Pretreatment multi-biomarker disease activity score and radiographic progression in early RA: results from the SWEFOT trial

被引:78
作者
Hambardzumyan, Karen [1 ]
Bolce, Rebecca [2 ]
Saevarsdottir, Saedis [1 ,3 ,4 ]
Cruickshank, Scott E. [5 ]
Sasso, Eric H. [2 ]
Chernoff, David [2 ]
Forslind, Kristina [6 ,7 ]
Petersson, Ingemar F. [6 ,8 ]
Geborek, Pierre [6 ]
van Vollenhoven, Ronald F. [1 ]
机构
[1] Karolinska Inst, Unit Clin Therapy Res, Inflammatory Dis ClinTRID, Stockholm, Sweden
[2] Crescendo Biosci Inc, San Francisco, CA USA
[3] Karolinska Univ Hosp, Dept Med, Rheumatol Unit, Stockholm, Sweden
[4] Karolinska Inst, Stockholm, Sweden
[5] Scott Cruickshank & Associates Inc, Santa Barbara, CA USA
[6] Univ Lund Hosp, Sect Rheumatol, Inst Clin Sci, S-22185 Lund, Sweden
[7] Helsingborg Hosp, Dept Med, Sect Rheumatol, Helsingborg, Sweden
[8] Lund Univ, Inst Clin Sci, Dept Orthopaed, Lund, Sweden
关键词
Rheumatoid Arthritis; Disease Activity; Anti-TNF; Cytokines; Patient perspective; EARLY RHEUMATOID-ARTHRITIS; ACR/EULAR REMISSION CRITERIA; JOINT DAMAGE; RISK MODEL; METHOTREXATE; PREDICTION; VALIDATION; INFLIXIMAB; ANTIBODIES; MARKERS;
D O I
10.1136/annrheumdis-2013-204986
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives Prediction of radiographic progression (RP) in early rheumatoid arthritis (eRA) would be very useful for optimal choice among available therapies. We evaluated a multi-biomarker disease activity (MBDA) score, based on 12 serum biomarkers as a baseline predictor for 1-year RP in eRA. Methods Baseline disease activity score based on erythrocyte sedimentation rate (DAS28-ESR), disease activity score based on C-reactive protein (DAS28-CRP), CRP, MBDA scores and DAS28-ESR at 3months were analysed for 235 patients with eRA from the Swedish Farmacotherapy (SWEFOT) clinical trial. RP was defined as an increase in the Van der Heijde-modified Sharp score by more than five points over 1year. Associations between baseline disease activity measures, the MBDA score, and 1-year RP were evaluated using univariate and multivariate logistic regression, adjusted for potential confounders. Results Among 235 patients with eRA, 5 had low and 29 moderate MBDA scores at baseline. None of the former and only one of the latter group (3.4%) had RP during 1year, while the proportion of patients with RP among those with high MBDA score was 20.9% (p=0.021). Among patients with low/moderate CRP, moderate DAS28-CRP or moderate DAS28-ESR at baseline, progression occurred in 14%, 15%, 14% and 15%, respectively. MBDA score was an independent predictor of RP as a continuous (OR=1.05, 95% CI 1.02 to 1.08) and dichotomised variable (high versus low/moderate, OR=3.86, 95% CI 1.04 to 14.26). Conclusions In patients with eRA, the MBDA score at baseline was a strong independent predictor of 1-year RP. These results suggest that when choosing initial treatment in eRA the MBDA test may be clinically useful to identify a subgroup of patients at low risk of RP. Trial registration number WHO database at the Karolinska Institute: CT20080004; and clinicaltrials.gov: NCT00764725.
引用
收藏
页码:1102 / 1109
页数:8
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