Serum chemokine levels as prognostic markers in patients with early systemic sclerosis: a multicenter, prospective, observational study
Authors:
- Minoru HasegawaMHMinoru Hasegawa
- Yoshihide AsanoYAYoshihide Asano
- Hirahito EndoHEHirahito Endo
- Manabu FujimotoMFManabu Fujimoto
- Daisuke GotoDGDaisuke Goto
- Hironobu IhnHIHironobu Ihn
- Katsumi InoueKIKatsumi Inoue
- Osamu IshikawaOIOsamu Ishikawa
- Yasushi KawaguchiYKYasushi Kawaguchi
- Masataka KuwanaMKMasataka Kuwana
- Fumihide OgawaFOFumihide Ogawa
- Hiroki TakahashiHTHiroki Takahashi
- 23 November 2012
- journal article
- research article
- Published by Oxford University Press (OUP) in Modern Rheumatology
- Vol. 23 (6) , 1076-84
Abstract
To assess the utility of serum chemokine levels as a prognostic indicator of disease progression in systemic sclerosis (SSc) patients with early onset disease. Seventy Japanese patients with early onset SSc presenting with diffuse skin sclerosis and/or interstitial lung disease were registered in a multicenter, observational study. Concentrations of CCL2, CCL5, CXCL8, CXCL9, and CXCL10 in serum samples from all patients were measured using cytometric beads array. In 33 patients, chemokine levels were measured each year for 4 years. The ability of baseline chemokine levels to predict changes in clinical features were evaluated statistically by multiple regression analysis. At their first visit, serum levels of CCL2, CCL5, CXCL8, CXCL9, and CXCL10 were significantly elevated in patients with SSc compared with healthy controls. There were significant associations between CCL2 and CXCL8 levels and between CXCL9 and CXCL10 levels in patients. The initial serum CXCL8 levels were significantly associated with the HAQ-DI at the fourth year while the %VC of baseline tended to be negatively associated with HAQ-DI at the fourth year. Initial chemokine levels were not associated with other clinical features including skin thickness score and the respiratory function. Serum CXCL8 level may serve as a prognostic indicator of the physical dysfunction in SSc. Further longitudinal studies of larger populations are needed to confirm these findings.Keywords
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