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Association between age and the host response in critically ill patients with sepsis
BACKGROUND: The association of ageing with increased sepsis mortality is well established. Nonetheless, current investigations on the influence of age on host response aberrations are largely limited to plasma cytokine levels while neglecting other pathophysiological sepsis domains like endothelial...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747080/ https://www.ncbi.nlm.nih.gov/pubmed/36514130 http://dx.doi.org/10.1186/s13054-022-04266-9 |
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author | Michels, Erik H. A. Butler, Joe M. Reijnders, Tom D. Y. Cremer, Olaf L. Scicluna, Brendon P. Uhel, Fabrice Peters-Sengers, Hessel Schultz, Marcus J. Knight, Julian C. van Vught, Lonneke A. van der Poll, Tom |
author_facet | Michels, Erik H. A. Butler, Joe M. Reijnders, Tom D. Y. Cremer, Olaf L. Scicluna, Brendon P. Uhel, Fabrice Peters-Sengers, Hessel Schultz, Marcus J. Knight, Julian C. van Vught, Lonneke A. van der Poll, Tom |
author_sort | Michels, Erik H. A. |
collection | PubMed |
description | BACKGROUND: The association of ageing with increased sepsis mortality is well established. Nonetheless, current investigations on the influence of age on host response aberrations are largely limited to plasma cytokine levels while neglecting other pathophysiological sepsis domains like endothelial cell activation and function, and coagulation activation. The primary objective of this study was to gain insight into the association of ageing with aberrations in key host response pathways and blood transcriptomes in sepsis. METHODS: We analysed the clinical outcome (n = 1952), 16 plasma biomarkers providing insight in deregulation of specific pathophysiological domains (n = 899), and blood leukocyte transcriptomes (n = 488) of sepsis patients stratified according to age decades. Blood transcriptome results were validated in an independent sepsis cohort and compared with healthy individuals. RESULTS: Older age was associated with increased mortality independent of comorbidities and disease severity. Ageing was associated with lower endothelial cell activation and dysfunction, and similar inflammation and coagulation activation, despite higher disease severity scores. Blood leukocytes of patients ≥ 70 years, compared to patients < 50 years, showed decreased expression of genes involved in cytokine signaling, and innate and adaptive immunity, and increased expression of genes involved in hemostasis and endothelial cell activation. The diminished expression of gene pathways related to innate immunity and cytokine signaling in subjects ≥ 70 years was sepsis-induced, as healthy subjects ≥ 70 years showed enhanced expression of these pathways compared to healthy individuals < 50 years. CONCLUSIONS: This study provides novel evidence that older age is associated with relatively mitigated sepsis-induced endothelial cell activation and dysfunction, and a blood leukocyte transcriptome signature indicating impaired innate immune and cytokine signaling. These data suggest that age should be considered in patient selection in future sepsis trials targeting the immune system and/or the endothelial cell response. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-022-04266-9. |
format | Online Article Text |
id | pubmed-9747080 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-97470802022-12-14 Association between age and the host response in critically ill patients with sepsis Michels, Erik H. A. Butler, Joe M. Reijnders, Tom D. Y. Cremer, Olaf L. Scicluna, Brendon P. Uhel, Fabrice Peters-Sengers, Hessel Schultz, Marcus J. Knight, Julian C. van Vught, Lonneke A. van der Poll, Tom Crit Care Research BACKGROUND: The association of ageing with increased sepsis mortality is well established. Nonetheless, current investigations on the influence of age on host response aberrations are largely limited to plasma cytokine levels while neglecting other pathophysiological sepsis domains like endothelial cell activation and function, and coagulation activation. The primary objective of this study was to gain insight into the association of ageing with aberrations in key host response pathways and blood transcriptomes in sepsis. METHODS: We analysed the clinical outcome (n = 1952), 16 plasma biomarkers providing insight in deregulation of specific pathophysiological domains (n = 899), and blood leukocyte transcriptomes (n = 488) of sepsis patients stratified according to age decades. Blood transcriptome results were validated in an independent sepsis cohort and compared with healthy individuals. RESULTS: Older age was associated with increased mortality independent of comorbidities and disease severity. Ageing was associated with lower endothelial cell activation and dysfunction, and similar inflammation and coagulation activation, despite higher disease severity scores. Blood leukocytes of patients ≥ 70 years, compared to patients < 50 years, showed decreased expression of genes involved in cytokine signaling, and innate and adaptive immunity, and increased expression of genes involved in hemostasis and endothelial cell activation. The diminished expression of gene pathways related to innate immunity and cytokine signaling in subjects ≥ 70 years was sepsis-induced, as healthy subjects ≥ 70 years showed enhanced expression of these pathways compared to healthy individuals < 50 years. CONCLUSIONS: This study provides novel evidence that older age is associated with relatively mitigated sepsis-induced endothelial cell activation and dysfunction, and a blood leukocyte transcriptome signature indicating impaired innate immune and cytokine signaling. These data suggest that age should be considered in patient selection in future sepsis trials targeting the immune system and/or the endothelial cell response. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13054-022-04266-9. BioMed Central 2022-12-13 /pmc/articles/PMC9747080/ /pubmed/36514130 http://dx.doi.org/10.1186/s13054-022-04266-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Michels, Erik H. A. Butler, Joe M. Reijnders, Tom D. Y. Cremer, Olaf L. Scicluna, Brendon P. Uhel, Fabrice Peters-Sengers, Hessel Schultz, Marcus J. Knight, Julian C. van Vught, Lonneke A. van der Poll, Tom Association between age and the host response in critically ill patients with sepsis |
title | Association between age and the host response in critically ill patients with sepsis |
title_full | Association between age and the host response in critically ill patients with sepsis |
title_fullStr | Association between age and the host response in critically ill patients with sepsis |
title_full_unstemmed | Association between age and the host response in critically ill patients with sepsis |
title_short | Association between age and the host response in critically ill patients with sepsis |
title_sort | association between age and the host response in critically ill patients with sepsis |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9747080/ https://www.ncbi.nlm.nih.gov/pubmed/36514130 http://dx.doi.org/10.1186/s13054-022-04266-9 |
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