Table 4

Correlation of original BASDAI and mini-BASDAI with patient global, BASFI, physician global and CRP in GESPIC, TNFα trial population and NSAID trial population

AS (sub)populationParametersCorrelation of original BASDAI with parameterCorrelation of mini-BASDAI with parameter
GESPIC, baselineTotal groupPatient global0.760.77
BASFI0.770.70
Physician global0.550.54
CRP0.110.09
“P−” groupPatient global0.760.78
BASFI0.740.69
Physician global0.550.56
CRP0.150.13
“P+” groupPatient global0.700.70
BASFI0.760.67
Physician global0.440.42
CRP−0.03−0.01
TNFα trial population, baselineTotal groupPatient global0.560.47
BASFI0.800.71
Physician global0.400.25
CRP0.090.01
“P−” groupPatient global0.590.41
BASFI0.720.69
Physician global0.270.23
CRP0.130.03
“P+” groupPatient global0.490.46
BASFI0.860.70
Physician global0.410.21
CRP0.04−0.04
TNFα trial population, week 12Total groupPatient global0.900.87
BASFI0.890.85
Physician global0.700.65
CRP0.250.21
“P−” groupPatient global0.890.85
BASFI0.890.85
Physician global0.800.79
CRP0.310.28
“P+” groupPatient global0.920.88
BASFI0.880.84
Physician global0.610.54
CRP0.250.18
NSAID trial population, baselineTotal groupPatient global0.520.54
BASFI0.530.53
Physician global0.350.36
CRP0.050.06
NSAID trial population, week 12Total groupPatient global0.830.85
BASFI0.800.77
Physician global0.720.74
CRP0.100.11
  • “P−”, subgroup of ankylosing spondylitis (AS) patients without peripheral involvement at baseline, 70.6% in the German Spondyloarthritis Inception Cohort (GESPIC) and 39.6% in the tumour necrosis factor alpha (TNFα) trial population. “P+”, subgroup of AS patients with peripheral involvement at baseline, 29.4% in the GESPIC and 61.4% in the TNFα trial population. BASDAI, Bath Ankylosing Spondylitis Disease Activity Index; mini-BASDAI, BASDAI without Q3arthritis and Q4enthesitis; BASFI, Bath Ankylosing Spondylitis Functional Index; CRP, C-reactive protein; NSAID, non-steroidal anti-inflammatory drug.