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Transcriptomic biomarkers of the response of hospitalized geriatric patients with infectious diseases
BACKGROUND: Infectious diseases are significant causes of morbidity and mortality among elderly populations. However, the relationship between oxidative stress, immune function and inflammatory response in acute phase of the infectious disease is poorly understood. RESULTS: Herein the abundance of a...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2933667/ https://www.ncbi.nlm.nih.gov/pubmed/20716329 http://dx.doi.org/10.1186/1742-4933-7-9 |
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author | Vo, Thi Kim Duy Godard, Patrice de Saint-Hubert, Marie Morrhaye, Gabriel Swine, Christian Geenen, Vincent Martens, Henri J Debacq-Chainiaux, Florence Toussaint, Olivier |
author_facet | Vo, Thi Kim Duy Godard, Patrice de Saint-Hubert, Marie Morrhaye, Gabriel Swine, Christian Geenen, Vincent Martens, Henri J Debacq-Chainiaux, Florence Toussaint, Olivier |
author_sort | Vo, Thi Kim Duy |
collection | PubMed |
description | BACKGROUND: Infectious diseases are significant causes of morbidity and mortality among elderly populations. However, the relationship between oxidative stress, immune function and inflammatory response in acute phase of the infectious disease is poorly understood. RESULTS: Herein the abundance of a selection of 148 transcripts involved in immunosenescence and stress response was compared in total RNA of PBMC of 28 healthy aged probands and 39 aged patients in acute phase of infectious disease (day 2-4 after hospitalization) or in convalescence phase (day 7-10). This study provides a list of 24 differentially abundant transcript species in the acute phase versus healthy aged. For instance, transcripts associated with inflammatory and anti-inflammatory reactions (TNFRSF1A, IL1R1, IL1R2, IL10RB) and with oxidative stress (HMOX1, GPX1, SOD2, PRDX6) were more abundant while those associated with T-cell functions (CD28, CD69, LCK) were less abundant in acute phase. The abundance of seven of these transcripts (CD28, CD69, LCK, CTSD, HMOX1, TNFRSF1A and PRDX6) was already known to be altered in healthy aged probands compared to healthy young ones and was further affected in aged patients in acute phase, compromising an efficient response. CONCLUSION: This work provides insights of the state of acute phase response to infections in elderly patients and could explain further the lack of appropriate response in the elderly compared to younger persons. |
format | Text |
id | pubmed-2933667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29336672010-09-07 Transcriptomic biomarkers of the response of hospitalized geriatric patients with infectious diseases Vo, Thi Kim Duy Godard, Patrice de Saint-Hubert, Marie Morrhaye, Gabriel Swine, Christian Geenen, Vincent Martens, Henri J Debacq-Chainiaux, Florence Toussaint, Olivier Immun Ageing Research BACKGROUND: Infectious diseases are significant causes of morbidity and mortality among elderly populations. However, the relationship between oxidative stress, immune function and inflammatory response in acute phase of the infectious disease is poorly understood. RESULTS: Herein the abundance of a selection of 148 transcripts involved in immunosenescence and stress response was compared in total RNA of PBMC of 28 healthy aged probands and 39 aged patients in acute phase of infectious disease (day 2-4 after hospitalization) or in convalescence phase (day 7-10). This study provides a list of 24 differentially abundant transcript species in the acute phase versus healthy aged. For instance, transcripts associated with inflammatory and anti-inflammatory reactions (TNFRSF1A, IL1R1, IL1R2, IL10RB) and with oxidative stress (HMOX1, GPX1, SOD2, PRDX6) were more abundant while those associated with T-cell functions (CD28, CD69, LCK) were less abundant in acute phase. The abundance of seven of these transcripts (CD28, CD69, LCK, CTSD, HMOX1, TNFRSF1A and PRDX6) was already known to be altered in healthy aged probands compared to healthy young ones and was further affected in aged patients in acute phase, compromising an efficient response. CONCLUSION: This work provides insights of the state of acute phase response to infections in elderly patients and could explain further the lack of appropriate response in the elderly compared to younger persons. BioMed Central 2010-08-17 /pmc/articles/PMC2933667/ /pubmed/20716329 http://dx.doi.org/10.1186/1742-4933-7-9 Text en Copyright ©2010 Vo 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 Vo, Thi Kim Duy Godard, Patrice de Saint-Hubert, Marie Morrhaye, Gabriel Swine, Christian Geenen, Vincent Martens, Henri J Debacq-Chainiaux, Florence Toussaint, Olivier Transcriptomic biomarkers of the response of hospitalized geriatric patients with infectious diseases |
title | Transcriptomic biomarkers of the response of hospitalized geriatric patients with infectious diseases |
title_full | Transcriptomic biomarkers of the response of hospitalized geriatric patients with infectious diseases |
title_fullStr | Transcriptomic biomarkers of the response of hospitalized geriatric patients with infectious diseases |
title_full_unstemmed | Transcriptomic biomarkers of the response of hospitalized geriatric patients with infectious diseases |
title_short | Transcriptomic biomarkers of the response of hospitalized geriatric patients with infectious diseases |
title_sort | transcriptomic biomarkers of the response of hospitalized geriatric patients with infectious diseases |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2933667/ https://www.ncbi.nlm.nih.gov/pubmed/20716329 http://dx.doi.org/10.1186/1742-4933-7-9 |
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