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. 2021 Feb 28;204(2):267–282. doi: 10.1111/cei.13581

Table 1.

Selected characteristics of the study participants

Active stage of GPA Remission Control
n 26 29 31
Age (mean ± s.d.) 56·1 ± 13·2 53·2 ± 13·1 52·1 ± 12·3
Gender (F/M) 14/12 16/13 16/15
BVAS (min–max) VDI 6–32 0
VDI (min–max) 0–5 1–7
GC treatment (yes/no) 15/11 25/4
GC dose (mg/day) (min–max) 3–20 2–8
CYC cumulative dose 0–33 10–25
IgG anti‐PR3 (RU/ml) (min‐max) 20–200 < 20–140 < 20
CRP (mg/ml) < 5·0–130 < 5·0–6·9 < 5·0
Procalcitonin (ng/ml) < 0·05 < 0·05 < 0·05
PBMC (103/µl) 10·9 ± 3·8* 8·3 ± 1·9 6·2 ± 3·5
PMN (103/µl) 7·69 ± 4·8* 5·8 ± 2·5 3·9 ± 2·6
PLT (103/µl) 255 ± 231·6* 221·6 ± 70·9* 209·9 ± 33·5
LDH U/l 550 ± 156 506 ± 226 360 ± 48

BVAS = Birmingham Vasculitis Activity Score; VDI = Vasculitis Damage Index, * P < 0·05 in comparison with controls; GC = glucocorticosteroids; GPA = granulomatosis with polyangiitis; PBMC = peripheral blood mononuclear cells; CRP = C‐reactive protein; PMN = polymorphonuclear cells; PLT = platelet; Ig = immunoglobulin; s.d. = standard deviation. Platelet count results presented as median and interquartile range. Nine patients in the active‐GPA group were treated with cyclophosphamide (cumulative dose 25 g [9, 32]); all patients with inactive‐GPA previously received cyclophosphamide.