UV Fluorescence-Based Determination of Urinary Advanced Glycation End Products in Patients with Chronic Kidney Disease

Advanced glycation end products (AGEs) are a class of proteins or lipids that are non-enzymatically glycated and oxidized after contact with aldose sugars. The accumulation of AGEs results in carbonyl stress, which is characteristic for diabetes mellitus, uremia, atherosclerosis and vascular dysfunc...

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Main Authors: Mieke Steenbeke, Sander De Bruyne, Elisabeth Van Aken, Griet Glorieux, Wim Van Biesen, Jonas Himpe, Gilles De Meester, Marijn Speeckaert, Joris Delanghe
Format: Article
Language:English
Published: MDPI AG 2020-01-01
Series:Diagnostics
Subjects:
Online Access:https://www.mdpi.com/2075-4418/10/1/34
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spelling doaj-25f7ec83c4364f8cbd77f05c1ccbf2492020-11-25T03:35:39ZengMDPI AGDiagnostics2075-44182020-01-011013410.3390/diagnostics10010034diagnostics10010034UV Fluorescence-Based Determination of Urinary Advanced Glycation End Products in Patients with Chronic Kidney DiseaseMieke Steenbeke0Sander De Bruyne1Elisabeth Van Aken2Griet Glorieux3Wim Van Biesen4Jonas Himpe5Gilles De Meester6Marijn Speeckaert7Joris Delanghe8Department of Nephrology, Ghent University Hospital, 9000 Ghent, BelgiumDepartment of Laboratory Medicine, Clinical Chemistry, Ghent University Hospital, 9000 Ghent, BelgiumDepartment of Ophthalmology, Sint-Elisabeth Ziekenhuis, 9620 Zottegem, BelgiumDepartment of Nephrology, Ghent University Hospital, 9000 Ghent, BelgiumDepartment of Nephrology, Ghent University Hospital, 9000 Ghent, BelgiumDepartment of Laboratory Medicine, Clinical Chemistry, Ghent University Hospital, 9000 Ghent, BelgiumDepartment of Laboratory Medicine, Clinical Chemistry, Ghent University Hospital, 9000 Ghent, BelgiumDepartment of Nephrology, Ghent University Hospital, 9000 Ghent, BelgiumDepartment of Diagnostic Sciences, Ghent University, 9000 Ghent, BelgiumAdvanced glycation end products (AGEs) are a class of proteins or lipids that are non-enzymatically glycated and oxidized after contact with aldose sugars. The accumulation of AGEs results in carbonyl stress, which is characteristic for diabetes mellitus, uremia, atherosclerosis and vascular dysfunction. In recent decades, several innovative methods have been developed to measure the concentration of AGEs in blood or urine. In the present study, we evaluated the use of UV fluorescence as an alternative tool to detect urinary AGEs in four groups of well characterized chronic kidney disease (CKD) patients over a wide range of kidney insufficiency and in a group of healthy subjects. Using an excitation wavelength of 365 nm, the fluorescence spectra of urinary AGEs were recorded in the 400–620 nm emission range. When considering the emission peaks at 440 nm and 490 nm, a significantly higher AGE-specific fluorescence intensity was detected in CKD patients compared to healthy subjects (<i>p</i> &lt; 0.0001 and <i>p</i> = 0.0001, respectively). The urinary creatinine adjusted fluorescence emission spectra in the group of CKD patients with diabetes mellitus were comparable with those of CKD patients without diabetes mellitus. Creatinine-adjusted fluorescence emission spectra were highest in CKD patients with proteinuria, moderate in CKD patients without proteinuria and lowest in healthy controls (<i>p</i> &lt; 0.0001 at both emission wavelengths). In a multiple regression analysis, age, CRP and insulin treatment were predictors of fluorescence intensity at the emission wavelength of 440 nm. Age and insulin treatment were predictors at 490 nm. The presented method is a simple, cheap, alternative method to monitor the AGE-load in the CKD population.https://www.mdpi.com/2075-4418/10/1/34advanced glycation end productschronic kidney diseasediabetes mellitusurineuv-fluorescence
