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. 2019 Jan 24;5(3):182–188. doi: 10.1159/000495751

Table 1.

Demographic and clinical data at renal biopsy and over the follow-up in 174 children <18 years old enrolled in the VALIGA cohort

Clinical data at biopsy
Female gender 49 (28.16)
Age, years 12.72±3.63
eGFR, mL/min/1.73 m2 117.02 (96.17–120)
Proteinuria, g/day/1.73 m2 0.84 (0.34–2.18)
MAP, mm Hg 87.53±11.35

Biopsy features
M1 38 (21.84)
E1 24 (13.79)
S1 74 (42.53)
T1–2 11 (6.32)

Follow-up data
Duration of follow-up, years 4.63 (2.48–7.35)
TA MAP, mm Hg 86.64±8.54
TA proteinuria, g/day/1.73 m2 0.56 (0.27–1.02)
RASB treatment 116 (66.67)
CsA/IS treatment 88 (50.57)
ΔeGFR, mL/min/1.73 m2 2.01±15.38
ΔMAP, mm Hg −1.29±11.75
ΔProteinuria, g/day/1.73 m2 −1.31±3.99

Clinical outcomes
Rate of eGFR loss, mL/min/1.73 m2/year 0 (−1.72 to 0.76)
15-year survival free from combined event 163 (93.68)
TA proteinuria ≤0.5 in patients with baseline proteinuria >0.5 g/day/1.73 m2 4/53 (7.54)

Values are n (%), means ± standard deviations, or medians (interquartile ranges). eGFR, estimated glomerular filtration rate; MAP, mean arterial pressure; M1, mesangial hypercellularity (>50 of glomeruli with mesangial hypercellularity); E1, presence of endocapillary hypercellularity; S1, presence of segmental glomerular sclerosis; T1–2, tubular atrophy/interstitial fibrosis in >25% of renal biopsy tissues; TA, time-average; RASB, renin-angiotensin blockade; CsA, cyclosporine A; IS, steroid/immunosuppressive drugs.