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Role of Age-Related Changes in DNA Methylation in the Disproportionate Susceptibility and Worse Outcomes of Sepsis in Older Adults

Sepsis, a complex multisystem disorder, is among the top causes of hospitalization and mortality in older adults. However, the mechanisms underlying the disproportionate susceptibility to sepsis and worse outcomes in the elderly are not well understood. Recently, changes in DNA methylation have been...

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Autores principales: Lang, Xiabing, Shen, Lingling, Zhu, Tingting, Zhao, Wenjun, Chen, Yang, Zhu, Chaohong, Su, Qun, Wang, Cuili, Wang, Yucheng, Neri, Francesco, Jiang, Hong, Chen, Jianghua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8886726/
https://www.ncbi.nlm.nih.gov/pubmed/35242787
http://dx.doi.org/10.3389/fmed.2022.822847
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author Lang, Xiabing
Shen, Lingling
Zhu, Tingting
Zhao, Wenjun
Chen, Yang
Zhu, Chaohong
Su, Qun
Wang, Cuili
Wang, Yucheng
Neri, Francesco
Jiang, Hong
Chen, Jianghua
author_facet Lang, Xiabing
Shen, Lingling
Zhu, Tingting
Zhao, Wenjun
Chen, Yang
Zhu, Chaohong
Su, Qun
Wang, Cuili
Wang, Yucheng
Neri, Francesco
Jiang, Hong
Chen, Jianghua
author_sort Lang, Xiabing
collection PubMed
description Sepsis, a complex multisystem disorder, is among the top causes of hospitalization and mortality in older adults. However, the mechanisms underlying the disproportionate susceptibility to sepsis and worse outcomes in the elderly are not well understood. Recently, changes in DNA methylation have been shown to be linked to aging processes and age-related diseases. Thus, we postulated that age-related changes in DNA methylation may play a role in the onset and prognosis of sepsis in elderly patients. Here, we performed genome-wide methylation profiling of peripheral blood from patients with sepsis and controls. Among the CpG sites whose methylation changes may contribute to an increase in sepsis susceptibility or mortality, 241 sites that possessed age-related changes in DNA methylation in controls may partly explain the increased risk of sepsis in older adults, and 161 sites whose methylation significantly correlated with age in sepsis group may be the potential mechanisms underlying the worse outcomes of elderly septic patients. Finally, an independent cohort was used to validate our findings. Together, our study demonstrates that age-related changes in DNA methylation may explain in part the disproportionate susceptibility and worse outcomes of sepsis in older adults.
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spelling pubmed-88867262022-03-02 Role of Age-Related Changes in DNA Methylation in the Disproportionate Susceptibility and Worse Outcomes of Sepsis in Older Adults Lang, Xiabing Shen, Lingling Zhu, Tingting Zhao, Wenjun Chen, Yang Zhu, Chaohong Su, Qun Wang, Cuili Wang, Yucheng Neri, Francesco Jiang, Hong Chen, Jianghua Front Med (Lausanne) Medicine Sepsis, a complex multisystem disorder, is among the top causes of hospitalization and mortality in older adults. However, the mechanisms underlying the disproportionate susceptibility to sepsis and worse outcomes in the elderly are not well understood. Recently, changes in DNA methylation have been shown to be linked to aging processes and age-related diseases. Thus, we postulated that age-related changes in DNA methylation may play a role in the onset and prognosis of sepsis in elderly patients. Here, we performed genome-wide methylation profiling of peripheral blood from patients with sepsis and controls. Among the CpG sites whose methylation changes may contribute to an increase in sepsis susceptibility or mortality, 241 sites that possessed age-related changes in DNA methylation in controls may partly explain the increased risk of sepsis in older adults, and 161 sites whose methylation significantly correlated with age in sepsis group may be the potential mechanisms underlying the worse outcomes of elderly septic patients. Finally, an independent cohort was used to validate our findings. Together, our study demonstrates that age-related changes in DNA methylation may explain in part the disproportionate susceptibility and worse outcomes of sepsis in older adults. Frontiers Media S.A. 2022-02-15 /pmc/articles/PMC8886726/ /pubmed/35242787 http://dx.doi.org/10.3389/fmed.2022.822847 Text en Copyright © 2022 Lang, Shen, Zhu, Zhao, Chen, Zhu, Su, Wang, Wang, Neri, Jiang and Chen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Lang, Xiabing
Shen, Lingling
Zhu, Tingting
Zhao, Wenjun
Chen, Yang
Zhu, Chaohong
Su, Qun
Wang, Cuili
Wang, Yucheng
Neri, Francesco
Jiang, Hong
Chen, Jianghua
Role of Age-Related Changes in DNA Methylation in the Disproportionate Susceptibility and Worse Outcomes of Sepsis in Older Adults
title Role of Age-Related Changes in DNA Methylation in the Disproportionate Susceptibility and Worse Outcomes of Sepsis in Older Adults
title_full Role of Age-Related Changes in DNA Methylation in the Disproportionate Susceptibility and Worse Outcomes of Sepsis in Older Adults
title_fullStr Role of Age-Related Changes in DNA Methylation in the Disproportionate Susceptibility and Worse Outcomes of Sepsis in Older Adults
title_full_unstemmed Role of Age-Related Changes in DNA Methylation in the Disproportionate Susceptibility and Worse Outcomes of Sepsis in Older Adults
title_short Role of Age-Related Changes in DNA Methylation in the Disproportionate Susceptibility and Worse Outcomes of Sepsis in Older Adults
title_sort role of age-related changes in dna methylation in the disproportionate susceptibility and worse outcomes of sepsis in older adults
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8886726/
https://www.ncbi.nlm.nih.gov/pubmed/35242787
http://dx.doi.org/10.3389/fmed.2022.822847
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