Table 1

Characteristics of patients and controls. Age, CRP and prednisolone dose are shown as mean (±SD)

RA (N=53)PsA/SpA (N=46)HC (N=169)
Age (years)56.15 (±11.80)51.33 (±12.92)46.18 (±12.56)
Female68% (n=36)48% (n=22)59% (n=100)
Male32% (n=17)52% (n=24)41% (n=69)
csDMARD
Methotrexate3024None
Leflunomide32None
Azathioprine2None
Hydroxycholorquine4None
Salazopyrin22None
TNF inhibitor
Adalimumab413None
Certolizumab2None
Etanercept23None
Golimumab65None
Infliximab22None
IL-17 inhibitor
Secukinumab5None
Ixekizumab4None
IL-6 inhibitor
Tocilizumab3None
JAK inhibitor
Baricitinib3None
Upadacitinib12None
Filgotinib1None
Apremilast2None
 No therapy22169
 Disease duration in years12.53 (±10.75)10.26 (±8.8)
 Treatment duration in months61.25 (±65.35)44.79 (±49.8)
Disease activity
SJ count (28)
SJ=0: 63%
SJ ≥1: 37%
1.24 (±2.34)0.64 (±1.23)
TJ count (28)2.71 (±3.55)4.15 (±8.59)
CRP0.35 mg/dL (±0.63)0.30 mg/dL (±0.38)
SeropositiveN=24
Prednisolone dose
Patients without prednisoloneN=39N=38N=169
Patients with daily prednisolone at 1. vaccinationN=7
Mean dose: 5.53 mg/day (±4.19)
N=3
Mean dose: 8.33 mg/day (±3.82)
None
Patients without prednisoloneN=38N=38N=169
Patients with daily prednisolone at 2. vaccination7.31 mg/day (±7.73) N=88.33 mg/day (±3.81) N=3None
  • CRP, C-reactive protein; csDMARD, conventional synthetic DMARD; HC, healthy controls; IL, interleukin; JAK, Janus kinase; PsA, psoriatic arthritis; RA, rheumatoid arthritis; SJ, swollen joint; SpA, seronegative spondyloarthritis; TJ, tender joint; TNF, tumour necrosis factor.