The Utility of Myositis Specific Antibodies in Clinical Practice.
Kathryn BiddleMatthew D TaylorSarah E LinsteadPatrick D W KielyPublished in: The journal of applied laboratory medicine (2022)
Clinical practice is likely to be refined, with diagnosis and classification of the idiopathic inflammatory myositides based primarily on myositis-specific antibody, rather than directed by muscle histology or the broader clinical characteristics of polymyositis and dermatomyositis. All patients newly presenting with idiopathic inflammatory myositis should be routinely screened for myositis-specific antibodies. A positive result will usefully provide diagnostic and prognostic information, guide selection of therapy, and prompt surveillance for potential organ involvement and other features, such as cancer, throughout the disease course.
Keyphrases
- interstitial lung disease
- clinical practice
- systemic sclerosis
- rheumatoid arthritis
- end stage renal disease
- idiopathic pulmonary fibrosis
- myasthenia gravis
- chronic kidney disease
- oxidative stress
- ejection fraction
- newly diagnosed
- machine learning
- public health
- skeletal muscle
- peritoneal dialysis
- papillary thyroid
- healthcare
- patient reported outcomes
- young adults
- health information
- patient reported
- squamous cell