Clinical Characteristics and Management of Statin-Associated Anti-3-Hydroxy-3-Methylglutaryl-Coenzyme A Reductase Immune-Mediated Necrotizing Myopathy.

IF 2.9 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Jiyeol Yoon, Seung Woo Kim, Se Hoon Kim, Jason Jungsik Song, Yong-Beom Park, Hee Jin Park, Ha Young Shin, Se Hee Park, Yumie Rhee
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引用次数: 0

Abstract

Background: Immune-mediated necrotizing myopathy (IMNM) associated with anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) antibody is a rare but critical complication usually triggered by statin use. However, the comprehensive characterization and long-term outcomes of anti-HMGCR-positive IMNM remain underexplored. This study aimed to examine the clinical characteristics, diagnostic challenges, treatment responses, and long-term outcomes of patients with anti-HMGCR-positive IMNM. Methods: A retrospective review was conducted at a single institution between 2019 and 2025 to analyze the data of patients diagnosed with anti-HMGCR-positive IMNM. Diagnoses were confirmed by detecting anti-HMGCR antibodies and meeting the criteria for IMNM of the European Neuromuscular Center. The analyzed data included demographics, clinical presentation, laboratory findings, imaging results, muscle biopsy characteristics, treatment regimens, and follow-up outcomes. Results: Ten patients (six women and four men) with a median age of 58 (range, 33-86) years were included. Nine patients had a history of statin use for a median duration of two years. The average diagnostic delay was 233 days after the onset of symptoms. The initial creatine kinase (CK) levels ranged from 1438 to over 13,000 IU/L. Muscle biopsies revealed necrosis and regeneration of muscle fibers. CK levels fluctuated and trended downward over 180 days post-treatment. Treatment included corticosteroids, methotrexate, azathioprine, tacrolimus, mycophenolate, intravenous immunoglobulin, and rituximab. Delayed treatment initiation from symptom onset was correlated with prolonged treatment time until the first remission. Conclusions: The prognosis of anti-HMGCR-positive IMNM is less favorable when treatment is delayed after symptom onset. Further research is warranted to identify poor prognostic markers and develop relevant treatments.

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他汀类药物相关抗3-羟基-3-甲基戊二酰辅酶A还原酶免疫介导的坏死性肌病的临床特点和治疗
背景:免疫介导的坏死性肌病(IMNM)伴抗3-羟基-3-甲基戊二酰辅酶A还原酶(HMGCR)抗体是一种罕见但关键的并发症,通常由他汀类药物引起。然而,抗hmgcr阳性IMNM的综合表征和长期结果仍未得到充分探讨。本研究旨在探讨抗hmgcr阳性IMNM患者的临床特征、诊断挑战、治疗反应和长期预后。方法:回顾性分析2019年至2025年在单一机构诊断为抗hmgcr阳性IMNM患者的数据。通过检测抗hmgcr抗体并符合欧洲神经肌肉中心的IMNM标准,确诊。分析的数据包括人口统计学、临床表现、实验室结果、影像学结果、肌肉活检特征、治疗方案和随访结果。结果:纳入10例患者(6女4男),中位年龄58岁(33-86岁)。9例患者有他汀类药物使用史,平均持续时间为2年。平均诊断延迟时间为症状出现后233天。初始肌酸激酶(CK)水平在1438到13000 IU/L之间。肌肉活检显示肌纤维坏死和再生。CK水平在处理后180 d内波动并呈下降趋势。治疗包括皮质类固醇、甲氨蝶呤、硫唑嘌呤、他克莫司、霉酚酸酯、静脉注射免疫球蛋白和利妥昔单抗。从症状开始延迟治疗与延长治疗时间直到第一次缓解相关。结论:抗hmgcr阳性IMNM在症状出现后延迟治疗,预后较差。有必要进一步研究以确定不良预后标志物并开发相关治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Clinical Medicine
Journal of Clinical Medicine MEDICINE, GENERAL & INTERNAL-
CiteScore
5.70
自引率
7.70%
发文量
6468
审稿时长
16.32 days
期刊介绍: Journal of Clinical Medicine (ISSN 2077-0383), is an international scientific open access journal, providing a platform for advances in health care/clinical practices, the study of direct observation of patients and general medical research. This multi-disciplinary journal is aimed at a wide audience of medical researchers and healthcare professionals. Unique features of this journal: manuscripts regarding original research and ideas will be particularly welcomed.JCM also accepts reviews, communications, and short notes. There is no limit to publication length: our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible.
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