Table 1

Baseline characteristics of the study population, according to smoking status

SmokerNon-smokerp Value
Male sex (N=647)123 (51.0%)174 (42.9%)0.04
Mean age at onset of IBP (years) (N=628)31.1±8.332.6±9.00.04
Mean duration of axial symptoms (years) (N=628)1.6±1.01.5±0.90.44
Mean age at onset of peripheral arthritis (years) (N=359)31.3±8.833.1±9.70.08
Mean age at onset of enthesitis (years) (N=324)31.6±8.533.4±9.00.08
Caucasian race (N=646)220 (91.7%)360 (88.7%)0.22
Drinker (N=644)55 (23.1%)40 (9.9%)<0.001
Family history of ankylosing spondyloarthritis (N=640)63 (26.4%)106 (26.4%)0.98
HLA-B27 positive (N=641)157 (65.7%)244 (60.7%)0.21
History of peripheral arthritis (N=645)137 (57.3%)241 (59.4%)0.61
Signs of peripheral arthritis (N=386)46 (32.9%)99 (40.2%)0.15
History of enthesitis (N=647)125 (51.9%)218 (53.7%)0.65
NSAID user (N=647)271 (66.7%)173 (71.8%)0.18
Steroid user (N=647)53 (13.1%)29 (12.0%)0.71
DMARD user (N=648)40 (9.9%)19 (7.9%)0.40
Analgesics user (N=647)258 (63.5%)152 (63.1%)0.90
Mean CRP (mg/l) (N=626)8.0±13.77.7±14.00.78
Patients with elevated CRP (N=626)106 (27.0%)80 (34.3%)0.051
Mean ESR (mm/h) (621)12.9±14.714.8±16.60.14
Patients with elevated ESR (N=618)79 (20.5%)45 (19.4%)0.75
Patients with elevated CRP or ESR131 (34.4%)89 (38.9%)0.26
Patients with extra-articular features (N=647)116 (28.6%)63 (26.1%)0.50
BASDAI (N=641)4.6±1.94.3±2.10.06
BASDAI ≥4 (N=641)150 (63.3%)238 (58.9%)0.27
ASDAS–CRP (N=618)2.6±1.02.4±1.10.051
BASFI (N=634)3.4±2.22.8±2.30.001
BASFI ≥4 (N=634)96 (40.5%)121 (30.5%)0.01
Intensity of axial pain in last 2 days (NRS) (N=644)5.2±2.84.7±2.70.03
Intensity of peripheral joints pain in last 2 days (NRS) (N=643)3.3±2.83.2±2.80.76
Tender joint count (out of 53 joints) (N=647)5.0±9.54.1±7.90.22
Swollen joint count (out of 28 joints) (N=645)0.2±1.00.2±0.80.56
BASMI (N=616)1.6±1.21.5±1.10.12
Chest expansion (cm) (N=645)5.7±2.05.7±2.20.99
Euro-quality of life questionnaire (N=645)10.4±4.88.7±5.0<0.001
HAQ–AS – disability index (N=644)1.0±0.70.9±0.70.06
SF-36 mental health component score (N=642)46.2±20.252.7±20.5<0.001
SF-36 physical health component score (N=642)35.6±15.840.5±16.9<0.001
Patients with MRI inflammatory lesions in sacroiliac joints (N=610)104 (46.8%)123 (31.7%)<0.001
Patients with MRI inflammatory lesions in spine (N=605)72 (32.9%)64 (16.6%)<0.001
Patients with MRI structural lesions in sacroiliac joints (N=610)78 (35.1%)92 (23.7%)0.002
Patients with MRI structural lesions in spine (N=601)28 (12.8%)26 (6.8%)0.01
Patients with MRI inflammation, spine or sacroiliac joints (N=608)125 (56.6%)149 (38.5%)<0.001
Patients with MRI structural lesions, spine or sacroiliac joints (N=604)88 (40.2%)108 (28.1%)0.002
mSASSS (N=623)1.4±3.30.9±2.60.09
Patients with mSASSS >0 (N=623)66 (28.6%)92 (23.5%)0.16
Patients with radiographic sacroiliitis (N=625)78 (33.8%)103 (26.1%)0.04
Missing workdays (N=555)45.6±79.627.3±61.40.003
  • ASDAS–CRP, ankylosing spondylitis disease activity score, C-reactive protein based; BASDAI, Bath ankylosing spondylitis disease activity index; BASFI, Bath ankylosing spondylitis functional index; BASMI, Bath ankylosing spondylitis metrology index; CRP, C-reactive protein; DMARD, disease-modifying antirheumatic drug; ESR, erythrocyte sedimentation rate; HAQ–AS, health assessment questionnaire for ankylosing spondylitis; HLA, human leucocyte antigen; IBP, inflammatory back pain; mSASSS, modified Stoke ankylosing spondylitis spine score; NRS, numerical rating scale; NSAID, non-steroidal anti-inflammatory drug; SF-36, short form 36.