TY - JOUR
T1 - A multi-biomarker disease activity score tracks clinical response consistently in patients with rheumatoid arthritis treated with diff Erent anti-tumor necrosis factor therapies
T2 - A retrospective observational study
AU - Hirata, Shintaro
AU - Li, Wanying
AU - Defranoux, Nadine
AU - Cavet, Guy
AU - Bolce, Rebecca
AU - Yamaoka, Kunihiro
AU - Saito, Kazuyoshi
AU - Tanaka, Yoshiya
N1 - Funding Information:
This work was supported in part by Crescendo Bioscience, who supported shipment and testing of the serum samples. No other funding by Crescendo Bioscience was received for this study. The study was also supported in part by a Research Grant-In-Aid for Scientific Research by the Ministry of Health, Labor and Welfare of Japan, the Ministry of Education, Culture, Sports, Science and Technology of Japan, and the University of Occupational and Environmental Health, Japan.
Publisher Copyright:
© 2013 Japan College of Rheumatology.
PY - 2015
Y1 - 2015
N2 - Objectives. To assess the ability of a multi-biomarker disease activity (MBDA) score to track clinical response in patients with rheumatoid arthritis (RA) treated with different TNF inhibitors. Methods. The study included 147 patients who had received adalimumab, etanercept, or infliximab for a year or more, during routine clinical care at the University Hospital of Occupational and Environmental Health, Japan. MBDA scores and clinical measures of disease activity were evaluated at baseline and, after 24 weeks (N = 84) and 52 weeks of treatment. Relationships between the changes (Δ) in MBDA score and changes in clinical measures or EULAR response categories were evaluated. Results. The median disease activity was 5.7 by DAS28-ESR and 64 by MBDA score at baseline, and decreased significantly with treatment. Δ MBDA scores over 1 year correlated with Δ DAS28-ESR (r = 0.48) and Δ DAS28-CRP (r = 0.46). Linear relationships between Δ MBDA scores and Δ DAS28-ESR or Δ DAS28-CRP were not signifi cantly diff erent between TNF inhibitors. The MBDA scores declined significantly more in good responders (median change: - 29) than moderate (– 21), and more in moderate than in non-responders (+ 2), by the EULAR criteria. Conclusions. MBDA scores tracked disease activity and treatment response in patients with RA treated with three TNF inhibitors. The relationships between Δ MBDA scores and Δ DAS28-ESR or Δ DAS28-CRP were consistent across the three TNF inhibitor groups.
AB - Objectives. To assess the ability of a multi-biomarker disease activity (MBDA) score to track clinical response in patients with rheumatoid arthritis (RA) treated with different TNF inhibitors. Methods. The study included 147 patients who had received adalimumab, etanercept, or infliximab for a year or more, during routine clinical care at the University Hospital of Occupational and Environmental Health, Japan. MBDA scores and clinical measures of disease activity were evaluated at baseline and, after 24 weeks (N = 84) and 52 weeks of treatment. Relationships between the changes (Δ) in MBDA score and changes in clinical measures or EULAR response categories were evaluated. Results. The median disease activity was 5.7 by DAS28-ESR and 64 by MBDA score at baseline, and decreased significantly with treatment. Δ MBDA scores over 1 year correlated with Δ DAS28-ESR (r = 0.48) and Δ DAS28-CRP (r = 0.46). Linear relationships between Δ MBDA scores and Δ DAS28-ESR or Δ DAS28-CRP were not signifi cantly diff erent between TNF inhibitors. The MBDA scores declined significantly more in good responders (median change: - 29) than moderate (– 21), and more in moderate than in non-responders (+ 2), by the EULAR criteria. Conclusions. MBDA scores tracked disease activity and treatment response in patients with RA treated with three TNF inhibitors. The relationships between Δ MBDA scores and Δ DAS28-ESR or Δ DAS28-CRP were consistent across the three TNF inhibitor groups.
KW - Biomarkers
KW - Disease activity
KW - Rheumatoid arthritis
KW - TNF inhibitor
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U2 - 10.3109/14397595.2014.958893
DO - 10.3109/14397595.2014.958893
M3 - Article
C2 - 25295918
AN - SCOPUS:84929472825
SN - 1439-7595
VL - 25
SP - 344
EP - 349
JO - Japanese Journal of Rheumatology
JF - Japanese Journal of Rheumatology
IS - 3
ER -