Department of Cardiology, The First Hospital of China Medical University, Shenyang 110001, China.
Lipoprotein Metabolism Laboratory, Translational Vascular Medicine Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892, USA.
J Clin Endocrinol Metab. 2023 Aug 18;108(9):2424-2434. doi: 10.1210/clinem/dgad153.
Statins are the lipid-lowering therapy of choice for the prevention of atherosclerotic cardiovascular disease (ASCVD) but their effectiveness in lowering low-density lipoprotein cholesterol (LDL-C) can substantially differ between individuals. In this mini-review, we describe the different causes for a suboptimal statin response and an algorithm for the diagnosis and clinical management of these patients.
A PubMed search using the terms "statin resistance," "statin sensitivity," "statin pharmacokinetics," "cardiovascular disease," and "lipid-lowering therapies" was performed. Published papers in the past 10 years that were relevant to the topic were examined to provide content for this mini-review.
Suboptimal lowering of LDL-C by statins is a major problem in the clinical management of patients and limits the value of this therapeutic approach. There are multiple causes of statin hyporesponsiveness with compliance being the most common explanation. Other causes, such as analytical issues with LDL-C measurement and the presence of common lipid disorders (familial hypercholesterolemia, elevated lipoprotein[a] and secondary dyslipidemias) should be excluded before considering primary statin resistance from rare genetic variants in lipoprotein-related or drug-metabolism genes. A wide variety of nonstatin lipid-lowering drugs are now available and can be added to statins to achieve more effective LDL-C lowering.
The evaluation of statin hyporesponsiveness is a multistep process that can lead to the optimization of lipid-lowering therapy for the prevention of ASCVD. It may also lead to the identification of distinct types of dyslipidemias that require specific therapies and/or the genetic screening of family members.
他汀类药物是预防动脉粥样硬化性心血管疾病(ASCVD)的首选降脂治疗药物,但个体之间降低低密度脂蛋白胆固醇(LDL-C)的效果差异很大。在本篇迷你综述中,我们描述了他汀类药物反应不佳的不同原因,并提出了这些患者的诊断和临床管理算法。
使用术语“他汀类药物抵抗”、“他汀类药物敏感性”、“他汀类药物药代动力学”、“心血管疾病”和“降脂治疗”进行了 PubMed 搜索。查阅了过去 10 年中与该主题相关的已发表论文,为本篇迷你综述提供内容。
他汀类药物不能充分降低 LDL-C 是患者临床管理中的一个主要问题,限制了这种治疗方法的价值。他汀类药物低反应性有多种原因,最常见的解释是依从性差。其他原因,如 LDL-C 测量的分析问题和常见脂质紊乱(家族性高胆固醇血症、脂蛋白[a]升高和继发性血脂异常)的存在,应在考虑脂蛋白相关或药物代谢基因中罕见遗传变异导致的原发性他汀类药物抵抗之前排除。现在有多种非他汀类降脂药物可供选择,可以与他汀类药物联合使用以实现更有效的 LDL-C 降低。
他汀类药物低反应性的评估是一个多步骤的过程,可以优化降脂治疗以预防 ASCVD。它还可能导致识别出需要特定治疗的不同类型的血脂异常,以及对家庭成员进行基因筛查。