Table 1

Baseline demographic and clinical characteristics of included patients with axial spondyloarthritis

ParameterAll patients (n=208)r-axSpA (n=115)nr-axSpA (n=93)
Age, years37.3±10.636.1±11.038.6±10.0
Duration of symptoms, years4.2±2.75.0±2.83.1±2.2
Male sex, n (%)106 (51)75 (65.2)31 (33.3)
HLA-B27 carrier, n (%)165 (79.3)97 (84.3)68 (73.9)
Peripheral arthritis, n (%)31 (14.9)15 (13.0)16 (17.2)
Enthesitis*, n (%)45 (21.6)23 (20.5)22 (23.9)
Uveitis ever, n (%)45 (21.6)27 (23.5)18 (19.4)
Psoriasis ever, n (%)28 (13.5)18 (15.7)10 (10.8)
IBD ever, n (%)4 (1.9)3 (2.6)1 (1.1)
Family history of SpA, n (%)35 (16.8)19 (16.5)16 (17.2)
BASDAI, points NRS (0–10)3.9±2.13.8±2.24.1±2.0
BASFI, points NRS (0–10)2.9±2.33.0±2.42.8±2.2
BASMI, points (0–10)1.8±1.62.0±1.71.5±1.5
CRPbaseline, mg/L7.48±8.69.64±9.94.82±5.6
mSASSS, points4.3±8.45.9±10.32.3±4.3
Smoking, n (%)63 (30.3)39 (33.9)24 (25.8)
Treatment with NSAIDs, n (%)139 (66.8)76 (66.1)63 (67.7)
Treatment with DMARDs, n (%)53 (25.5)31 (26.9)22 (23.6)
Treatment with systemic steroids, n (%)12 (5.8)6 (5.2)6 (6.4)
Treatment with a TNF-α inhibitor, n (%)5 (2.4)4 (3.7)1 (1.1)
  • *The Berlin score assesses 12 enthesitis sites of lower limbs plus optional sites elsewhere. Continuous variables are presented as mean±SD.

  • BASDAI, bath ankylosing spondylitis disease activity index; BASFI, bath ankylosing spondylitis functional index; BASMI, bath ankylosing spondylitis metrology index; CRPbaseline, C-reactive protein level at baseline; DMARD, disease-modifying anti-rheumatic drug; IBD, inflammatory bowel disease; mSASSS, modified Stoke Ankylosing Spondylitis Spinal Score; nr-axSpA, non-radiographic axial spondyloarthritis at baseline; NSAID, non-steroidal anti-inflammatory drug; r-axSpA, radiographic axial spondyloarthritis at baseline; TNF-α, tumour necrosis factor alpha.