Backes James M, Ruisinger Janelle F, Gibson Cheryl A, Moriarty Patrick M
Department of Pharmacy Practice, Atherosclerosis and LDL-Apheresis Center, Kansas University Medical Center, Kansas City, KS, USA; Department of Medicine, Atherosclerosis and LDL-Apheresis Center, Kansas University Medical Center, Kansas City, KS, USA.
Department of Pharmacy Practice, Atherosclerosis and LDL-Apheresis Center, Kansas University Medical Center, Kansas City, KS, USA; Department of Medicine, Atherosclerosis and LDL-Apheresis Center, Kansas University Medical Center, Kansas City, KS, USA.
J Clin Lipidol. 2017 Jan-Feb;11(1):24-33. doi: 10.1016/j.jacl.2017.01.006. Epub 2017 Jan 18.
Musculoskeletal symptoms are the most commonly reported adverse effects associated with statin therapy. Yet, certain data indicate that these symptoms often present in populations with underlying musculoskeletal complaints and are not likely statin related. Switching statins or using lower doses resolves muscle complaints in most patients. However, there is a growing population of individuals who experience intolerable musculoskeletal symptoms with multiple statins, regardless of the individual agent or prescribed dose. Recent randomized, placebo-controlled trials enrolling highly intolerant subjects provide significant insight regarding statin-associated muscle symptoms (SAMS). Notable findings include the inconsistency with reproducing muscle complaints, as approximately 40% of subjects report SAMS when taking a statin but not while receiving placebo, but a substantial cohort reports intolerable muscle symptoms with placebo but none when on a statin. These data validate SAMS for those likely experiencing true intolerance, but for others, suggest a psychosomatic component or misattribution of the source of pain and highlights the importance of differentiating from the musculoskeletal symptoms caused by concomitant factors. Managing the highly intolerant requires candid patient counseling, shared decision-making, eliminating contributing factors, careful clinical assessment and the use of a myalgia index score, and isolating potential muscle-related adverse events by gradually reintroducing drug therapy with the utilization of intermittent dosing of lipid-altering agents. We provide a review of recent data and therapeutic guidance involving a focused step-by-step approach for managing SAMS among the highly intolerant. Such strategies usually allow for clinically meaningful reductions in low-density lipoprotein cholesterol and an overall lowering of cardiovascular risk.
肌肉骨骼症状是与他汀类药物治疗相关的最常见不良反应。然而,某些数据表明,这些症状常在有潜在肌肉骨骼问题的人群中出现,不太可能与他汀类药物有关。大多数患者换用他汀类药物或使用较低剂量可缓解肌肉问题。然而,越来越多的人对多种他汀类药物都出现无法耐受的肌肉骨骼症状,无论使用何种药物或规定剂量。最近针对高度不耐受受试者开展的随机、安慰剂对照试验为他汀类药物相关肌肉症状(SAMS)提供了重要见解。显著发现包括肌肉问题再现的不一致性,约40%的受试者在服用他汀类药物时报告有SAMS,但服用安慰剂时没有,然而相当一部分受试者报告服用安慰剂时有无法耐受的肌肉症状,而服用他汀类药物时没有。这些数据证实了SAMS在那些可能真正不耐受的患者中的存在,但对其他患者而言,提示存在心身因素或疼痛来源的错误归因,并凸显了与伴随因素引起的肌肉骨骼症状相鉴别的重要性。管理高度不耐受患者需要与患者坦诚沟通、共同决策、消除促成因素、进行仔细的临床评估并使用肌痛指数评分,通过逐步重新引入药物治疗并采用间断给药的调脂药物来分离潜在的肌肉相关不良事件。我们综述了近期数据及治疗指导,其中涉及一种针对高度不耐受患者管理SAMS的重点明确的逐步方法。此类策略通常能在临床上显著降低低密度脂蛋白胆固醇水平并总体降低心血管风险。