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Advanced glycation endproducts in sepsis and mechanical ventilation: extra or leading man?

Advanced glycation endproducts (AGEs) are primarily known as a complication in diabetic patients through their mediation of the inflammatory response. However, a variety of studies have demonstrated enhanced formation of AGEs in cardiovascular disorders. Despite the large number of AGEs produced dur...

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Detalles Bibliográficos
Autor principal: Baumann, Marcus
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2750142/
https://www.ncbi.nlm.nih.gov/pubmed/19664173
http://dx.doi.org/10.1186/cc7939
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author Baumann, Marcus
author_facet Baumann, Marcus
author_sort Baumann, Marcus
collection PubMed
description Advanced glycation endproducts (AGEs) are primarily known as a complication in diabetic patients through their mediation of the inflammatory response. However, a variety of studies have demonstrated enhanced formation of AGEs in cardiovascular disorders. Despite the large number of AGEs produced during the Maillard reaction, recent focus is on the major non-crosslinking AGE N(ε)-carboxymethyllysine. Kneyber and colleagues focused on sepsis-induced cardiac dysfunction and investigated whether myocardial inflammation is associated with enhanced cardiac AGE deposition and whether this is further enhanced by mechanical ventilation. They showed that both conditions are associated with enhanced AGE deposition and myocardial inflammation. Therefore, AGEs may participate in the inflammatory response related to cardiac dysfunction in critically ill patients. Moreover, life-saving ventilation stimulates AGE formation in these patients. This interesting study raises the question of whether AGEs in critically ill patients are a driving force of the disease.
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spelling pubmed-27501422010-07-14 Advanced glycation endproducts in sepsis and mechanical ventilation: extra or leading man? Baumann, Marcus Crit Care Commentary Advanced glycation endproducts (AGEs) are primarily known as a complication in diabetic patients through their mediation of the inflammatory response. However, a variety of studies have demonstrated enhanced formation of AGEs in cardiovascular disorders. Despite the large number of AGEs produced during the Maillard reaction, recent focus is on the major non-crosslinking AGE N(ε)-carboxymethyllysine. Kneyber and colleagues focused on sepsis-induced cardiac dysfunction and investigated whether myocardial inflammation is associated with enhanced cardiac AGE deposition and whether this is further enhanced by mechanical ventilation. They showed that both conditions are associated with enhanced AGE deposition and myocardial inflammation. Therefore, AGEs may participate in the inflammatory response related to cardiac dysfunction in critically ill patients. Moreover, life-saving ventilation stimulates AGE formation in these patients. This interesting study raises the question of whether AGEs in critically ill patients are a driving force of the disease. BioMed Central 2009 2009-07-14 /pmc/articles/PMC2750142/ /pubmed/19664173 http://dx.doi.org/10.1186/cc7939 Text en Copyright ©2009 BioMed Central Ltd
spellingShingle Commentary
Baumann, Marcus
Advanced glycation endproducts in sepsis and mechanical ventilation: extra or leading man?
title Advanced glycation endproducts in sepsis and mechanical ventilation: extra or leading man?
title_full Advanced glycation endproducts in sepsis and mechanical ventilation: extra or leading man?
title_fullStr Advanced glycation endproducts in sepsis and mechanical ventilation: extra or leading man?
title_full_unstemmed Advanced glycation endproducts in sepsis and mechanical ventilation: extra or leading man?
title_short Advanced glycation endproducts in sepsis and mechanical ventilation: extra or leading man?
title_sort advanced glycation endproducts in sepsis and mechanical ventilation: extra or leading man?
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2750142/
https://www.ncbi.nlm.nih.gov/pubmed/19664173
http://dx.doi.org/10.1186/cc7939
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