Adenine Nucleotide Metabolites in Uremic Erythrocytes as Metabolic Markers of Chronic Kidney Disease in Children

Chronic kidney disease (CKD) is associated with multifaceted pathophysiological lesions including metabolic pathways in red blood cells (RBC). The aim of the study was to determine the concentration of adenine nucleotide metabolites, i.e., nicotinamide adenine dinucleotide (NAD)-oxidized form, nicot...

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Autores principales: Joanna Piechowicz, Andrzej Gamian, Danuta Zwolińska, Dorota Polak-Jonkisz
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:679930869e894bcca669766c4a58965f2021-11-11T17:48:46ZAdenine Nucleotide Metabolites in Uremic Erythrocytes as Metabolic Markers of Chronic Kidney Disease in Children10.3390/jcm102152082077-0383https://doaj.org/article/679930869e894bcca669766c4a58965f2021-11-01T00:00:00Zhttps://www.mdpi.com/2077-0383/10/21/5208https://doaj.org/toc/2077-0383Chronic kidney disease (CKD) is associated with multifaceted pathophysiological lesions including metabolic pathways in red blood cells (RBC). The aim of the study was to determine the concentration of adenine nucleotide metabolites, i.e., nicotinamide adenine dinucleotide (NAD)-oxidized form, nicotinamide adenine dinucleotide hydrate (NADH)-reduced form, nicotinic acid mononucleotide (NAMN), β-nicotinamide mononucleotide (NMN), nicotinic acid adenine dinucleotide (NAAD), nicotinic acid (NA) and nicotinamide (NAM) in RBC and to determine a relationship between NAD metabolites and CKD progression. Forty-eight CKD children and 33 age-matched controls were examined. Patients were divided into groups depending on the CKD stages (Group II-stage II, Group III- stage III, Group IV- stage IV and Group RRT children on dialysis). To determine the above-mentioned metabolites concentrations in RBC liquid chromatography-mass spectrometry was used. Results: the only difference between the groups was shown concerning NAD in RBC, although the values did not differ significantly from controls. The lowest NAD values were found in Group II (188.6 ± 124.49 nmol/mL, the highest in group IV (324.94 ± 63.06 nmol/mL. Between Groups II and IV, as well as III and IV, the differences were statistically significant (<i>p</i> < 0.032, <i>p</i> < 0.046 respectively). Conclusions. CKD children do not have evident abnormalities of RBC metabolism with respect to adenine nucleotide metabolites. The significant differences in erythrocyte NAD concentrations between CKD stages may suggest the activation of adaptive defense mechanisms aimed at erythrocyte metabolic stabilization. It seems that the implementation of RRT has a positive impact on RBC NAD metabolism, but further research performed on a larger population is needed to confirm it.Joanna PiechowiczAndrzej GamianDanuta ZwolińskaDorota Polak-JonkiszMDPI AGarticleadenine nucleotide metaboliteschronic renal failurechildrenMedicineRENJournal of Clinical Medicine, Vol 10, Iss 5208, p 5208 (2021)
institution DOAJ
collection DOAJ
language EN
topic adenine nucleotide metabolites
chronic renal failure
children
Medicine
R
spellingShingle adenine nucleotide metabolites
chronic renal failure
children
Medicine
R
Joanna Piechowicz
Andrzej Gamian
Danuta Zwolińska
Dorota Polak-Jonkisz
Adenine Nucleotide Metabolites in Uremic Erythrocytes as Metabolic Markers of Chronic Kidney Disease in Children
description Chronic kidney disease (CKD) is associated with multifaceted pathophysiological lesions including metabolic pathways in red blood cells (RBC). The aim of the study was to determine the concentration of adenine nucleotide metabolites, i.e., nicotinamide adenine dinucleotide (NAD)-oxidized form, nicotinamide adenine dinucleotide hydrate (NADH)-reduced form, nicotinic acid mononucleotide (NAMN), β-nicotinamide mononucleotide (NMN), nicotinic acid adenine dinucleotide (NAAD), nicotinic acid (NA) and nicotinamide (NAM) in RBC and to determine a relationship between NAD metabolites and CKD progression. Forty-eight CKD children and 33 age-matched controls were examined. Patients were divided into groups depending on the CKD stages (Group II-stage II, Group III- stage III, Group IV- stage IV and Group RRT children on dialysis). To determine the above-mentioned metabolites concentrations in RBC liquid chromatography-mass spectrometry was used. Results: the only difference between the groups was shown concerning NAD in RBC, although the values did not differ significantly from controls. The lowest NAD values were found in Group II (188.6 ± 124.49 nmol/mL, the highest in group IV (324.94 ± 63.06 nmol/mL. Between Groups II and IV, as well as III and IV, the differences were statistically significant (<i>p</i> < 0.032, <i>p</i> < 0.046 respectively). Conclusions. CKD children do not have evident abnormalities of RBC metabolism with respect to adenine nucleotide metabolites. The significant differences in erythrocyte NAD concentrations between CKD stages may suggest the activation of adaptive defense mechanisms aimed at erythrocyte metabolic stabilization. It seems that the implementation of RRT has a positive impact on RBC NAD metabolism, but further research performed on a larger population is needed to confirm it.
format article
author Joanna Piechowicz
Andrzej Gamian
Danuta Zwolińska
Dorota Polak-Jonkisz
author_facet Joanna Piechowicz
Andrzej Gamian
Danuta Zwolińska
Dorota Polak-Jonkisz
author_sort Joanna Piechowicz
title Adenine Nucleotide Metabolites in Uremic Erythrocytes as Metabolic Markers of Chronic Kidney Disease in Children
title_short Adenine Nucleotide Metabolites in Uremic Erythrocytes as Metabolic Markers of Chronic Kidney Disease in Children
title_full Adenine Nucleotide Metabolites in Uremic Erythrocytes as Metabolic Markers of Chronic Kidney Disease in Children
title_fullStr Adenine Nucleotide Metabolites in Uremic Erythrocytes as Metabolic Markers of Chronic Kidney Disease in Children
title_full_unstemmed Adenine Nucleotide Metabolites in Uremic Erythrocytes as Metabolic Markers of Chronic Kidney Disease in Children
title_sort adenine nucleotide metabolites in uremic erythrocytes as metabolic markers of chronic kidney disease in children
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/679930869e894bcca669766c4a58965f
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AT danutazwolinska adeninenucleotidemetabolitesinuremicerythrocytesasmetabolicmarkersofchronickidneydiseaseinchildren
AT dorotapolakjonkisz adeninenucleotidemetabolitesinuremicerythrocytesasmetabolicmarkersofchronickidneydiseaseinchildren
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