Current approach to diagnosis of inflammatory myopathies: Clinical features and myositis antibody profiles

Indian J Pathol Microbiol. 2022 May;65(Supplement):S252-S258. doi: 10.4103/ijpm.ijpm_1082_21.

Abstract

Diagnosis of inflammatory myositis has been made easier with the availability of commercial assays for myositis-specific and myositis-associated antibodies. Clinico-serological association studies have permitted a better definition of clinical subsets. Myositis-specific auto-antibodies are highly specific and non-overlapping, whereas myositis-associated antibodies are those seen also in other connective tissue disorders such as systemic lupus erythematosus, primary Sjogren's syndrome, and idiopathic pulmonary auto-immune fibrosis. Their value is pronounced when clinical features are subtle or non-specific or when the muscle is not the primary organ involved. Overall, the muscle-specific and myositis-associated antibodies have changed the landscape in terms of diagnostic utility, prognostication, and the approach to organ-specific evaluation and management of idiopathic inflammatory myopathies (IIMs).

Keywords: Clinical features; inflammatory myopathy; myositis profile.

Publication types

  • Review

MeSH terms

  • Autoantibodies
  • Connective Tissue Diseases*
  • Humans
  • Myositis* / diagnosis

Substances

  • Autoantibodies