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Multiple gene-to-gene interactions in children with sepsis: a combination of five gene variants predicts outcome of life-threatening sepsis

INTRODUCTION: The aim of the study was to identify the dependency structure of genetic variants that can influence the outcome for paediatric patients with sepsis. METHODS: We evaluated the role of single nucleotide polymorphisms for five genes: bactericidal permeability increasing protein (BPI; rs5...

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Autores principales: Jabandziev, Petr, Smerek, Michal, Michalek, Jaroslav, Fedora, Michal, Kosinova, Lucie, Hubacek, Jaroslav A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056441/
https://www.ncbi.nlm.nih.gov/pubmed/24383711
http://dx.doi.org/10.1186/cc13174
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author Jabandziev, Petr
Smerek, Michal
Michalek, Jaroslav
Fedora, Michal
Kosinova, Lucie
Hubacek, Jaroslav A
Michalek, Jaroslav
author_facet Jabandziev, Petr
Smerek, Michal
Michalek, Jaroslav
Fedora, Michal
Kosinova, Lucie
Hubacek, Jaroslav A
Michalek, Jaroslav
author_sort Jabandziev, Petr
collection PubMed
description INTRODUCTION: The aim of the study was to identify the dependency structure of genetic variants that can influence the outcome for paediatric patients with sepsis. METHODS: We evaluated the role of single nucleotide polymorphisms for five genes: bactericidal permeability increasing protein (BPI; rs5743507), lipopolysaccharide-binding protein (LBP; rs2232618), toll-like receptor 4 (TLR4; rs4986790), heat shock protein 70 (HSP 70; rs2227956), and interleukin 6 (IL-6; rs1800795) in 598 children aged 0 to 19 years that were admitted to a paediatric intensive care unit with fever, systemic inflammatory response syndrome, sepsis, severe sepsis, septic shock, or multiple organ dysfunction syndrome. A control group of 529 healthy individuals was included. Multi-way contingency tables were constructed and statistically evaluated using log-linear models. Typical gene combinations were found for both study groups. RESULTS: Detailed analyses of the five studied gene profiles revealed significant differences in sepsis survival. Stratification into high-risk, intermediate-risk, and low-risk groups of paediatric patients can predict the severity of sepsis. CONCLUSIONS: Analysis of single nucleotide polymorphisms for five genes can be used as a predictor of sepsis outcome in children.
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spelling pubmed-40564412014-06-14 Multiple gene-to-gene interactions in children with sepsis: a combination of five gene variants predicts outcome of life-threatening sepsis Jabandziev, Petr Smerek, Michal Michalek, Jaroslav Fedora, Michal Kosinova, Lucie Hubacek, Jaroslav A Michalek, Jaroslav Crit Care Research INTRODUCTION: The aim of the study was to identify the dependency structure of genetic variants that can influence the outcome for paediatric patients with sepsis. METHODS: We evaluated the role of single nucleotide polymorphisms for five genes: bactericidal permeability increasing protein (BPI; rs5743507), lipopolysaccharide-binding protein (LBP; rs2232618), toll-like receptor 4 (TLR4; rs4986790), heat shock protein 70 (HSP 70; rs2227956), and interleukin 6 (IL-6; rs1800795) in 598 children aged 0 to 19 years that were admitted to a paediatric intensive care unit with fever, systemic inflammatory response syndrome, sepsis, severe sepsis, septic shock, or multiple organ dysfunction syndrome. A control group of 529 healthy individuals was included. Multi-way contingency tables were constructed and statistically evaluated using log-linear models. Typical gene combinations were found for both study groups. RESULTS: Detailed analyses of the five studied gene profiles revealed significant differences in sepsis survival. Stratification into high-risk, intermediate-risk, and low-risk groups of paediatric patients can predict the severity of sepsis. CONCLUSIONS: Analysis of single nucleotide polymorphisms for five genes can be used as a predictor of sepsis outcome in children. BioMed Central 2014 2014-01-02 /pmc/articles/PMC4056441/ /pubmed/24383711 http://dx.doi.org/10.1186/cc13174 Text en Copyright © 2014 Jabandziev 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
Jabandziev, Petr
Smerek, Michal
Michalek, Jaroslav
Fedora, Michal
Kosinova, Lucie
Hubacek, Jaroslav A
Michalek, Jaroslav
Multiple gene-to-gene interactions in children with sepsis: a combination of five gene variants predicts outcome of life-threatening sepsis
title Multiple gene-to-gene interactions in children with sepsis: a combination of five gene variants predicts outcome of life-threatening sepsis
title_full Multiple gene-to-gene interactions in children with sepsis: a combination of five gene variants predicts outcome of life-threatening sepsis
title_fullStr Multiple gene-to-gene interactions in children with sepsis: a combination of five gene variants predicts outcome of life-threatening sepsis
title_full_unstemmed Multiple gene-to-gene interactions in children with sepsis: a combination of five gene variants predicts outcome of life-threatening sepsis
title_short Multiple gene-to-gene interactions in children with sepsis: a combination of five gene variants predicts outcome of life-threatening sepsis
title_sort multiple gene-to-gene interactions in children with sepsis: a combination of five gene variants predicts outcome of life-threatening sepsis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4056441/
https://www.ncbi.nlm.nih.gov/pubmed/24383711
http://dx.doi.org/10.1186/cc13174
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