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Accelerated maturation in functional connectivity following early life stress: Circuit specific or broadly distributed?
Psychosocial acceleration theory and other frameworks adapted from life history predict a link between early life stress and accelerated maturation in several physiological systems. Those findings led researchers to suggest that the emotion-regulatory brain circuits of previously-institutionalized (...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848776/ https://www.ncbi.nlm.nih.gov/pubmed/33517108 http://dx.doi.org/10.1016/j.dcn.2021.100922 |
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author | Herzberg, Max P. McKenzie, Kelly Jedd Hodel, Amanda S. Hunt, Ruskin H. Mueller, Bryon A. Gunnar, Megan R. Thomas, Kathleen M. |
author_facet | Herzberg, Max P. McKenzie, Kelly Jedd Hodel, Amanda S. Hunt, Ruskin H. Mueller, Bryon A. Gunnar, Megan R. Thomas, Kathleen M. |
author_sort | Herzberg, Max P. |
collection | PubMed |
description | Psychosocial acceleration theory and other frameworks adapted from life history predict a link between early life stress and accelerated maturation in several physiological systems. Those findings led researchers to suggest that the emotion-regulatory brain circuits of previously-institutionalized (PI) youth are more mature than youth raised in their biological families (non-adopted, or NA, youth) during emotion tasks. Whether this accelerated maturation is evident during resting-state fMRI has not yet been established. Resting-state fMRI data from 83 early adolescents (M(age) = 12.9 years, SD = 0.57 years) including 41 PI and 42 NA youth, were used to examine seed-based functional connectivity between the amygdala and ventromedial prefrontal cortex (vmPFC). Additional whole-brain analyses assessed group differences in functional connectivity and associations with cognitive performance and behavior. We found group differences in amygdala – vmPFC connectivity that may be consistent with accelerated maturation following early life stress. Further, whole-brain connectivity analyses revealed group differences associated with internalizing and externalizing symptoms. However, the majority of whole-brain results were not consistent with an accelerated maturation framework. Our results suggest early life stress in the form of institutional care is associated with circuit-specific alterations to a frontolimbic emotion-regulatory system, while revealing limited differences in more broadly distributed networks. |
format | Online Article Text |
id | pubmed-7848776 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-78487762021-02-04 Accelerated maturation in functional connectivity following early life stress: Circuit specific or broadly distributed? Herzberg, Max P. McKenzie, Kelly Jedd Hodel, Amanda S. Hunt, Ruskin H. Mueller, Bryon A. Gunnar, Megan R. Thomas, Kathleen M. Dev Cogn Neurosci Original Research Psychosocial acceleration theory and other frameworks adapted from life history predict a link between early life stress and accelerated maturation in several physiological systems. Those findings led researchers to suggest that the emotion-regulatory brain circuits of previously-institutionalized (PI) youth are more mature than youth raised in their biological families (non-adopted, or NA, youth) during emotion tasks. Whether this accelerated maturation is evident during resting-state fMRI has not yet been established. Resting-state fMRI data from 83 early adolescents (M(age) = 12.9 years, SD = 0.57 years) including 41 PI and 42 NA youth, were used to examine seed-based functional connectivity between the amygdala and ventromedial prefrontal cortex (vmPFC). Additional whole-brain analyses assessed group differences in functional connectivity and associations with cognitive performance and behavior. We found group differences in amygdala – vmPFC connectivity that may be consistent with accelerated maturation following early life stress. Further, whole-brain connectivity analyses revealed group differences associated with internalizing and externalizing symptoms. However, the majority of whole-brain results were not consistent with an accelerated maturation framework. Our results suggest early life stress in the form of institutional care is associated with circuit-specific alterations to a frontolimbic emotion-regulatory system, while revealing limited differences in more broadly distributed networks. Elsevier 2021-01-20 /pmc/articles/PMC7848776/ /pubmed/33517108 http://dx.doi.org/10.1016/j.dcn.2021.100922 Text en © 2021 Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Original Research Herzberg, Max P. McKenzie, Kelly Jedd Hodel, Amanda S. Hunt, Ruskin H. Mueller, Bryon A. Gunnar, Megan R. Thomas, Kathleen M. Accelerated maturation in functional connectivity following early life stress: Circuit specific or broadly distributed? |
title | Accelerated maturation in functional connectivity following early life stress: Circuit specific or broadly distributed? |
title_full | Accelerated maturation in functional connectivity following early life stress: Circuit specific or broadly distributed? |
title_fullStr | Accelerated maturation in functional connectivity following early life stress: Circuit specific or broadly distributed? |
title_full_unstemmed | Accelerated maturation in functional connectivity following early life stress: Circuit specific or broadly distributed? |
title_short | Accelerated maturation in functional connectivity following early life stress: Circuit specific or broadly distributed? |
title_sort | accelerated maturation in functional connectivity following early life stress: circuit specific or broadly distributed? |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848776/ https://www.ncbi.nlm.nih.gov/pubmed/33517108 http://dx.doi.org/10.1016/j.dcn.2021.100922 |
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