Abstract
We screened anti-signal recognition particle (SRP) and anti-3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) antibodies among 42 patients who had undiagnosed chronic myopathy from six national hospitals. Anti-SRP and anti-HMGCR antibodies were determined by RNA immuneprecipitation and enzyme-linked immune-sorbent assay (ELISA), respectively. We identified two patients with anti-SRP antibodies (4.7%) and, two with anti-HMGCR antibodies (4.7%). Both of anti-SRP-positive patients showed dysphagia with a high level of creatine kinase. Anti-HMGCR antibodies were associated with mild muscle weakness with a relatively late disease onset. Our study suggests the importance of autoantibody testing among undiagnosed chronic myopathy.
Original language | English |
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Pages (from-to) | 562-566 |
Number of pages | 5 |
Journal | Clinical Neurology |
Volume | 57 |
Issue number | 10 |
DOIs | |
Publication status | Published - 2017 |
Keywords
- Anti-HMGCR antibody
- Anti-SRP antibody
- Chronic myopathy
- Immune-mediated necrotizing myopathy
ASJC Scopus subject areas
- Clinical Neurology