Table 1

Adalimumab and methotrexate (MTX) data divided into four groups at start of adalimumab (Ada)

Ada+10 mg MTX (36)Ada+15 mg MTX (104)Ada+20 mg MTX (85)Ada+25 mg MTX (146)p Value
Mean age (SD), years56.5 (12.9)54.7 (11.9)54.1 (12.4)50.6 (13.1)0.015
Female77.8% (28)69.2% (72)64.7% (85)69.9% (102)0.556
Median disease duration (IQR)5.4 (2.6–10.2)5.1 (1.9–11.2)5.1 (1.8–13.4)3.2 (0.9–8.1)0.027
RF+80.6% (29)76.0% (76)68.3% (56)63.8% (90)0.099
Erosive72.4% (21)72.6% (61)66.7% (42)51.1% (48)0.001
No. of DMARDs* 0.802
 158.3% (21)65.4% (68)63.5% (54)58.9% (86)
 233.3% (12)27.9% (29)30.6% (26)34.2% (50)
 35.6% (2)6.7% (7)5.9% (5)5.5% (8)
 42.8% (1)0.0% (0)0.0% (0)1.4% (2)
DAS28 (SD)5.15 (1.29)4.76 (1.29)4.60 (1.40)4.55 (1.34)0.142
HAQ-DI (SD)1.35 (0.65)1.22 (0.58)1.13 (0.62)1.17 (0.61)0.410
Oral MTX62.9% (22)52.4% (54)54.1% (46)51.4% (75)0.671
  • The 444 patients received the following MTX doses: 2.5 mg (1), 5 mg (6), 7.5 mg (10), 10 mg (36), 12.5 mg (11), 15 mg (104), 17.5 mg (2), 20 mg (85), 22.5 mg (0), 25 mg (146), 27.5 mg (0), 30 mg (19) and ≥35 mg (10).

  • *Number of DMARDs as comedication next to adalimumab. This includes methotrexate. Other possible DMARDs are sulfasalazine, hydroxychloroquine, leflunomide, aurothiomalaat and azathioprine.

  • DAS28, disease activity score in 28 joints; DMARDs, disease-modifying antirheumatic drugs; HAQ-DI, health assessment questionnaire disability index; RF+, rheumatoid factor positive.