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Genetic Polymorphisms and Posttraumatic Complications

Major trauma is the leading cause of death in young adults. Despite advances in prehospital system and treatment in hospital, mortality rates have not improved significantly over the past decades. Victims of severe injuries who survive the initial hours have great risk for additional life-threatenin...

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Detalles Bibliográficos
Autores principales: Gu, Wei, Jiang, Jianxin
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025375/
https://www.ncbi.nlm.nih.gov/pubmed/21274447
http://dx.doi.org/10.1155/2010/814086
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author Gu, Wei
Jiang, Jianxin
author_facet Gu, Wei
Jiang, Jianxin
author_sort Gu, Wei
collection PubMed
description Major trauma is the leading cause of death in young adults. Despite advances in prehospital system and treatment in hospital, mortality rates have not improved significantly over the past decades. Victims of severe injuries who survive the initial hours have great risk for additional life-threatening complicaitons, including uncontrollable infection (sepsis) and multiple organ dysfunction syndrome (MODS). Single nucleotide polymorphisms (SNPs) have been shown to affect susceptibility to the course of numerous diseases. Accumulating evidence suggests that genetic backgrounds also play important roles in posttraumatic complications. Genetic polymorphisms may become powerful biomarkers for diagnosis and prognosis of trauma-induced complications. Recent advances in studies on associations between genetic polymorphisms and sepsis or MODS have led to better understanding of posttraumatic complications. Here we summarise recent findings on genetic variations in molecules of the innate immune system and other systems as well as their connection with susceptibility to posttraumatic complications.
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spelling pubmed-30253752011-01-27 Genetic Polymorphisms and Posttraumatic Complications Gu, Wei Jiang, Jianxin Comp Funct Genomics Review Article Major trauma is the leading cause of death in young adults. Despite advances in prehospital system and treatment in hospital, mortality rates have not improved significantly over the past decades. Victims of severe injuries who survive the initial hours have great risk for additional life-threatening complicaitons, including uncontrollable infection (sepsis) and multiple organ dysfunction syndrome (MODS). Single nucleotide polymorphisms (SNPs) have been shown to affect susceptibility to the course of numerous diseases. Accumulating evidence suggests that genetic backgrounds also play important roles in posttraumatic complications. Genetic polymorphisms may become powerful biomarkers for diagnosis and prognosis of trauma-induced complications. Recent advances in studies on associations between genetic polymorphisms and sepsis or MODS have led to better understanding of posttraumatic complications. Here we summarise recent findings on genetic variations in molecules of the innate immune system and other systems as well as their connection with susceptibility to posttraumatic complications. Hindawi Publishing Corporation 2010 2011-01-11 /pmc/articles/PMC3025375/ /pubmed/21274447 http://dx.doi.org/10.1155/2010/814086 Text en Copyright © 2010 W. Gu and J. Jiang. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Gu, Wei
Jiang, Jianxin
Genetic Polymorphisms and Posttraumatic Complications
title Genetic Polymorphisms and Posttraumatic Complications
title_full Genetic Polymorphisms and Posttraumatic Complications
title_fullStr Genetic Polymorphisms and Posttraumatic Complications
title_full_unstemmed Genetic Polymorphisms and Posttraumatic Complications
title_short Genetic Polymorphisms and Posttraumatic Complications
title_sort genetic polymorphisms and posttraumatic complications
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3025375/
https://www.ncbi.nlm.nih.gov/pubmed/21274447
http://dx.doi.org/10.1155/2010/814086
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