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. 2022 Jun 30;22:168. doi: 10.1186/s12902-022-01082-8

Table 3.

Pathological types in Non-diabetic kidney disease

Type All (n = 244) NDKD Group (n = 112) MIX Group (n = 14)
IgA N, n( %) 69 (28.28) 59 (52.68) 10 (71.43)
MN, n( %) 23 (9.43) 21 (18.75) 2 (14.29)
MCD, n( %) 6 (2.46) 6 (5.36) 0
MsPGN, n( %) 5 (2.05) 5 (4.46) 0
Hypertensive nephropathy, n( %) 5 (2.05) 4 (3.57) 1 (7.14)
HSPN, n( %) 5 (2.05) 5 (4.46) 0
PsG, n( %) 3 (1.23) 3 (2.68) 0
Amyloid nephropathy, n( %) 4 (1.64) 3 (2.68) 1 (7.14)
ANCA relative glomerulonephritis, n( %) 4 (1.64) 4 (3.57) 0
FSGS, n( %) 3 (1.23) 3 (2.68) 0
LN, n( %) 3 (1.23) 3 (2.68) 0
MPGN, n( %) 1 (0.41) 1 (0.89) 0
C3G, n( %) 1 (0.41) 1 (0.89) 0
OaG, n( %) 1 (0.41) 1 (0.89) 0

The data were presented as the frequency (%). NDKD Non-diabetic kidney disease; MIX Group, NDKD superimposed DKD, IgA N IgA nephropathy, MN Membranous nephropathy, MCD Minimal change disease, MsPGN Mesangial proliferative glomerulonephritis, HSPN Henoch-Schonlein purpura nephritis, PsG Proliferative-sclerosing glomerulonephritis, FSGS Focal segmental glomerulosclerosis, LN Lupus nephritis, MPGN Membranoproliferative glomerulonephritis, C3G C3 glomerulopathy, OaG Obesity-associated glomerulomegaly. Six patients were diagnosed as IgA N combined with MN, and one patients was diagnosed as MCD combined with hypertensive nephropathy