Diagnostics (May 2022)

A New Method for the Assessment of Myalgia in Interstitial Lung Disease: Association with Positivity for Myositis-Specific and Myositis-Associated Antibodies

  • Gianluca Sambataro,
  • Chiara Alfia Ferrara,
  • Carla Spadaro,
  • Sebastiano Emanuele Torrisi,
  • Giovanna Vignigni,
  • Ada Vancheri,
  • Giuseppe Muscato,
  • Nicoletta Del Papa,
  • Michele Colaci,
  • Lorenzo Malatino,
  • Stefano Palmucci,
  • Lorenzo Cavagna,
  • Giovanni Zanframundo,
  • Francesco Ferro,
  • Chiara Baldini,
  • Domenico Sambataro,
  • Carlo Vancheri

DOI
https://doi.org/10.3390/diagnostics12051139
Journal volume & issue
Vol. 12, no. 5
p. 1139

Abstract

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In this study, it was found that myositis-specific and myositis-associated antibodies (MSAs and MAAs) improved the recognition of idiopathic inflammatory myopathies (IIMs) in interstitial lung disease (ILD) patients. The objective of this study is to propose a clinical method to evaluate myalgia in respiratory settings as a possible tool for the recognition of MSA/MAA positivity in ILD patients. We prospectively enrolled 167 ILD patients with suspected myositis, of which 63 had myalgia evoked at specific points (M+ILD+). We also enrolled in a 174 patients with only myalgia (M+ILD-) in a rheumatological setting. The patients were assessed jointly by rheumatologists and pulmonologists and were tested for autoantibodies. M+ILD+ patients were positive for at least one MAA/MSA in 68.3% of cases, as were M-ILD+ patients in 48.1% of cases and M+ILD- patients in 17.2% of cases (p = 0.01 and p = 0.02). Myalgia was significantly associated with positivity for MSA/MAAs in ILD patients (p = 0.01, X2: 6.47). In conclusion, myalgia in ILD patients with suspected myositis is associated with MSA/MAA positivity, and could support a diagnosis of IIM. A significant proportion of M+ILD- patients also had MSA/MAA positivity, a phenomenon warranting further study to evaluate its clinical meaning.

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