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Experience-Driven Differences in Childhood Cortisol Predict Affect-Relevant Brain Function and Coping in Adolescent Monozygotic Twins

Stress and emotion involve diverse developmental and individual differences. Partially attributed to the development of the prefrontal cortex (PFC), the amygdala, and hypothalamic-pituitary-adrenal axis, the precise genetic and experiential contributions remain unknown. In previous work, childhood b...

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Autores principales: Burghy, Cory A., Fox, Michelle E., Cornejo, M. Daniela, Stodola, Diane E., Sommerfeldt, Sasha L., Westbrook, Cecilia A., Van Hulle, Carol, Schmidt, Nicole L., Goldsmith, H. Hill, Davidson, Richard J., Birn, Rasmus M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5181835/
https://www.ncbi.nlm.nih.gov/pubmed/27872489
http://dx.doi.org/10.1038/srep37081
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author Burghy, Cory A.
Fox, Michelle E.
Cornejo, M. Daniela
Stodola, Diane E.
Sommerfeldt, Sasha L.
Westbrook, Cecilia A.
Van Hulle, Carol
Schmidt, Nicole L.
Goldsmith, H. Hill
Davidson, Richard J.
Birn, Rasmus M.
author_facet Burghy, Cory A.
Fox, Michelle E.
Cornejo, M. Daniela
Stodola, Diane E.
Sommerfeldt, Sasha L.
Westbrook, Cecilia A.
Van Hulle, Carol
Schmidt, Nicole L.
Goldsmith, H. Hill
Davidson, Richard J.
Birn, Rasmus M.
author_sort Burghy, Cory A.
collection PubMed
description Stress and emotion involve diverse developmental and individual differences. Partially attributed to the development of the prefrontal cortex (PFC), the amygdala, and hypothalamic-pituitary-adrenal axis, the precise genetic and experiential contributions remain unknown. In previous work, childhood basal cortisol function predicted adolescent resting-state functional connectivity (rs-FC) and psychopathology. To parse experience-driven (non-genetic) contributions, we investigated these relations with a monozygotic (MZ) twin design. Specifically, we examined whether intrapair differences in childhood afternoon cortisol levels predicted cotwin differences in adolescent brain function and coping. As expected, intrapair differences in childhood cortisol forecast amygdala-perigenual PFC rs-FC (R(2) = 0.84, FWE-corrected p = 0.01), and amygdala recovery following unpleasant images (R(2) = 0.40, FWE-corrected p < 0.05), such that the cotwin with higher childhood cortisol evinced relatively lower rs-FC and poorer amygdala recovery in adolescence. Cotwin differences in amygdala recovery also predicted coping styles. These data highlight experience-dependent change in childhood and adolescence.
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spelling pubmed-51818352016-12-29 Experience-Driven Differences in Childhood Cortisol Predict Affect-Relevant Brain Function and Coping in Adolescent Monozygotic Twins Burghy, Cory A. Fox, Michelle E. Cornejo, M. Daniela Stodola, Diane E. Sommerfeldt, Sasha L. Westbrook, Cecilia A. Van Hulle, Carol Schmidt, Nicole L. Goldsmith, H. Hill Davidson, Richard J. Birn, Rasmus M. Sci Rep Article Stress and emotion involve diverse developmental and individual differences. Partially attributed to the development of the prefrontal cortex (PFC), the amygdala, and hypothalamic-pituitary-adrenal axis, the precise genetic and experiential contributions remain unknown. In previous work, childhood basal cortisol function predicted adolescent resting-state functional connectivity (rs-FC) and psychopathology. To parse experience-driven (non-genetic) contributions, we investigated these relations with a monozygotic (MZ) twin design. Specifically, we examined whether intrapair differences in childhood afternoon cortisol levels predicted cotwin differences in adolescent brain function and coping. As expected, intrapair differences in childhood cortisol forecast amygdala-perigenual PFC rs-FC (R(2) = 0.84, FWE-corrected p = 0.01), and amygdala recovery following unpleasant images (R(2) = 0.40, FWE-corrected p < 0.05), such that the cotwin with higher childhood cortisol evinced relatively lower rs-FC and poorer amygdala recovery in adolescence. Cotwin differences in amygdala recovery also predicted coping styles. These data highlight experience-dependent change in childhood and adolescence. Nature Publishing Group 2016-11-22 /pmc/articles/PMC5181835/ /pubmed/27872489 http://dx.doi.org/10.1038/srep37081 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Burghy, Cory A.
Fox, Michelle E.
Cornejo, M. Daniela
Stodola, Diane E.
Sommerfeldt, Sasha L.
Westbrook, Cecilia A.
Van Hulle, Carol
Schmidt, Nicole L.
Goldsmith, H. Hill
Davidson, Richard J.
Birn, Rasmus M.
Experience-Driven Differences in Childhood Cortisol Predict Affect-Relevant Brain Function and Coping in Adolescent Monozygotic Twins
title Experience-Driven Differences in Childhood Cortisol Predict Affect-Relevant Brain Function and Coping in Adolescent Monozygotic Twins
title_full Experience-Driven Differences in Childhood Cortisol Predict Affect-Relevant Brain Function and Coping in Adolescent Monozygotic Twins
title_fullStr Experience-Driven Differences in Childhood Cortisol Predict Affect-Relevant Brain Function and Coping in Adolescent Monozygotic Twins
title_full_unstemmed Experience-Driven Differences in Childhood Cortisol Predict Affect-Relevant Brain Function and Coping in Adolescent Monozygotic Twins
title_short Experience-Driven Differences in Childhood Cortisol Predict Affect-Relevant Brain Function and Coping in Adolescent Monozygotic Twins
title_sort experience-driven differences in childhood cortisol predict affect-relevant brain function and coping in adolescent monozygotic twins
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5181835/
https://www.ncbi.nlm.nih.gov/pubmed/27872489
http://dx.doi.org/10.1038/srep37081
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