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The Developing Human Connectome Project: typical and disrupted perinatal functional connectivity

The Developing Human Connectome Project is an Open Science project that provides the first large sample of neonatal functional MRI data with high temporal and spatial resolution. These data enable mapping of intrinsic functional connectivity between spatially distributed brain regions under normal a...

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Autores principales: Eyre, Michael, Fitzgibbon, Sean P, Ciarrusta, Judit, Cordero-Grande, Lucilio, Price, Anthony N, Poppe, Tanya, Schuh, Andreas, Hughes, Emer, O’Keeffe, Camilla, Brandon, Jakki, Cromb, Daniel, Vecchiato, Katy, Andersson, Jesper, Duff, Eugene P, Counsell, Serena J, Smith, Stephen M, Rueckert, Daniel, Hajnal, Joseph V, Arichi, Tomoki, O’Muircheartaigh, Jonathan, Batalle, Dafnis, Edwards, A David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370420/
https://www.ncbi.nlm.nih.gov/pubmed/33734321
http://dx.doi.org/10.1093/brain/awab118
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author Eyre, Michael
Fitzgibbon, Sean P
Ciarrusta, Judit
Cordero-Grande, Lucilio
Price, Anthony N
Poppe, Tanya
Schuh, Andreas
Hughes, Emer
O’Keeffe, Camilla
Brandon, Jakki
Cromb, Daniel
Vecchiato, Katy
Andersson, Jesper
Duff, Eugene P
Counsell, Serena J
Smith, Stephen M
Rueckert, Daniel
Hajnal, Joseph V
Arichi, Tomoki
O’Muircheartaigh, Jonathan
Batalle, Dafnis
Edwards, A David
author_facet Eyre, Michael
Fitzgibbon, Sean P
Ciarrusta, Judit
Cordero-Grande, Lucilio
Price, Anthony N
Poppe, Tanya
Schuh, Andreas
Hughes, Emer
O’Keeffe, Camilla
Brandon, Jakki
Cromb, Daniel
Vecchiato, Katy
Andersson, Jesper
Duff, Eugene P
Counsell, Serena J
Smith, Stephen M
Rueckert, Daniel
Hajnal, Joseph V
Arichi, Tomoki
O’Muircheartaigh, Jonathan
Batalle, Dafnis
Edwards, A David
author_sort Eyre, Michael
collection PubMed
description The Developing Human Connectome Project is an Open Science project that provides the first large sample of neonatal functional MRI data with high temporal and spatial resolution. These data enable mapping of intrinsic functional connectivity between spatially distributed brain regions under normal and adverse perinatal circumstances, offering a framework to study the ontogeny of large-scale brain organization in humans. Here, we characterize in unprecedented detail the maturation and integrity of resting state networks (RSNs) at term-equivalent age in 337 infants (including 65 born preterm). First, we applied group independent component analysis to define 11 RSNs in term-born infants scanned at 43.5–44.5 weeks postmenstrual age (PMA). Adult-like topography was observed in RSNs encompassing primary sensorimotor, visual and auditory cortices. Among six higher-order, association RSNs, analogues of the adult networks for language and ocular control were identified, but a complete default mode network precursor was not. Next, we regressed the subject-level datasets from an independent cohort of infants scanned at 37–43.5 weeks PMA against the group-level RSNs to test for the effects of age, sex and preterm birth. Brain mapping in term-born infants revealed areas of positive association with age across four of six association RSNs, indicating active maturation in functional connectivity from 37 to 43.5 weeks PMA. Female infants showed increased connectivity in inferotemporal regions of the visual association network. Preterm birth was associated with striking impairments of functional connectivity across all RSNs in a dose-dependent manner; conversely, connectivity of the superior parietal lobules within the lateral motor network was abnormally increased in preterm infants, suggesting a possible mechanism for specific difficulties such as developmental coordination disorder, which occur frequently in preterm children. Overall, we found a robust, modular, symmetrical functional brain organization at normal term age. A complete set of adult-equivalent primary RSNs is already instated, alongside emerging connectivity in immature association RSNs, consistent with a primary-to-higher order ontogenetic sequence of brain development. The early developmental disruption imposed by preterm birth is associated with extensive alterations in functional connectivity.
