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. Author manuscript; available in PMC: 2010 Aug 26.
Published in final edited form as: Proteomics Clin Appl. 2009 Aug 26;3(9):1029–1043. doi: 10.1002/prca.200800243

Table 1.

Classification of proteinuria and main causes.

Type Category Specific diagnosis
Glomerular Primary glomerulonephritis Minimal-change disease
Membranous glomerulonephritis
Focal segmental glomerulosclerosis
Membranoproliferative glomerulonephritis
IgA nephropathy
Glomerular injury secondary to
systemic disorder
Diabetes mellitus
Systemic lupus erythematosus
Amyloidosis
Infection (e.g., HIV, hepatitis B and C,
streptococcus, syphilis, malaria and
endocarditis)
Lymphoma
Hypertensive nephrosclerosis
Drug-induced injury Heroin
Non-steroidal anti-inflammatory drugs
Gold components
Antibiotics
Lithium
Heavy metals
Tubular Tubulointerstitial disease Uric acid nephropathy
Interstitial nephritis
Fanconi syndrome
Sickle cell disease
Drug-induced Non-steroidal anti-inflammatory drugs
Antibiotics
Heavy metals
Overflow Hemoglobinuria, Myoglobinuria
Multiple myeloma
Amyloidosis
Leukemia
Myelodysplastic syndromes
Tissue
proteinuria
Acute inflammation of urinary tract
Uroepithelial tumors
Renal allograft Cell-mediated rejection
Antibody-mediated rejection