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Renal Tubular Damage Marker, Urinary N-acetyl-β-DGlucosaminidase, as a Predictive Marker of Hepatic Fibrosis in Type 2 Diabetes Mellitus.

Authors :
Hae Kyung Kim
Minyoung Lee
Yong-ho Lee
Eun Seok Kang
Bong-Soo Cha
Byung-Wan Lee
Source :
Diabetes & Metabolism Journal; Jan2022, Vol. 46 Issue 1, p104-116, 21p
Publication Year :
2022

Abstract

Background: Non-alcoholic steatohepatitis is closely associated with the progression of diabetic kidney disease (DKD) in type 2 diabetes mellitus (T2DM). We investigated whether urinary N-acetyl-β-D-glucosaminidase (u-NAG), an early renal tubular damage biomarker in DKD, could be related to the degree of hepatic fibrosis in patients with T2DM. Methods: A total of 300 patients with T2DM were enrolled in this study. Hepatic steatosis and fibrosis were determined using transient elastography. The levels of urinary biomarkers, including u-NAG, albumin, protein, and creatinine, and glucometabolic parameters were measured. Results: Based on the median value of the u-NAG to creatinine ratio (u-NCR), subjects were divided into low and high u-NCR groups. The high u-NCR group showed a significantly longer duration of diabetes, worsened hyperglycemia, and a more enhanced hepatic fibrosis index. A higher u-NCR was associated with a greater odds ratio for the risk of higher hepatic fibrosis stage (F2: odds ratio, 1.99; 95% confidence interval [CI], 1.04 to 3.82). Also, u-NCR was an independent predictive marker for more advanced hepatic fibrosis, even after adjusting for several confounding factors (β=1.58, P<0.01). Conclusion: The elevation of u-NAG was independently associated with a higher degree of hepatic fibrosis in patients with T2DM. Considering the common metabolic milieu of renal and hepatic fibrosis in T2DM, the potential use of u-NAG as an effective urinary biomarker reflecting hepatic fibrosis in T2DM needs to be validated in the future. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
22336079
Volume :
46
Issue :
1
Database :
Complementary Index
Journal :
Diabetes & Metabolism Journal
Publication Type :
Academic Journal
Accession number :
154992169
Full Text :
https://doi.org/10.4093/dmj.2020.0273