Increased serum levels of B cell activating factor (BAFF) in subsets of patients with idiopathic inflammatory myopathies
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
18628284
DOI
10.1136/ard.2008.091405
PII: S0003-4967(24)21749-0
Knihovny.cz E-resources
- MeSH
- Analysis of Variance MeSH
- Antibodies, Antinuclear blood MeSH
- Autoantibodies blood immunology MeSH
- C-Reactive Protein analysis MeSH
- Dermatomyositis blood drug therapy immunology MeSH
- Child MeSH
- Adult MeSH
- B-Cell Activating Factor blood MeSH
- Glucocorticoids therapeutic use MeSH
- Creatine Kinase blood MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Myositis blood drug therapy immunology MeSH
- Statistics, Nonparametric MeSH
- Polymyositis blood drug therapy immunology MeSH
- Tumor Necrosis Factor Ligand Superfamily Member 13 blood MeSH
- Aged MeSH
- Case-Control Studies MeSH
- Check Tag
- Child MeSH
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Adolescent MeSH
- Young Adult MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Antibodies, Antinuclear MeSH
- Autoantibodies MeSH
- C-Reactive Protein MeSH
- B-Cell Activating Factor MeSH
- Glucocorticoids MeSH
- Jo-1 antibody MeSH Browser
- Creatine Kinase MeSH
- Tumor Necrosis Factor Ligand Superfamily Member 13 MeSH
OBJECTIVE: To investigate serum levels of B cell activating factor (BAFF) in patients with myositis and correlate these to autoantibody profile, clinical phenotype and treatment. METHODS: BAFF levels in sera from 49 patients with dermatomyositis, 44 with polymyositis, 6 with inclusion body myositis and 30 matched controls were measured by ELISA. Specific autoantibodies were detected by line blot and western blot assays. RESULTS: Serum levels of BAFF were significantly higher in patients compared to healthy controls (p = 0.003). Patients with anti-Jo-1 autoantibodies had higher BAFF levels than control individuals (p<0.003) or patients without any specific autoantibodies (p<0.05). Patients with dermatomyositis had higher BAFF levels compared to polymyositis (p<0.05). Patients with interstitial lung disease (ILD) had higher BAFF levels than patients without ILD (p<0.05) or controls (p<0.01) but this could be explained by presence of anti-Jo-1 autoantibodies. BAFF levels correlated with serum creatine kinase (CK) (rs = 0.365, p = 0.0005) but not with C-reactive protein (CRP) levels. A negative correlation of BAFF levels with glucocorticoid daily dose for all patients (rs = -0.292, p = 0.003) and with cumulative glucocorticoid doses in early myositis cases (rs = -0.659, p<0.001) was recorded. CONCLUSION: Our finding of elevated serum levels of BAFF in patients with myositis with described phenotypes together with the correlations between levels of BAFF and CK and a negative correlation with dose of glucocorticoids, indicate that BAFF could be a potential therapeutic target in such cases.
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