Cargando…
Early life adversity predicts brain-gut alterations associated with increased stress and mood
Alterations in the brain-gut system have been implicated in various disease states, but little is known about how early-life adversity (ELA) impacts development and adult health as mediated by brain-gut interactions. We hypothesize that ELA disrupts components of the brain-gut system, thereby increa...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8170500/ https://www.ncbi.nlm.nih.gov/pubmed/34113697 http://dx.doi.org/10.1016/j.ynstr.2021.100348 |
_version_ | 1783702259144589312 |
---|---|
author | Coley, Elena J.L. Mayer, Emeran A. Osadchiy, Vadim Chen, Zixi Subramanyam, Vishvak Zhang, Yurui Hsiao, Elaine Y. Gao, Kan Bhatt, Ravi Dong, Tien Vora, Priten Naliboff, Bruce Jacobs, Jonathan P. Gupta, Arpana |
author_facet | Coley, Elena J.L. Mayer, Emeran A. Osadchiy, Vadim Chen, Zixi Subramanyam, Vishvak Zhang, Yurui Hsiao, Elaine Y. Gao, Kan Bhatt, Ravi Dong, Tien Vora, Priten Naliboff, Bruce Jacobs, Jonathan P. Gupta, Arpana |
author_sort | Coley, Elena J.L. |
collection | PubMed |
description | Alterations in the brain-gut system have been implicated in various disease states, but little is known about how early-life adversity (ELA) impacts development and adult health as mediated by brain-gut interactions. We hypothesize that ELA disrupts components of the brain-gut system, thereby increasing susceptibility to disordered mood. In a sample of 128 healthy adult participants, a history of ELA and current stress, depression, and anxiety were assessed using validated questionnaires. Fecal metabolites were measured using liquid chromatography tandem mass spectrometry-based untargeted metabolomic profiling. Functional brain connectivity was evaluated by magnetic resonance imaging. Sparse partial least squares-discriminant analysis, controlling for sex, body mass index, age, and diet was used to predict brain-gut alterations as a function of ELA. ELA was correlated with four gut-regulated metabolites within the glutamate pathway (5-oxoproline, malate, urate, and glutamate gamma methyl ester) and alterations in functional brain connectivity within primarily sensorimotor, salience, and central executive networks. Integrated analyses revealed significant associations between these metabolites, functional brain connectivity, and scores for perceived stress, anxiety, and depression. This study reveals a novel association between a history of ELA, alterations in the brain-gut axis, and increased vulnerability to negative mood and stress. Results from the study raise the hypothesis that select gut-regulated metabolites may contribute to the adverse effects of critical period stress on neural development via pathways related to glutamatergic excitotoxicity and oxidative stress. |
format | Online Article Text |
id | pubmed-8170500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-81705002021-06-09 Early life adversity predicts brain-gut alterations associated with increased stress and mood Coley, Elena J.L. Mayer, Emeran A. Osadchiy, Vadim Chen, Zixi Subramanyam, Vishvak Zhang, Yurui Hsiao, Elaine Y. Gao, Kan Bhatt, Ravi Dong, Tien Vora, Priten Naliboff, Bruce Jacobs, Jonathan P. Gupta, Arpana Neurobiol Stress Original Research Article Alterations in the brain-gut system have been implicated in various disease states, but little is known about how early-life adversity (ELA) impacts development and adult health as mediated by brain-gut interactions. We hypothesize that ELA disrupts components of the brain-gut system, thereby increasing susceptibility to disordered mood. In a sample of 128 healthy adult participants, a history of ELA and current stress, depression, and anxiety were assessed using validated questionnaires. Fecal metabolites were measured using liquid chromatography tandem mass spectrometry-based untargeted metabolomic profiling. Functional brain connectivity was evaluated by magnetic resonance imaging. Sparse partial least squares-discriminant analysis, controlling for sex, body mass index, age, and diet was used to predict brain-gut alterations as a function of ELA. ELA was correlated with four gut-regulated metabolites within the glutamate pathway (5-oxoproline, malate, urate, and glutamate gamma methyl ester) and alterations in functional brain connectivity within primarily sensorimotor, salience, and central executive networks. Integrated analyses revealed significant associations between these metabolites, functional brain connectivity, and scores for perceived stress, anxiety, and depression. This study reveals a novel association between a history of ELA, alterations in the brain-gut axis, and increased vulnerability to negative mood and stress. Results from the study raise the hypothesis that select gut-regulated metabolites may contribute to the adverse effects of critical period stress on neural development via pathways related to glutamatergic excitotoxicity and oxidative stress. Elsevier 2021-05-25 /pmc/articles/PMC8170500/ /pubmed/34113697 http://dx.doi.org/10.1016/j.ynstr.2021.100348 Text en © 2021 The Authors. Published by Elsevier Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Original Research Article Coley, Elena J.L. Mayer, Emeran A. Osadchiy, Vadim Chen, Zixi Subramanyam, Vishvak Zhang, Yurui Hsiao, Elaine Y. Gao, Kan Bhatt, Ravi Dong, Tien Vora, Priten Naliboff, Bruce Jacobs, Jonathan P. Gupta, Arpana Early life adversity predicts brain-gut alterations associated with increased stress and mood |
title | Early life adversity predicts brain-gut alterations associated with increased stress and mood |
title_full | Early life adversity predicts brain-gut alterations associated with increased stress and mood |
title_fullStr | Early life adversity predicts brain-gut alterations associated with increased stress and mood |
title_full_unstemmed | Early life adversity predicts brain-gut alterations associated with increased stress and mood |
title_short | Early life adversity predicts brain-gut alterations associated with increased stress and mood |
title_sort | early life adversity predicts brain-gut alterations associated with increased stress and mood |
topic | Original Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8170500/ https://www.ncbi.nlm.nih.gov/pubmed/34113697 http://dx.doi.org/10.1016/j.ynstr.2021.100348 |
work_keys_str_mv | AT coleyelenajl earlylifeadversitypredictsbraingutalterationsassociatedwithincreasedstressandmood AT mayeremerana earlylifeadversitypredictsbraingutalterationsassociatedwithincreasedstressandmood AT osadchiyvadim earlylifeadversitypredictsbraingutalterationsassociatedwithincreasedstressandmood AT chenzixi earlylifeadversitypredictsbraingutalterationsassociatedwithincreasedstressandmood AT subramanyamvishvak earlylifeadversitypredictsbraingutalterationsassociatedwithincreasedstressandmood AT zhangyurui earlylifeadversitypredictsbraingutalterationsassociatedwithincreasedstressandmood AT hsiaoelainey earlylifeadversitypredictsbraingutalterationsassociatedwithincreasedstressandmood AT gaokan earlylifeadversitypredictsbraingutalterationsassociatedwithincreasedstressandmood AT bhattravi earlylifeadversitypredictsbraingutalterationsassociatedwithincreasedstressandmood AT dongtien earlylifeadversitypredictsbraingutalterationsassociatedwithincreasedstressandmood AT vorapriten earlylifeadversitypredictsbraingutalterationsassociatedwithincreasedstressandmood AT naliboffbruce earlylifeadversitypredictsbraingutalterationsassociatedwithincreasedstressandmood AT jacobsjonathanp earlylifeadversitypredictsbraingutalterationsassociatedwithincreasedstressandmood AT guptaarpana earlylifeadversitypredictsbraingutalterationsassociatedwithincreasedstressandmood |