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. 2018 Jun 11;33(10):1731–1739. doi: 10.1007/s00467-018-3988-1

Table 2.

Basic clinical characteristics of progressors and non-progressors at baseline and the end of follow-up

Progressors, N = 22 Non-progressors, N = 16 p value
At baseline
 uEGF/Cr (ng/mg) 10.59 ± 6.83 27.83 ± 12.67 0.0001
 Age (years) 11.18 ± 2.63 9.81 ± 2.32 NS
 eGFR (ml/min/1.73m2) 99.48 ± 37.99 137.80 ± 38.52 0.004
 24-h UP (g/24 h) 3.41 ± 2.51b 1.31 ± 1.23b 0.02
 Genotype XLAS (14/17) ARAS (3/17) XLAS (11/13) ARAS (2/13) NS
 Baseline CKD stage CKD1–2 (19/22) CKD3 (3/22) CKD1–2 (16/16) CKD3 (0/16) NS
At the end of follow-up
 eGFR (ml/min/1.73m2) 59.46 ± 25.63 113.50 ± 20.86 < 0.0001
 24-h UP (g/24 h) 4.34 ± 3.78b 1.89 ± 2.08b NS
 Time (months) a 23.64 ± 13.28 24.75 ± 5.94 NS

Data are shown as mean ± SD; NS no significance, p > 0.05, XLAS X-linked Alport syndrome, ARAS autosomal recessive Alport syndrome, uEGF/Cr urinary epidermal growth factor/creatinine, eGFR estimated glomerular filtration rate, CKD chronic kidney disease

a“Time” indicates time to stage advance for progressors and time of follow-up for non-progressors

bThe value for 24-h UP was an average value of n = 16 and 14 patients respectively for progressors and non-progressors