Table 1

Patient characteristics according to treatment modality

Initial MTX monotherapy (months 0–3, n=316)Add-on DMARD combination (months 3–12, n=55)Add-on TNF inhibitor (months 3–12, n=84)
Women (%)231 (73)45 (82)64 (76)
Disease duration, mean months (SD)6.2 (4.8)5.8 (3.0)6.2 (3.4)
Rheumatoid factor positive (%)213 (67)37 (67)53 (63)
Concurrent low-dose prednisolone (%)42 (13)6 (11)8 (10)
DAS28, mean (SD)5.7 (1.0)5.9 (1.0)6.0 (1.0)
DAS28 at 3 months, mean (SD)4.0 (1.4)4.7 (1.0)5.0 (1.0)
Erosions, n (%)*107 (38)22 (45)27 (36)
Median anti-CCP level, AU/mL (IQR)†811 (259–2147)874 (234–2556)743 (187–1883)
Median anti-CEP-1 level, U/mL (IQR)†50.7 (21.3–119.5)45.8 (20.8–113.7)46.0 (20.4–103.4)
Median anti-cVim level, U/mL (IQR)†22.7 (14.4–40.8)25.3 (11.2–31.6)20.4 (14.6–38.3)
Median anti-cFib level, U/mL (IQR)†32.6 (18.6–64.1)40.7 (18.2–64.1)23.3 (15.3–46.8)
Median number of ACPAs, median (range)2 (0–4)2 (0–4)1 (0–4)
  • Baseline values are given unless otherwise indicated.

  • *Data available from 282, 49 and 75 patients, respectively.

  • †Among positive patients only.

  • ACPA, anticitrullinated protein antibody; CCP, cyclic citrullinated peptide; CEP-1, citrullinated α-enolase peptide-1; cFib, citrullinated fibrinogen peptide; cVim, citrullinated vimentin peptide; DAS28, 28-joint disease activity score; DMARD, disease-modifying antirheumatic drugs; MTX, methotrexate; TNF, tumour necrosis factor.