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The Role of Corpus Callosum Development in Functional Connectivity and Cognitive Processing
The corpus callosum is hypothesized to play a fundamental role in integrating information and mediating complex behaviors. Here, we demonstrate that lack of normal callosal development can lead to deficits in functional connectivity that are related to impairments in specific cognitive domains. We e...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3411722/ https://www.ncbi.nlm.nih.gov/pubmed/22870191 http://dx.doi.org/10.1371/journal.pone.0039804 |
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author | Hinkley, Leighton B. N. Marco, Elysa J. Findlay, Anne M. Honma, Susanne Jeremy, Rita J. Strominger, Zoe Bukshpun, Polina Wakahiro, Mari Brown, Warren S. Paul, Lynn K. Barkovich, A. James Mukherjee, Pratik Nagarajan, Srikantan S. Sherr, Elliott H. |
author_facet | Hinkley, Leighton B. N. Marco, Elysa J. Findlay, Anne M. Honma, Susanne Jeremy, Rita J. Strominger, Zoe Bukshpun, Polina Wakahiro, Mari Brown, Warren S. Paul, Lynn K. Barkovich, A. James Mukherjee, Pratik Nagarajan, Srikantan S. Sherr, Elliott H. |
author_sort | Hinkley, Leighton B. N. |
collection | PubMed |
description | The corpus callosum is hypothesized to play a fundamental role in integrating information and mediating complex behaviors. Here, we demonstrate that lack of normal callosal development can lead to deficits in functional connectivity that are related to impairments in specific cognitive domains. We examined resting-state functional connectivity in individuals with agenesis of the corpus callosum (AgCC) and matched controls using magnetoencephalographic imaging (MEG-I) of coherence in the alpha (8–12 Hz), beta (12–30 Hz) and gamma (30–55 Hz) bands. Global connectivity (GC) was defined as synchronization between a region and the rest of the brain. In AgCC individuals, alpha band GC was significantly reduced in the dorsolateral pre-frontal (DLPFC), posterior parietal (PPC) and parieto-occipital cortices (PO). No significant differences in GC were seen in either the beta or gamma bands. We also explored the hypothesis that, in AgCC, this regional reduction in functional connectivity is explained primarily by a specific reduction in interhemispheric connectivity. However, our data suggest that reduced connectivity in these regions is driven by faulty coupling in both inter- and intrahemispheric connectivity. We also assessed whether the degree of connectivity correlated with behavioral performance, focusing on cognitive measures known to be impaired in AgCC individuals. Neuropsychological measures of verbal processing speed were significantly correlated with resting-state functional connectivity of the left medial and superior temporal lobe in AgCC participants. Connectivity of DLPFC correlated strongly with performance on the Tower of London in the AgCC cohort. These findings indicate that the abnormal callosal development produces salient but selective (alpha band only) resting-state functional connectivity disruptions that correlate with cognitive impairment. Understanding the relationship between impoverished functional connectivity and cognition is a key step in identifying the neural mechanisms of language and executive dysfunction in common neurodevelopmental and psychiatric disorders where disruptions of callosal development are consistently identified. |
format | Online Article Text |
id | pubmed-3411722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-34117222012-08-06 The Role of Corpus Callosum Development in Functional Connectivity and Cognitive Processing Hinkley, Leighton B. N. Marco, Elysa J. Findlay, Anne M. Honma, Susanne Jeremy, Rita J. Strominger, Zoe Bukshpun, Polina Wakahiro, Mari Brown, Warren S. Paul, Lynn K. Barkovich, A. James Mukherjee, Pratik Nagarajan, Srikantan S. Sherr, Elliott H. PLoS One Research Article The corpus callosum is hypothesized to play a fundamental role in integrating information and mediating complex behaviors. Here, we demonstrate that lack of normal callosal development can lead to deficits in functional connectivity that are related to impairments in specific cognitive domains. We examined resting-state functional connectivity in individuals with agenesis of the corpus callosum (AgCC) and matched controls using magnetoencephalographic imaging (MEG-I) of coherence in the alpha (8–12 Hz), beta (12–30 Hz) and gamma (30–55 Hz) bands. Global connectivity (GC) was defined as synchronization between a region and the rest of the brain. In AgCC individuals, alpha band GC was significantly reduced in the dorsolateral pre-frontal (DLPFC), posterior parietal (PPC) and parieto-occipital cortices (PO). No significant differences in GC were seen in either the beta or gamma bands. We also explored the hypothesis that, in AgCC, this regional reduction in functional connectivity is explained primarily by a specific reduction in interhemispheric connectivity. However, our data suggest that reduced connectivity in these regions is driven by faulty coupling in both inter- and intrahemispheric connectivity. We also assessed whether the degree of connectivity correlated with behavioral performance, focusing on cognitive measures known to be impaired in AgCC individuals. Neuropsychological measures of verbal processing speed were significantly correlated with resting-state functional connectivity of the left medial and superior temporal lobe in AgCC participants. Connectivity of DLPFC correlated strongly with performance on the Tower of London in the AgCC cohort. These findings indicate that the abnormal callosal development produces salient but selective (alpha band only) resting-state functional connectivity disruptions that correlate with cognitive impairment. Understanding the relationship between impoverished functional connectivity and cognition is a key step in identifying the neural mechanisms of language and executive dysfunction in common neurodevelopmental and psychiatric disorders where disruptions of callosal development are consistently identified. Public Library of Science 2012-08-03 /pmc/articles/PMC3411722/ /pubmed/22870191 http://dx.doi.org/10.1371/journal.pone.0039804 Text en © 2012 Hinkley et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Hinkley, Leighton B. N. Marco, Elysa J. Findlay, Anne M. Honma, Susanne Jeremy, Rita J. Strominger, Zoe Bukshpun, Polina Wakahiro, Mari Brown, Warren S. Paul, Lynn K. Barkovich, A. James Mukherjee, Pratik Nagarajan, Srikantan S. Sherr, Elliott H. The Role of Corpus Callosum Development in Functional Connectivity and Cognitive Processing |
title | The Role of Corpus Callosum Development in Functional Connectivity and Cognitive Processing |
title_full | The Role of Corpus Callosum Development in Functional Connectivity and Cognitive Processing |
title_fullStr | The Role of Corpus Callosum Development in Functional Connectivity and Cognitive Processing |
title_full_unstemmed | The Role of Corpus Callosum Development in Functional Connectivity and Cognitive Processing |
title_short | The Role of Corpus Callosum Development in Functional Connectivity and Cognitive Processing |
title_sort | role of corpus callosum development in functional connectivity and cognitive processing |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3411722/ https://www.ncbi.nlm.nih.gov/pubmed/22870191 http://dx.doi.org/10.1371/journal.pone.0039804 |
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