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. 2018 Jan 1;15(1):10–15. doi: 10.7150/ijms.22812

Table 1.

Demographic and clinicopathological features of the study cases

IFX group
n=66
ADM group
n=37
Total series
n=103
Gender, n (%) Female 30 (45.4) 24 (64.8) 54 (52.4)
Age, mean [±SD] Years 44.1 [14.6] 43.2 [11.8] 43.7 [13.6]
Weight, mean [±SD] Kg 70.4 [15.0] 70.0 [15.7] 70.2 [15.2]
IBD disease, n (%) CD 49 (74.2) 31 (83.8) 80 (77.7)
UC 17 (25.8) 6 (16.2) 23 (22.3)
mAb Naïve, n (%) Yes 54 (81.8) 20 (54) 74 (71.8)
Immunomodulator, n (%) AZA 23 (34.8) 13 (35.1) 36 (35.0)
MCP 2 (3) 1 (0.9) 3 (2.9)
MTX 3 (4.5) 2 (5.4) 5 (4.9)
None 38 (57.5) 21 (20.8) 59 (57.3)
Anti-TNF intensification Positive 23 (34.8) 10 (27) 33 (32.0)
Duration anti-TNF, mean [± SD] Years 4.2 [2.3] 3.6 [1.6] 4.0 [2.1]
Albumin, mean [± SD] mg/dL 3.9 [0.5] 4.1 [0.4] 4.0 [0.5]
C reactive protein, mean [± SD] mg/dL 0.9 [1.3] 0.6 [0.6] 0.8 [1.1]
TNF, mean [± SD] pg/mL 283.1 [516.6] 442.6 [362.9] 341.1 [471.0]
ADA production, n (%) Positive 11 (16.7) 2 (5.4) 13 (12.6)
FCGR3 V158F polymorphism, n (%) FF 21 (31.8) 19 (51.4) 40 (38.8)
FV 33 (50.0) 14 (37.8) 47 (44.6)
VV 12 (18.2) 4 (10.8) 16 (15.5)

IFX: infliximab, ADA: adalimmab, SD: Standard deviation, CD: Crohn's disease, UC: Ulcerative colitis, AZA, Azacytidine, MCP: Mercaptopurine, MTX: Methotrextate, ADA: Anti-drug antibody