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.
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Kuru, S., Suzuki, S., Ogata, K., Kobayashi, M., Ishida, C., Watanabe, C., & Matsumura, T. (2017). Screening of autoantibodies associated with necrotizing myopathy among undiagnosed chronic myopathy. Clinical Neurology, 57(10), 562–566. https://doi.org/10.5692/clinicalneurol.cn-001075
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