Cargando…

Evaluation of mRNA Biomarkers to Identify Risk of Hospital Acquired Infections in Children Admitted to Paediatric Intensive Care Unit

OBJECTIVES: Hospital-acquired infections (HAI) are associated with significant mortality and morbidity and prolongation of hospital stay, adding strain on limited hospital resources. Despite stringent infection control practices some children remain at high risk of developing HAI. The development of...

Descripción completa

Detalles Bibliográficos
Autores principales: Peronnet, Estelle, Nguyen, Kha, Cerrato, Elisabeth, Guhadasan, Rathi, Venet, Fabienne, Textoris, Julien, Pachot, Alexandre, Monneret, Guillaume, Carrol, Enitan Delphine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807819/
https://www.ncbi.nlm.nih.gov/pubmed/27015534
http://dx.doi.org/10.1371/journal.pone.0152388
_version_ 1782423425039466496
author Peronnet, Estelle
Nguyen, Kha
Cerrato, Elisabeth
Guhadasan, Rathi
Venet, Fabienne
Textoris, Julien
Pachot, Alexandre
Monneret, Guillaume
Carrol, Enitan Delphine
author_facet Peronnet, Estelle
Nguyen, Kha
Cerrato, Elisabeth
Guhadasan, Rathi
Venet, Fabienne
Textoris, Julien
Pachot, Alexandre
Monneret, Guillaume
Carrol, Enitan Delphine
author_sort Peronnet, Estelle
collection PubMed
description OBJECTIVES: Hospital-acquired infections (HAI) are associated with significant mortality and morbidity and prolongation of hospital stay, adding strain on limited hospital resources. Despite stringent infection control practices some children remain at high risk of developing HAI. The development of biomarkers which could identify these patients would be useful. In this study our objective was to evaluate mRNA candidate biomarkers for HAI prediction in a pediatric intensive care unit. DESIGN: Serial blood samples were collected from patients admitted to pediatric intensive care unit between March and June 2012. Candidate gene expression (IL1B, TNF, IL10, CD3D, BCL2, BID) was quantified using RT-qPCR. Comparisons of relative gene expression between those that did not develop HAI versus those that did were performed using Mann Whitney U-test. PATIENTS: Exclusion criteria were: age <28 days or ≥16 years, expected length of stay < 24 hours, expected survival < 28 days, end-stage renal disease and end-stage liver disease. Finally, 45 children were included in this study. MAIN RESULTS: The overall HAI rate was 30% of which 62% were respiratory infections. Children who developed HAI had a three-fold increase in hospital stay compared to those who did not (27 days versus 9 days, p<0.001). An increased expression of cytokine genes (IL1B and IL10) was observed in patients who developed HAI, as well as a pro-apoptosis pattern (higher expression of BID and lower expression of BCL2). CD3D, a key TCR co-factor was also significantly down-modulated in patients who developed HAI. CONCLUSIONS: To our knowledge, this is the first study of mRNA biomarkers of HAI in the paediatric population. Increased mRNA expressions of anti-inflammatory cytokine and modulation of apoptotic genes suggest the development of immunosuppression in critically ill children. Immune monitoring using a panel of genes may offer a novel stratification tool to identify HAI risk.
format Online
Article
Text
id pubmed-4807819
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-48078192016-04-05 Evaluation of mRNA Biomarkers to Identify Risk of Hospital Acquired Infections in Children Admitted to Paediatric Intensive Care Unit Peronnet, Estelle Nguyen, Kha Cerrato, Elisabeth Guhadasan, Rathi Venet, Fabienne Textoris, Julien Pachot, Alexandre Monneret, Guillaume Carrol, Enitan Delphine PLoS One Research Article OBJECTIVES: Hospital-acquired infections (HAI) are associated with significant mortality and morbidity and prolongation of hospital stay, adding strain on limited hospital resources. Despite stringent infection control practices some children remain at high risk of developing HAI. The development of biomarkers which could identify these patients would be useful. In this study our objective was to evaluate mRNA candidate biomarkers for HAI prediction in a pediatric intensive care unit. DESIGN: Serial blood samples were