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Investigating the impact of early-life adversity on physiological, immune, and gene expression responses to acute stress: A pilot feasibility study

OBJECTIVE: Exposure to early-life adversity (ELA) can result in long-term changes to physiological systems, which predispose individuals to negative health outcomes. This biological embedding of stress-responsive systems may operate via dysregulation of physiological resources in response to common...

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Autores principales: Shalev, Idan, Hastings, Waylon J., Etzel, Laura, Israel, Salomon, Russell, Michael A., Hendrick, Kelsie A., Zinobile, Megan, Siegel, Sue Rutherford
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7122782/
https://www.ncbi.nlm.nih.gov/pubmed/32243432
http://dx.doi.org/10.1371/journal.pone.0221310
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author Shalev, Idan
Hastings, Waylon J.
Etzel, Laura
Israel, Salomon
Russell, Michael A.
Hendrick, Kelsie A.
Zinobile, Megan
Siegel, Sue Rutherford
author_facet Shalev, Idan
Hastings, Waylon J.
Etzel, Laura
Israel, Salomon
Russell, Michael A.
Hendrick, Kelsie A.
Zinobile, Megan
Siegel, Sue Rutherford
author_sort Shalev, Idan
collection PubMed
description OBJECTIVE: Exposure to early-life adversity (ELA) can result in long-term changes to physiological systems, which predispose individuals to negative health outcomes. This biological embedding of stress-responsive systems may operate via dysregulation of physiological resources in response to common stressors. The present pilot study outlines a novel experimental design to test how young adults’ exposure to ELA influences neuroendocrine and inflammatory responses to acute stress. MATERIALS AND METHODS: Participants were 12 males (mean age = 21.25), half of whom endorsed at least three significant adverse events up to age 18 years (‘ELA group’), and half who confirmed zero (‘controls’). Using a randomized within-subjects, between-groups experimental design, we induced acute psychosocial stress (Trier Social Stress Test, TSST), and included a no-stress control condition one week apart. During these sessions, we obtained repeated measurements of physiological reactivity, gene expression of the glucocorticoid receptor (NR3C1), and plasma levels of pro-inflammatory cytokines (IL-1β, IL-6, IL-8 and TNFα) over a 4-hour window post-test. RESULTS: In this pilot study, the ELA group evinced higher cortisol response and blunted NR3C1 gene expression in response to the TSST compared with controls, while no differences were observed in the no-stress condition. For pro-inflammatory cytokines, only IL-6 increased significantly in response to the TSST, with no differences between the two groups. CONCLUSION: Overall, this pilot feasibility study provides a framework to investigate the biological embedding of early-adversity via dysregulation across physiological and genomic systems in response to acute psychosocial stress. ELA may program such systems in a maladaptive manner more likely to manifest during times of duress, predisposing individuals to the negative health consequences of everyday stressors. Future studies with larger sample size including both males and females are needed to replicate and expand upon these preliminary findings.
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spelling pubmed-71227822020-04-09 Investigating the impact of early-life adversity on physiological, immune, and gene expression responses to acute stress: A pilot feasibility study Shalev, Idan Hastings, Waylon J. Etzel, Laura Israel, Salomon Russell, Michael A. Hendrick, Kelsie A. Zinobile, Megan Siegel, Sue Rutherford PLoS One Research Article OBJECTIVE: Exposure to early-life adversity (ELA) can result in long-term changes to physiological systems, which predispose individuals to negative health outcomes. This biological embedding of stress-responsive systems may operate via dysregulation of physiological resources in response to common stressors. The present pilot study outlines a novel experimental design to test how young adults’ exposure to ELA influences neuroendocrine and inflammatory responses to acute stress. MATERIALS AND METHODS: Participants were 12 males (mean age = 21.25), half of whom endorsed at least three significant adverse events up to age 18 years (‘ELA group’), and half who confirmed zero (‘controls’). Using a randomized within-subjects, between-groups experimental design, we induced acute psychosocial stress (Trier Social Stress Test, TSST), and included a no-stress control condition one week apart. During these sessions, we obtained repeated measurements of physiological reactivity, gene expression of the glucocorticoid receptor (NR3C1), and plasma levels of pro-inflammatory cytokines (IL-1β, IL-6, IL-8 and TNFα) over a 4-hour window post-test. RESULTS: In this pilot study, the ELA group evinced higher cortisol response and blunted NR3C1 gene expression in response to the TSST compared with controls, while no differences were observed in the no-stress condition. For pro-inflammatory cytokines, only IL-6 increased significantly in response to the TSST, with no differences between the two groups. CONCLUSION: Overall, this pilot feasibility study provides a framework to investigate the biological embedding of early-adversity via dysregulation across physiological and genomic systems in response to acute psychosocial stress. ELA may program such systems in a maladaptive manner more likely to manifest during times of duress, predisposing individuals to the negative health consequences of everyday stressors. Future studies with larger sample size including both males and females are needed to replicate and expand upon these preliminary findings. Public Library of Science 2020-04-03 /pmc/articles/PMC7122782/ /pubmed/32243432 http://dx.doi.org/10.1371/journal.pone.0221310 Text en © 2020 Shalev 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
Shalev, Idan
Hastings, Waylon J.
Etzel, Laura
Israel, Salomon
Russell, Michael A.
Hendrick, Kelsie A.
Zinobile, Megan
Siegel, Sue Rutherford
Investigating the impact of early-life adversity on physiological, immune, and gene expression responses to acute stress: A pilot feasibility study
title Investigating the impact of early-life adversity on physiological, immune, and gene expression responses to acute stress: A pilot feasibility study
title_full Investigating the impact of early-life adversity on physiological, immune, and gene expression responses to acute stress: A pilot feasibility study
title_fullStr Investigating the impact of early-life adversity on physiological, immune, and gene expression responses to acute stress: A pilot feasibility study
title_full_unstemmed Investigating the impact of early-life adversity on physiological, immune, and gene expression responses to acute stress: A pilot feasibility study
title_short Investigating the impact of early-life adversity on physiological, immune, and gene expression responses to acute stress: A pilot feasibility study
title_sort investigating the impact of early-life adversity on physiological, immune, and gene expression responses to acute stress: a pilot feasibility study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7122782/
https://www.ncbi.nlm.nih.gov/pubmed/32243432
http://dx.doi.org/10.1371/journal.pone.0221310
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