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. Author manuscript; available in PMC: 2019 Aug 1.
Published in final edited form as: Pediatr Nephrol. 2018 Sep 7;34(2):261–267. doi: 10.1007/s00467-018-4072-6

Table 1.

Demographic and clinical characteristics

Participants
N (%)
Sex (N = 370)
  Male 227 (61.4%)
Race/ethnicity (N =311)
  White 145 (46.6%)
  Hispanic 62 (19.9%)
  Black 70 (22.5%)
  Other 34 (10.9%)
Clinical pattern of NS (N = 354)
  Steroid sensitive-infrequently relapsing 104 (29.4%)
  Steroid sensitive-frequently relapsing or 146 (41.2%)
  steroid dependent 99 (28.0%)
  Steroid-resistant 5 (1.4%)
  Congenital or infantile
Biopsy diagnosis (N = 370)
  Minimal change disease (± mild mesangial 111 (30.0%)
  hypercellularity) 85 (23.0%)
  FSGS or FGGS 24 (6.5%)
  Membranous, MPGN, others 150 (40.5%)
  No biopsy

FGGS focal global glomerulosclerosis, FSGS focal segmental glomerulosclerosis, MPGN membranoproliferative glomerulonephritis, NS nephrotic syndrome