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Altered myelination in youth born with congenital heart disease

Brain injury and dysmaturation is common in fetuses and neonates with congenital heart disease (CHD) and is hypothesized to result in persistent myelination deficits. This study aimed to quantify and compare myelin content in vivo between youth born with CHD and healthy controls. Youth aged 16 to 24...

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Autores principales: Easson, Kaitlyn, Gilbert, Guillaume, Rohlicek, Charles V., Saint‐Martin, Christine, Descoteaux, Maxime, Deoni, Sean C. L., Brossard‐Racine, Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248320/
https://www.ncbi.nlm.nih.gov/pubmed/35411995
http://dx.doi.org/10.1002/hbm.25866
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author Easson, Kaitlyn
Gilbert, Guillaume
Rohlicek, Charles V.
Saint‐Martin, Christine
Descoteaux, Maxime
Deoni, Sean C. L.
Brossard‐Racine, Marie
author_facet Easson, Kaitlyn
Gilbert, Guillaume
Rohlicek, Charles V.
Saint‐Martin, Christine
Descoteaux, Maxime
Deoni, Sean C. L.
Brossard‐Racine, Marie
author_sort Easson, Kaitlyn
collection PubMed
description Brain injury and dysmaturation is common in fetuses and neonates with congenital heart disease (CHD) and is hypothesized to result in persistent myelination deficits. This study aimed to quantify and compare myelin content in vivo between youth born with CHD and healthy controls. Youth aged 16 to 24 years born with CHD and healthy age‐ and sex‐matched controls underwent brain magnetic resonance imaging including multicomponent driven equilibrium single pulse observation of T(1) and T(2) (mcDESPOT). Average myelin water fraction (MWF) values for 33 white matter tracts, as well as a summary measure of average white matter MWF, the White Matter Myelination Index, were calculated and compared between groups. Tract‐average MWF was lower throughout the corpus callosum and in many bilateral association tracts and left hemispheric projection tracts in youth with CHD (N = 44) as compared to controls (N = 45). The White Matter Myelination Index was also lower in the CHD group. As such, this study provides specific evidence of widespread myelination deficits in youth with CHD, likely representing a long‐lasting consequence of early‐life brain dysmaturation in this population. This deficient myelination may underlie the frequent neurodevelopmental impairments experienced by CHD survivors and could eventually serve as a biomarker of neuropsychological function.
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spelling pubmed-92483202022-07-05 Altered myelination in youth born with congenital heart disease Easson, Kaitlyn Gilbert, Guillaume Rohlicek, Charles V. Saint‐Martin, Christine Descoteaux, Maxime Deoni, Sean C. L. Brossard‐Racine, Marie Hum Brain Mapp Research Articles Brain injury and dysmaturation is common in fetuses and neonates with congenital heart disease (CHD) and is hypothesized to result in persistent myelination deficits. This study aimed to quantify and compare myelin content in vivo between youth born with CHD and healthy controls. Youth aged 16 to 24 years born with CHD and healthy age‐ and sex‐matched controls underwent brain magnetic resonance imaging including multicomponent driven equilibrium single pulse observation of T(1) and T(2) (mcDESPOT). Average myelin water fraction (MWF) values for 33 white matter tracts, as well as a summary measure of average white matter MWF, the White Matter Myelination Index, were calculated and compared between groups. Tract‐average MWF was lower throughout the corpus callosum and in many bilateral association tracts and left hemispheric projection tracts in youth with CHD (N = 44) as compared to controls (N = 45). The White Matter Myelination Index was also lower in the CHD group. As such, this study provides specific evidence of widespread myelination deficits in youth with CHD, likely representing a long‐lasting consequence of early‐life brain dysmaturation in this population. This deficient myelination may underlie the frequent neurodevelopmental impairments experienced by CHD survivors and could eventually serve as a biomarker of neuropsychological function. John Wiley & Sons, Inc. 2022-04-12 /pmc/articles/PMC9248320/ /pubmed/35411995 http://dx.doi.org/10.1002/hbm.25866 Text en © 2022 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Easson, Kaitlyn
Gilbert, Guillaume
Rohlicek, Charles V.
Saint‐Martin, Christine
Descoteaux, Maxime
Deoni, Sean C. L.
Brossard‐Racine, Marie
Altered myelination in youth born with congenital heart disease
title Altered myelination in youth born with congenital heart disease
title_full Altered myelination in youth born with congenital heart disease
title_fullStr Altered myelination in youth born with congenital heart disease
title_full_unstemmed Altered myelination in youth born with congenital heart disease
title_short Altered myelination in youth born with congenital heart disease
title_sort altered myelination in youth born with congenital heart disease
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248320/
https://www.ncbi.nlm.nih.gov/pubmed/35411995
http://dx.doi.org/10.1002/hbm.25866
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