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. 2006 Nov 1;66(3):302–307. doi: 10.1136/ard.2006.060608

Table 1 Demographic and clinical characteristic of patients included in the study.

Total patients (n = 132) Infliximab (n = 63) Etanercept (n = 35) Adalimumab (n = 34)
Age (years) 57.28 (12.46) 59.12 (10.86) 58.4 (11.99) 52.57 (14.87)
Female/male 101/31 46/17 28/7 27/7
Disease duration (years) 8.3 (6.93) 9.08 (8.11) 6.15 (4.72) 9.58 (6.65)
Tender joints (68) 15.96 (9.9) 18.1 (10.3) 16.65 (9.7) 11.03 (7.36)
Swollen joints (66) 9.59 (5.7) 7.9 (4.88) 13.17 (7.46) 9.36 (3.21)
Erosions (%) 100 100 100 100
DAS 28 5.87 (0.99) 5.93 (1.08) 5.95 (1.08) 5.52 (0.7)
HAQ 1.598 (0.69) 1.73 (0.57) 1.74 (0.77) 1.11 (0.66)
Responders (%)* 66 61 65 76
Previous DMARDs, n of patients (%)
 Methotrexate 131 (99.24) 63 (100) 34 (97.14) 34 (100)
 Hydroxycloroquine 93 (70.45) 53 (84.12) 22 (62.85) 19 (55.88)
 Sulfasalazine 61 (46.21) 32 (50.79) 16 (47.71) 13 (38.23)
 Ciclosporin A 48 (36.36) 29 (46.03) 12 (34.28) 7 (20.58)
 Others 34 (25.75) 14 (22.22) 9 (25.71) 11 (32.35)
DMARDs associated, n of patients (%)
 Methotrexate 115 (87.12) 63 (100) 29 (82.85) 23 (67.64)
 Leflunomide 2 (1.51) 0 0 2 (5.88)
 None 15 (11.36) 0 6 (17.14) 9 (26.47)

DAS 28, disease activity score including 28 joint counts; DMARD, disease‐modifying antirheumatic drug; HAQ, Health Assessment Questionnaire.

Where applicable, the values are expressed as mean (SD).

*126 patients evaluable for clinical response.