Tumour necrosis factor alpha and its soluble receptors in juvenile chronicarthritis

Citation
M. Rooney et al., Tumour necrosis factor alpha and its soluble receptors in juvenile chronicarthritis, RHEUMATOLOG, 39(4), 2000, pp. 432-438
Citations number
40
Categorie Soggetti
Rheumatology
Journal title
RHEUMATOLOGY
ISSN journal
14620324 → ACNP
Volume
39
Issue
4
Year of publication
2000
Pages
432 - 438
Database
ISI
SICI code
1462-0324(200004)39:4<432:TNFAAI>2.0.ZU;2-S
Abstract
Objective. To identify possible imbalance of tumour necrosis factor alpha ( TNF alpha) and its soluble receptors in the different subgroups of juvenile chronic arthritis (JCA). Methods. Serum and synovial fluid samples from 45 children were examined, 2 5 pauciarticular JCA, 13 polyarticular JCA and seven spondyloarthropathy. T NF alpha, sTNFRI and sTNFRII levels were measured by EASIA and enzyme-linke d immunosorbent assay (ELISA). Analysis of the results was carried out usin g non-parametric tests: Kruskal-Wallis one-way analysis of variance was use d to compare the three clinical subgroups: the MannWhitney U-test was used to compare group medians. Results. Thirty-three serum samples were assayed for TNF alpha. There was n o significant difference between the three groups using the Kruskal-Wallis analysis of variance. Analysis of synovial fluid TNF levels showed signific antly lower levels in the spondyloarthropathy group compared with the pauci articular JCA (P = 0.01) and the polyarticular group (P = 0.001). Significa ntly higher levels of sTNFRI were observed in the synovial fluid of the pol yarticular JCA group compared with the pauciarticular JCA group (P = 0.004) and similarly for sTNFRII (P = 0.03). Molar ratios were calculated for TNF , vs sTNFRI. The sTNFRI/TNF alpha ratio was significantly higher in the spo ndyloarthropathy group compared with the pauci(P = 0.003) and the polyartic ular JCA subgroups (P = 0.003). The combined soluble receptor levels expres sed as molar ratio to TNF again showed a significantly higher ratio in the spondyloarthropathy group compared with the pauciarticular group (P = 0.01) and compared with the polyarticular group (P = 0.05). Conclusion. These results suggest that the increased joint destruction obse rved ill polyarticular disease compared with the other two subtypes may be related to the lower sTNFR/TNF alpha ratios observed.