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Clinical relevance of the interleukin 10 promoter polymorphisms in Chinese Han patients with major trauma: genetic association studies

INTRODUCTION: An excessive inflammatory response is thought to account for the pathogenesis of sepsis and multiple organ dysfunction syndrome (MODS) after severe trauma. The interleukin-10 (IL-10) is a potent anti-inflammatory cytokine. The objectives of this prospective study were to investigate th...

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Autores principales: Zeng, Ling, Gu, Wei, Chen, Kehong, Jiang, Dongpo, Zhang, Lianyang, Du, Dingyuan, Hu, Ping, Liu, Qing, Huang, Suna, Jiang, Jianxin
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2811917/
https://www.ncbi.nlm.nih.gov/pubmed/19939284
http://dx.doi.org/10.1186/cc8182
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author Zeng, Ling
Gu, Wei
Chen, Kehong
Jiang, Dongpo
Zhang, Lianyang
Du, Dingyuan
Hu, Ping
Liu, Qing
Huang, Suna
Jiang, Jianxin
author_facet Zeng, Ling
Gu, Wei
Chen, Kehong
Jiang, Dongpo
Zhang, Lianyang
Du, Dingyuan
Hu, Ping
Liu, Qing
Huang, Suna
Jiang, Jianxin
author_sort Zeng, Ling
collection PubMed
description INTRODUCTION: An excessive inflammatory response is thought to account for the pathogenesis of sepsis and multiple organ dysfunction syndrome (MODS) after severe trauma. The interleukin-10 (IL-10) is a potent anti-inflammatory cytokine. The objectives of this prospective study were to investigate the distribution of IL-10 promoter polymorphisms in a cohort of 308 Chinese Han patients with major trauma, and to identify associations of IL-10 promoter polymorphisms with IL-10 production and incidence of sepsis and MODS. METHODS: A total of 308 patients with major trauma were included in this study. The genotypes of polymorphisms -1082, -819 and -592 were determined by polymerase chain reaction-restriction fragment length polymorphism. The IL-10 levels in the supernatants were determined with enzyme-linked immunoabsorbent assay. RESULTS: The -1082A and -592A alleles were significantly associated with lower lipopolysaccharide-induced IL-10 production in an allele-dose dependent fashion. There was no significant difference for the -819 polymorphism. Except for the -1082 polymorphism, the -819 and -592 polymorphisms were not significantly associated with sepsis morbidity rate and MOD scores. CONCLUSIONS: Our results further confirm the functionality of the IL-10 promoter single nucleotide polymorphisms in relation to IL-10 production. They also suggest that individual difference in IL-10 production in trauma patients might be at least in part related to genetic variations in the IL-10 promoter region.
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spelling pubmed-28119172010-01-28 Clinical relevance of the interleukin 10 promoter polymorphisms in Chinese Han patients with major trauma: genetic association studies Zeng, Ling Gu, Wei Chen, Kehong Jiang, Dongpo Zhang, Lianyang Du, Dingyuan Hu, Ping Liu, Qing Huang, Suna Jiang, Jianxin Crit Care Research INTRODUCTION: An excessive inflammatory response is thought to account for the pathogenesis of sepsis and multiple organ dysfunction syndrome (MODS) after severe trauma. The interleukin-10 (IL-10) is a potent anti-inflammatory cytokine. The objectives of this prospective study were to investigate the distribution of IL-10 promoter polymorphisms in a cohort of 308 Chinese Han patients with major trauma, and to identify associations of IL-10 promoter polymorphisms with IL-10 production and incidence of sepsis and MODS. METHODS: A total of 308 patients with major trauma were included in this study. The genotypes of polymorphisms -1082, -819 and -592 were determined by polymerase chain reaction-restriction fragment length polymorphism. The IL-10 levels in the supernatants were determined with enzyme-linked immunoabsorbent assay. RESULTS: The -1082A and -592A alleles were significantly associated with lower lipopolysaccharide-induced IL-10 production in an allele-dose dependent fashion. There was no significant difference for the -819 polymorphism. Except for the -1082 polymorphism, the -819 and -592 polymorphisms were not significantly associated with sepsis morbidity rate and MOD scores. CONCLUSIONS: Our results further confirm the functionality of the IL-10 promoter single nucleotide polymorphisms in relation to IL-10 production. They also suggest that individual difference in IL-10 production in trauma patients might be at least in part related to genetic variations in the IL-10 promoter region. BioMed Central 2009 2009-11-26 /pmc/articles/PMC2811917/ /pubmed/19939284 http://dx.doi.org/10.1186/cc8182 Text en Copyright ©2009 Zeng 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
Zeng, Ling
Gu, Wei
Chen, Kehong
Jiang, Dongpo
Zhang, Lianyang
Du, Dingyuan
Hu, Ping
Liu, Qing
Huang, Suna
Jiang, Jianxin
Clinical relevance of the interleukin 10 promoter polymorphisms in Chinese Han patients with major trauma: genetic association studies
title Clinical relevance of the interleukin 10 promoter polymorphisms in Chinese Han patients with major trauma: genetic association studies
title_full Clinical relevance of the interleukin 10 promoter polymorphisms in Chinese Han patients with major trauma: genetic association studies
title_fullStr Clinical relevance of the interleukin 10 promoter polymorphisms in Chinese Han patients with major trauma: genetic association studies
title_full_unstemmed Clinical relevance of the interleukin 10 promoter polymorphisms in Chinese Han patients with major trauma: genetic association studies
title_short Clinical relevance of the interleukin 10 promoter polymorphisms in Chinese Han patients with major trauma: genetic association studies
title_sort clinical relevance of the interleukin 10 promoter polymorphisms in chinese han patients with major trauma: genetic association studies
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2811917/
https://www.ncbi.nlm.nih.gov/pubmed/19939284
http://dx.doi.org/10.1186/cc8182
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