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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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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. |
format | Online Article Text |
id | pubmed-9248320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
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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