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Development of human white matter pathways in utero over the second and third trimester

During the second and third trimesters of human gestation, rapid neurodevelopment is underpinned by fundamental processes including neuronal migration, cellular organization, cortical layering, and myelination. In this time, white matter growth and maturation lay the foundation for an efficient netw...

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Autores principales: Wilson, Siân, Pietsch, Maximilian, Cordero-Grande, Lucilio, Price, Anthony N., Hutter, Jana, Xiao, Jiaxin, McCabe, Laura, Rutherford, Mary A., Hughes, Emer J., Counsell, Serena J., Tournier, Jacques-Donald, Arichi, Tomoki, Hajnal, Joseph V., Edwards, A. David, Christiaens, Daan, O’Muircheartaigh, Jonathan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157930/
https://www.ncbi.nlm.nih.gov/pubmed/33972435
http://dx.doi.org/10.1073/pnas.2023598118
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author Wilson, Siân
Pietsch, Maximilian
Cordero-Grande, Lucilio
Price, Anthony N.
Hutter, Jana
Xiao, Jiaxin
McCabe, Laura
Rutherford, Mary A.
Hughes, Emer J.
Counsell, Serena J.
Tournier, Jacques-Donald
Arichi, Tomoki
Hajnal, Joseph V.
Edwards, A. David
Christiaens, Daan
O’Muircheartaigh, Jonathan
author_facet Wilson, Siân
Pietsch, Maximilian
Cordero-Grande, Lucilio
Price, Anthony N.
Hutter, Jana
Xiao, Jiaxin
McCabe, Laura
Rutherford, Mary A.
Hughes, Emer J.
Counsell, Serena J.
Tournier, Jacques-Donald
Arichi, Tomoki
Hajnal, Joseph V.
Edwards, A. David
Christiaens, Daan
O’Muircheartaigh, Jonathan
author_sort Wilson, Siân
collection PubMed
description During the second and third trimesters of human gestation, rapid neurodevelopment is underpinned by fundamental processes including neuronal migration, cellular organization, cortical layering, and myelination. In this time, white matter growth and maturation lay the foundation for an efficient network of structural connections. Detailed knowledge about this developmental trajectory in the healthy human fetal brain is limited, in part, due to the inherent challenges of acquiring high-quality MRI data from this population. Here, we use state-of-the-art high-resolution multishell motion-corrected diffusion-weighted MRI (dMRI), collected as part of the developing Human Connectome Project (dHCP), to characterize the in utero maturation of white matter microstructure in 113 fetuses aged 22 to 37 wk gestation. We define five major white matter bundles and characterize their microstructural features using both traditional diffusion tensor and multishell multitissue models. We found unique maturational trends in thalamocortical fibers compared with association tracts and identified different maturational trends within specific sections of the corpus callosum. While linear maturational increases in fractional anisotropy were seen in the splenium of the corpus callosum, complex nonlinear trends were seen in the majority of other white matter tracts, with an initial decrease in fractional anisotropy in early gestation followed by a later increase. The latter is of particular interest as it differs markedly from the trends previously described in ex utero preterm infants, suggesting that this normative fetal data can provide significant insights into the abnormalities in connectivity which underlie the neurodevelopmental impairments associated with preterm birth.
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spelling pubmed-81579302021-05-28 Development of human white matter pathways in utero over the second and third trimester Wilson, Siân Pietsch, Maximilian Cordero-Grande, Lucilio Price, Anthony N. Hutter, Jana Xiao, Jiaxin McCabe, Laura Rutherford, Mary A. Hughes, Emer J. Counsell, Serena J. Tournier, Jacques-Donald Arichi, Tomoki Hajnal, Joseph V. Edwards, A. David Christiaens, Daan O’Muircheartaigh, Jonathan Proc Natl Acad Sci U S A Biological Sciences During the second and third trimesters of human gestation, rapid neurodevelopment is underpinned by fundamental processes including neuronal migration, cellular organization, cortical layering, and myelination. In this time, white matter growth and maturation lay the foundation for an efficient network of structural connections. Detailed knowledge about this developmental trajectory in the healthy human fetal brain is limited, in part, due to the inherent challenges of acquiring high-quality MRI data from this population. Here, we use state-of-the-art high-resolution multishell motion-corrected diffusion-weighted MRI (dMRI), collected as part of the developing Human Connectome Project (dHCP), to characterize the in utero maturation of white matter microstructure in 113 fetuses aged 22 to 37 wk gestation. We define five major white matter bundles and characterize their microstructural features using both traditional diffusion tensor and multishell multitissue models. We found unique maturational trends in thalamocortical fibers compared with association tracts and identified different maturational trends within specific sections of the corpus callosum. While linear maturational increases in fractional anisotropy were seen in the splenium of the corpus callosum, complex nonlinear trends were seen in the majority of other white matter tracts, with an initial decrease in fractional anisotropy in early gestation followed by a later increase. The latter is of particular interest as it differs markedly from the trends previously described in ex utero preterm infants, suggesting that this normative fetal data can provide significant insights into the abnormalities in connectivity which underlie the neurodevelopmental impairments associated with preterm birth. National Academy of Sciences 2021-05-18 2021-05-10 /pmc/articles/PMC8157930/ /pubmed/33972435 http://dx.doi.org/10.1073/pnas.2023598118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Wilson, Siân
Pietsch, Maximilian
Cordero-Grande, Lucilio
Price, Anthony N.
Hutter, Jana
Xiao, Jiaxin
McCabe, Laura
Rutherford, Mary A.
Hughes, Emer J.
Counsell, Serena J.
Tournier, Jacques-Donald
Arichi, Tomoki
Hajnal, Joseph V.
Edwards, A. David
Christiaens, Daan
O’Muircheartaigh, Jonathan
Development of human white matter pathways in utero over the second and third trimester
title Development of human white matter pathways in utero over the second and third trimester
title_full Development of human white matter pathways in utero over the second and third trimester
title_fullStr Development of human white matter pathways in utero over the second and third trimester
title_full_unstemmed Development of human white matter pathways in utero over the second and third trimester
title_short Development of human white matter pathways in utero over the second and third trimester
title_sort development of human white matter pathways in utero over the second and third trimester
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8157930/
https://www.ncbi.nlm.nih.gov/pubmed/33972435
http://dx.doi.org/10.1073/pnas.2023598118
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