| IFX + MTX | MTX | PL | P value |
---|---|---|---|---|
Number of patients (n) | 38 | 36 | 16 | 0.4440 |
Female | 26 (68.4%) | 28 (77.8%) | 9 (56.3%) | 0.2833 |
Age (years), mean ± SD | 52.1 ± 14.1 | 52.9 ± 14.0 | 54.4 ± 11.2 | 0.9170 |
Symptom duration (weeks)a, mean ± SD | 10.3 ± 2.3 | 9.4 ± 2.3 | 9.8 ± 1.8 | 0.0722 |
Rheumatoid factor positive | 13 (34.2%) | 13 (36.1%) | 7 (43.8%) | 0.7988 |
Patients who used steroids prior to the study | 24 (63.2%) | 22 (61.1%) | 9 (56.3%) | 0.8931 |
Anti-citrullinated protein antibody positive | 18 (47.4%) | 16 (44.4%) | 7 (43.8%) | 0.9563 |
Patients who meet the ACR/EULAR 2010 classification criteria for RA, 2010 [25] | 26 (68%) | 19 (53%) | 12 (75%) | 0.2135 |
Patients who meet the 1987 ARA classification criteria for RA [35] | 22 (58%) | 19 (53%) | 9 (56%) | 0.9049 |
Health Assessment Questionnaire (0–3) | 0.9 ± 0.7 | 0.9 ± 0.6 | 0.7 ± 0.7 | 0.2903 |
Disease Activity Score 28 (DAS28; based on ESR) | 5.0 ± 1.4 | 4.8 ± 1.3 | 4.7 ± 1.1 | 0.8464 |
Simplified Disease Activity Index (SDAI) | 34.3 ± 23.8 | 31.1 ± 14.4 | 27.5 ± 20.0 | 0.4771 |
Clinical Disease Activity Index (CDAI) | 25.1 ± 14.7 | 26.2 ± 13.9 | 23.5 ± 11.9 | 0.8951 |
Swollen joint count (0–28) | 7.2 ± 5.7 | 6.50 ± 5.1 | 7.4 ± 4.6 | 0.7048 |
Tender joint count (0–28) | 9.2 ± 7.3 | 10.3 ± 7.2 | 7.8 ± 5.6 | 0.5263 |
Visual analogue scale pain (mm) | 44.0 ± 29.3 | 44.2 ± 24.3 | 44.6 ± 22.7 | 0.9595 |
Patient global assessment (mm) | 48.6 ± 29.0 | 47.8 ± 24.7 | 39.6 ± 21.0 | 0.5274 |
Evaluator/physician global assessment (mm) | 38.6 ± 18.3 | 46.3 ± 22.3 | 44.6 ± 20.7 | 0.3627 |
C-reactive protein (mg/dl) | 1.71 ± 2.40 | 1.18 ± 1.88 | 0.98 ± 1.28 | 0.5567 |
Erythrocyte sedimentation rate (ESR; mm/h) | 23.2 ± 20.3 | 20.3 ± 21.2 | 20.4 ± 12.6 | 0.8129 |
Total Sharp-van-der-Heide score | 2.8 ± 5.4 | 3 ± 3.8 | 4.6 ± 8.6 | 0.4816 |
Erosion score | 1.2 ± 1.8 | 1.6 ± 2.2 | 2.2 ± 4.2 | 0.6019 |
Joint space narrowing score | 1.6 ± 3.8 | 1.4 ± 2.2 | 2.4 ± 4.4 | 0.5658 |