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Does hyperglycemia affect arginine metabolites in critically ill patients? A prospective cohort and in vitro study

BACKGROUND: Changes in the arginine metabolites asymmetric dimethyl-L-arginine (ADMA) and L-homoarginine and acute blood glucose concentrations have been shown to cause endothelial dysfunction and be independently associated with mortality in Intensive Care Unit (ICU) patients. The aim of this study...

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Autores principales: Lee, Tien F., Tommasi, Sara, Bersten, Andrew, Heilbronn, Leonie K., Sotgia, Salvatore, Zinellu, Angelo, Carru, Ciriaco, Mangoni, Arduino A., Burt, Morton G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067243/
https://www.ncbi.nlm.nih.gov/pubmed/37005603
http://dx.doi.org/10.1186/s13098-023-01035-8
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author Lee, Tien F.
Tommasi, Sara
Bersten, Andrew
Heilbronn, Leonie K.
Sotgia, Salvatore
Zinellu, Angelo
Carru, Ciriaco
Mangoni, Arduino A.
Burt, Morton G.
author_facet Lee, Tien F.
Tommasi, Sara
Bersten, Andrew
Heilbronn, Leonie K.
Sotgia, Salvatore
Zinellu, Angelo
Carru, Ciriaco
Mangoni, Arduino A.
Burt, Morton G.
author_sort Lee, Tien F.
collection PubMed
description BACKGROUND: Changes in the arginine metabolites asymmetric dimethyl-L-arginine (ADMA) and L-homoarginine and acute blood glucose concentrations have been shown to cause endothelial dysfunction and be independently associated with mortality in Intensive Care Unit (ICU) patients. The aim of this study was to investigate whether hyperglycemia potentially modulates these arginine metabolite concentrations to provide a mechanism that may link hyperglycemia and mortality in this patient group. METHODS: A clinical and in vitro study were undertaken. Glucose, glycosylated hemoglobin-A1c (HbA1c) and the stress hyperglycemia ratio (SHR) (to quantify absolute, chronic and relative hyperglycemia respectively) were measured in 1155 acutely unwell adult patients admitted to a mixed medical-surgical ICU. SHR was calculated by dividing the admission glucose by the estimated average glucose over the last 3 months, which was derived from HbA1c. ADMA and l-homoarginine were measured in a plasma sample collected at admission to ICU by liquid chromatography tandem mass spectrometry. The activity of dimethylarginine-dimethylaminohydrolase 1 (DDAH1), the main enzyme regulating ADMA concentrations, was assessed at varying glucose concentrations in vitro by quantifying the conversion of ADMA to citrulline in HEK293 cells that overexpress DDAH1. RESULTS: In the clinical study, plasma ADMA was not significantly associated with any measure of hyperglycemia. L-homoarginine was positively associated with glucose (β = 0.067, p = 0.018) and SHR (β = 0.107, p < 0.001) after correction for glomerular filtration rate. However, as l-homoarginine is a negative predictor of mortality, the direction of these associations are the opposite of those expected if hyperglycemia was affecting mortality via changes in l-homoarginine. In vitro DDAH1 activity was not significantly influenced by glucose concentrations (p = 0.506). CONCLUSION: In critically ill patients the association between relative hyperglycemia and mortality is not mediated by changes in ADMA or L-homoarginine. Trial registration ANZCTR Trial ID ACTRN12615001164583.
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spelling pubmed-100672432023-04-03 Does hyperglycemia affect arginine metabolites in critically ill patients? A prospective cohort and in vitro study Lee, Tien F. Tommasi, Sara Bersten, Andrew Heilbronn, Leonie K. Sotgia, Salvatore Zinellu, Angelo Carru, Ciriaco Mangoni, Arduino A. Burt, Morton G. Diabetol Metab Syndr Research BACKGROUND: Changes in the arginine metabolites asymmetric dimethyl-L-arginine (ADMA) and L-homoarginine and acute blood glucose concentrations have been shown to cause endothelial dysfunction and be independently associated with mortality in Intensive Care Unit (ICU) patients. The aim of this study was to investigate whether hyperglycemia potentially modulates these arginine metabolite concentrations to provide a mechanism that may link hyperglycemia and mortality in this patient group. METHODS: A clinical and in vitro study were undertaken. Glucose, glycosylated hemoglobin-A1c (HbA1c) and the stress hyperglycemia ratio (SHR) (to quantify absolute, chronic and relative hyperglycemia respectively) were measured in 1155 acutely unwell adult patients admitted to a mixed medical-surgical ICU. SHR was calculated by dividing the admission glucose by the estimated average glucose over the last 3 months, which was derived from HbA1c. ADMA and l-homoarginine were measured in a plasma sample collected at admission to ICU by liquid chromatography tandem mass spectrometry. The activity of dimethylarginine-dimethylaminohydrolase 1 (DDAH1), the main enzyme regulating ADMA concentrations, was assessed at varying glucose concentrations in vitro by quantifying the conversion of ADMA to citrulline in HEK293 cells that overexpress DDAH1. RESULTS: In the clinical study, plasma ADMA was not significantly associated with any measure of hyperglycemia. L-homoarginine was positively associated with glucose (β = 0.067, p = 0.018) and SHR (β = 0.107, p < 0.001) after correction for glomerular filtration rate. However, as l-homoarginine is a negative predictor of mortality, the direction of these associations are the opposite of those expected if hyperglycemia was affecting mortality via changes in l-homoarginine. In vitro DDAH1 activity was not significantly influenced by glucose concentrations (p = 0.506). CONCLUSION: In critically ill patients the association between relative hyperglycemia and mortality is not mediated by changes in ADMA or L-homoarginine. Trial registration ANZCTR Trial ID ACTRN12615001164583. BioMed Central 2023-04-01 /pmc/articles/PMC10067243/ /pubmed/37005603 http://dx.doi.org/10.1186/s13098-023-01035-8 Text en © The Author(s) 2023 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
Lee, Tien F.
Tommasi, Sara
Bersten, Andrew
Heilbronn, Leonie K.
Sotgia, Salvatore
Zinellu, Angelo
Carru, Ciriaco
Mangoni, Arduino A.
Burt, Morton G.
Does hyperglycemia affect arginine metabolites in critically ill patients? A prospective cohort and in vitro study
title Does hyperglycemia affect arginine metabolites in critically ill patients? A prospective cohort and in vitro study
title_full Does hyperglycemia affect arginine metabolites in critically ill patients? A prospective cohort and in vitro study
title_fullStr Does hyperglycemia affect arginine metabolites in critically ill patients? A prospective cohort and in vitro study
title_full_unstemmed Does hyperglycemia affect arginine metabolites in critically ill patients? A prospective cohort and in vitro study
title_short Does hyperglycemia affect arginine metabolites in critically ill patients? A prospective cohort and in vitro study
title_sort does hyperglycemia affect arginine metabolites in critically ill patients? a prospective cohort and in vitro study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10067243/
https://www.ncbi.nlm.nih.gov/pubmed/37005603
http://dx.doi.org/10.1186/s13098-023-01035-8
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