Inflammatory myopathies

The pattern of MHC class I expression in muscle biopsies from patients with myositis and other neuromuscular disorders

Rheumatology (Oxford)Published Cross-sectional study

Authors' conclusion

MHC-I immunostaining was useful to distinguish IIMs from non-inflammatory myopathies or neurogenic disorders.

Study context

Population
Diagnostic muscle biopsies processed at the Johns Hopkins Neuromuscular Pathology Laboratory, August 2013 to January 2017
Participants
357 muscle biopsies
Exposure
MHC-I immunostaining across normal biopsies, idiopathic inflammatory myopathies (IIMs), non-inflammatory myopathies and neurogenic disorders
  • Normaln = 31reference
  • IIMsn = 170
  • Non-inflammatory myopathiesn = 60
  • Neurogenic disordersn = 96
Outcome
Prevalence and patterns of abnormal MHC-I immunostaining
Methodological detailsretrospective, single-centre
  • Retrospective
  • Single-centre

Main finding

As reported in the abstract

Abnormal MHC-I immunostaining

Observational data: associations, not effects.

Further findings

OutcomeValues
Diagnostic accuracy of abnormal MHC-I immunostaining for IIMsAbnormal MHC-I immunostaining sensitivity 0.95 · specificity 0.82
Perifascicular MHC-I pattern in DM biopsies without perifascicular atrophy (n = 18)DM without perifascicular atrophy 50%

MHC-I staining patterns

Focal pattern associated with immune-mediated necrotizing myopathy (IMNM)
Global pattern more prevalent in sporadic IBM (sIBM)
Perifascicular pattern significantly more common in DM
Sarcoplasmic upregulation more common than sarcolemmal staining across all groups

Original publication

The pattern of MHC class I expression in muscle biopsies from patients with myositis and other neuromuscular disorders. Rheumatology (Oxford). Published 27 January 2023. doi:10.1093/rheumatology/kead052

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