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. 2020 Apr 14;50(8):1209–1219. doi: 10.1002/eji.201948502

Table 1.

Clinical and demographic characteristics of the study group

Variable HC (N = 42) RA (N = 16) PsA (N = 25) AS (N = 15)
Age in years – median (range) 45 (23–65) 61 (26–73) 54 (31–73) 42 (19–65)
Female sex – No. (%) 20 (48) 12 (75) 6 (24) 4 (27)
Disease duration in years – median (range) n.a. 10 (1–28) 11 (1–28) 9 (0.5–30)
Age of disease onset in years – median (range) n.a. 46 (14–69) 44 (24–66) 33 (13–57)
HLA‐B27+ – No. (%) n.a. n.a. 0 (0) 12 (80)
RF+ – No. (%) n.a. 11 (69) 1 (4) 0 (0)
Axial involvement – No. (%) n.a. n.a. 1 (4) 15 (100)
ESR in mm/hour – median (range) n.a. 7 (5–47) 8 (1–42) 13 (1–42)
TJC, of 76 – median (range) n.a. 4 (0–13) 1 (0–26) 0 (0–4)
SJC, of 78 – median (range) n.a. 3 (0–13) 0 (0–13) 0 (0–4)
Systemic immunomodulatory medicationa) – No. (%) n.a. 16 (100) 18 (72) 3 (20)

RF, rheumatoid factor; ESR, erythrocyte sedimentation rate; TJR, ender joint count; SJC, swollen joint count; BASDAI, Bath Ankylosing Spondylitis Disease Activity Index.

a

Systemic immunomodulatory medication consisted of methotrexate (MTX; 10 patients with RA, 16 patients with PsA, one patient with AS), leflunomide (two patients with PsA), hydroxychloroquine (HCQ; one patient with RA), prednisone (one patient with PsA), sulfalazine (SSZ; two patients with AS), MTX + HCQ (five patients with RA), and SSZ + prednisone (one RA patient).