Table 1

 Patient characteristics at the start of the study for all subjects and when first entering as anti-TNF exposed and not exposed respectively

VariablesAll (n = 1430)At entry to the study
Anti-TNF exposed (n = 921)Not anti-TNF exposed (n = 652)
AllMen (n = 211)Women (n = 710)AllMen (n = 178)Women (n = 474)
COPD, chronic obstructive pulmonary disease; CVD, cardiovascular disease; DMARD, disease-modifying antirheumatic drug; HAQ, Health Assessment Questionnaire; TNF, tumour necrosis factor; VAS, visual analogue scale.
Results are presented as means (SD) unless otherwise mentioned.
Age57.8 (13.3)55.1 (12.8)57.3 (11.5)54.4 (13.0)61.1 (13.0)62.5 (11.8)60.5 (13.4)
Female (n, %)1067 (74.6)710 (77.1)474 (72.7)
HAQ (score limit 0–3)1.28 (0.72)1.45 (0.63)1.20 (0.60)1.53 (0.62)1.12 (0.79)0.87 (0.74)1.22 (0.78)
VAS patient global assessment54.1 (26.3)63.4 (21.5)58.6 (23.1)64.7 (20.9)43.1 (27.6)39.5 (27.4)44.5 (27.6)
VAS pain54.2 (26.5)62.5 (22.1)57.7 (24.0)63.9 (21.1)45.0 (28.6)39.8 (29.2)46.9 (28.1)
Disease duration (years)13.2 (11.3)12.7 (9.6)12.3 (9.6)12.9 (10.0)14.6 (12.6)14.0 (12.6)14.8 (12.8)
Present prednisolone treatment (n, %)696 (48.7)646 (70.1)159 (75.4)487 (68.6)140 (21.5)41 (23.0)99 (20.9)
Previous DMARD treatment (number of drugs)2.8 (1.9)3.6 (2.0)3.2 (1.6)3.7 (2.0)2,2 (1.7)1.8 (1.5)2.3 (1.8)
Comorbidity before first visit
    COPD (n, %)20 (1.4)13 (1.4)3 (1.4)10 (1.4)8 (1.2)6 (3.4)2 (0.4)
    Diabetes (n, %)51 (3.6)40 (4.3)15 (7.1)25 (3.5)14 (2.1)6 (3.4)8 (1.7)
    CVD (n, %)105 (7.3)59 (6.4)27 (12.8)32 (4.5)54 (8.2)23 (12.9)31 (6.5)
Any of the comorbidities154 (10.8)94 (10.2)37 (17.5)57 (8.0)71 (10.9)31 (17.4)40 (8.4)