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新的希望?心脏结局预防评估 3 期的经验教训。

A New HOPE? Lessons from Heart Outcomes Prevention Evaluation-3.

机构信息

Northwestern University, Chicago, Ill.

Northwestern University, Chicago, Ill.

出版信息

Am J Med. 2018 Feb;131(2):134-140. doi: 10.1016/j.amjmed.2017.10.012. Epub 2017 Oct 23.

Abstract

Lifestyle modification is the cornerstone of preventing atherosclerotic cardiovascular disease. When this is not sufficient in reducing risk, statin therapy is first line. Heart Outcomes Prevention Evaluation (HOPE-3) was a randomized controlled trial of rosuvastatin versus placebo, which demonstrated a significant net benefit in a lower-risk population without known atherosclerotic cardiovascular disease. There were many novel characteristics about this trial that should not be overlooked. It contained a diverse population and was the first trial to base inclusion solely on easily ascertainable metabolic risk factors. It had high adherence in the statin arm, likely due to several factors, including a run-in phase, close follow-up, and low intolerance of moderate-dose rosuvastatin. Attempting to simulate these could increase adherence among clinic populations. Although HOPE-3 did not demonstrate a significant decrease in cardiovascular events among women, meta-analysis including prior randomized controlled trials still demonstrates significant benefit, supporting prior guidelines for statin therapy in this group. Finally, HOPE-3 provides data that potentially support the legacy effect of statins. Understanding these key points provides additional insight into the benefits of statin therapy.

摘要

生活方式的改变是预防动脉粥样硬化性心血管疾病的基石。当这种方法不足以降低风险时,首先使用他汀类药物治疗。心脏结局预防评估 3 期临床试验(HOPE-3)是一项比较瑞舒伐他汀与安慰剂的随机对照试验,结果表明在无已知动脉粥样硬化性心血管疾病的低危人群中,瑞舒伐他汀具有显著的净获益。该试验有许多值得关注的新颖特征。它包含了一个多样化的人群,并且是第一个仅基于易于确定的代谢危险因素来确定纳入标准的试验。在他汀类药物治疗组中,患者的依从性很高,这可能是由于多种因素共同作用的结果,包括导入期、密切随访和对中等剂量瑞舒伐他汀的低耐受性。尝试模拟这些因素可能会提高临床人群的依从性。尽管 HOPE-3 并未显示在女性中心血管事件显著减少,但包括先前随机对照试验的荟萃分析仍表明存在显著获益,支持了先前针对该人群他汀类药物治疗的指南。最后,HOPE-3 提供的数据可能支持他汀类药物的遗留效应。了解这些关键点可以更深入地了解他汀类药物治疗的益处。

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