Immune-Mediated Necrotizing Myopathies: Current Landscape

被引:3
作者
Koumas, Christoforos [1 ]
Michelassi, Francesco [1 ]
机构
[1] Columbia Univ, Dept Neurol, Med Ctr, New York, NY 10019 USA
关键词
Immune-mediated necrotizing myopathy; Myositis; HMGCR; Signal recognition particle (SRP); IDIOPATHIC INFLAMMATORY MYOPATHIES; CANCER-ASSOCIATED DERMATOMYOSITIS; SIGNAL RECOGNITION PARTICLE; CLINICAL-FEATURES; AUTOANTIBODIES; ANTIBODIES; ANTI-3-HYDROXY-3-METHYLGLUTARYL-COENZYME; POLYMYOSITIS; RITUXIMAB; EXPOSURE;
D O I
10.1007/s11910-024-01337-y
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose of ReviewImmune-mediated necrotizing myopathy (IMNM), characterized by acute or subacute onset, severe weakness, and elevated creatine kinase levels, poses diagnostic and therapeutic challenges. This article provides a succinct overview of IMNM, including clinical features, diagnostic strategies, and treatment approaches.Recent FindingsRecent insights highlight the different clinical presentations and therapeutic options of IMNM stratified by autoantibody positivity and type. Additionally, recent findings call into question the reported link between statin use and IMNM.SummaryThis review synthesizes current knowledge on IMNM, emphasizing its distinct clinical features and challenging management. The evolving understanding of IMNM underscores the need for a comprehensive diagnostic approach that utilizes a growing range of modalities. Early and aggressive immunomodulatory therapy remains pivotal. Ongoing research aims to refine diagnostic tools and therapeutic interventions for this challenging muscle disorder, underscoring the importance of advancing our understanding to enhance patient outcomes.
引用
收藏
页码:141 / 150
页数:10
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