Tractography of the corpus callosum in Huntington's disease.

White matter abnormalities have been shown in presymptomatic and symptomatic Huntington's disease (HD) subjects using Magnetic Resonance Imaging (MRI) and Diffusion Tensor Imaging (DTI) methods. The largest white matter tract, the corpus callosum (CC), has been shown to be particularly vulnerab...

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Main Authors: Owen Phillips, Cristina Sanchez-Castaneda, Francesca Elifani, Vittorio Maglione, Alba Di Pardo, Carlo Caltagirone, Ferdinando Squitieri, Umberto Sabatini, Margherita Di Paola
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0073280&type=printable
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author Owen Phillips
Cristina Sanchez-Castaneda
Francesca Elifani
Vittorio Maglione
Alba Di Pardo
Carlo Caltagirone
Ferdinando Squitieri
Umberto Sabatini
Margherita Di Paola
author_facet Owen Phillips
Cristina Sanchez-Castaneda
Francesca Elifani
Vittorio Maglione
Alba Di Pardo
Carlo Caltagirone
Ferdinando Squitieri
Umberto Sabatini
Margherita Di Paola
author_sort Owen Phillips
collection DOAJ
description White matter abnormalities have been shown in presymptomatic and symptomatic Huntington's disease (HD) subjects using Magnetic Resonance Imaging (MRI) and Diffusion Tensor Imaging (DTI) methods. The largest white matter tract, the corpus callosum (CC), has been shown to be particularly vulnerable; however, little work has been done to investigate the regional specificity of tract abnormalities in the CC. Thus, this study examined the major callosal tracts by applying DTI-based tractography. Using TrackVis, a previously defined region of interest tractography method parcellating CC into seven major tracts based on target region was applied to 30 direction DTI data collected from 100 subjects: presymptomatic HD (Pre-HD) subjects (n=25), HD patients (n=25) and healthy control subjects (n=50). Tractography results showed decreased fractional anisotropy (FA) and increased radial diffusivity (RD) across broad regions of the CC in Pre-HD subjects. Similar though more severe deficits were seen in HD patients. In Pre-HD and HD, callosal FA and RD were correlated with Disease Burden/CAG repeat length as well as motor (UHDRSI) and cognitive (URDRS2) assessments. These results add evidence that CC pathways are compromised prior to disease onset with possible demyelination occurring early in the disease and suggest that CAG repeat length is a contributing factor to connectivity deficits. Furthermore, disruption of these callosal pathways potentially contributes to the disturbances of motor and cognitive processing that characterize HD.
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spelling doaj-art-6bb43314a849488b9ed021e7dd14873a2025-08-20T03:46:23ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0189e7328010.1371/journal.pone.0073280Tractography of the corpus callosum in Huntington's disease.Owen PhillipsCristina Sanchez-CastanedaFrancesca ElifaniVittorio MaglioneAlba Di PardoCarlo CaltagironeFerdinando SquitieriUmberto SabatiniMargherita Di PaolaWhite matter abnormalities have been shown in presymptomatic and symptomatic Huntington's disease (HD) subjects using Magnetic Resonance Imaging (MRI) and Diffusion Tensor Imaging (DTI) methods. The largest white matter tract, the corpus callosum (CC), has been shown to be particularly vulnerable; however, little work has been done to investigate the regional specificity of tract abnormalities in the CC. Thus, this study examined the major callosal tracts by applying DTI-based tractography. Using TrackVis, a previously defined region of interest tractography method parcellating CC into seven major tracts based on target region was applied to 30 direction DTI data collected from 100 subjects: presymptomatic HD (Pre-HD) subjects (n=25), HD patients (n=25) and healthy control subjects (n=50). Tractography results showed decreased fractional anisotropy (FA) and increased radial diffusivity (RD) across broad regions of the CC in Pre-HD subjects. Similar though more severe deficits were seen in HD patients. In Pre-HD and HD, callosal FA and RD were correlated with Disease Burden/CAG repeat length as well as motor (UHDRSI) and cognitive (URDRS2) assessments. These results add evidence that CC pathways are compromised prior to disease onset with possible demyelination occurring early in the disease and suggest that CAG repeat length is a contributing factor to connectivity deficits. Furthermore, disruption of these callosal pathways potentially contributes to the disturbances of motor and cognitive processing that characterize HD.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0073280&type=printable
spellingShingle Owen Phillips
Cristina Sanchez-Castaneda
Francesca Elifani
Vittorio Maglione
Alba Di Pardo
Carlo Caltagirone
Ferdinando Squitieri
Umberto Sabatini
Margherita Di Paola
Tractography of the corpus callosum in Huntington's disease.
PLoS ONE
title Tractography of the corpus callosum in Huntington's disease.
title_full Tractography of the corpus callosum in Huntington's disease.
title_fullStr Tractography of the corpus callosum in Huntington's disease.
title_full_unstemmed Tractography of the corpus callosum in Huntington's disease.
title_short Tractography of the corpus callosum in Huntington's disease.
title_sort tractography of the corpus callosum in huntington s disease
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0073280&type=printable
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