Table 2.
Index | Baseline (mean ± SD) | Post-treatment (mean ± SD) | t/Z | P |
---|---|---|---|---|
Patients treated by anti-TNF alone (n = 18)a | ||||
SPARCC | 27.76 ± 18.38 | 14.38 ± 14.91 | 2.681 | 0.011 |
ASDAS | 2.56 ± 1.24 | 1.83 ± 0.71 | 4.231 | 0.006 |
ESRb | 27.94 ± 33.24 | 5.72 ± 7.06 | –2.763 | 0.009 |
CRPb | 16.29 ± 23.05 | 2.70 ± 2.55 | –2.470 | 0.022 |
Patients treated by anti-TNF combined with DMARDs (n = 21)c | ||||
SPARCC | 39.53 ± 19.21 | 20.71 ± 15.98 | 5.110 | 0.000 |
ASDAS | 3.58 ± 1.05 | 1.88 ± 0.74 | 4.278 | 0.003 |
ESRb | 38.49 ± 38.50 | 9.02 ± 13.29 | –2.703 | 0.010 |
CRPb | 26.29 ± 28.02 | 8.43 ± 15.79 | –2.329 | 0.053 |
Patients treated by DMARDs alone (n = 17)d | ||||
SPARCC | 28.67 ± 15.51 | 21.66 ± 11.23 | 0.820 | 0.419 |
ASDAS | 2.21 ± 1.03 | 1.99 ± 0.47 | 1.301 | 0.261 |
ESRb | 12.14 ± 8.43 | 4.65 ± 4.27 | –2.396 | 0.013 |
CRPb | 7.919 ± 5.60 | 5.55 ± 4.46 | –1.911 | 0.056 |
aBaseline of clinical practices from patients in anti-TNF group: 85.7 % male; age, 23.3 ± 6.43; symptom duration, 3.15 ± 2.98; HLA-B27-positive, 100 %
bNot normally distributed, compared by paired rank test
cBaseline of clinical practices from patients in combination group: 82.35 % male; age, 21.6 ± 3.36; symptom duration, 2.97 ± 2.69; HLA-B27-positive, 88.2 %
dBaseline of clinical practices from patients in DMARD group: 80 % male; age, 20.5 ± 2.75; symptom duration, 3.0 ± 2.66; HLA-B27-positive, 90 %
ASDAS Ankylosing Spondylitis Disease Activity Indices, CRP C-reactive protein, DMARD disease-modifying anti-rheumatic drug, ESR erythrocyte sedimentation rate, SD standard deviation, SPARCC Spondyloarthritis Research Consortium Canada, TNF tumor necrosis factor