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Different brain profiles in children with prenatal alcohol exposure with or without early adverse exposures

Prenatal alcohol exposure (PAE) can alter brain development and impact mental health outcomes, and often occurs in conjunction with postnatal adversity (e.g., maltreatment). However, it is unclear how postnatal adverse exposures may moderate mental health and brain outcomes in children with PAE. T1‐...

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Detalles Bibliográficos
Autores principales: Andre, Quinn R., McMorris, Carly A., Kar, Preeti, Ritter, Chantel, Gibbard, W. Ben, Tortorelli, Christina, Lebel, Catherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7502833/
https://www.ncbi.nlm.nih.gov/pubmed/32659051
http://dx.doi.org/10.1002/hbm.25130
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author Andre, Quinn R.
McMorris, Carly A.
Kar, Preeti
Ritter, Chantel
Gibbard, W. Ben
Tortorelli, Christina
Lebel, Catherine
author_facet Andre, Quinn R.
McMorris, Carly A.
Kar, Preeti
Ritter, Chantel
Gibbard, W. Ben
Tortorelli, Christina
Lebel, Catherine
author_sort Andre, Quinn R.
collection PubMed
description Prenatal alcohol exposure (PAE) can alter brain development and impact mental health outcomes, and often occurs in conjunction with postnatal adversity (e.g., maltreatment). However, it is unclear how postnatal adverse exposures may moderate mental health and brain outcomes in children with PAE. T1‐weighted and diffusion magnetic resonance imaging were obtained from 66 participants aged 7–16 years. Twenty‐one participants had PAE and adverse postnatal exposures (PAE+), 12 had PAE without adverse postnatal exposures (PAE−), and 33 were age‐ and gender‐matched controls unexposed to either prenatal alcohol or postnatal adversity. Internalizing and externalizing mental health symptoms were assessed using the Behavioral Assessment System for Children II, Parent‐Rating Scale. ANCOVAs were used to compare mental health symptoms, limbic and prefrontal cortical volumes, and diffusion parameters of cortico‐limbic white matter tracts between groups, and to assess brain‐mental health relationships. Both PAE groups had worse externalizing behavior (higher scores) than controls. The PAE− group had lower fractional anisotropy (FA) in the bilateral cingulum and left uncinate fasciculus, and smaller volumes in the left anterior cingulate cortex than controls and the PAE+ group. The PAE− group also had higher mean diffusivity (MD) in the left uncinate than the PAE+ group, and smaller right anterior cingulate and superior frontal gyrus volumes than controls. These findings show different brain structure and mental health symptom profiles in children with PAE with and without postnatal adversity, highlighting the need to consider adverse postnatal exposures in individuals with PAE.
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spelling pubmed-75028332020-09-28 Different brain profiles in children with prenatal alcohol exposure with or without early adverse exposures Andre, Quinn R. McMorris, Carly A. Kar, Preeti Ritter, Chantel Gibbard, W. Ben Tortorelli, Christina Lebel, Catherine Hum Brain Mapp Research Articles Prenatal alcohol exposure (PAE) can alter brain development and impact mental health outcomes, and often occurs in conjunction with postnatal adversity (e.g., maltreatment). However, it is unclear how postnatal adverse exposures may moderate mental health and brain outcomes in children with PAE. T1‐weighted and diffusion magnetic resonance imaging were obtained from 66 participants aged 7–16 years. Twenty‐one participants had PAE and adverse postnatal exposures (PAE+), 12 had PAE without adverse postnatal exposures (PAE−), and 33 were age‐ and gender‐matched controls unexposed to either prenatal alcohol or postnatal adversity. Internalizing and externalizing mental health symptoms were assessed using the Behavioral Assessment System for Children II, Parent‐Rating Scale. ANCOVAs were used to compare mental health symptoms, limbic and prefrontal cortical volumes, and diffusion parameters of cortico‐limbic white matter tracts between groups, and to assess brain‐mental health relationships. Both PAE groups had worse externalizing behavior (higher scores) than controls. The PAE− group had lower fractional anisotropy (FA) in the bilateral cingulum and left uncinate fasciculus, and smaller volumes in the left anterior cingulate cortex than controls and the PAE+ group. The PAE− group also had higher mean diffusivity (MD) in the left uncinate than the PAE+ group, and smaller right anterior cingulate and superior frontal gyrus volumes than controls. These findings show different brain structure and mental health symptom profiles in children with PAE with and without postnatal adversity, highlighting the need to consider adverse postnatal exposures in individuals with PAE. John Wiley & Sons, Inc. 2020-07-13 /pmc/articles/PMC7502833/ /pubmed/32659051 http://dx.doi.org/10.1002/hbm.25130 Text en © 2020 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Andre, Quinn R.
McMorris, Carly A.
Kar, Preeti
Ritter, Chantel
Gibbard, W. Ben
Tortorelli, Christina
Lebel, Catherine
Different brain profiles in children with prenatal alcohol exposure with or without early adverse exposures
title Different brain profiles in children with prenatal alcohol exposure with or without early adverse exposures
title_full Different brain profiles in children with prenatal alcohol exposure with or without early adverse exposures
title_fullStr Different brain profiles in children with prenatal alcohol exposure with or without early adverse exposures
title_full_unstemmed Different brain profiles in children with prenatal alcohol exposure with or without early adverse exposures
title_short Different brain profiles in children with prenatal alcohol exposure with or without early adverse exposures
title_sort different brain profiles in children with prenatal alcohol exposure with or without early adverse exposures
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7502833/
https://www.ncbi.nlm.nih.gov/pubmed/32659051
http://dx.doi.org/10.1002/hbm.25130
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