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Microstructural White Matter Changes in the Corpus Callosum of Young People with Bipolar Disorder: A Diffusion Tensor Imaging Study

To date, most studies of white matter changes in Bipolar Disorder (BD) have been conducted in older subjects and with well-established disorders. Studies of young people who are closer to their illness onset may help to identify core neurobiological characteristics and separate these from consequenc...

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Autores principales: Lagopoulos, Jim, Hermens, Daniel F., Hatton, Sean N., Tobias-Webb, Juliette, Griffiths, Kristi, Naismith, Sharon L., Scott, Elizabeth M., Hickie, Ian B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602458/
https://www.ncbi.nlm.nih.gov/pubmed/23527101
http://dx.doi.org/10.1371/journal.pone.0059108
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author Lagopoulos, Jim
Hermens, Daniel F.
Hatton, Sean N.
Tobias-Webb, Juliette
Griffiths, Kristi
Naismith, Sharon L.
Scott, Elizabeth M.
Hickie, Ian B.
author_facet Lagopoulos, Jim
Hermens, Daniel F.
Hatton, Sean N.
Tobias-Webb, Juliette
Griffiths, Kristi
Naismith, Sharon L.
Scott, Elizabeth M.
Hickie, Ian B.
author_sort Lagopoulos, Jim
collection PubMed
description To date, most studies of white matter changes in Bipolar Disorder (BD) have been conducted in older subjects and with well-established disorders. Studies of young people who are closer to their illness onset may help to identify core neurobiological characteristics and separate these from consequences of repeated illness episodes or prolonged treatment. Diffusion tensor imaging (DTI) was used to examine white matter microstructural changes in 58 young patients with BD (mean age 23 years; range 16–30 years) and 40 controls. Whole brain voxelwise measures of fractional anisotropy (FA), parallel diffusivity (λ//) and radial diffusivity (λ⊥) were calculated for all subjects. White matter microstructure differences (decreased FA corrected p<.05) were found between the patients with BD and controls in the genu, body and splenium of the corpus callosum as well as the superior and anterior corona radiata. In addition, significantly increased radial diffusivity (p<.01) was found in the BD group. Neuroimaging studies of young patients with BD may help to clarify neurodevelopmental aspects of the illness and for identifying biomarkers of disease onset and progression. Our findings provide evidence of microstructural white matter changes early in the course of illness within the corpus callosum and the nature of these changes suggest they are associated with abnormalities in the myelination of axons.
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spelling pubmed-36024582013-03-22 Microstructural White Matter Changes in the Corpus Callosum of Young People with Bipolar Disorder: A Diffusion Tensor Imaging Study Lagopoulos, Jim Hermens, Daniel F. Hatton, Sean N. Tobias-Webb, Juliette Griffiths, Kristi Naismith, Sharon L. Scott, Elizabeth M. Hickie, Ian B. PLoS One Research Article To date, most studies of white matter changes in Bipolar Disorder (BD) have been conducted in older subjects and with well-established disorders. Studies of young people who are closer to their illness onset may help to identify core neurobiological characteristics and separate these from consequences of repeated illness episodes or prolonged treatment. Diffusion tensor imaging (DTI) was used to examine white matter microstructural changes in 58 young patients with BD (mean age 23 years; range 16–30 years) and 40 controls. Whole brain voxelwise measures of fractional anisotropy (FA), parallel diffusivity (λ//) and radial diffusivity (λ⊥) were calculated for all subjects. White matter microstructure differences (decreased FA corrected p<.05) were found between the patients with BD and controls in the genu, body and splenium of the corpus callosum as well as the superior and anterior corona radiata. In addition, significantly increased radial diffusivity (p<.01) was found in the BD group. Neuroimaging studies of young patients with BD may help to clarify neurodevelopmental aspects of the illness and for identifying biomarkers of disease onset and progression. Our findings provide evidence of microstructural white matter changes early in the course of illness within the corpus callosum and the nature of these changes suggest they are associated with abnormalities in the myelination of axons. Public Library of Science 2013-03-19 /pmc/articles/PMC3602458/ /pubmed/23527101 http://dx.doi.org/10.1371/journal.pone.0059108 Text en © 2013 Lagopoulos 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
Lagopoulos, Jim
Hermens, Daniel F.
Hatton, Sean N.
Tobias-Webb, Juliette
Griffiths, Kristi
Naismith, Sharon L.
Scott, Elizabeth M.
Hickie, Ian B.
Microstructural White Matter Changes in the Corpus Callosum of Young People with Bipolar Disorder: A Diffusion Tensor Imaging Study
title Microstructural White Matter Changes in the Corpus Callosum of Young People with Bipolar Disorder: A Diffusion Tensor Imaging Study
title_full Microstructural White Matter Changes in the Corpus Callosum of Young People with Bipolar Disorder: A Diffusion Tensor Imaging Study
title_fullStr Microstructural White Matter Changes in the Corpus Callosum of Young People with Bipolar Disorder: A Diffusion Tensor Imaging Study
title_full_unstemmed Microstructural White Matter Changes in the Corpus Callosum of Young People with Bipolar Disorder: A Diffusion Tensor Imaging Study
title_short Microstructural White Matter Changes in the Corpus Callosum of Young People with Bipolar Disorder: A Diffusion Tensor Imaging Study
title_sort microstructural white matter changes in the corpus callosum of young people with bipolar disorder: a diffusion tensor imaging study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3602458/
https://www.ncbi.nlm.nih.gov/pubmed/23527101
http://dx.doi.org/10.1371/journal.pone.0059108
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