Table 1

 Baseline characteristics of patients at initiation of anti-TNF therapy

Disease characteristics*Adalimumab (ADL) (n = 317)Infliximab (INF) (n = 362)Etanercept (ETN) (n = 519)p Value†
*Values are given as means with 95% confidence intervals (CI) if not otherwise indicated. When not normally distributed variables, medians and interquartile ranges (IQRs) are reported; †one way analysis of variance (ANOVA) of means or medians for continuous variables. χ2 Test for dichotomous variables; ‡for patients with follow up data only, respectively n = 107, n = 295, n = 425.
DAS28, Disease Activity Score based on 28 joints; RADAI, Rheumatoid Arthritis Disease Activity Index; HAQ, Health Assessment Questionnaire; DMARD classical disease modifying antirheumatic drug; rheumatoid factor+, proportion of rheumatoid factor positive patients.
Anti-TNF dose, median (IQR)40 mg/2 wk (40–40)3.2 mg/kg×8 wk (3.0–3.75)50 mg/wk (50–50)
Female (%)7475740.89
Age (years)53.0 (51.4 to 54.7)53.1 (51.7 to 54.5)54.4 (53.2 to 55.6)0.24
Disease duration (years), median (IQR)10.1 (5.6–17.5)10.2 (5.0–16.5)10.3 (5.7–15.9)0.97
Rheumatoid factor+ (%)8281780.33
Follow up (mo)‡, median (IQR)10.7 (5.8–12.3)18.8 (11.5–28.3)23.7 (12.6–35.8)<0.001
Previous failure of anti-TNF agent (%)39127<0.001
Disease activity score (DAS28)4.19 (4.02 to 4.36)4.54 (4.38 to 4.7)4.72 (4.59 to 4.85)<0.001
RADAI4.02 (3.6 to 4.5)4.59 (4.37 to 4.81)4.85 (4.67 to 5.03)<0.001
Function disability (HAQ)1.25 (1.18 to 1.33)1.37 (1.29 to 1.44)1.37 (1.31 to 1.43)0.04
Concomitant DMARD use (%)539364
    Methotrexate (%)377040
    Leflunomide (%)101010
    Sulfasalazine (%)466
    Other DMARD (%)278
Glucocorticoid use (%)415660<0.001