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Excess circulating angiopoietin-2 levels in sepsis: harbinger of death in the intensive care unit?

The early recognition and management of sepsis remain the greatest challenges in the field of critical care medicine. Endothelial injury is one of the hallmarks of sepsis, leading to capillary leak, microcirculatory dysfunction, organ failure, and eventual death in many critically ill patients. The...

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Detalles Bibliográficos
Autores principales: Giuliano, John S, Wheeler, Derek S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2688109/
https://www.ncbi.nlm.nih.gov/pubmed/19226440
http://dx.doi.org/10.1186/cc7685
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author Giuliano, John S
Wheeler, Derek S
author_facet Giuliano, John S
Wheeler, Derek S
author_sort Giuliano, John S
collection PubMed
description The early recognition and management of sepsis remain the greatest challenges in the field of critical care medicine. Endothelial injury is one of the hallmarks of sepsis, leading to capillary leak, microcirculatory dysfunction, organ failure, and eventual death in many critically ill patients. The angiogenic growth factors, angiopoietin (angpt)-1 and angpt-2, act upon the Tie-2 receptor in opposing roles. Angpt-2 has been found in abundance in septic patients when compared with healthy controls. In the study by Kümpers and colleagues in the previous issue of Critical Care, angpt-2 levels correlated with markers of tissue hypoxia, disease severity, and mortality in septic adults. However, the temporal kinetics of the angiopoietins were not assessed. It remains to be seen whether angpt-2 levels will function solely as an early marker of sepsis or whether the manipulation of the angpt/Tie-2 system will become a rational therapeutic target for the management of sepsis.
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spelling pubmed-26881092010-01-27 Excess circulating angiopoietin-2 levels in sepsis: harbinger of death in the intensive care unit? Giuliano, John S Wheeler, Derek S Crit Care Commentary The early recognition and management of sepsis remain the greatest challenges in the field of critical care medicine. Endothelial injury is one of the hallmarks of sepsis, leading to capillary leak, microcirculatory dysfunction, organ failure, and eventual death in many critically ill patients. The angiogenic growth factors, angiopoietin (angpt)-1 and angpt-2, act upon the Tie-2 receptor in opposing roles. Angpt-2 has been found in abundance in septic patients when compared with healthy controls. In the study by Kümpers and colleagues in the previous issue of Critical Care, angpt-2 levels correlated with markers of tissue hypoxia, disease severity, and mortality in septic adults. However, the temporal kinetics of the angiopoietins were not assessed. It remains to be seen whether angpt-2 levels will function solely as an early marker of sepsis or whether the manipulation of the angpt/Tie-2 system will become a rational therapeutic target for the management of sepsis. BioMed Central 2009 2009-01-27 /pmc/articles/PMC2688109/ /pubmed/19226440 http://dx.doi.org/10.1186/cc7685 Text en Copyright © 2009 BioMed Central Ltd
spellingShingle Commentary
Giuliano, John S
Wheeler, Derek S
Excess circulating angiopoietin-2 levels in sepsis: harbinger of death in the intensive care unit?
title Excess circulating angiopoietin-2 levels in sepsis: harbinger of death in the intensive care unit?
title_full Excess circulating angiopoietin-2 levels in sepsis: harbinger of death in the intensive care unit?
title_fullStr Excess circulating angiopoietin-2 levels in sepsis: harbinger of death in the intensive care unit?
title_full_unstemmed Excess circulating angiopoietin-2 levels in sepsis: harbinger of death in the intensive care unit?
title_short Excess circulating angiopoietin-2 levels in sepsis: harbinger of death in the intensive care unit?
title_sort excess circulating angiopoietin-2 levels in sepsis: harbinger of death in the intensive care unit?
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2688109/
https://www.ncbi.nlm.nih.gov/pubmed/19226440
http://dx.doi.org/10.1186/cc7685
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