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 language | English (US) |
|---|---|
| Title of host publication | Managing Myositis |
| Subtitle of host publication | A Practical Guide |
| Publisher | Springer International Publishing |
| Pages | 225-235 |
| Number of pages | 11 |
| ISBN (Electronic) | 9783030158200 |
| ISBN (Print) | 9783030158194 |
| DOIs | |
| State | Published - 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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