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Statin-induced necrotizing myositis – A discrete autoimmune entity within the statin-induced myopathy spectrum

机译:他汀类药物引起的坏死性肌炎–他汀类药物引起的肌病谱内的离散自身免疫实体

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摘要

Statin-induced necrotizing myositis is increasingly being recognised as part of the “statin-induced myopathy spectrum”. As in other immune-mediated necrotizing myopathies, statin-induced myositis is characterised by proximal muscle weakness with marked serum creatine kinase elevations and histological evidence of myonecrosis, and with little or no inflammatory cell infiltration. Unlike other necrotizing myopathies, statin-induced myopathy is associated with the presence of autoantibodies directed against 3-hydroxy-3-methylglutaryl-coenzyme A reductase (the enzyme target of statin therapies), and with HLA-DRB1*11. This article summarises the clinical presentation, investigations and management of this rare, but serious complication of statin therapy.
机译:他汀类药物引起的坏死性肌炎越来越被认为是“他汀类药物引起的肌病谱”的一部分。与其他免疫介导的坏死性肌病一样,他汀类药物诱发的肌炎的特点是近端肌无力,血清肌酸激酶明显升高,并有组织坏死的组织学证据,几乎没有炎症细胞浸润。与其他坏死性肌病不同,他汀类药物引起的肌病与针对3-羟基-3-甲基戊二酰辅酶A还原酶(他汀类药物疗法的酶靶标)的自身抗体以及HLA-DRB1 * 11相关。本文总结了这种罕见但严重的他汀类药物疗法的临床表现,研究和处理。

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