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Immune-Mediated Necrotizing Myopathy (IMNM)

Research output: Chapter in Book/Report/Conference proceedingChapter

Abstract

Immune-mediated necrotizing myopathy (IMNM) is a distinct subset of the idiopathic inflammatory myopathies, characterized by proximal muscle weakness and muscle atrophy, markedly elevated CK levels, and myocyte necrosis with minimal inflammatory infiltrate on muscle biopsy. The two most common antibodies associated with IMNM are anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (anti-HMGCR) and anti-signal recognition particle (anti-SRP), although in one-third of cases there are no identifiable autoantibodies. The greatest risk factor for anti-HMGCR myopathy is statin exposure, although it can occur independently of statins, especially in younger patients.

Original languageEnglish (US)
Title of host publicationManaging Myositis
Subtitle of host publicationA Practical Guide
PublisherSpringer International Publishing
Pages225-235
Number of pages11
ISBN (Electronic)9783030158200
ISBN (Print)9783030158194
DOIs
StatePublished - Jan 1 2019

Keywords

  • 3-Hydroxy-3-methylglutaryl-coenzyme A reductase
  • HMGCR
  • Immune-mediated necrotizing myopathy
  • Myositis
  • Necrotizing autoimmune myopathy
  • Signal recognition particle
  • SRP
  • Statin-induced myopathy

ASJC Scopus subject areas

  • General Medicine
  • General Neuroscience

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