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Urinary N-acetyl-beta-d-glucosaminidase levels in diabetic adults

Diabetes mellitus (DM) is known to be one of the most common causes of end-stage renal disease. The disease is usually not detected on time, because of the large functioning reserve of the kidney. Currently used markers (serum creatinine, creatinine clearance, urea, and electrolytes) remain relative...

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Autores principales: Omozee, Eiya Bibiana, Okaka, Enajit Ibiene, Edo, Andrew Efosa, Obika, Leonard Fedinard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6437819/
https://www.ncbi.nlm.nih.gov/pubmed/30983794
http://dx.doi.org/10.4103/JLP.JLP_164_17
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author Omozee, Eiya Bibiana
Okaka, Enajit Ibiene
Edo, Andrew Efosa
Obika, Leonard Fedinard
author_facet Omozee, Eiya Bibiana
Okaka, Enajit Ibiene
Edo, Andrew Efosa
Obika, Leonard Fedinard
author_sort Omozee, Eiya Bibiana
collection PubMed
description Diabetes mellitus (DM) is known to be one of the most common causes of end-stage renal disease. The disease is usually not detected on time, because of the large functioning reserve of the kidney. Currently used markers (serum creatinine, creatinine clearance, urea, and electrolytes) remain relatively normal even when more than 50% of the renal nephron is not functioning. The aim of this study was to determine the level of urinary N-acetyl-beta-d-glucosaminidase (NAG) in diabetic adults in comparison with some currently used markers. A total of 56 diabetic patients between the ages of 23 and 63 were used for this study and 30 nondiabetic between the ages of 18 and 62 were used as control. The diabetic patients were classified into three groups based on how long they have been diagnosed: <2 years (25), 2–5 years (30), and >5 years (25). Spot midstream urine samples were collected into sterile containers, and blood samples were collected into plain tubes. All the analyses were done spectrophotometrically. Creatinine clearance was calculated using the Cockcroft–Gault Equation. There was a significant increase (P < 0.01) in NAG values of 2–5 years and above 5 years and control. The urinary microalbumin concentration of controls was significantly different (P < 0.05) only with those who have had DM for <2 years. Urinary creatinine concentration of control was significantly higher (P < 0.05) than values of all the diabetic groups. There was a significant increase (P < 0.01) in creatinine clearance of control group and those who have had DM for <2 years. It is thus concluded that urinary NAG can be used as an early marker in the diagnosis of diabetic nephropathy since urinary NAG increases first before the other markers analyzed in this current study begins to increase.
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spelling pubmed-64378192019-04-12 Urinary N-acetyl-beta-d-glucosaminidase levels in diabetic adults Omozee, Eiya Bibiana Okaka, Enajit Ibiene Edo, Andrew Efosa Obika, Leonard Fedinard J Lab Physicians Review Article Diabetes mellitus (DM) is known to be one of the most common causes of end-stage renal disease. The disease is usually not detected on time, because of the large functioning reserve of the kidney. Currently used markers (serum creatinine, creatinine clearance, urea, and electrolytes) remain relatively normal even when more than 50% of the renal nephron is not functioning. The aim of this study was to determine the level of urinary N-acetyl-beta-d-glucosaminidase (NAG) in diabetic adults in comparison with some currently used markers. A total of 56 diabetic patients between the ages of 23 and 63 were used for this study and 30 nondiabetic between the ages of 18 and 62 were used as control. The diabetic patients were classified into three groups based on how long they have been diagnosed: <2 years (25), 2–5 years (30), and >5 years (25). Spot midstream urine samples were collected into sterile containers, and blood samples were collected into plain tubes. All the analyses were done spectrophotometrically. Creatinine clearance was calculated using the Cockcroft–Gault Equation. There was a significant increase (P < 0.01) in NAG values of 2–5 years and above 5 years and control. The urinary microalbumin concentration of controls was significantly different (P < 0.05) only with those who have had DM for <2 years. Urinary creatinine concentration of control was significantly higher (P < 0.05) than values of all the diabetic groups. There was a significant increase (P < 0.01) in creatinine clearance of control group and those who have had DM for <2 years. It is thus concluded that urinary NAG can be used as an early marker in the diagnosis of diabetic nephropathy since urinary NAG increases first before the other markers analyzed in this current study begins to increase. Wolters Kluwer - Medknow 2019 /pmc/articles/PMC6437819/ /pubmed/30983794 http://dx.doi.org/10.4103/JLP.JLP_164_17 Text en Copyright: © 2019 Journal of Laboratory Physicians http://creativecommons.org/licenses/by-nc-sa/4.0 This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Review Article
Omozee, Eiya Bibiana
Okaka, Enajit Ibiene
Edo, Andrew Efosa
Obika, Leonard Fedinard
Urinary N-acetyl-beta-d-glucosaminidase levels in diabetic adults
title Urinary N-acetyl-beta-d-glucosaminidase levels in diabetic adults
title_full Urinary N-acetyl-beta-d-glucosaminidase levels in diabetic adults
title_fullStr Urinary N-acetyl-beta-d-glucosaminidase levels in diabetic adults
title_full_unstemmed Urinary N-acetyl-beta-d-glucosaminidase levels in diabetic adults
title_short Urinary N-acetyl-beta-d-glucosaminidase levels in diabetic adults
title_sort urinary n-acetyl-beta-d-glucosaminidase levels in diabetic adults
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6437819/
https://www.ncbi.nlm.nih.gov/pubmed/30983794
http://dx.doi.org/10.4103/JLP.JLP_164_17
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