone in select populations. Others have demonstrated no benefit, with potential for side effects, such as new-onset atrial fibrillation. Both EPA and DHA have favorable impact on lipids and inflammation, suggesting some biological plausibility for CV risk reduction. However, clinical trials of these agents have produced mixed results. Based on available evidence, EPA may work better for CV risk than DHA and EPA combined. The benefit of EPA seems to be dose dependent, though higher doses may have more side effects. Further research is needed to define the role of EPA and DHA in the landscape of CV risk reduction.
ω-3 脂肪酸(二十碳五烯酸[EPA]和二十二碳六烯酸[DHA])在降低心血管(CV)风险方面的应用一直存在争议。
最近 EPA 和 DHA 的试验提供了相互矛盾的证据。一些研究表明,在特定人群中单独使用 EPA 可降低 CV 风险。其他研究则表明,EPA 和 DHA 没有益处,反而可能有副作用,如新发性心房颤动。EPA 和 DHA 均可改善血脂和炎症,提示其具有降低 CV 风险的生物学可能性。然而,这些药物的临床试验结果不一。基于现有证据,EPA 可能比 DHA 和 EPA 联合应用对 CV 风险的降低效果更好。EPA 的获益似乎与剂量相关,但高剂量可能有更多副作用。需要进一步研究来明确 EPA 和 DHA 在 CV 风险降低中的作用。