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依泽替米贝对吸烟人群心血管结局的潜在影响:REDUCE-IT 吸烟研究。

Potential effects of icosapent ethyl on cardiovascular outcomes in cigarette smokers: REDUCE-IT smoking.

机构信息

Corporal Michael J. Crescenz Veterans Affairs Medical Center and Hospital, University of Pennsylvania, Philadelphia, PA 19104, USA.

Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

出版信息

Eur Heart J Cardiovasc Pharmacother. 2023 Feb 2;9(2):129-137. doi: 10.1093/ehjcvp/pvac045.

Abstract

AIMS

Cigarette smoking is among the most well-established risk factors for adverse cardiovascular outcomes. We sought to determine whether icosapent ethyl (IPE), a highly purified form of eicosapentaenoic acid with antiatherothrombotic properties, may reduce the excessive risk of cardiovascular disease (CVD) attributable to smoking.

METHODS AND RESULTS

Reduction of Cardiovascular Events with Icosapent Ethyl Trial (REDUCE-IT) was a multinational, double-blind trial that randomized 8179 statin-treated patients with elevated triglycerides and CV risk to IPE or placebo, with a median follow-up period of 4.9 years. Icosapent ethyl reduced the primary composite endpoint [CV death, non-fatal myocardial infarction (MI), non-fatal stroke, coronary revascularization, or hospitalization for unstable angina] by 25% (P < 0.0001). In the current analyses, the effect of IPE was evaluated in REDUCE-IT using post hoc analyses based on smoking history. Groups were classified as current smokers (n = 1241), former smokers (n = 3672), and never smokers (n = 3264). Compared with placebo, IPE use in combined current and former smokers (n = 4913) was associated with significant reductions in time to the primary composite endpoint {hazard ratio: 0.77 [95% confidence interval (CI): 0.68-0.87]; P < 0.0001} and in total events [rate ratio: 0.71 (95% CI: 0.61-0.82); P < 0.0001]. These benefits remained significant when subdivided into current and former smokers (P = 0.04, P = 0.005), with reductions in the key secondary composite endpoint (P < 0.0001) and in the individual components of CV death or non-fatal MI (P = 0.04, P = 0.01) and fatal or non-fatal MI (P = 0.009, P = 0.01), respectively. Benefits were consistent and significant in non-smokers as well. Overall, there were similar estimated rates of first occurrences of primary CVD endpoints in current smokers (23.8%) and former smokers (23.0%) assigned to IPE compared with never smokers on placebo (25.7%).

CONCLUSION

In REDUCE-IT, IPE treatment was associated with a reduced risk of CV events in current and former smokers to levels observed in never smokers. While smoking cessation should always be recommended, these data raise the possibility that IPE treatment may attenuate CV hazards attributable to smoking.

摘要

目的

吸烟是导致不良心血管结局的最确定的危险因素之一。我们试图确定 icosapent ethyl(IPE)是否可以降低因吸烟而导致的心血管疾病(CVD)的过度风险,IPE 是一种具有抗动脉粥样血栓形成特性的高度纯化形式的二十碳五烯酸。

方法和结果

用依泽替米贝降低心血管风险(REDUCE-IT)试验是一项多中心、双盲试验,将 8179 名服用他汀类药物且甘油三酯升高和心血管风险升高的患者随机分为 IPE 或安慰剂组,中位随访时间为 4.9 年。IPE 降低了主要复合终点[心血管死亡、非致死性心肌梗死(MI)、非致死性卒、冠状动脉血运重建或不稳定型心绞痛住院]25%(P<0.0001)。在目前的分析中,根据吸烟史,使用 REDUCE-IT 中的事后分析评估了 IPE 的效果。将患者分为当前吸烟者(n=1241)、曾经吸烟者(n=3672)和从不吸烟者(n=3264)。与安慰剂相比,IPE 联合当前和曾经吸烟者(n=4913)的使用与主要复合终点时间的显著减少相关[风险比:0.77[95%置信区间(CI):0.68-0.87];P<0.0001]和总事件[发生率比:0.71(95%CI:0.61-0.82);P<0.0001]。当细分为当前吸烟者和曾经吸烟者时,这些益处仍然显著(P=0.04,P=0.005),主要次要复合终点(P<0.0001)和心血管死亡或非致死性 MI(P=0.04,P=0.01)和致命或非致命性 MI(P=0.009,P=0.01)的关键次要复合终点的发生率降低。非吸烟者也有类似的益处。总体而言,与从未吸烟者相比,当前吸烟者(23.8%)和曾经吸烟者(23.0%)在 IPE 治疗组中首次发生主要 CVD 终点的估计发生率相似。

结论

在 REDUCE-IT 中,IPE 治疗与当前和曾经吸烟者的心血管事件风险降低相关,降至从不吸烟者的水平。虽然应始终建议戒烟,但这些数据表明,IPE 治疗可能会减轻吸烟引起的心血管危害。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87d5/9892866/7b286942e019/pvac045fig1.jpg

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