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. 2021 Sep 24;12:738481. doi: 10.3389/fimmu.2021.738481

Table 2.

Comparison of clinical and laboratory parameters at baseline and after 3-month treatment with tofacitinib and csDMARDs.

Before, median (IQR) After 3 months, median (IQR) p
Swollen joint count, 0-46 7 (6-9) 2 (0-3) <0.001
Tender joint count, 0-46 11 (5-17) 1 (0-8) <0.001
Swollen joint count, 0-28 5 (4-7) 1 (0-2) <0.001
Tender joint count, 0-28 4 (2-10) 1 (0-3) <0.001
General health, VAS, 0-100 mm 51 (37-65) 16 (7-29) 0.001
Pain, VAS, 0-100 mm 43 (22-64) 12 (5-38) 0.002
Physician’s assessment, VAS, 0-100 mm 35 (31-46) 13 (11-18) <0.001
HAQ disability index, 0-3 0.813 (0.625-1.253) 0.130 (0-0.813) 0.011
DAS28 4.4 (3.6-4.9) 2.6 (1.9-2.9) <0.001
Plasma C-reactive protein, mg/l 5 (3-17) 3 (3-4) 0.042
Blood hemoglobin, g/l 129 (126-140) 132 (126-145) 0.775
Blood leukocyte count, ×109/l 8.3 (6.1-9.1) 5.3 (4.3-6.9) 0.003
Blood neutrophil count, ×109/l 5.32 (4.02-6.34) 2.88 (2.32-3.91) 0.003
Blood lymphocyte count, ×109/l 1.40 (1.07-1.94) 1.41 (1.20-1.83) 0.959
Blood platelet count, ×109/l 297 (274-334) 281 (225-302) <0.001
Plasma alanine aminotransferase, U/l 20 (15-26) 21 (19-28) 0.224
Plasma creatinine, µmol/l 63 (56-83) 68 (56-86) 0.615

p-values are calculated using Wilcoxon test and shown in bold when p ≤ 0.05.

DAS28, composite Disease Activity Score for 28 joints based on the C-reactive protein level (DAS28-4[CRP]); csDMARD, conventional systemic disease-modifying antirheumatic drug; HAQ, Health Assessment Questionnaire; IQR, interquartile range; VAS, visual analogue scale.