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Whole body protein kinetics during hypocaloric and normocaloric feeding in critically ill patients
INTRODUCTION: Optimal feeding of critically ill patients in the ICU is controversial. Existing guidelines rest on rather weak evidence. Whole body protein kinetics may be an attractive technique for assessing optimal protein intake. In this study, critically ill patients were investigated during hyp...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057244/ https://www.ncbi.nlm.nih.gov/pubmed/23883571 http://dx.doi.org/10.1186/cc12837 |
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author | Berg, Agneta Rooyackers, Olav Bellander, Bo-Michael Wernerman, Jan |
author_facet | Berg, Agneta Rooyackers, Olav Bellander, Bo-Michael Wernerman, Jan |
author_sort | Berg, Agneta |
collection | PubMed |
description | INTRODUCTION: Optimal feeding of critically ill patients in the ICU is controversial. Existing guidelines rest on rather weak evidence. Whole body protein kinetics may be an attractive technique for assessing optimal protein intake. In this study, critically ill patients were investigated during hypocaloric and normocaloric IV nutrition. METHODS: Neurosurgical patients on mechanical ventilation (n = 16) were studied during a 48-hour period. In random order 50% and 100% of measured energy expenditure was given as IV nutrition during 24 hours, corresponding to hypocaloric and normocaloric nutrition, respectively. At the end of each period, whole body protein turnover was measured using d5-phenylalanine and 13C-leucine tracers. RESULTS: The phenylalanine tracer indicated that whole-body protein synthesis was lower during hypocaloric feeding, while whole-body protein degradation and amino acid oxidation were unaltered, which resulted in a more negative protein balance, namely −1.9 ± 2.1 versus −0.7 ± 1.3 mg phenylalanine/kg/h (P = 0.014). The leucine tracer indicated that whole body protein synthesis and degradation and amino acid oxidation were unaltered, but the protein balance was negative during hypocaloric feeding, namely −0.3 ± 0.5 versus 0.6 ± 0.5 mg leucine/kg/h (P < 0.001). CONCLUSION: In the patient group studied, hypocaloric feeding was associated with a more negative protein balance, but the amino acid oxidation was not different. The protein kinetics measurements and the study’s investigational protocol were useful for assessing the efficacy of nutrition support on protein metabolism in critically ill patients. |
format | Online Article Text |
id | pubmed-4057244 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40572442014-06-16 Whole body protein kinetics during hypocaloric and normocaloric feeding in critically ill patients Berg, Agneta Rooyackers, Olav Bellander, Bo-Michael Wernerman, Jan Crit Care Research INTRODUCTION: Optimal feeding of critically ill patients in the ICU is controversial. Existing guidelines rest on rather weak evidence. Whole body protein kinetics may be an attractive technique for assessing optimal protein intake. In this study, critically ill patients were investigated during hypocaloric and normocaloric IV nutrition. METHODS: Neurosurgical patients on mechanical ventilation (n = 16) were studied during a 48-hour period. In random order 50% and 100% of measured energy expenditure was given as IV nutrition during 24 hours, corresponding to hypocaloric and normocaloric nutrition, respectively. At the end of each period, whole body protein turnover was measured using d5-phenylalanine and 13C-leucine tracers. RESULTS: The phenylalanine tracer indicated that whole-body protein synthesis was lower during hypocaloric feeding, while whole-body protein degradation and amino acid oxidation were unaltered, which resulted in a more negative protein balance, namely −1.9 ± 2.1 versus −0.7 ± 1.3 mg phenylalanine/kg/h (P = 0.014). The leucine tracer indicated that whole body protein synthesis and degradation and amino acid oxidation were unaltered, but the protein balance was negative during hypocaloric feeding, namely −0.3 ± 0.5 versus 0.6 ± 0.5 mg leucine/kg/h (P < 0.001). CONCLUSION: In the patient group studied, hypocaloric feeding was associated with a more negative protein balance, but the amino acid oxidation was not different. The protein kinetics measurements and the study’s investigational protocol were useful for assessing the efficacy of nutrition support on protein metabolism in critically ill patients. BioMed Central 2013 2013-07-24 /pmc/articles/PMC4057244/ /pubmed/23883571 http://dx.doi.org/10.1186/cc12837 Text en Copyright © 2013 Berg et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Berg, Agneta Rooyackers, Olav Bellander, Bo-Michael Wernerman, Jan Whole body protein kinetics during hypocaloric and normocaloric feeding in critically ill patients |
title | Whole body protein kinetics during hypocaloric and normocaloric feeding in critically ill patients |
title_full | Whole body protein kinetics during hypocaloric and normocaloric feeding in critically ill patients |
title_fullStr | Whole body protein kinetics during hypocaloric and normocaloric feeding in critically ill patients |
title_full_unstemmed | Whole body protein kinetics during hypocaloric and normocaloric feeding in critically ill patients |
title_short | Whole body protein kinetics during hypocaloric and normocaloric feeding in critically ill patients |
title_sort | whole body protein kinetics during hypocaloric and normocaloric feeding in critically ill patients |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4057244/ https://www.ncbi.nlm.nih.gov/pubmed/23883571 http://dx.doi.org/10.1186/cc12837 |
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