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Cardiometabolic disease risk markers are increased following burn injury in children

INTRODUCTION: Burn injury in children causes prolonged systemic effects on physiology and metabolism leading to increased morbidity and mortality, yet much remains undefined regarding the metabolic trajectory towards specific health outcomes. METHODS: A multi-platform strategy was implemented to eva...

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Autores principales: Begum, Sofina, Lodge, Samantha, Hall, Drew, Johnson, Blair Z., Bong, Sze How, Whiley, Luke, Gray, Nicola, Fear, Vanessa S., Fear, Mark W., Holmes, Elaine, Wood, Fiona M., Nicholson, Jeremy K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275366/
https://www.ncbi.nlm.nih.gov/pubmed/37333522
http://dx.doi.org/10.3389/fpubh.2023.1105163
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author Begum, Sofina
Lodge, Samantha
Hall, Drew
Johnson, Blair Z.
Bong, Sze How
Whiley, Luke
Gray, Nicola
Fear, Vanessa S.
Fear, Mark W.
Holmes, Elaine
Wood, Fiona M.
Nicholson, Jeremy K.
author_facet Begum, Sofina
Lodge, Samantha
Hall, Drew
Johnson, Blair Z.
Bong, Sze How
Whiley, Luke
Gray, Nicola
Fear, Vanessa S.
Fear, Mark W.
Holmes, Elaine
Wood, Fiona M.
Nicholson, Jeremy K.
author_sort Begum, Sofina
collection PubMed
description INTRODUCTION: Burn injury in children causes prolonged systemic effects on physiology and metabolism leading to increased morbidity and mortality, yet much remains undefined regarding the metabolic trajectory towards specific health outcomes. METHODS: A multi-platform strategy was implemented to evaluate the long-term immuno-metabolic consequences of burn injury combining metabolite, lipoprotein, and cytokine panels. Plasma samples from 36 children aged 4–8 years were collected 3 years after a burn injury together with 21 samples from non-injured age and sex matched controls. Three different (1)H Nuclear Magnetic Resonance spectroscopic experiments were applied to capture information on plasma low molecular weight metabolites, lipoproteins, and α-1-acid glycoprotein. RESULTS: Burn injury was characterized by underlying signatures of hyperglycaemia, hypermetabolism and inflammation, suggesting disruption of multiple pathways relating to glycolysis, tricarboxylic acid cycle, amino acid metabolism and the urea cycle. In addition, very low-density lipoprotein sub-components were significantly reduced in participants with burn injury whereas small-dense low density lipoprotein particles were significantly elevated in the burn injured patient plasma compared to uninjured controls, potentially indicative of modified cardiometabolic risk after a burn. Weighted-node Metabolite Correlation Network Analysis was restricted to the significantly differential features (q <0.05) between the children with and without burn injury and demonstrated a striking disparity in the number of statistical correlations between cytokines, lipoproteins, and small molecular metabolites in the injured groups, with increased correlations between these groups. DISCUSSION: These findings suggest a ‘metabolic memory’ of burn defined by a signature of interlinked and perturbed immune and metabolic function. Burn injury is associated with a series of adverse metabolic changes that persist chronically and are independent of burn severity and this study demonstrates increased risk of cardiovascular disease in the long-term. These findings highlight a crucial need for improved longer term monitoring of cardiometabolic health in a vulnerable population of children that have undergone burn injury.
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spelling pubmed-102753662023-06-17 Cardiometabolic disease risk markers are increased following burn injury in children Begum, Sofina Lodge, Samantha Hall, Drew Johnson, Blair Z. Bong, Sze How Whiley, Luke Gray, Nicola Fear, Vanessa S. Fear, Mark W. Holmes, Elaine Wood, Fiona M. Nicholson, Jeremy K. Front Public Health Public Health INTRODUCTION: Burn injury in children causes prolonged systemic effects on physiology and metabolism leading to increased morbidity and mortality, yet much remains undefined regarding the metabolic trajectory towards specific health outcomes. METHODS: A multi-platform strategy was implemented to evaluate the long-term immuno-metabolic consequences of burn injury combining metabolite, lipoprotein, and cytokine panels. Plasma samples from 36 children aged 4–8 years were collected 3 years after a burn injury together with 21 samples from non-injured age and sex matched controls. Three different (1)H Nuclear Magnetic Resonance spectroscopic experiments were applied to capture information on plasma low molecular weight metabolites, lipoproteins, and α-1-acid glycoprotein. RESULTS: Burn injury was characterized by underlying signatures of hyperglycaemia, hypermetabolism and inflammation, suggesting disruption of multiple pathways relating to glycolysis, tricarboxylic acid cycle, amino acid metabolism and the urea cycle. In addition, very low-density lipoprotein sub-components were significantly reduced in participants with burn injury whereas small-dense low density lipoprotein particles were significantly elevated in the burn injured patient plasma compared to uninjured controls, potentially indicative of modified cardiometabolic risk after a burn. Weighted-node Metabolite Correlation Network Analysis was restricted to the significantly differential features (q <0.05) between the children with and without burn injury and demonstrated a striking disparity in the number of statistical correlations between cytokines, lipoproteins, and small molecular metabolites in the injured groups, with increased correlations between these groups. DISCUSSION: These findings suggest a ‘metabolic memory’ of burn defined by a signature of interlinked and perturbed immune and metabolic function. Burn injury is associated with a series of adverse metabolic changes that persist chronically and are independent of burn severity and this study demonstrates increased risk of cardiovascular disease in the long-term. These findings highlight a crucial need for improved longer term monitoring of cardiometabolic health in a vulnerable population of children that have undergone burn injury. Frontiers Media S.A. 2023-06-02 /pmc/articles/PMC10275366/ /pubmed/37333522 http://dx.doi.org/10.3389/fpubh.2023.1105163 Text en Copyright © 2023 Begum, Lodge, Hall, Johnson, Bong, Whiley, Gray, Fear, Fear, Holmes, Wood and Nicholson. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Public Health
Begum, Sofina
Lodge, Samantha
Hall, Drew
Johnson, Blair Z.
Bong, Sze How
Whiley, Luke
Gray, Nicola
Fear, Vanessa S.
Fear, Mark W.
Holmes, Elaine
Wood, Fiona M.
Nicholson, Jeremy K.
Cardiometabolic disease risk markers are increased following burn injury in children
title Cardiometabolic disease risk markers are increased following burn injury in children
title_full Cardiometabolic disease risk markers are increased following burn injury in children
title_fullStr Cardiometabolic disease risk markers are increased following burn injury in children
title_full_unstemmed Cardiometabolic disease risk markers are increased following burn injury in children
title_short Cardiometabolic disease risk markers are increased following burn injury in children
title_sort cardiometabolic disease risk markers are increased following burn injury in children
topic Public Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10275366/
https://www.ncbi.nlm.nih.gov/pubmed/37333522
http://dx.doi.org/10.3389/fpubh.2023.1105163
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