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

Ann Rheum Dis. 2015 Jun;74(6):1102-9. doi: 10.1136/annrheumdis-2013-204986. Epub 2014 May 8.

Abstract

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 3 months 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 1 year. 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 1 year, 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.

Keywords: Anti-TNF; Cytokines; Disease Activity; Patient perspective; Rheumatoid Arthritis.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipokines / metabolism
  • Antibodies, Monoclonal / therapeutic use
  • Antirheumatic Agents / therapeutic use
  • Arthritis, Rheumatoid / diagnostic imaging
  • Arthritis, Rheumatoid / drug therapy
  • Arthritis, Rheumatoid / metabolism*
  • Biomarkers / metabolism*
  • C-Reactive Protein / metabolism
  • Chitinase-3-Like Protein 1
  • Disease Progression
  • Drug Therapy, Combination
  • Epidermal Growth Factor / metabolism
  • Female
  • Foot Joints / diagnostic imaging
  • Hand Joints / diagnostic imaging
  • Humans
  • Hydroxychloroquine / therapeutic use
  • Infliximab
  • Interleukin-6 / metabolism
  • Lectins / metabolism
  • Leptin / metabolism
  • Logistic Models
  • Male
  • Matrix Metalloproteinase 1 / metabolism
  • Matrix Metalloproteinase 3 / metabolism
  • Methotrexate / therapeutic use
  • Multivariate Analysis
  • Prognosis
  • Radiography
  • Receptors, Tumor Necrosis Factor, Type I / metabolism
  • Resistin / metabolism
  • Serum Amyloid A Protein / metabolism
  • Severity of Illness Index
  • Sulfasalazine / therapeutic use
  • Treatment Outcome
  • Vascular Cell Adhesion Molecule-1 / metabolism
  • Vascular Endothelial Growth Factor A / metabolism

Substances

  • Adipokines
  • Antibodies, Monoclonal
  • Antirheumatic Agents
  • Biomarkers
  • CHI3L1 protein, human
  • Chitinase-3-Like Protein 1
  • IL6 protein, human
  • Interleukin-6
  • Lectins
  • Leptin
  • Receptors, Tumor Necrosis Factor, Type I
  • Resistin
  • Serum Amyloid A Protein
  • Vascular Cell Adhesion Molecule-1
  • Vascular Endothelial Growth Factor A
  • Sulfasalazine
  • Hydroxychloroquine
  • Epidermal Growth Factor
  • C-Reactive Protein
  • Infliximab
  • MMP3 protein, human
  • Matrix Metalloproteinase 3
  • MMP1 protein, human
  • Matrix Metalloproteinase 1
  • Methotrexate

Associated data

  • ClinicalTrials.gov/NCT00764725