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. 2022 Nov 16;23(22):14139. doi: 10.3390/ijms232214139

Table 2.

Summary of patients’ diagnosis regarding the whole cohort included in the study.

Diagnosis Patients Number (%)
Diabetic nephropathy 3625 (40.7)
CKD without specifying the underlying cause 2675 (30.1)
IgA nephropathy 362 (4.1)
Renal transplant recipients 313 (3.5)
Lupus nephritis 106 (1.2)
Systemic lupus erythematosus 75 (0.8)
Generically reported as biopsy-proven renal fibrosis 58 (0.6)
Acute kidney injury 50 (0.5)
ANCA-associated vasculitis 47 (0.5)
Unilateral hydronephrosis 45 children (0.5)
Membranous nephropathy 45 (0.5)
HIV-positive CKD 25 (0.3)
Minimal change disease 23 (0.25)
Obstructive uropathy 23 (0.25)
Hypertensive nephrosclerosis 21 (0.2)
Focal segmental glomerulosclerosis 17 (0.2)
Hypo/dysplastic kidney 15 (0.2)
Reflux nephropathy 14 (0.15)
ANCA-associated nephritis 12 (0.1)
Minor histopathologic abnormality 11 (0.1)
Renal amyloidosis 6 (0.05)
Cast nephropathy 5 (0.05)
Polycystic kidney disease 4 (0.05)
Thin basement membrane disease 3 (0.03)
Thrombotic microangiopathy 2 (0.02)
Membranous proliferative glomerulonephritis 2 (0.02)
Post-infectious glomerulonephritis 1 (0.01)
Crescentic glomerulonephritis 1 (0.01)
Uric acid nephropathy 1 (0.01)
General population (prospectively followed) 1302 (14.6)