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Rationale and design of REDUCE‐IT: Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial

机译:REDUCE-IT的原理和设计:使用二十碳五烯酸乙酯干预试验减少心血管事件

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摘要

Residual cardiovascular risk persists despite statins, yet outcome studies of lipid‐targeted therapies beyond low‐density lipoprotein cholesterol (LDL‐C) have not demonstrated added benefit. Triglyceride elevation is an independent risk factor for cardiovascular events. High‐dose eicosapentaenoic acid (EPA) reduces triglyceride‐rich lipoproteins without raising LDL‐C. Omega‐3s have postulated pleiotropic cardioprotective benefits beyond triglyceride‐lowering. To date, no large, multinational, randomized clinical trial has proved that lowering triglycerides on top of statin therapy improves cardiovascular outcomes. The Reduction of Cardiovascular Events with Icosapent Ethyl–Intervention Trial (REDUCE‐IT; ) is a phase 3b randomized, double‐blinded, placebo‐controlled trial of icosapent ethyl, a highly purified ethyl ester of EPA, vs placebo. The main objective is to evaluate whether treatment with icosapent ethyl reduces ischemic events in statin‐treated patients with high triglycerides at elevated cardiovascular risk. REDUCE‐IT enrolled men or women age ≥45 years with established cardiovascular disease or age ≥50 years with diabetes mellitus and 1 additional risk factor. Randomization required fasting triglycerides ≥150 mg/dL and <500 mg/dL and LDL‐C >40 mg/dL and ≤100 mg/dL with stable statin (± ezetimibe) ≥4 weeks prior to qualifying measurements. The primary endpoint is a composite of cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, coronary revascularization, or unstable angina. The key secondary endpoint is the composite of cardiovascular death, nonfatal myocardial infarction, or nonfatal stroke. Several secondary, tertiary, and exploratory endpoints will be assessed. Approximately 8000 patients have been randomized at approximately 470 centers worldwide. Follow‐up will continue in this event‐driven trial until approximately 1612 adjudicated primary‐efficacy endpoint events have occurred.
机译:尽管他汀类药物仍然存在残留的心血管风险,但是,针对脂类靶向疗法(低密度脂蛋白胆固醇(LDL-C)以外)的结局研究并未显示出其他益处。甘油三酸酯升高是心血管事件的独立危险因素。大剂量二十碳五烯酸(EPA)可降低富含甘油三酸酯的脂蛋白,而不会升高LDL-C。除了降低甘油三酸酯外,Omega-3还具有多效性的心脏保护作用。迄今为止,尚无大型,跨国,随机的临床试验证明在他​​汀类药物治疗的基础上降低甘油三酯可改善心血管疾病的预后。二十碳五烯乙基干预试验(REDUCE-IT;)减少心血管事件是一项3b期随机,双盲,安慰剂对照试验,涉及二十碳五烯酸乙酯(一种EPA的高纯度乙酯)与安慰剂。主要目的是评估在心血管风险升高的情况下,用二十碳五烯酸乙酯治疗是否可以降低他汀类药物治疗的高甘油三酸酯患者的缺血事件。 REDUCE‐IT纳入了患有心血管疾病的年龄≥45岁的男性或女性,或患有糖尿病和1个其他危险因素的年龄≥50岁的男性或女性。随机分组要求在合格检查前几周禁食甘油三酯≥150μg/ dL和<500μmg/ dL,LDL-C>40μmg/ dL和≤100μmg/ dL,且稳定的他汀类药物(±依泽替米贝)≥4μl。主要终点指标是心血管死亡,非致命性心肌梗塞,非致命性中风,冠状动脉血运重建或不稳定型心绞痛的综合表现。主要的次要终点是心血管死亡,非致命性心肌梗塞或非致命性中风的综合。将评估几个次要,第三级和探索性终点。全球约有470个中心将约8000名患者随机分组。在该事件驱动的试验中,将继续随访,直到发生大约1612个已判定的主要疗效终点事件。

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