» Articles » PMID: 25717442

Urinary Biomarker N-acetyl-β-D-glucosaminidase Can Predict Severity of Renal Damage in Diabetic Nephropathy

Overview
Specialty Endocrinology
Date 2015 Feb 27
PMID 25717442
Citations 29
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Diabetic nephropathy is a clinical diagnosis where proteinuria is present in a patient with diabetes. Early intervention can significantly improve the prognosis. However, imprecision of the currently available biomarkers have impaired effective therapies in a timely manner. Urinary N-acetyl-β-D-glucosaminidase (NAG) is excreted in abnormally high amounts in many renal diseases. The aim of this study was to evaluate urinary NAG as an early biomarker in detection of diabetic nephropathy and whether it parallels the severity of kidney damage in different stages of diabetic nephropathy.

Methods: Fifty patients with type 2 DM were classified into 3 groups (normoalbuminurea, microalbuminurea and macroalbuminurea) and 10 healthy subjects served as a control group. Urinary NAG, albumin and creatinine were measured. Blood urea, serum creatinine, serum albumin, total proteins, serum cholesterol, alanine aminotransferase (ALT), aspartate aminotransferase (AST), fasting and postprandial blood glucose, HbA1c and creatinine clearance were measured for all subjects.

Results: All diabetic patients had a significantly higher level of urinary NAG compared to control. NAG value increased in parallel with the severity of renal involvement.

Conclusion: Urinary NAG expresses the degree of renal impairment in diabetic nephropathy.

Citing Articles

Hydrogen gas inhalation ameliorates glomerular enlargement after hypoxic-ischemic insult in asphyxiated piglet model.

Iwaki T, Nakamura S, Wakabayashi T, Nakao Y, Htun Y, Tsuchiya T Sci Rep. 2025; 15(1):1677.

PMID: 39799178 PMC: 11724992. DOI: 10.1038/s41598-025-85231-8.


Urinary N-acetyl-D-glucosaminidase can predict bleeding after a percutaneous kidney biopsy.

Goto H, Kobayashi Y, Sato H, Fukunaga T, Tanoue K, Yamashiro A BMC Nephrol. 2024; 25(1):234.

PMID: 39039446 PMC: 11265090. DOI: 10.1186/s12882-024-03658-z.


Diabetes and Renal Complications: An Overview on Pathophysiology, Biomarkers and Therapeutic Interventions.

Jha R, Lopez-Trevino S, Kankanamalage H, Jha J Biomedicines. 2024; 12(5).

PMID: 38791060 PMC: 11118045. DOI: 10.3390/biomedicines12051098.


Pathomechanisms of Diabetic Kidney Disease.

Sinha S, Nicholas S J Clin Med. 2023; 12(23).

PMID: 38068400 PMC: 10707303. DOI: 10.3390/jcm12237349.


Association between continuous glucose monitoring-derived glycemic control indices and urinary biomarkers of diabetic kidney disease: Hyogo Diabetes Hypoglycemia Cognition Complications study.

Takagi A, Kusunoki Y, Ohigashi M, Osugi K, Inoue C, Inoue M Acta Diabetol. 2023; 61(4):413-423.

PMID: 38006524 PMC: 10963564. DOI: 10.1007/s00592-023-02214-9.


References
1.
Vaidya V, Niewczas M, Ficociello L, Johnson A, Collings F, Warram J . Regression of microalbuminuria in type 1 diabetes is associated with lower levels of urinary tubular injury biomarkers, kidney injury molecule-1, and N-acetyl-β-D-glucosaminidase. Kidney Int. 2010; 79(4):464-70. PMC: 3033751. DOI: 10.1038/ki.2010.404. View

2.
. Standards of medical care in diabetes--2007. Diabetes Care. 2006; 30 Suppl 1:S4-S41. DOI: 10.2337/dc07-S004. View

3.
Bagshaw S, Bellomo R . Early diagnosis of acute kidney injury. Curr Opin Crit Care. 2007; 13(6):638-44. DOI: 10.1097/MCC.0b013e3282f07570. View

4.
Kuzniar J, Marchewka Z, Lembas-Bogaczyk J, Kuzniar T, Klinger M . Etiology of increased enzymuria in different morphological forms of glomerulonephritis. Nephron Physiol. 2004; 98(1):p8-14. DOI: 10.1159/000079932. View

5.
Navarro J, Mora C, Muros M, Maca M, Garca J . Effects of pentoxifylline administration on urinary N-acetyl-beta-glucosaminidase excretion in type 2 diabetic patients: a short-term, prospective, randomized study. Am J Kidney Dis. 2003; 42(2):264-70. DOI: 10.1016/s0272-6386(03)00651-6. View