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Impact of tight glucose control on circulating 3-hydroxybutyrate in critically ill patients

BACKGROUND: Recent evidence suggests a potentially protective effect of increasing ketone body availability via accepting low macronutrient intake early after onset of critical illness. The impact of blood glucose control with insulin on circulating ketones is unclear. Whereas lowering blood glucose...

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Autores principales: Gunst, Jan, De Bruyn, Astrid, Casaer, Michael P., Vander Perre, Sarah, Langouche, Lies, Van den Berghe, Greet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547101/
https://www.ncbi.nlm.nih.gov/pubmed/34696774
http://dx.doi.org/10.1186/s13054-021-03772-6
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author Gunst, Jan
De Bruyn, Astrid
Casaer, Michael P.
Vander Perre, Sarah
Langouche, Lies
Van den Berghe, Greet
author_facet Gunst, Jan
De Bruyn, Astrid
Casaer, Michael P.
Vander Perre, Sarah
Langouche, Lies
Van den Berghe, Greet
author_sort Gunst, Jan
collection PubMed
description BACKGROUND: Recent evidence suggests a potentially protective effect of increasing ketone body availability via accepting low macronutrient intake early after onset of critical illness. The impact of blood glucose control with insulin on circulating ketones is unclear. Whereas lowering blood glucose may activate ketogenesis, high insulin concentrations may have the opposite effect. We hypothesized that the previously reported protective effects of tight glucose control in critically ill patients receiving early parenteral nutrition may have been mediated in part by activation of ketogenesis. METHODS: This is a secondary analysis of 3 randomized controlled trials on tight versus liberal blood glucose control in the intensive care unit, including 700 critically ill children and 2748 critically ill adults. All patients received early parenteral nutrition as part of the contemporary standard of care. Before studying a potential mediator role of circulating ketones in improving outcome, we performed a time course analysis to investigate whether tight glucose control significantly affected ketogenesis and to identify a day of maximal effect, if any. We quantified plasma/serum 3-hydroxybutyrate concentrations from intensive care unit admission until day 3 in 2 matched subsets of 100 critically ill children and 100 critically ill adults. Univariable differences between groups were investigated by Kruskal-Wallis test. Differences in 3-hydroxybutyrate concentrations between study days were investigated by Wilcoxon signed-rank test. RESULTS: In critically ill children and adults receiving early parenteral nutrition, tight glucose control, as compared with liberal glucose control, lowered mean morning blood glucose on days 1–3 (P < 0.0001) via infusing insulin at a higher dose (P < 0.0001). Throughout the study period, caloric intake was not different between groups. In both children and adults, tight glucose control did not affect 3-hydroxybutyrate concentrations, which were suppressed on ICU days 1–3 and significantly lower than the ICU admission values for both groups (P < 0.0001). CONCLUSION: Tight versus liberal glucose control in the context of early parenteral nutrition did not affect 3-hydroxybutyrate concentrations in critically ill patients. Hence, the protective effects of tight glucose control in this context cannot be attributed to increased ketone body availability. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-021-03772-6.
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spelling pubmed-85471012021-10-26 Impact of tight glucose control on circulating 3-hydroxybutyrate in critically ill patients Gunst, Jan De Bruyn, Astrid Casaer, Michael P. Vander Perre, Sarah Langouche, Lies Van den Berghe, Greet Crit Care Research BACKGROUND: Recent evidence suggests a potentially protective effect of increasing ketone body availability via accepting low macronutrient intake early after onset of critical illness. The impact of blood glucose control with insulin on circulating ketones is unclear. Whereas lowering blood glucose may activate ketogenesis, high insulin concentrations may have the opposite effect. We hypothesized that the previously reported protective effects of tight glucose control in critically ill patients receiving early parenteral nutrition may have been mediated in part by activation of ketogenesis. METHODS: This is a secondary analysis of 3 randomized controlled trials on tight versus liberal blood glucose control in the intensive care unit, including 700 critically ill children and 2748 critically ill adults. All patients received early parenteral nutrition as part of the contemporary standard of care. Before studying a potential mediator role of circulating ketones in improving outcome, we performed a time course analysis to investigate whether tight glucose control significantly affected ketogenesis and to identify a day of maximal effect, if any. We quantified plasma/serum 3-hydroxybutyrate concentrations from intensive care unit admission until day 3 in 2 matched subsets of 100 critically ill children and 100 critically ill adults. Univariable differences between groups were investigated by Kruskal-Wallis test. Differences in 3-hydroxybutyrate concentrations between study days were investigated by Wilcoxon signed-rank test. RESULTS: In critically ill children and adults receiving early parenteral nutrition, tight glucose control, as compared with liberal glucose control, lowered mean morning blood glucose on days 1–3 (P < 0.0001) via infusing insulin at a higher dose (P < 0.0001). Throughout the study period, caloric intake was not different between groups. In both children and adults, tight glucose control did not affect 3-hydroxybutyrate concentrations, which were suppressed on ICU days 1–3 and significantly lower than the ICU admission values for both groups (P < 0.0001). CONCLUSION: Tight versus liberal glucose control in the context of early parenteral nutrition did not affect 3-hydroxybutyrate concentrations in critically ill patients. Hence, the protective effects of tight glucose control in this context cannot be attributed to increased ketone body availability. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-021-03772-6. BioMed Central 2021-10-25 /pmc/articles/PMC8547101/ /pubmed/34696774 http://dx.doi.org/10.1186/s13054-021-03772-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Gunst, Jan
De Bruyn, Astrid
Casaer, Michael P.
Vander Perre, Sarah
Langouche, Lies
Van den Berghe, Greet
Impact of tight glucose control on circulating 3-hydroxybutyrate in critically ill patients
title Impact of tight glucose control on circulating 3-hydroxybutyrate in critically ill patients
title_full Impact of tight glucose control on circulating 3-hydroxybutyrate in critically ill patients
title_fullStr Impact of tight glucose control on circulating 3-hydroxybutyrate in critically ill patients
title_full_unstemmed Impact of tight glucose control on circulating 3-hydroxybutyrate in critically ill patients
title_short Impact of tight glucose control on circulating 3-hydroxybutyrate in critically ill patients
title_sort impact of tight glucose control on circulating 3-hydroxybutyrate in critically ill patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547101/
https://www.ncbi.nlm.nih.gov/pubmed/34696774
http://dx.doi.org/10.1186/s13054-021-03772-6
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