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Maternal cortisol is associated with neonatal amygdala microstructure and connectivity in a sexually dimorphic manner

The mechanisms linking maternal stress in pregnancy with infant neurodevelopment in a sexually dimorphic manner are poorly understood. We tested the hypothesis that maternal hypothalamic-pituitary-adrenal axis activity, measured by hair cortisol concentration (HCC), is associated with microstructure...

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Autores principales: Stoye, David Q, Blesa, Manuel, Sullivan, Gemma, Galdi, Paola, Lamb, Gillian J, Black, Gill S, Quigley, Alan J, Thrippleton, Michael J, Bastin, Mark E, Reynolds, Rebecca M, Boardman, James P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685701/
https://www.ncbi.nlm.nih.gov/pubmed/33228850
http://dx.doi.org/10.7554/eLife.60729
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author Stoye, David Q
Blesa, Manuel
Sullivan, Gemma
Galdi, Paola
Lamb, Gillian J
Black, Gill S
Quigley, Alan J
Thrippleton, Michael J
Bastin, Mark E
Reynolds, Rebecca M
Boardman, James P
author_facet Stoye, David Q
Blesa, Manuel
Sullivan, Gemma
Galdi, Paola
Lamb, Gillian J
Black, Gill S
Quigley, Alan J
Thrippleton, Michael J
Bastin, Mark E
Reynolds, Rebecca M
Boardman, James P
author_sort Stoye, David Q
collection PubMed
description The mechanisms linking maternal stress in pregnancy with infant neurodevelopment in a sexually dimorphic manner are poorly understood. We tested the hypothesis that maternal hypothalamic-pituitary-adrenal axis activity, measured by hair cortisol concentration (HCC), is associated with microstructure, structural connectivity, and volume of the infant amygdala. In 78 mother-infant dyads, maternal hair was sampled postnatally, and infants underwent magnetic resonance imaging at term-equivalent age. We found a relationship between maternal HCC and amygdala development that differed according to infant sex. Higher HCC was associated with higher left amygdala fractional anisotropy (β = 0.677, p=0.010), lower left amygdala orientation dispersion index (β = −0.597, p=0.034), and higher fractional anisotropy in connections between the right amygdala and putamen (β = 0.475, p=0.007) in girls compared to boys. Furthermore, altered amygdala microstructure was only observed in boys, with connectivity changes restricted to girls. Maternal cortisol during pregnancy is related to newborn amygdala architecture and connectivity in a sexually dimorphic manner. Given the fundamental role of the amygdala in the emergence of emotion regulation, these findings offer new insights into mechanisms linking maternal health with neuropsychiatric outcomes of children.
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spelling pubmed-76857012020-11-30 Maternal cortisol is associated with neonatal amygdala microstructure and connectivity in a sexually dimorphic manner Stoye, David Q Blesa, Manuel Sullivan, Gemma Galdi, Paola Lamb, Gillian J Black, Gill S Quigley, Alan J Thrippleton, Michael J Bastin, Mark E Reynolds, Rebecca M Boardman, James P eLife Neuroscience The mechanisms linking maternal stress in pregnancy with infant neurodevelopment in a sexually dimorphic manner are poorly understood. We tested the hypothesis that maternal hypothalamic-pituitary-adrenal axis activity, measured by hair cortisol concentration (HCC), is associated with microstructure, structural connectivity, and volume of the infant amygdala. In 78 mother-infant dyads, maternal hair was sampled postnatally, and infants underwent magnetic resonance imaging at term-equivalent age. We found a relationship between maternal HCC and amygdala development that differed according to infant sex. Higher HCC was associated with higher left amygdala fractional anisotropy (β = 0.677, p=0.010), lower left amygdala orientation dispersion index (β = −0.597, p=0.034), and higher fractional anisotropy in connections between the right amygdala and putamen (β = 0.475, p=0.007) in girls compared to boys. Furthermore, altered amygdala microstructure was only observed in boys, with connectivity changes restricted to girls. Maternal cortisol during pregnancy is related to newborn amygdala architecture and connectivity in a sexually dimorphic manner. Given the fundamental role of the amygdala in the emergence of emotion regulation, these findings offer new insights into mechanisms linking maternal health with neuropsychiatric outcomes of children. eLife Sciences Publications, Ltd 2020-11-24 /pmc/articles/PMC7685701/ /pubmed/33228850 http://dx.doi.org/10.7554/eLife.60729 Text en © 2020, Stoye et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Stoye, David Q
Blesa, Manuel
Sullivan, Gemma
Galdi, Paola
Lamb, Gillian J
Black, Gill S
Quigley, Alan J
Thrippleton, Michael J
Bastin, Mark E
Reynolds, Rebecca M
Boardman, James P
Maternal cortisol is associated with neonatal amygdala microstructure and connectivity in a sexually dimorphic manner
title Maternal cortisol is associated with neonatal amygdala microstructure and connectivity in a sexually dimorphic manner
title_full Maternal cortisol is associated with neonatal amygdala microstructure and connectivity in a sexually dimorphic manner
title_fullStr Maternal cortisol is associated with neonatal amygdala microstructure and connectivity in a sexually dimorphic manner
title_full_unstemmed Maternal cortisol is associated with neonatal amygdala microstructure and connectivity in a sexually dimorphic manner
title_short Maternal cortisol is associated with neonatal amygdala microstructure and connectivity in a sexually dimorphic manner
title_sort maternal cortisol is associated with neonatal amygdala microstructure and connectivity in a sexually dimorphic manner
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7685701/
https://www.ncbi.nlm.nih.gov/pubmed/33228850
http://dx.doi.org/10.7554/eLife.60729
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