随机试验评估联合治疗在二级预防中的疗效方案和基线特征:随机对照试验和观察性生物标志物研究的组合——瑞舒伐他汀和二十碳五烯酸的二次预防效果评价研究(RESPECT-EPA)。

Study protocol and baseline characteristics of Randomized trial for Evaluation in Secondary Prevention Efficacy of Combination Therapy-Statin and Eicosapentaenoic Acid: RESPECT-EPA, the combination of a randomized control trial and an observational biomarker study.

机构信息

Department of Cardiovascular Biology and Medicine, Juntendo University Graduate School of Medicine, Bunkyo, Tokyo, Japan.

Japan Red Cross Society, Nasu Red Cross Hospital, Otawara, Tochigi, Japan; Dokkyo Medical University, Mibu, Tochigi, Japan.

出版信息

Am Heart J. 2023 Mar;257:1-8. doi: 10.1016/j.ahj.2022.11.008. Epub 2022 Nov 11.

Abstract

BACKGROUND

Omega-3 polyunsaturated fatty acids (PUFAs) have been a hot topic since the Japan EPA Lipid Intervention Study (JELIS), the first landmark study using a highly purified eicosapentaenoic acid (EPA), indicated that EPA could decrease the incidence of cardiovascular events. Over 20 years have passed since the JELIS was conducted, and the standard treatment for dyslipidemia has altered significantly since then. The JELIS subjects did not undertake the current risk management especially current standard statins and did not exclusively target secondary prevention patients. In addition, the subjects included are relatively high EPA population. Furthermore, the clinical implication of the plasma EPA/arachidonic acid (AA) ratio as a biomarker has not yet been validated. Therefore, the Randomized trial for Evaluation in Secondary Prevention Efficacy of Combination Therapy - Statin and EPA (RESPECT-EPA) was planned and is currently underway in Japan.

METHODS

The RESPECT-EPA comprises two parts: the open-label randomized controlled trial (RCT) and biomarker study (prospective cohort study design). The RCT included patients with a low EPA/AA ratio. These patients were then randomized to highly purified EPA (1800 mg/day) or control groups. The primary endpoint was cardiovascular death, non-fatal myocardial infarction, non-fatal ischemic stroke, unstable angina pectoris, and clinically indicated coronary revascularization. The biomarker study assesses the EPA/AA ratio's usefulness as a biomarker for cardiovascular events prediction.

RESULTS

In the RCT, a total of 2,460 patients were enrolled in 95 sites in Japan. Patients' baseline characteristics were similar between intervention and control groups in the RCT. The baseline median EPA/AA ratio was 0.243 and 0.235, respectively. A total of 1,314 patients were participated in the observational part, and the baseline median EPA/AA ratio was 0.577.

CONCLUSIONS

After this study is completed, we will have further evidence on whether a highly purified EPA is effective in reducing cardiovascular events for secondary prevention or not, as well as whether if EPA/AA ratio is a predictor for future cardiovascular events. This study was registered in the University Hospital Medical Information Network Clinical Trials Registry (UMIN000012069).

摘要

背景

自日本 EPA 脂质干预研究(JELIS)以来,ω-3 多不饱和脂肪酸(PUFAs)一直是一个热门话题,该研究首次使用高度纯化的二十碳五烯酸(EPA)表明 EPA 可降低心血管事件的发生率。自 JELIS 开展以来已经过去了 20 多年,自那时以来,血脂异常的标准治疗方法已经发生了很大变化。JELIS 研究对象没有接受当前的风险管理,特别是当前的标准他汀类药物治疗,也没有专门针对二级预防患者。此外,研究对象中 EPA 含量相对较高。此外,作为生物标志物的血浆 EPA/花生四烯酸(AA)比值的临床意义尚未得到验证。因此,计划并正在日本开展随机试验,评估联合治疗 - 他汀类药物和 EPA 的二级预防疗效(RESPECT-EPA)。

方法

RESPECT-EPA 由两部分组成:开放标签随机对照试验(RCT)和生物标志物研究(前瞻性队列研究设计)。RCT 纳入了 EPA/AA 比值低的患者。这些患者随后被随机分为高度纯化的 EPA(1800mg/天)组或对照组。主要终点是心血管死亡、非致死性心肌梗死、非致死性缺血性卒中和不稳定型心绞痛以及有临床指征的冠状动脉血运重建。生物标志物研究评估 EPA/AA 比值作为心血管事件预测的生物标志物的有用性。

结果

在 RCT 中,共有 2460 名患者在日本的 95 个地点入组。RCT 中干预组和对照组患者的基线特征相似。RCT 中患者的基线中位 EPA/AA 比值分别为 0.243 和 0.235。共有 1314 名患者参加了观察部分,基线中位 EPA/AA 比值为 0.577。

结论

这项研究完成后,我们将进一步了解高度纯化的 EPA 是否对二级预防的心血管事件有降低作用,以及 EPA/AA 比值是否是未来心血管事件的预测指标。本研究在大学医院医疗信息网络临床试验注册中心(UMIN000012069)注册。

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