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指南建议、临床试验数据以及新出现的治疗方法。

Guideline recommendations, clinical trial data, and new and emerging therapies.

机构信息

Clinical pharmacy specialist, Cardiac Care Unit, Johns Hopkins Hospital, Baltimore, MD. Email:

出版信息

Am J Manag Care. 2021 Mar;27(4 Suppl):S70-S75. doi: 10.37765/ajmc.2021.88607.

DOI:10.37765/ajmc.2021.88607
PMID:33710846
Abstract

Nearly 93 million American adults have hyperlipidemia, a major risk factor for the development of atherosclerotic cardiovascular disease. Use of HMG-CoA reductase inhibitors (ie, statins) and ezetimibe have decreased hypercholesterolemia's prevalence in the past decade, but poor adherence is common and leads to scenarios where patients do not derive the greatest possible benefit. In addition, statin resistance may play a role when patients' LDL-C levels are not lowered to the expected extent despite good medication adherence. When statins fail to control hyperlipidemia, guidelines recommend furthering treatment by adding ezetimibe or a PCSK9 inhibitor. In November 2018, the American College of Cardiology and the American Heart Association updated their hyperlipidemia guideline. This revision recommends a more aggressive approach to hyperlipidemia. In patients who fail to respond to or cannot tolerate statins or ezetimibe, PCSK9 inhibitors are a reasonable treatment option. Large outcomes trials have compared the currently approved PCSK9 inhibitors with placebo and established that PCSK9 inhibitors lowered LDL-C by more than 50% below the statin-treated baseline and reduce cardiovascular outcomes. In addition, bempedoic acid, lomitapide, and evinacumab are available options that may be instituted in select patients. In development is inclisiran, a small interfering RNA molecule, which antagonizes PCSK9 production. With good adherence and the use of a greater assortment of medications, patients may experience atherogenic lipoprotein lowering, leading to a decrease in cardiovascular disease.

摘要

近 9300 万美国成年人患有高脂血症,这是动脉粥样硬化性心血管疾病发展的一个主要危险因素。在过去十年中,使用羟甲基戊二酰辅酶 A 还原酶抑制剂(即他汀类药物)和依折麦布降低了高胆固醇血症的患病率,但普遍存在用药依从性差的情况,导致患者无法获得最大可能的获益。此外,当患者的 LDL-C 水平尽管药物依从性良好但并未降低到预期水平时,他汀类药物耐药可能起作用。当他汀类药物不能控制高脂血症时,指南建议通过添加依折麦布或 PCSK9 抑制剂来进一步治疗。2018 年 11 月,美国心脏病学会和美国心脏协会更新了他们的高脂血症指南。该修订建议采取更积极的高脂血症治疗方法。对于不能耐受或不能耐受他汀类药物或依折麦布的患者,PCSK9 抑制剂是合理的治疗选择。大型结局试验比较了目前批准的 PCSK9 抑制剂与安慰剂,并证实 PCSK9 抑制剂使 LDL-C 降低了 50%以上,且优于他汀类药物治疗的基线水平,并降低了心血管结局。此外,在某些患者中,还可以选择苯扎贝特酸、洛美他派和依库珠单抗。正在开发的inclisiran 是一种小干扰 RNA 分子,可拮抗 PCSK9 的产生。通过良好的依从性和使用更多种类的药物,患者可能会经历致动脉粥样硬化脂蛋白降低,从而降低心血管疾病的风险。

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