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解读他汀类药物相关肌肉症状的复杂性。

Decoding the Intricacies of Statin-Associated Muscle Symptoms.

机构信息

Johns Hopkins Myositis Center, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Department of Internal Medicine, Texas Tech University Health Science Center, Amarillo, TX, USA.

出版信息

Curr Rheumatol Rep. 2024 Jul;26(7):260-268. doi: 10.1007/s11926-024-01143-y. Epub 2024 Apr 5.

DOI:10.1007/s11926-024-01143-y
PMID:38575845
Abstract

PURPOSE OF REVIEW

Hyperlipidemia is the major cardiovascular morbidity and mortality risk factor. Statins are the first-line treatment for hyperlipidemia. Statin-associated muscle symptoms (SAMS) are the main reason for the discontinuation of statins among patients. The purpose of this review is to guide clinicians to recognize the difference between self-limited and autoimmune statin myopathy in addition to the factors that potentiate them. Finally, treatment strategies will be discussed. This review mostly focuses on new data in the past 3 years.

RECENT FINDINGS

Recent findings suggest that SAMS is a complex and multifactorial condition that involves mitochondrial dysfunction, oxidative stress, and immune-mediated mechanisms. Effective management of SAMS requires a thorough evaluation of the patient's symptoms, risk factors, and medication history, as well as consideration of alternative treatment options. While statins are effective in reducing the risk of cardiovascular events, their use is associated with a range of adverse effects, including SAMS.

摘要

目的综述

高脂血症是主要的心血管发病率和死亡率的危险因素。他汀类药物是治疗高脂血症的一线药物。他汀类药物相关肌肉症状(SAMS)是导致患者停止使用他汀类药物的主要原因。本综述的目的是指导临床医生除了增强因素外,还能识别自限性和自身免疫性他汀类药物肌病之间的差异。最后,将讨论治疗策略。本综述主要关注过去 3 年中的新数据。

最近的发现

最近的研究结果表明,SAMS 是一种复杂的多因素疾病,涉及线粒体功能障碍、氧化应激和免疫介导的机制。SAMS 的有效管理需要对患者的症状、风险因素和药物治疗史进行全面评估,并考虑替代治疗方案。虽然他汀类药物在降低心血管事件风险方面非常有效,但它们的使用与一系列不良反应有关,包括 SAMS。

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本文引用的文献

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Prolonged Moderate-Intensity Exercise Does Not Increase Muscle Injury Markers in Symptomatic or Asymptomatic Statin Users.长期中等强度运动不会增加有症状或无症状他汀类药物使用者的肌肉损伤标志物。
J Am Coll Cardiol. 2023 Apr 11;81(14):1353-1364. doi: 10.1016/j.jacc.2023.01.043.
2
Bempedoic Acid and Cardiovascular Outcomes in Statin-Intolerant Patients.贝匹地酸在他汀类药物不耐受患者中的心血管结局。
N Engl J Med. 2023 Apr 13;388(15):1353-1364. doi: 10.1056/NEJMoa2215024. Epub 2023 Mar 4.
3
Limb girdle muscular disease caused by mutation and statin myopathy treatable with mevalonolactone.
由 突变引起的肢带型肌肉疾病和他汀类药物肌病可用美伐他汀治疗。
Proc Natl Acad Sci U S A. 2023 Feb 14;120(7):e2217831120. doi: 10.1073/pnas.2217831120. Epub 2023 Feb 6.
4
Global, regional and national trends in statin utilisation in high-income and low/middle-income countries, 2015-2020.2015-2020 年高收入和低收入/中等收入国家他汀类药物使用的全球、区域和国家趋势。
BMJ Open. 2022 Sep 8;12(9):e061350. doi: 10.1136/bmjopen-2022-061350.
5
Statin-Associated Muscle Symptoms Among New Statin Users Randomly Assigned to Vitamin D or Placebo.新使用他汀类药物的患者中随机分配维生素 D 或安慰剂的他汀类药物相关肌肉症状。
JAMA Cardiol. 2023 Jan 1;8(1):74-80. doi: 10.1001/jamacardio.2022.4250.
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Necrotizing myopathy with elevated anti-HMGCR antibodies following exposure to the supplement Bacopa.接触补充剂假马齿苋后出现抗HMGCR抗体升高的坏死性肌病。
Muscle Nerve. 2023 Feb;67(2):E1-E3. doi: 10.1002/mus.27758. Epub 2022 Dec 5.
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Mushroom supplements triggering a flare of HMGCR immune mediated necrotising myopathy.蘑菇补充剂引发 HMGCR 免疫介导的坏死性肌病发作。
BMJ Case Rep. 2022 May 23;15(5):e248880. doi: 10.1136/bcr-2022-248880.
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Statin-associated immune-mediated necrotizing myositis in Native Americans.美洲原住民中与他汀类药物相关的免疫介导坏死性肌炎。
Rheumatology (Oxford). 2022 Nov 28;61(12):4855-4862. doi: 10.1093/rheumatology/keac198.
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A systematic review of the drug-drug interaction between statins and colchicine: Patient characteristics, etiologies, and clinical management strategies.他汀类药物与秋水仙碱相互作用的系统评价:患者特征、病因和临床管理策略。
Pharmacotherapy. 2022 Apr;42(4):320-333. doi: 10.1002/phar.2674. Epub 2022 Feb 25.
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Ascorbic Acid Significantly Decreases Creatine Kinase Plasma Levels in an Animal Model of Statin/Fibrate-Induced Myopathy.在他汀类药物/贝特类药物诱导的肌病动物模型中,抗坏血酸显著降低肌酸激酶血浆水平。
Adv Pharmacol Pharm Sci. 2021 Dec 29;2021:5539595. doi: 10.1155/2021/5539595. eCollection 2021.