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. 2020 Jul 28;15(8):1103–1111. doi: 10.2215/CJN.14561119

Table 1.

Baseline characteristics of the validation cohort according to histopathologic class

Baseline Characteristics Focal, n=52 Crescentic, n=37 Mixed, n=39 Sclerotic, n=17
Age at biopsy, yr, mean ± SD 60±13 62±11 61±14 66±12
Men (%) 33 (64) 24 (65) 18 (46) 8 (47)
Diagnosis (%)a
 Granulomatosis with polyangiitis 33 (63) 14 (40) 8 (21) 8 (50)
 Microscopic polyangiitis 17 (33) 19 (54) 27 (73) 8 (50)
 Eosinophilic granulomatosis with polyangiitis 1 (2) 0 (0.0) 1 (3) 0 (0)
 Kidney limited vasculitis 1 (2) 2 (6) 1 (3) 0 (0)
ANCA specificity (%)b
 PR3 23 (48) 13 (37) 7 (20) 7 (44)
 MPO 19 (40) 21 (60) 25 (69) 8 (50)
 Negative 3 (6) 0 (0) 3 (8) 0 (0)
 Double positive 3 (6) 1 (3) 1 (3) 1 (6)
Diagnostic delay, mo, mean ± SD 4.7±12.9 1.4±2.7 2.4±3.2 3.6±11.5
eGFR0, ml/min per 1.73 m2, mean ± SD 50±29 18±16 27±19 19±12
Proteinuria class at biopsy (%)c
 Normal 4 (9) 1 (3) 2 (5) 0 (0)
 Moderately increased 18 (39) 4 (13) 3 (8) 3 (19)
 Severely increased 24 (52) 27 (84) 33 (87) 13 (81)

PR3, proteinase-3; MPO, myeloperoxidase.

a

The diagnosis was specified in 140 patients.

b

ELISA test results were available in 135 patients.

c

In accordance with the Kidney Disease Improving Global Outcomes clinical guidelines, normal level of proteinuria was defined as protein excretion of <0.15 g/d or as a negative protein dipstick test, moderately increased proteinuria was defined as a protein excretion rate of 0.15–0.50 g/d or as trace on protein dipstick test, and severely increased proteinuria was defined as total protein excretion >0.50 g/d or as + or more on protein dipstick. The proteinuria class could be determined in 132 patients.