Table 2

Baseline patient characteristics of GC and COBRA cohorts

GC cohort (n=9)COBRA cohort (n=19)
Age (years)52 (8)51 (14)
Female, n (%)5 (56)12 (63)
DAS286.3 (1.0)5.3 (0.9)
Erosive disease, n (%)*8 (89)10 (67)
RF, n (%)5 (71)13 (72)
ACPA, n (%)4 (57)13 (75)
ESR (mm/h)45 (18–80)34 (26)
CRP (mg/dl)15 (4–60)16 (8–30)
Disease duration (months)10 (6–29)3.2 (4.4)
Leptin (ng/ml)39 (13–120)12 (10–37)
Resistin (ng/ml)31 (24–39)16.9 (13.5–22.0)
Adiponectin (mg/ml)72 (43–91)15.7 (15.2–16.3)
Visfatin (ng/ml)5.6 (4.3–7.7)1.4 (1.1–3.7)
Vaspin (ng/ml)0.30 (0.22–0.64)0.51 (0.16–0.72)
  • Data are represented as mean (SD), median (IQR) or n (%), as appropriate. Baseline values of patients with RA treated with an oral GC (60 mg prednisolone daily for 1 week followed by 40 mg prednisolone daily for 1 week; GC cohort), or combination of oral dosages of hydroxychloroquine (400 mg/day), sulfasalazine (2 g/day), methotrexate (10 mg/week) and step-down high-dose prednisolone (tapered in 6 weeks from 60 to 7.5 mg/day (thereafter until end of trial); COBRA cohort). Presence of erosive joint disease was determined by x-ray. Presence of IgM-RF was defined as serum levels ≥12.5 IU/ml for the GC cohort and ≥30 IU/ml for the COBRA cohort.

  • ACPA, anticitrullinated peptide antibody; CRP, C reactive protein; DAS28, disease activity score evaluated in 28 joints; ESR, erythrocyte sedimentation rate; GC, glucocorticoid; RF, IgM rheumatoid factor.