Abstract
The discovery of an increased repertoire of autoantibodies associated with idiopathic inflammatory myositis has important implications for enabling earlier diagnosis. Either a myositis-specific or a myositis-associated autoantibody is present in about 70% of adult and juvenile cases and in many cases identify specific patterns of disease and co-morbidities. In the future, it is likely that knowledge of a myositis autoantibody profile will be more fully incorporated into diagnostic and classification criteria and lessen the need for more invasive investigative procedures. In the meantime, there is a need for standardisation of commercial assays that are becoming more available, awareness of the reliability of initial autoantibody screening procedures, and guidance on how to interpret myositis autoantibody results in a given clinical context.
| Original language | English |
|---|---|
| Title of host publication | Managing Myositis |
| Subtitle of host publication | A Practical Guide |
| Editors | R. Aggarwal, C. Oddis |
| Place of Publication | Cham, Switzerland |
| Publisher | Springer International Publishing |
| Pages | 167-174 |
| Number of pages | 8 |
| ISBN (Electronic) | 9783030158200 |
| ISBN (Print) | 9783030158194 |
| DOIs | |
| Publication status | Published - 15 Dec 2019 |
Keywords
- Autoantibody
- Diagnosis
- Myositis
ASJC Scopus subject areas
- General Medicine
- General Neuroscience
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