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Early-life and pubertal stress differentially modulate grey matter development in human adolescents
Animal and human studies have shown that both early-life traumatic events and ongoing stress episodes affect neurodevelopment, however, it remains unclear whether and how they modulate normative adolescent neuro-maturational trajectories. We characterized effects of early-life (age 0–5) and ongoing...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003940/ https://www.ncbi.nlm.nih.gov/pubmed/29907813 http://dx.doi.org/10.1038/s41598-018-27439-5 |
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author | Tyborowska, Anna Volman, Inge Niermann, Hannah C. M. Pouwels, J. Loes Smeekens, Sanny Cillessen, Antonius H. N. Toni, Ivan Roelofs, Karin |
author_facet | Tyborowska, Anna Volman, Inge Niermann, Hannah C. M. Pouwels, J. Loes Smeekens, Sanny Cillessen, Antonius H. N. Toni, Ivan Roelofs, Karin |
author_sort | Tyborowska, Anna |
collection | PubMed |
description | Animal and human studies have shown that both early-life traumatic events and ongoing stress episodes affect neurodevelopment, however, it remains unclear whether and how they modulate normative adolescent neuro-maturational trajectories. We characterized effects of early-life (age 0–5) and ongoing stressors (age 14–17) on longitudinal changes (age 14 to17) in grey matter volume (GMV) of healthy adolescents (n = 37). Timing and stressor type were related to differential GMV changes. More personal early-life stressful events were associated with larger developmental reductions in GMV over anterior prefrontal cortex, amygdala and other subcortical regions; whereas ongoing stress from the adolescents’ social environment was related to smaller reductions over the orbitofrontal and anterior cingulate cortex. These findings suggest that early-life stress accelerates pubertal development, whereas an adverse adolescent social environment disturbs brain maturation with potential mental health implications: delayed anterior cingulate maturation was associated with more antisocial traits – a juvenile precursor of psychopathy. |
format | Online Article Text |
id | pubmed-6003940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-60039402018-06-26 Early-life and pubertal stress differentially modulate grey matter development in human adolescents Tyborowska, Anna Volman, Inge Niermann, Hannah C. M. Pouwels, J. Loes Smeekens, Sanny Cillessen, Antonius H. N. Toni, Ivan Roelofs, Karin Sci Rep Article Animal and human studies have shown that both early-life traumatic events and ongoing stress episodes affect neurodevelopment, however, it remains unclear whether and how they modulate normative adolescent neuro-maturational trajectories. We characterized effects of early-life (age 0–5) and ongoing stressors (age 14–17) on longitudinal changes (age 14 to17) in grey matter volume (GMV) of healthy adolescents (n = 37). Timing and stressor type were related to differential GMV changes. More personal early-life stressful events were associated with larger developmental reductions in GMV over anterior prefrontal cortex, amygdala and other subcortical regions; whereas ongoing stress from the adolescents’ social environment was related to smaller reductions over the orbitofrontal and anterior cingulate cortex. These findings suggest that early-life stress accelerates pubertal development, whereas an adverse adolescent social environment disturbs brain maturation with potential mental health implications: delayed anterior cingulate maturation was associated with more antisocial traits – a juvenile precursor of psychopathy. Nature Publishing Group UK 2018-06-15 /pmc/articles/PMC6003940/ /pubmed/29907813 http://dx.doi.org/10.1038/s41598-018-27439-5 Text en © The Author(s) 2018 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tyborowska, Anna Volman, Inge Niermann, Hannah C. M. Pouwels, J. Loes Smeekens, Sanny Cillessen, Antonius H. N. Toni, Ivan Roelofs, Karin Early-life and pubertal stress differentially modulate grey matter development in human adolescents |
title | Early-life and pubertal stress differentially modulate grey matter development in human adolescents |
title_full | Early-life and pubertal stress differentially modulate grey matter development in human adolescents |
title_fullStr | Early-life and pubertal stress differentially modulate grey matter development in human adolescents |
title_full_unstemmed | Early-life and pubertal stress differentially modulate grey matter development in human adolescents |
title_short | Early-life and pubertal stress differentially modulate grey matter development in human adolescents |
title_sort | early-life and pubertal stress differentially modulate grey matter development in human adolescents |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6003940/ https://www.ncbi.nlm.nih.gov/pubmed/29907813 http://dx.doi.org/10.1038/s41598-018-27439-5 |
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