Diffusional kurtosis imaging of the corpus callosum in autism

Abstract Background The corpus callosum is implicated in the pathophysiology of autism spectrum disorder (ASD). However, specific structural deficits and underlying mechanisms are yet to be well defined. Methods We employed diffusional kurtosis imaging (DKI) metrics to characterize white matter prop...

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Main Authors: Yu Veronica Sui, Jeffrey Donaldson, Laura Miles, James S. Babb, Francisco Xavier Castellanos, Mariana Lazar
Format: Article
Language:English
Published: BMC 2018-12-01
Series:Molecular Autism
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13229-018-0245-1
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author Yu Veronica Sui
Jeffrey Donaldson
Laura Miles
James S. Babb
Francisco Xavier Castellanos
Mariana Lazar
author_facet Yu Veronica Sui
Jeffrey Donaldson
Laura Miles
James S. Babb
Francisco Xavier Castellanos
Mariana Lazar
author_sort Yu Veronica Sui
collection DOAJ
description Abstract Background The corpus callosum is implicated in the pathophysiology of autism spectrum disorder (ASD). However, specific structural deficits and underlying mechanisms are yet to be well defined. Methods We employed diffusional kurtosis imaging (DKI) metrics to characterize white matter properties within five discrete segments of the corpus callosum in 17 typically developing (TD) adults and 16 age-matched participants with ASD without co-occurring intellectual disability (ID). The DKI metrics included axonal water fraction (f axon) and intra-axonal diffusivity (D axon), which reflect axonal density and caliber, and extra-axonal radial (RDextra) and axial (ADextra) diffusivities, which reflect myelination and microstructural organization of the extracellular space. The relationships between DKI metrics and processing speed, a cognitive feature known to be impaired in ASD, were also examined. Results ASD group had significantly decreased callosal f axon and D axon (p = .01 and p = .045), particularly in the midbody, isthmus, and splenium. Regression analysis showed that variation in DKI metrics, primarily in the mid and posterior callosal regions explained up to 70.7% of the variance in processing speed scores for TD (p = .001) but not for ASD (p > .05). Conclusion Decreased DKI metrics suggested that ASD may be associated with axonal deficits such as reduced axonal caliber and density in the corpus callosum, especially in the mid and posterior callosal areas. These data suggest that impaired interhemispheric connectivity may contribute to decreased processing speed in ASD participants.
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spelling doaj.art-06fd420e974148aca469653a2d9025da2022-12-21T19:44:35ZengBMCMolecular Autism2040-23922018-12-019111210.1186/s13229-018-0245-1Diffusional kurtosis imaging of the corpus callosum in autismYu Veronica Sui0Jeffrey Donaldson1Laura Miles2James S. Babb3Francisco Xavier Castellanos4Mariana Lazar5Department of Radiology, New York University School of MedicineDepartment of Radiology, New York University School of MedicineDepartment of Radiology, New York University School of MedicineDepartment of Radiology, New York University School of MedicineDepartment of Child and Adolescent Psychiatry, Hassenfeld Children’s Hospital at NYU LangoneDepartment of Radiology, New York University School of MedicineAbstract Background The corpus callosum is implicated in the pathophysiology of autism spectrum disorder (ASD). However, specific structural deficits and underlying mechanisms are yet to be well defined. Methods We employed diffusional kurtosis imaging (DKI) metrics to characterize white matter properties within five discrete segments of the corpus callosum in 17 typically developing (TD) adults and 16 age-matched participants with ASD without co-occurring intellectual disability (ID). The DKI metrics included axonal water fraction (f axon) and intra-axonal diffusivity (D axon), which reflect axonal density and caliber, and extra-axonal radial (RDextra) and axial (ADextra) diffusivities, which reflect myelination and microstructural organization of the extracellular space. The relationships between DKI metrics and processing speed, a cognitive feature known to be impaired in ASD, were also examined. Results ASD group had significantly decreased callosal f axon and D axon (p = .01 and p = .045), particularly in the midbody, isthmus, and splenium. Regression analysis showed that variation in DKI metrics, primarily in the mid and posterior callosal regions explained up to 70.7% of the variance in processing speed scores for TD (p = .001) but not for ASD (p > .05). Conclusion Decreased DKI metrics suggested that ASD may be associated with axonal deficits such as reduced axonal caliber and density in the corpus callosum, especially in the mid and posterior callosal areas. These data suggest that impaired interhemispheric connectivity may contribute to decreased processing speed in ASD participants.http://link.springer.com/article/10.1186/s13229-018-0245-1AutismCorpus callosumDiffusional kurtosis imagingProcessing speedInterhemispheric connectivity
spellingShingle Yu Veronica Sui
Jeffrey Donaldson
Laura Miles
James S. Babb
Francisco Xavier Castellanos
Mariana Lazar
Diffusional kurtosis imaging of the corpus callosum in autism
Molecular Autism
Autism
Corpus callosum
Diffusional kurtosis imaging
Processing speed
Interhemispheric connectivity
title Diffusional kurtosis imaging of the corpus callosum in autism
title_full Diffusional kurtosis imaging of the corpus callosum in autism
title_fullStr Diffusional kurtosis imaging of the corpus callosum in autism
title_full_unstemmed Diffusional kurtosis imaging of the corpus callosum in autism
title_short Diffusional kurtosis imaging of the corpus callosum in autism
title_sort diffusional kurtosis imaging of the corpus callosum in autism
topic Autism
Corpus callosum
Diffusional kurtosis imaging
Processing speed
Interhemispheric connectivity
url http://link.springer.com/article/10.1186/s13229-018-0245-1
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