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Adiponectin, retinol-binding protein 4, and leptin in protracted critical illness of pulmonary origin

INTRODUCTION: Critically ill patients requiring intensive care uniformly develop insulin resistance. This is most pronounced in patients with sepsis. Recently, several hormones secreted by adipose tissue have been identified to be involved in overall insulin sensitivity in metabolic syndrome-related...

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Autores principales: Langouche, Lies, Vander Perre, Sarah, Frystyk, Jan, Flyvbjerg, Allan, Hansen, Troels Krarup, Van den Berghe, Greet
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2750156/
https://www.ncbi.nlm.nih.gov/pubmed/19589139
http://dx.doi.org/10.1186/cc7956
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author Langouche, Lies
Vander Perre, Sarah
Frystyk, Jan
Flyvbjerg, Allan
Hansen, Troels Krarup
Van den Berghe, Greet
author_facet Langouche, Lies
Vander Perre, Sarah
Frystyk, Jan
Flyvbjerg, Allan
Hansen, Troels Krarup
Van den Berghe, Greet
author_sort Langouche, Lies
collection PubMed
description INTRODUCTION: Critically ill patients requiring intensive care uniformly develop insulin resistance. This is most pronounced in patients with sepsis. Recently, several hormones secreted by adipose tissue have been identified to be involved in overall insulin sensitivity in metabolic syndrome-related conditions. However, little is known about these adipokines in critical illness. METHODS: We studied circulating levels of the adipokines adiponectin, retinol-binding protein 4 (RBP4), and leptin during critical illness, and the impact of intensive insulin therapy, a therapy shown to affect insulin sensitivity, in serum samples from prolonged critically ill patients with a respiratory critical illness (n = 318). For comparison, we studied healthy subjects (n = 22) and acutely stressed patients (n = 22). RESULTS: During acute critical illness, circulating levels of adiponectin, RBP4, and leptin were low. Patients with sepsis had lower levels of leptin and RBP4 than did nonseptic patients. When critical illness was sustained, adipokine levels returned to normal reference values. Insulin therapy enhanced adiponectin, blunted the rise of RBP4, and did not alter leptin levels. CONCLUSIONS: Acute critical illness is associated with immediate, but transiently low serum adipokine levels. Adiponectin and RBP4 are associated with altered insulin resistance in critical illness.
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spelling pubmed-27501562009-09-25 Adiponectin, retinol-binding protein 4, and leptin in protracted critical illness of pulmonary origin Langouche, Lies Vander Perre, Sarah Frystyk, Jan Flyvbjerg, Allan Hansen, Troels Krarup Van den Berghe, Greet Crit Care Research INTRODUCTION: Critically ill patients requiring intensive care uniformly develop insulin resistance. This is most pronounced in patients with sepsis. Recently, several hormones secreted by adipose tissue have been identified to be involved in overall insulin sensitivity in metabolic syndrome-related conditions. However, little is known about these adipokines in critical illness. METHODS: We studied circulating levels of the adipokines adiponectin, retinol-binding protein 4 (RBP4), and leptin during critical illness, and the impact of intensive insulin therapy, a therapy shown to affect insulin sensitivity, in serum samples from prolonged critically ill patients with a respiratory critical illness (n = 318). For comparison, we studied healthy subjects (n = 22) and acutely stressed patients (n = 22). RESULTS: During acute critical illness, circulating levels of adiponectin, RBP4, and leptin were low. Patients with sepsis had lower levels of leptin and RBP4 than did nonseptic patients. When critical illness was sustained, adipokine levels returned to normal reference values. Insulin therapy enhanced adiponectin, blunted the rise of RBP4, and did not alter leptin levels. CONCLUSIONS: Acute critical illness is associated with immediate, but transiently low serum adipokine levels. Adiponectin and RBP4 are associated with altered insulin resistance in critical illness. BioMed Central 2009 2009-07-09 /pmc/articles/PMC2750156/ /pubmed/19589139 http://dx.doi.org/10.1186/cc7956 Text en Copyright ©2009 Langouche 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
Langouche, Lies
Vander Perre, Sarah
Frystyk, Jan
Flyvbjerg, Allan
Hansen, Troels Krarup
Van den Berghe, Greet
Adiponectin, retinol-binding protein 4, and leptin in protracted critical illness of pulmonary origin
title Adiponectin, retinol-binding protein 4, and leptin in protracted critical illness of pulmonary origin
title_full Adiponectin, retinol-binding protein 4, and leptin in protracted critical illness of pulmonary origin
title_fullStr Adiponectin, retinol-binding protein 4, and leptin in protracted critical illness of pulmonary origin
title_full_unstemmed Adiponectin, retinol-binding protein 4, and leptin in protracted critical illness of pulmonary origin
title_short Adiponectin, retinol-binding protein 4, and leptin in protracted critical illness of pulmonary origin
title_sort adiponectin, retinol-binding protein 4, and leptin in protracted critical illness of pulmonary origin
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2750156/
https://www.ncbi.nlm.nih.gov/pubmed/19589139
http://dx.doi.org/10.1186/cc7956
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