Table 3.
Δ SPARCC SIJ | Δ CRP | ||||
---|---|---|---|---|---|
N | R | N | R | ||
ASDAS | Week 12 Δ | 94 | 0.35† | 98 | 0.61† |
Week 48 Δ | 88 | 0.58† | 89 | 0.58† | |
BASDAI | Week 12 Δ | 97 | 0.27* | 100 | 0.22‡ |
Week 48 Δ | 90 | 0.42† | 90 | 0.30* | |
BASMI | Week 12 Δ | 94 | 0.07 | 97 | 0.34† |
Week 48 Δ | 88 | 0.14 | 88 | 0.28* | |
BASFI | Week 12 Δ | 97 | 0.17 | 100 | 0.20‡ |
Week 48 Δ | 90 | 0.35† | 90 | 0.20 | |
Total back pain | Week 12 Δ | 97 | 0.28* | 100 | 0.20‡ |
Week 48 Δ | 90 | 0.45† | 90 | 0.20 | |
CRP | Week 12 Δ | 96 | 0.31* | ||
Week 48 Δ | 89 | 0.37† | |||
ASAS40 | Week 12 Δ | 97 | −0.30* | 100 | −0.19 |
Week 48 Δ | 90 | −0.39† | 90 | −0.16 | |
SSS Fat metaplasia | Week 48 Δ | 88 | −0.28* | 87 | −0.07 |
SSS Erosion | Week 48 Δ | 88 | 0.57† | 87 | 0.25‡ |
SSS Ankylosis | Week 48 Δ | 88 | 0.11 | 87 | −0.08 |
SSS Backfill | Week 48 Δ | 88 | −0.61† | 87 | −0.20 |
*p<0.01, †p<0.001, ‡p<0.05.
Clinical measures used observed case population. SSS scores include baseline and week 48; no values from an early termination visit were included.
For change from baseline to week 12 in the PBO/ETN group, the significant correlations were R=0.37 for CRP/ASDAS and R=0.22 for SPARCC SIJ/CRP. For change from baseline to week 48 in the PBO/ETN group, the significant correlations were: R=0.24 for SPARCC SIJ/ASDAS; R=0.32 for SPARCC SIJ/CRP; R=−0.46 for SPARCC SIJ/fat metaplasia; R=0.55 for SPARCC SIJ/erosion; R=−0.43 for SPARCC SIJ/backfill; R=0.62 for CRP/ASDAS; R=0.31 for CRP/BASDAI; and R=0.30 for CRP/BASFI.
ASAS40, Assessment of SpondyloArthritis international Society 40; ASDAS, Ankylosing Spondylitis Disease Activity Score; BASDAI, Bath Ankylosing Spondylitis Disease Activity Index; BASFI, Bath Ankylosing Spondylitis Functional Index; BASMI, Bath Ankylosing Spondylitis Metrology Index; CRP, C-reactive protein; ETN, etanercept; PBO, placebo; R, Spearman correlation; SIJ, sacroiliac joint; SPARCC, Spondylitis Research Consortium of Canada; SSS, SPARCC MRI SIJ structural score.