Abstract | OBJECTIVES: METHODS: Cross-sectional data on patients with JDM documented in the National Paediatric Rheumatologic Database in Germany between 2014 and 2016 were analysed. In a subgroup of the cohort, MSAs were determined with a commercial multiplex array, and a retrospective chart review was conducted to specify the clinical phenotype and patient outcome. RESULTS: The total cohort consisted of 196 patients with JDM (mean age 12.2±4.0 years, mean disease duration 5.1±3.8 years, 70% female). Apart from typical skin changes and muscle weakness, 41% of patients also had arthritis and/or contractures, 27% had calcinosis and approximately 10% had interstitial lung disease. Immunoblot testing was performed on the sera of 91 (46%) patients, detecting MSAs in 44% of patients. Patient groups with specific MSAs differed in clinical characteristics such as calcinosis, dysphagia, and lung and joint involvement. The extent of muscle weakness evaluated by the Childhood Myositis Assessment Scale was significantly associated with an increased level of creatine kinase. Patients with anti-MDA5 were particularly affected by polyarthritis of the small joints. After 5 years, 51 patients of the MSA cohort (56.0%) achieved an inactive disease state, 12/51 (23.5%) were off therapy. CONCLUSIONS: Patients with JDM in Germany show a broad spectrum of clinical manifestations that can be grouped into homogeneous groups using MSA, which also helps to predict the course and prognosis of the disease.
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Authors | Svea Horn, Kirsten Minden, Fabian Speth, Tobias Schwarz, Frank Dressler, Nadine Grösch, Johannes-Peter Haas, Claas Hinze, Gerd Horneff, Anton Hospach, Tilmann Kallinich, Jens Klotsche, Katharina Köstner, Christian Meisel, Martina Niewerth, Prasad Thomas Oommen, Catharina Schütz, Frank Weller-Heinemann, Nadine Unterwalder, Claudia Sengler |
Journal | Clinical and experimental rheumatology
(Clin Exp Rheumatol)
Vol. 40
Issue 2
Pg. 433-442
(Feb 2022)
ISSN: 0392-856X [Print] Italy |
PMID | 33124555
(Publication Type: Journal Article)
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Chemical References |
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Topics |
- Adolescent
- Autoantibodies
- Child
- Cross-Sectional Studies
- Dermatomyositis
(complications)
- Female
- Humans
- Male
- Myositis
(complications)
- Phenotype
- Retrospective Studies
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