TY - JOUR
T1 - Structural mediation of the default-mode network in children with callosal agenesis
AU - Provins, Céline
AU - Tarun Nahalka, Anjali
AU - Schmidt, Léa
AU - Anderson, Vicki
AU - McIlroy, Alissandra
AU - Wood, Amanda
AU - Esteban, Oscar
AU - Leventer, Richard
AU - Spencer-Smith, Megan
AU - Van De Ville, Dimitri
AU - Siffredi, Vanessa
N1 - Copyright © The Author(s) 2025. Published by Oxford University Press.
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which
permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
PY - 2025/7/26
Y1 - 2025/7/26
N2 - Agenesis of the corpus callosum is a neurodevelopmental condition characterized by the partial or complete absence of the corpus callosum, the largest white matter bundle connecting the cerebral hemispheres. The default-mode network comprises bilateral frontal, temporal, and parietal regions that exhibit correlated activity at rest. Previous studies show that individuals with agenesis of the corpus callosum show overall preserved default-mode network functional connectivity, suggesting compensatory mechanisms for maintaining bilaterally correlated activity. In this study, we aimed to explore white matter pathways that support default-mode network-related networks in 15 children with agenesis of the corpus callosum and 27 typically developing controls, using combined diffusion and functional magnetic resonance imaging. A seed-based and dynamic functional connectivity approach enabled us to examine default-mode network spatial and temporal properties and their white matter substrates. While spatial default-mode network patterns were similar across groups, we found differences in temporal dynamics of 1 network and in white matter–default-mode network correspondence. These differences were either observed in white matter tracts directly associated with complete or partial absence of the corpus callosum or in white matter tracts such as the fornix and the anterior and posterior commissures, which have been previously implicated in neuroplasticity in agenesis of the corpus callosum. Our findings show that default-mode network dynamics can remain functionally preserved despite significant white matter alterations.
AB - Agenesis of the corpus callosum is a neurodevelopmental condition characterized by the partial or complete absence of the corpus callosum, the largest white matter bundle connecting the cerebral hemispheres. The default-mode network comprises bilateral frontal, temporal, and parietal regions that exhibit correlated activity at rest. Previous studies show that individuals with agenesis of the corpus callosum show overall preserved default-mode network functional connectivity, suggesting compensatory mechanisms for maintaining bilaterally correlated activity. In this study, we aimed to explore white matter pathways that support default-mode network-related networks in 15 children with agenesis of the corpus callosum and 27 typically developing controls, using combined diffusion and functional magnetic resonance imaging. A seed-based and dynamic functional connectivity approach enabled us to examine default-mode network spatial and temporal properties and their white matter substrates. While spatial default-mode network patterns were similar across groups, we found differences in temporal dynamics of 1 network and in white matter–default-mode network correspondence. These differences were either observed in white matter tracts directly associated with complete or partial absence of the corpus callosum or in white matter tracts such as the fornix and the anterior and posterior commissures, which have been previously implicated in neuroplasticity in agenesis of the corpus callosum. Our findings show that default-mode network dynamics can remain functionally preserved despite significant white matter alterations.
KW - corpus callosum agenesis
KW - default-mode network
KW - neuroimaging
KW - neuroplasticity
KW - structure-function relationship
UR - https://academic.oup.com/cercor/article/35/7/bhaf190/8213922
UR - http://www.scopus.com/inward/record.url?scp=105011623885&partnerID=8YFLogxK
U2 - 10.1093/cercor/bhaf190
DO - 10.1093/cercor/bhaf190
M3 - Article
SN - 1047-3211
VL - 35
JO - Cerebral Cortex
JF - Cerebral Cortex
IS - 7
M1 - bhaf190
ER -