Table 1

Patient characteristics at baseline

M-arm (Maintenance) (n=73)S-arm (Injection spacing) (n=64)
Age, years56.4±12.054.3±10.7
Female sex, n (%)54 (74.0)53 (82.8)
Disease duration, years11.0±10.38.3±5.4
IgM RF positivity, n (%)42 (67.7)37 (68.5)
ACPA positivity, n (%)46 (76.7)45 (80.4)
Erosive disease on X-rays (%)64 (87.7)57 (89.1)
ACR 1987 criteria, n (%)73 (100)64 (100)
ACR/EULAR 2010 criteria, n (%)*64 (100)60 (100)
Swollen joint count (28 joints)0.2±0.50.2±0.6
Tender joint count (28 joints)0.7±2.70.9±1.8
ESR, mm/1st hour12.5±10.712.6±8.3
CRP, mg/L2.9±2.02.6±1.9
DAS281.7±0.51.9±0.6
DAS441.0±0.51.1±0.5
HAQ score0.4±0.50.5±0.6
Total vSHS30.3±48.724.1±40.5
Satisfaction of remission criteria, n (%)
 DAS28≤2.873 (100)64 (100)
 CDAI≤2.847 (69)30 (50)
 SDAI≤3.350 (76)40 (67)
 Boolean remission53 (76.0)41 (64)
Previous RA treatment
 Number of previous DMARDs2.7±1.82.6±1.7
 Patients with previous biologic treatment18 (24.7)15 (23.4)
Ongoing treatment
 ADA (n=63)/ETA (n=74)34 (46.6)/39 (53.4)29 (45.3)/35 (54.7)
 Monotherapy (n=33)/combination (n=104)17 (23.3)/56 (76.7)16 (25.0)/48 (75.0)
 Patients receiving low-dose prednisone1 (1.4)1 (1.6)
  • Data are mean±SD or n (%).

  • *Data available for 64 and 60 patients in the M-arm and S-arm, respectively, for 2010 ACR/EULAR criteria assessment.

  • ACPA, anti-citrullinated peptides antibody; ACR, American College of Rheumatology; ADA, adalimumab; CDAI, Clinical Disease Activity Index (data available for 128 patients only); CRP, C-reactive protein; DAS, disease activity score; DMARD, disease-modifying anti-rheumatic drug; ESR, erythrocyte sedimentation rate; ETA, etanercept; EULAR, European League Against Rheumatism; HAQ, Health Assessment Questionnaire; IgM, immunoglobulin M; RA, rheumatoid arthritis; RF, rheumatoid factor; SDAI, Simplified Disease Activity Index (data available for 126 patients only); vSHS, van der Heijde-modified Sharp Score.