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spelling pubmed-83704202021-08-18 The Developing Human Connectome Project: typical and disrupted perinatal functional connectivity Eyre, Michael Fitzgibbon, Sean P Ciarrusta, Judit Cordero-Grande, Lucilio Price, Anthony N Poppe, Tanya Schuh, Andreas Hughes, Emer O’Keeffe, Camilla Brandon, Jakki Cromb, Daniel Vecchiato, Katy Andersson, Jesper Duff, Eugene P Counsell, Serena J Smith, Stephen M Rueckert, Daniel Hajnal, Joseph V Arichi, Tomoki O’Muircheartaigh, Jonathan Batalle, Dafnis Edwards, A David Brain Original Articles The Developing Human Connectome Project is an Open Science project that provides the first large sample of neonatal functional MRI data with high temporal and spatial resolution. These data enable mapping of intrinsic functional connectivity between spatially distributed brain regions under normal and adverse perinatal circumstances, offering a framework to study the ontogeny of large-scale brain organization in humans. Here, we characterize in unprecedented detail the maturation and integrity of resting state networks (RSNs) at term-equivalent age in 337 infants (including 65 born preterm). First, we applied group independent component analysis to define 11 RSNs in term-born infants scanned at 43.5–44.5 weeks postmenstrual age (PMA). Adult-like topography was observed in RSNs encompassing primary sensorimotor, visual and auditory cortices. Among six higher-order, association RSNs, analogues of the adult networks for language and ocular control were identified, but a complete default mode network precursor was not. Next, we regressed the subject-level datasets from an independent cohort of infants scanned at 37–43.5 weeks PMA against the group-level RSNs to test for the effects of age, sex and preterm birth. Brain mapping in term-born infants revealed areas of positive association with age across four of six association RSNs, indicating active maturation in functional connectivity from 37 to 43.5 weeks PMA. Female infants showed increased connectivity in inferotemporal regions of the visual association network. Preterm birth was associated with striking impairments of functional connectivity across all RSNs in a dose-dependent manner; conversely, connectivity of the superior parietal lobules within the lateral motor network was abnormally increased in preterm infants, suggesting a possible mechanism for specific difficulties such as developmental coordination disorder, which occur frequently in preterm children. Overall, we found a robust, modular, symmetrical functional brain organization at normal term age. A complete set of adult-equivalent primary RSNs is already instated, alongside emerging connectivity in immature association RSNs, consistent with a primary-to-higher order ontogenetic sequence of brain development. The early developmental disruption imposed by preterm birth is associated with extensive alterations in functional connectivity. Oxford University Press 2021-03-18 /pmc/articles/PMC8370420/ /pubmed/33734321 http://dx.doi.org/10.1093/brain/awab118 Text en © The Author(s) (2021). Published by Oxford University Press on behalf of the Guarantors of Brain. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Eyre, Michael
Fitzgibbon, Sean P
Ciarrusta, Judit
Cordero-Grande, Lucilio
Price, Anthony N
Poppe, Tanya
Schuh, Andreas
Hughes, Emer
O’Keeffe, Camilla
Brandon, Jakki
Cromb, Daniel
Vecchiato, Katy
Andersson, Jesper
Duff, Eugene P
Counsell, Serena J
Smith, Stephen M
Rueckert, Daniel
Hajnal, Joseph V
Arichi, Tomoki
O’Muircheartaigh, Jonathan
Batalle, Dafnis
Edwards, A David
The Developing Human Connectome Project: typical and disrupted perinatal functional connectivity
title The Developing Human Connectome Project: typical and disrupted perinatal functional connectivity
title_full The Developing Human Connectome Project: typical and disrupted perinatal functional connectivity
title_fullStr The Developing Human Connectome Project: typical and disrupted perinatal functional connectivity
title_full_unstemmed The Developing Human Connectome Project: typical and disrupted perinatal functional connectivity
title_short The Developing Human Connectome Project: typical and disrupted perinatal functional connectivity
title_sort developing human connectome project: typical and disrupted perinatal functional connectivity
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8370420/
https://www.ncbi.nlm.nih.gov/pubmed/33734321
http://dx.doi.org/10.1093/brain/awab118
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