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. 2020 Mar 4;22:41. doi: 10.1186/s13075-020-2122-5

Table 2.

Comparison of patient background characteristics between a TNFi insensitivity group and a poor response group. For each variable, p values of a simple comparison between the two groups using chi-squared test are shown

Category TNIi insensitivity Refractory Control p value*
N % N % N % P1 P2 P3
Gender Female 75 79.8 501 82.9 731 79.9 0.83 0.14 0.34
Male 19 20.2 103 17.1 184 20.1
Age group ≦50 23 24.5 129 21.4 228 24.9 0.62 0.41 0.48
51–60 26 27.7 149 24.7 205 22.4
61–70 19 20.2 165 27.3 246 26.9
71 26 27.7 161 26.7 236 25.8
Disease duration (year) < 0.5 22 23.4 75 12.4 165 18.0 0.45 < 0.01 0.01
0.5–2 31 33.0 163 27.0 284 31.0
2–5 17 18.1 117 19.4 159 17.4
≥ 5 24 25.5 247 40.9 306 33.4
DAS28-CRP at week 0 < 3.2 3 3.2 6 1.0 43 4.7 < 0.01 < 0.01 0.18
3.2–5.1 12 12.8 94 15.6 259 28.3
> 5.1 79 84.0 502 83.1 613 67.0
RF positivity** Negative 25 26.6 127 21.0 240 26.2 0.95 0.02 0.24
Positive 69 73.4 473 78.3 673 73.6
Use of GC No 66 70.2 393 65.1 708 77.4 0.13 < 0.01 0.30
Yes 28 29.8 211 34.9 207 22.6
Dose of MTX (mg/week) 0 13 13.8 81 13.4 83 9.1 0.22 < 0.01 0.47
1–6 10 10.6 74 12.3 79 8.6
7–9 22 23.4 189 31.3 218 23.8
10–15 32 34.0 176 29.1 294 32.1
> 15 17 18.1 84 13.9 241 26.3
Failure in > 2 csDMARDs No 44 46.8 301 49.8 365 39.9 0.16 < 0.01 0.66
Yes 50 53.2 303 50.2 550 60.1
Entry phase I 29 30.9 287 47.5 327 35.7 0.11 < 0.01 < 0.01
II 24 25.5 169 28.0 179 19.6
III 22 23.4 95 15.7 287 31.4
Drug type IFX 2 2.1 11 1.8 12 1.3 0.77 < 0.01 < 0.01
ETN 17 18.1 42 7.0 110 12.0
ADA 5 5.3 55 9.1 55 6.0
GLM 22 23.4 234 38.7 186 20.3
CZP 67 71.3 315 52.2 674 73.7

*P1, comparison between control and insensitivity; P2, comparison between control and refractory; P3, comparison between insensitivity and refractory

**RF > 20 IU/mL was defined as positive

p < 0.05

DAS28 disease activity score for 28 joints, CRP c-reactive protein, MTX methotrexate, IFX infliximab, ETA etanercept, ADA adalimumab, GLM golimumab, CZP certolizumab, csDMARDs conventional synthetic disease-modifying anti-rheumatic drugs