Autoantibodies in Myositis. How to Achieve a Comprehensive Strategy for Serological Testing.
autoantibodies
autoimmunity
dermatomyositis
inclusion body myositis
myositis
polymyositis
serology
Journal
Mediterranean journal of rheumatology
ISSN: 2529-198X
Titre abrégé: Mediterr J Rheumatol
Pays: Greece
ID NLM: 101730166
Informations de publication
Date de publication:
Sep 2019
Sep 2019
Historique:
received:
02
07
2019
revised:
23
07
2019
accepted:
30
07
2019
entrez:
19
3
2020
pubmed:
19
3
2020
medline:
19
3
2020
Statut:
epublish
Résumé
Myopathies are a rare type of acquired, chronic autoimmune diseases of the skeletal muscles and affect both children and adults. The hallmark symptoms of idiopathic inflammatory myopathies (IIM) are muscle inflammation, proximal muscle weakness and disability, arthritis, cutaneous rashes, calcinosis, ulceration, malignancy and interstitial lung disease (ILD). Subforms of IIM include polymyositis, dermatomyositis, cancer-related myositis and sporadic inclusion body myositis. Autoantibodies function as biomarkers for diagnosis of IIM and can be used to delimit clinically distinguishable IIM subforms. To maximise the diagnostic information it is essential to perform comprehensive multiparametric serological testing including both screening and confirmation tests.
Identifiants
pubmed: 32185358
doi: 10.31138/mjr.30.3.155
pii: MJR-30-3-155
pmc: PMC7045863
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
155-161Informations de copyright
© 2019 The Mediterranean Journal of Rheumatology (MJR).
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