Heparanase activity is dysregulated in children with steroid-sensitive nephrotic syndrome

• Published in: Kidney international Vol. 67; no. 1; pp. 122 - 129
• Main Authors: Holt, Richard C.L., Webb, Nicholas J.A., Ralph, Shirley, Davies, John, Short, Colin D., Brenchley, Paul E.C.
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Inc 01.01.2005; Nature Publishing; Elsevier Limited
• Subjects: Adult; Age Factors; Biological and medical sciences; Case-Control Studies; Child; Enzyme Activation; Female; Gene Expression Regulation, Enzymologic; Glomerulonephritis; Glucuronidase - genetics; Glucuronidase - metabolism; heparanase; Heparitin Sulfate - metabolism; Humans; Male; Medical sciences; Middle Aged; Nephrology. Urinary tract diseases; Nephropathies. Renovascular diseases. Renal failure; Nephrotic Syndrome - drug therapy; Nephrotic Syndrome - enzymology; Nephrotic Syndrome - genetics; Protein Processing, Post-Translational; proteinuria; Recurrence; RNA, Messenger - genetics; RNA, Messenger - metabolism; steroid sensitive nephrotic syndrome; Steroids - therapeutic use; Urinary system involvement in other diseases. Miscellaneous; Urinary tract. Prostate gland; steroid sensitive nephrotic syndrome; proteinuria; heparanase; Human; Glomerulonephritis; Kidney disease; Steroid; Nephrology; Urinary system disease; Activity; Nephrotic syndrome; Urology; Child; Proteinuria
• ISSN: 0085-2538; 1523-1755
• DOI: 10.1111/j.1523-1755.2005.00062.x

Heparanase activity is dysregulated in children with steroid-sensitive nephrotic syndrome. Immune cells express heparanase, an endoglycosidase, able to degrade heparan sulfate glycosaminoglycan (HSGAG) in the glomerular capillary wall (GCW) and potentially induce proteinuria. The aim of this study was to determine whether dysregulated heparanase expression is associated with the heavy proteinuria of childhood steroid-sensitive nephrotic syndrome (SSNS). Plasma and urinary heparanase activity and peripheral blood mononuclear cell (PBMC) mRNA heparanase levels [real-time polymerase chain reaction (PCR)] were measured in children with SSNS in relapse and remission. Plasma and urinary heparanase activity was determined in adult patients with nephrotic syndrome and in age- and gender-matched controls. Plasma heparanase activity was reduced in SSNS with relapse (811.2 units) compared to remission (1147.96 units) (P = 0.003) and control subjects (1390.51 units) (P < 0.001). In adult nephrotic syndrome, plasma heparanase activity was significantly lower in patients compared to controls. However, there was no difference between remission and relapse states. In children, urinary heparanase activity/urinary creatinine ratio was highest in SSNS relapse (14.26 units/mg) compared with remission (7.43 units/mg) (P = 0.016) and controls (2.29) (P < 0.001). However, PBMC heparanase mRNA expression was not different between these three groups. In adult nephrotic syndrome, urinary heparanase activity/urinary creatinine levels were lower in both remission and relapse compared to controls and there was no difference between remission and relapse states. In childhood SSNS, there is a qualitative and quantitative difference in urinary heparanase activity expression that is not paralleled in adult nephrotic syndrom. These data suggest that dysregulated heparanase expression may play a significant role in the pathogenesis of SSNS, possibly through an abnormality in post-translational control of latent heparanase activation.