collected from patients admitted to pediatric intensive care unit between March and June 2012. Candidate gene expression (IL1B, TNF, IL10, CD3D, BCL2, BID) was quantified using RT-qPCR. Comparisons of relative gene expression between those that did not develop HAI versus those that did were performed using Mann Whitney U-test. PATIENTS: Exclusion criteria were: age <28 days or ≥16 years, expected length of stay < 24 hours, expected survival < 28 days, end-stage renal disease and end-stage liver disease. Finally, 45 children were included in this study. MAIN RESULTS: The overall HAI rate was 30% of which 62% were respiratory infections. Children who developed HAI had a three-fold increase in hospital stay compared to those who did not (27 days versus 9 days, p<0.001). An increased expression of cytokine genes (IL1B and IL10) was observed in patients who developed HAI, as well as a pro-apoptosis pattern (higher expression of BID and lower expression of BCL2). CD3D, a key TCR co-factor was also significantly down-modulated in patients who developed HAI. CONCLUSIONS: To our knowledge, this is the first study of mRNA biomarkers of HAI in the paediatric population. Increased mRNA expressions of anti-inflammatory cytokine and modulation of apoptotic genes suggest the development of immunosuppression in critically ill children. Immune monitoring using a panel of genes may offer a novel stratification tool to identify HAI risk. Public Library of Science 2016-03-25 /pmc/articles/PMC4807819/ /pubmed/27015534 http://dx.doi.org/10.1371/journal.pone.0152388 Text en © 2016 Peronnet et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Peronnet, Estelle
Nguyen, Kha
Cerrato, Elisabeth
Guhadasan, Rathi
Venet, Fabienne
Textoris, Julien
Pachot, Alexandre
Monneret, Guillaume
Carrol, Enitan Delphine
Evaluation of mRNA Biomarkers to Identify Risk of Hospital Acquired Infections in Children Admitted to Paediatric Intensive Care Unit
title Evaluation of mRNA Biomarkers to Identify Risk of Hospital Acquired Infections in Children Admitted to Paediatric Intensive Care Unit
title_full Evaluation of mRNA Biomarkers to Identify Risk of Hospital Acquired Infections in Children Admitted to Paediatric Intensive Care Unit
title_fullStr Evaluation of mRNA Biomarkers to Identify Risk of Hospital Acquired Infections in Children Admitted to Paediatric Intensive Care Unit
title_full_unstemmed Evaluation of mRNA Biomarkers to Identify Risk of Hospital Acquired Infections in Children Admitted to Paediatric Intensive Care Unit
title_short Evaluation of mRNA Biomarkers to Identify Risk of Hospital Acquired Infections in Children Admitted to Paediatric Intensive Care Unit
title_sort evaluation of mrna biomarkers to identify risk of hospital acquired infections in children admitted to paediatric intensive care unit
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4807819/
https://www.ncbi.nlm.nih.gov/pubmed/27015534
http://dx.doi.org/10.1371/journal.pone.0152388
work_keys_str_mv AT peronnetestelle evaluationofmrnabiomarkerstoidentifyriskofhospitalacquiredinfectionsinchildrenadmittedtopaediatricintensivecareunit
AT nguyenkha evaluationofmrnabiomarkerstoidentifyriskofhospitalacquiredinfectionsinchildrenadmittedtopaediatricintensivecareunit
AT cerratoelisabeth evaluationofmrnabiomarkerstoidentifyriskofhospitalacquiredinfectionsinchildrenadmittedtopaediatricintensivecareunit
AT guhadasanrathi evaluationofmrnabiomarkerstoidentifyriskofhospitalacquiredinfectionsinchildrenadmittedtopaediatricintensivecareunit
AT venetfabienne evaluationofmrnabiomarkerstoidentifyriskofhospitalacquiredinfectionsinchildrenadmittedtopaediatricintensivecareunit
AT textorisjulien evaluationofmrnabiomarkerstoidentifyriskofhospitalacquiredinfectionsinchildrenadmittedtopaediatricintensivecareunit
AT pachotalexandre evaluationofmrnabiomarkerstoidentifyriskofhospitalacquiredinfectionsinchildrenadmittedtopaediatricintensivecareunit
AT monneretguillaume evaluationofmrnabiomarkerstoidentifyriskofhospitalacquiredinfectionsinchildrenadmittedtopaediatricintensivecareunit
AT carrolenitandelphine evaluationofmrnabiomarkerstoidentifyriskofhospitalacquiredinfectionsinchildrenadmittedtopaediatricintensivecareunit