collection DOAJ
language English
format Article
sources DOAJ
author Mieke Steenbeke
Sander De Bruyne
Elisabeth Van Aken
Griet Glorieux
Wim Van Biesen
Jonas Himpe
Gilles De Meester
Marijn Speeckaert
Joris Delanghe
spellingShingle Mieke Steenbeke
Sander De Bruyne
Elisabeth Van Aken
Griet Glorieux
Wim Van Biesen
Jonas Himpe
Gilles De Meester
Marijn Speeckaert
Joris Delanghe
UV Fluorescence-Based Determination of Urinary Advanced Glycation End Products in Patients with Chronic Kidney Disease
Diagnostics
advanced glycation end products
chronic kidney disease
diabetes mellitus
urine
uv-fluorescence
author_facet Mieke Steenbeke
Sander De Bruyne
Elisabeth Van Aken
Griet Glorieux
Wim Van Biesen
Jonas Himpe
Gilles De Meester
Marijn Speeckaert
Joris Delanghe
author_sort Mieke Steenbeke
title UV Fluorescence-Based Determination of Urinary Advanced Glycation End Products in Patients with Chronic Kidney Disease
title_short UV Fluorescence-Based Determination of Urinary Advanced Glycation End Products in Patients with Chronic Kidney Disease
title_full UV Fluorescence-Based Determination of Urinary Advanced Glycation End Products in Patients with Chronic Kidney Disease
title_fullStr UV Fluorescence-Based Determination of Urinary Advanced Glycation End Products in Patients with Chronic Kidney Disease
title_full_unstemmed UV Fluorescence-Based Determination of Urinary Advanced Glycation End Products in Patients with Chronic Kidney Disease
title_sort uv fluorescence-based determination of urinary advanced glycation end products in patients with chronic kidney disease
publisher MDPI AG
series Diagnostics
issn 2075-4418
publishDate 2020-01-01
description Advanced glycation end products (AGEs) are a class of proteins or lipids that are non-enzymatically glycated and oxidized after contact with aldose sugars. The accumulation of AGEs results in carbonyl stress, which is characteristic for diabetes mellitus, uremia, atherosclerosis and vascular dysfunction. In recent decades, several innovative methods have been developed to measure the concentration of AGEs in blood or urine. In the present study, we evaluated the use of UV fluorescence as an alternative tool to detect urinary AGEs in four groups of well characterized chronic kidney disease (CKD) patients over a wide range of kidney insufficiency and in a group of healthy subjects. Using an excitation wavelength of 365 nm, the fluorescence spectra of urinary AGEs were recorded in the 400–620 nm emission range. When considering the emission peaks at 440 nm and 490 nm, a significantly higher AGE-specific fluorescence intensity was detected in CKD patients compared to healthy subjects (<i>p</i> &lt; 0.0001 and <i>p</i> = 0.0001, respectively). The urinary creatinine adjusted fluorescence emission spectra in the group of CKD patients with diabetes mellitus were comparable with those of CKD patients without diabetes mellitus. Creatinine-adjusted fluorescence emission spectra were highest in CKD patients with proteinuria, moderate in CKD patients without proteinuria and lowest in healthy controls (<i>p</i> &lt; 0.0001 at both emission wavelengths). In a multiple regression analysis, age, CRP and insulin treatment were predictors of fluorescence intensity at the emission wavelength of 440 nm. Age and insulin treatment were predictors at 490 nm. The presented method is a simple, cheap, alternative method to monitor the AGE-load in the CKD population.
topic advanced glycation end products
chronic kidney disease
diabetes mellitus
urine
uv-fluorescence
url https://www.mdpi.com/2075-4418/10/1/34
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