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. 2022 Apr 1;24:81. doi: 10.1186/s13075-022-02761-6

Table 1.

Baseline demographics

All subjects (n = 23) Low dose (n = 13) High dose (n = 10)
Age in years (median; IQR) 40.5 (28.0–44.0) 35.0 (25.0–46.5) 41.0 (33.0–44.0)
Sex (M to F) 8:15 6:7 2:8
Disease (AAV to BD) 12:11 6:7 6:4
GPA 8 4 4
MPA 1 1 0
EGPA 3 1 2
BD 11 7 4
BVAS/WG score at entry (median; IQR) 4.0 (4.0–5.5) 4.0 (4.0–6.0) 4.5 (4.0–5.0)
Prior disease duration in months (median; IQR) 61.0 (42.0–102.5) 76.0 (52.0–115.0) 51.0 (40.0–68.5)
Number of previous treatments received (median; IQR) 4 (3–5) 5 (3–5) 4(3–4.75)
ANCA specificity (PR3:MPO:Neg) 7:1:15 4:1:8 3:0:7
Prior median cumulative cyclophosphamide dose (AAV only) in grams (n = 12) 9.1 (7–19.4) 6.4 (4.2–25.8) 9.6 (8.7–17.3)
Prior median cumulative rituximab dose (AAV only) in grams (n = 12) 4.5 (3–5.75) 5 (3–6) 4 (3–5)

AAV ANCA-associated vasculitis, BD Behçet’s disease, GPA granulomatosis with polyangiitis, MPA microscopic polyangiitis, eGPA eosinophilic granulomatosis with polyangiitis, IQR interquartile range, BVAS/WG Birmingham Vasculitis Activity Score for Wegener’s granulomatosis, PR3 proteinase 3, MPO myeloperoxidase