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Brain structural differences in children with fetal alcohol spectrum disorder and its subtypes

INTRODUCTION: The teratogenic effects of prenatal alcohol exposure (PAE) have been examined in animal models and humans. The current study extends the prior literature by quantifying differences in brain structure for individuals with a fetal alcohol spectrum disorder (FASD) compared to typically de...

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Autores principales: Boateng, Theresah, Beauchamp, Kathryn, Torres, Faerl, Ruffaner-Hanson, Chaselyn D., Pinner, John F. L., Vakamudi, Kishore, Cerros, Cassandra, Hill, Dina E., Stephen, Julia M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10445146/
https://www.ncbi.nlm.nih.gov/pubmed/37621716
http://dx.doi.org/10.3389/fnins.2023.1152038
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author Boateng, Theresah
Beauchamp, Kathryn
Torres, Faerl
Ruffaner-Hanson, Chaselyn D.
Pinner, John F. L.
Vakamudi, Kishore
Cerros, Cassandra
Hill, Dina E.
Stephen, Julia M.
author_facet Boateng, Theresah
Beauchamp, Kathryn
Torres, Faerl
Ruffaner-Hanson, Chaselyn D.
Pinner, John F. L.
Vakamudi, Kishore
Cerros, Cassandra
Hill, Dina E.
Stephen, Julia M.
author_sort Boateng, Theresah
collection PubMed
description INTRODUCTION: The teratogenic effects of prenatal alcohol exposure (PAE) have been examined in animal models and humans. The current study extends the prior literature by quantifying differences in brain structure for individuals with a fetal alcohol spectrum disorder (FASD) compared to typically developing controls, as well as examining FASD subtypes. We hypothesized the FASD group would reveal smaller brain volume, reduced cortical thickness, and reduced surface area compared to controls, with the partial fetal alcohol syndrome (pFAS)/fetal alcohol syndrome (FAS) subtypes showing the largest effects and the PAE/alcohol-related neurodevelopmental disorder (ARND) subtype revealing intermediate effects. METHODS: The sample consisted of 123 children and adolescents recruited from a single site including children with a diagnosis of FASD/PAE (26 males, 29 females) and controls (34 males, 34 females). Structural T1-weighted MRI scans were obtained on a 3T Trio TIM scanner and FreeSurfer v7.2 was used to quantify brain volume, cortical thickness, and surface area. Analyses examined effects by subgroup: pFAS/FAS (N = 32, M(age) = 10.7 years, SE(age) = 0.79), PAE/ARND (N = 23, M(age) = 10.8, SE(age) = 0.94), and controls (N = 68, M(age) = 11.1, SE(age) = 0.54). RESULTS: Total brain volume in children with an FASD was smaller relative to controls, but subtype analysis revealed only the pFAS/FAS group differed significantly from controls. Regional analyses similarly revealed reduced brain volume in frontal and temporal regions for children with pFAS/FAS, yet children diagnosed with PAE/ARND generally had similar volumes as controls. Notable differences to this pattern occurred in the cerebellum, caudate, and pallidum where children with pFAS/FAS and PAE/ARND revealed lower volume relative to controls. In the subset of participants who had neuropsychological testing, correlations between volume and IQ scores were observed. Goodness-of-Fit analysis by age revealed differences in developmental patterns (linear vs. quadratic) between groups in some cases. DISCUSSION: This study confirmed prior results indicating decreased brain volume in children with an FASD and extended the results by demonstrating differential effects by structure for FASD subtypes. It provides further evidence for a complex role of PAE in structural brain development that is likely related to the cognitive and behavioral effects experienced by children with an FASD.
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spelling pubmed-104451462023-08-24 Brain structural differences in children with fetal alcohol spectrum disorder and its subtypes Boateng, Theresah Beauchamp, Kathryn Torres, Faerl Ruffaner-Hanson, Chaselyn D. Pinner, John F. L. Vakamudi, Kishore Cerros, Cassandra Hill, Dina E. Stephen, Julia M. Front Neurosci Neuroscience INTRODUCTION: The teratogenic effects of prenatal alcohol exposure (PAE) have been examined in animal models and humans. The current study extends the prior literature by quantifying differences in brain structure for individuals with a fetal alcohol spectrum disorder (FASD) compared to typically developing controls, as well as examining FASD subtypes. We hypothesized the FASD group would reveal smaller brain volume, reduced cortical thickness, and reduced surface area compared to controls, with the partial fetal alcohol syndrome (pFAS)/fetal alcohol syndrome (FAS) subtypes showing the largest effects and the PAE/alcohol-related neurodevelopmental disorder (ARND) subtype revealing intermediate effects. METHODS: The sample consisted of 123 children and adolescents recruited from a single site including children with a diagnosis of FASD/PAE (26 males, 29 females) and controls (34 males, 34 females). Structural T1-weighted MRI scans were obtained on a 3T Trio TIM scanner and FreeSurfer v7.2 was used to quantify brain volume, cortical thickness, and surface area. Analyses examined effects by subgroup: pFAS/FAS (N = 32, M(age) = 10.7 years, SE(age) = 0.79), PAE/ARND (N = 23, M(age) = 10.8, SE(age) = 0.94), and controls (N = 68, M(age) = 11.1, SE(age) = 0.54). RESULTS: Total brain volume in children with an FASD was smaller relative to controls, but subtype analysis revealed only the pFAS/FAS group differed significantly from controls. Regional analyses similarly revealed reduced brain volume in frontal and temporal regions for children with pFAS/FAS, yet children diagnosed with PAE/ARND generally had similar volumes as controls. Notable differences to this pattern occurred in the cerebellum, caudate, and pallidum where children with pFAS/FAS and PAE/ARND revealed lower volume relative to controls. In the subset of participants who had neuropsychological testing, correlations between volume and IQ scores were observed. Goodness-of-Fit analysis by age revealed differences in developmental patterns (linear vs. quadratic) between groups in some cases. DISCUSSION: This study confirmed prior results indicating decreased brain volume in children with an FASD and extended the results by demonstrating differential effects by structure for FASD subtypes. It provides further evidence for a complex role of PAE in structural brain development that is likely related to the cognitive and behavioral effects experienced by children with an FASD. Frontiers Media S.A. 2023-08-09 /pmc/articles/PMC10445146/ /pubmed/37621716 http://dx.doi.org/10.3389/fnins.2023.1152038 Text en Copyright © 2023 Boateng, Beauchamp, Torres, Ruffaner-Hanson, Pinner, Vakamudi, Cerros, Hill and Stephen. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Boateng, Theresah
Beauchamp, Kathryn
Torres, Faerl
Ruffaner-Hanson, Chaselyn D.
Pinner, John F. L.
Vakamudi, Kishore
Cerros, Cassandra
Hill, Dina E.
Stephen, Julia M.
Brain structural differences in children with fetal alcohol spectrum disorder and its subtypes
title Brain structural differences in children with fetal alcohol spectrum disorder and its subtypes
title_full Brain structural differences in children with fetal alcohol spectrum disorder and its subtypes
title_fullStr Brain structural differences in children with fetal alcohol spectrum disorder and its subtypes
title_full_unstemmed Brain structural differences in children with fetal alcohol spectrum disorder and its subtypes
title_short Brain structural differences in children with fetal alcohol spectrum disorder and its subtypes
title_sort brain structural differences in children with fetal alcohol spectrum disorder and its subtypes
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10445146/
https://www.ncbi.nlm.nih.gov/pubmed/37621716
http://dx.doi.org/10.3389/fnins.2023.1152038
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