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. 2015 Jan 2;179(2):354–361. doi: 10.1111/cei.12461

Table 2.

Clinical and pathological data according to the evolution of kidney disease

Clinical and pathological data Progressive kidney disease (n = 20) Non-progressive kidney disease (n = 54) P-value
Age 45 ± 16 37 ± 13 0·053
Female 5 (25) 19 (35·2) 0·23
Hypertensive 18 (90) 26 (49·1) 0·001
Previous macroscopic haematuria 6 (33·3) 21 (40·4) 0·6
eGFR (ml/min per 1·73 m2) 31 ± 22 81 ± 31 <0·005
Proteinuria (g/day) 3·907 ± 2·155 1·835 ± 1·372 <0·005
Immunosuppressive therapy 5 (26·3) 11 (23·4) ≅1
IgM positivity 10 (50) 18 (34) 0·21
IgG positivity 5 (26·3) 14 (26·9) 0·96
C1q positivity 2 (10·5) 8 (16) 0·715
S1 score 8 (40) 29 (53·7) 0·295
E1 score 3 (15·0) 5 (9·3) 0·674
T1–2 score 17 (85) 8 (15·4) <0·005
C4d positivity 11 (55) 14 (27·5) 0·029
TGase-2 G score 1·35 ± 0·26 1·26 ± 0·29 0·19
High TGase-2 T score 16 (84·2) 15 (33·3) <0·005
p-ERK1/2 score 1·33 ± 0·68 1·32 ± 0·54 0·9
CD3 score 66 273 ± 39 311 19 322 ± 20 632 <0·005

For quantitative variables, values are expressed as the mean ± standard deviation. For qualitative variables, values are expressed as n (%). Progressive kidney disease, defined as a decline of at least 50% in the glomerular filtration rate (GFR) or progression to end-stage renal disease (ESRD) during the follow-up period. Immunoglobulin (Ig)M, IgG and C1q refer to the results of routine immunofluorescence data. S1, E1 and T1–2 according to the Oxford classification reanalysis of the biopsies. High TGase-2 T score (>25% staining). eGFR = estimated glomerular filtration rate.