Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, BC, Canada.
Lower Mainland Pharmacy Services, Chilliwack General Hospital, Chilliwack, BC, Canada.
Pharmacotherapy. 2021 Dec;41(12):1056-1065. doi: 10.1002/phar.2615. Epub 2021 Aug 30.
Marine-derived omega-3 fatty acids, docosahexaenoic acid (DHA) and eicosapentaenoic acid (EPA), are a type of polyunsaturated fatty acids with many purported beneficial health effects including the prevention of atherosclerotic cardiovascular disease (ASCVD) events. Omega-3 fatty acid intake may be supplemented via dietary sources, as well as prescription or non-prescription products. Omega-3 fatty acids have been shown to reduce serum triglycerides, but there remains ongoing debate regarding the effect of omega-3 fatty acids on major adverse cardiovascular events in patients with established, or at risk of, ASCVD. Recent evidence from randomized, placebo-controlled trials has demonstrated that low-dose (1 g daily or less) omega-3 fatty acids (DHA and EPA) do not reduce cardiovascular events or death in patients with or without established ASCVD. Contrarily, the REDUCE-IT trial demonstrated that a purified form of EPA ethyl esters (icosapent ethyl) at 4 g daily reduced cardiovascular events and death in patients with ASCVD (or diabetes and multiple cardiovascular risk factors) and elevated triglycerides on background statin therapy. However, 4 g daily of omega-3 carboxylic acids (DHA and EPA) did not show a cardiovascular benefit in the STRENGTH trial, which enrolled a similar population. The explanation for this observed discrepancy remains a source of contention and discourse. For now, icosapent ethyl has the most compelling evidence to support a cardiovascular benefit and should be considered in select patients who meet the REDUCE-IT criteria. Furthermore, alternative versions of omega-3 fatty acids should not be considered equivalent to icosapent ethyl. Patients taking an omega-3 fatty acid supplement should be monitored for potential adverse effects, including gastrointestinal disorders or bleeding, in addition to a possible increased risk of atrial fibrillation.
海洋衍生的 ω-3 脂肪酸,二十二碳六烯酸(DHA)和二十碳五烯酸(EPA),是一种多不饱和脂肪酸,具有许多据称有益的健康影响,包括预防动脉粥样硬化性心血管疾病(ASCVD)事件。ω-3 脂肪酸的摄入量可以通过饮食来源以及处方或非处方产品来补充。已经证明 ω-3 脂肪酸可以降低血清甘油三酯,但关于 ω-3 脂肪酸对已确诊或有 ASCVD 风险的患者的主要不良心血管事件的影响仍存在争议。最近来自随机、安慰剂对照试验的证据表明,低剂量(每天 1 克或更少)ω-3 脂肪酸(DHA 和 EPA)不会减少有或没有已确诊 ASCVD 的患者的心血管事件或死亡。相反,REDUCE-IT 试验表明,每天 4 克的纯化形式的 EPA 乙酯(二十碳五烯酸乙酯)可降低 ASCVD(或糖尿病和多种心血管危险因素)患者和在他汀类药物背景治疗下甘油三酯升高的心血管事件和死亡。然而,在 STRENGTH 试验中,每天 4 克的 ω-3 羧酸(DHA 和 EPA)并没有显示出心血管益处,该试验纳入了类似的人群。对这种观察到的差异的解释仍然是争议和讨论的来源。目前,二十碳五烯酸乙酯具有最有力的证据支持心血管获益,并且应该在符合 REDUCE-IT 标准的选择患者中考虑。此外,替代版本的 ω-3 脂肪酸不应被视为等同于二十碳五烯酸乙酯。服用 ω-3 脂肪酸补充剂的患者除了可能增加心房颤动的风险外,还应监测潜在的不良反应,包括胃肠道疾病或出血。