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. 2020 Oct 20;6(1):91–100. doi: 10.1016/j.ekir.2020.10.015

Table 1.

Characteristics of familial IgA nephropathy and sporadic IgA nephropathy patients at time of diagnosis

Parameters Familial IgAN (n = 348) Sporadic IgAN (n = 1116) P value
Male sex 175 (50) 593 (53) 0.35
Age at disease onset, yr, mean ± SD 35 ± 15 37 ± 12 0.03
Early-onset patients 137 (40) 358 (32) 0.003
Proteinuria, g/24 h, median (range) 0.55 (0.03–4.14) 1.46 (0.02–19.48) <0.001
Steroids and/or immunosuppressants 67 (19) 608 (54) <0.001
Severity of disease at diagnosis 0.32
 Preserved eGFR 201 (58) 612 (55)
 Nonpreserved eGFR 147 (42) 504 (45)
Oxford MEST-C n = 166 n = 713
 M1 38 (23) 257 (36) 0.002
 E1 31 (19) 236 (33) <0.001
 S1 113 (68) 571 (80) 0.001
 T1/2 41 (25) 323 (45) <0.001
 C1/2 73 (44) 348 (49) 0.31

eGFR, estimated glomerular filtration rate; IgAN, IgA nephropathy.

Values are n (%), unless otherwise noted.

Early-onset were patients with disease onset at age <30 years. Late-onset were patients with disease onset at age ≥30 years. Proteinuria at disease onset was presented with median (range) and transformed by log when compared in the 2 groups. Preserved eGFR group: patients with eGFR ≥60 ml/min per 1.73 m2. Nonpreserved eGFR group: patients with eGFR <60 ml/min per 1.73 m2.

Oxford MEST-C score: M, mesangial hypercellularity; E, presence of endocapillary proliferation; S, segmental glomerulosclerosis/adhesion; T, severity of tubular atrophy/interstitial fibrosis; C, presence of crescent.

Tests with P <0.05 are indicated in bold.