Cargando…

Reduced Fractional Anisotropy of Corpus Callosum Modulates Inter-Hemispheric Resting State Functional Connectivity in Migraine Patients without Aura

BACKGROUND: Diffusion tensor imaging (DTI) study revealed reduced fractional anisotropy (FA) values in the corpus callosum (CC) in migraine patients without aura. Abnormalities in white matter integrity, particularly in the CC, may affect inter-hemispheric resting state functional connectivity (RSFC...

Descripción completa

Detalles Bibliográficos
Autores principales: Yuan, Kai, Qin, Wei, Liu, Peng, Zhao, Ling, Yu, Dahua, Zhao, Limei, Dong, Minghao, Liu, Jixin, Yang, Xuejuan, von Deneen, Karen M., Liang, Fanrong, Tian, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3454437/
https://www.ncbi.nlm.nih.gov/pubmed/23029036
http://dx.doi.org/10.1371/journal.pone.0045476
_version_ 1782244506040532992
author Yuan, Kai
Qin, Wei
Liu, Peng
Zhao, Ling
Yu, Dahua
Zhao, Limei
Dong, Minghao
Liu, Jixin
Yang, Xuejuan
von Deneen, Karen M.
Liang, Fanrong
Tian, Jie
author_facet Yuan, Kai
Qin, Wei
Liu, Peng
Zhao, Ling
Yu, Dahua
Zhao, Limei
Dong, Minghao
Liu, Jixin
Yang, Xuejuan
von Deneen, Karen M.
Liang, Fanrong
Tian, Jie
author_sort Yuan, Kai
collection PubMed
description BACKGROUND: Diffusion tensor imaging (DTI) study revealed reduced fractional anisotropy (FA) values in the corpus callosum (CC) in migraine patients without aura. Abnormalities in white matter integrity, particularly in the CC, may affect inter-hemispheric resting state functional connectivity (RSFC). Unfortunately, relatively little is known about the alterations in functional interactions between the cerebral hemispheres during resting state in migraine patients without aura, and even less about how the inter-hemispheric RSFC are affected by the abnormalities of the CC. METHODS AND FINDINGS: Twenty-one migraine patients without aura and 21 healthy controls participated in this study, age-, sex-, and education-matched. Tract-based spatial statistics (TBSS) was employed to investigate the white matter alterations of the CC. Meanwhile, voxel-mirrored homotopic connectivity (VMHC) was used to compare the inter-hemispheric RSFC differences between the patients and controls. TBSS analysis revealed reduced FA values in the genu and the splenium of CC in patient group. VMHC analysis showed decreased inter-hemispheric RSFC of anterior cingulate cortex (ACC) in migraine patients without aura relative to that of the controls. Furthermore, in migraine patients without aura, the reduced FA values of the genu of CC correlated with the decreased inter-hemispheric RSFC of the ACC. CONCLUSIONS: Our findings demonstrated that the migraine patients without aura showed reduced FA values of the genu of CC and decreased inter-hemispheric RSFC of the ACC. The correlation between the above structural and functional changes suggested that the reduced fractional anisotropy (FA) of CC modulates inter-hemispheric VMHC in migraine patients without aura. Our results demonstrated that the VMHC alterations of ACC can reflect the FA changes of the genu of CC in migraine patients without aura.
format Online
Article
Text
id pubmed-3454437
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-34544372012-10-01 Reduced Fractional Anisotropy of Corpus Callosum Modulates Inter-Hemispheric Resting State Functional Connectivity in Migraine Patients without Aura Yuan, Kai Qin, Wei Liu, Peng Zhao, Ling Yu, Dahua Zhao, Limei Dong, Minghao Liu, Jixin Yang, Xuejuan von Deneen, Karen M. Liang, Fanrong Tian, Jie PLoS One Research Article BACKGROUND: Diffusion tensor imaging (DTI) study revealed reduced fractional anisotropy (FA) values in the corpus callosum (CC) in migraine patients without aura. Abnormalities in white matter integrity, particularly in the CC, may affect inter-hemispheric resting state functional connectivity (RSFC). Unfortunately, relatively little is known about the alterations in functional interactions between the cerebral hemispheres during resting state in migraine patients without aura, and even less about how the inter-hemispheric RSFC are affected by the abnormalities of the CC. METHODS AND FINDINGS: Twenty-one migraine patients without aura and 21 healthy controls participated in this study, age-, sex-, and education-matched. Tract-based spatial statistics (TBSS) was employed to investigate the white matter alterations of the CC. Meanwhile, voxel-mirrored homotopic connectivity (VMHC) was used to compare the inter-hemispheric RSFC differences between the patients and controls. TBSS analysis revealed reduced FA values in the genu and the splenium of CC in patient group. VMHC analysis showed decreased inter-hemispheric RSFC of anterior cingulate cortex (ACC) in migraine patients without aura relative to that of the controls. Furthermore, in migraine patients without aura, the reduced FA values of the genu of CC correlated with the decreased inter-hemispheric RSFC of the ACC. CONCLUSIONS: Our findings demonstrated that the migraine patients without aura showed reduced FA values of the genu of CC and decreased inter-hemispheric RSFC of the ACC. The correlation between the above structural and functional changes suggested that the reduced fractional anisotropy (FA) of CC modulates inter-hemispheric VMHC in migraine patients without aura. Our results demonstrated that the VMHC alterations of ACC can reflect the FA changes of the genu of CC in migraine patients without aura. Public Library of Science 2012-09-24 /pmc/articles/PMC3454437/ /pubmed/23029036 http://dx.doi.org/10.1371/journal.pone.0045476 Text en © 2012 Yuan 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
Yuan, Kai
Qin, Wei
Liu, Peng
Zhao, Ling
Yu, Dahua
Zhao, Limei
Dong, Minghao
Liu, Jixin
Yang, Xuejuan
von Deneen, Karen M.
Liang, Fanrong
Tian, Jie
Reduced Fractional Anisotropy of Corpus Callosum Modulates Inter-Hemispheric Resting State Functional Connectivity in Migraine Patients without Aura
title Reduced Fractional Anisotropy of Corpus Callosum Modulates Inter-Hemispheric Resting State Functional Connectivity in Migraine Patients without Aura
title_full Reduced Fractional Anisotropy of Corpus Callosum Modulates Inter-Hemispheric Resting State Functional Connectivity in Migraine Patients without Aura
title_fullStr Reduced Fractional Anisotropy of Corpus Callosum Modulates Inter-Hemispheric Resting State Functional Connectivity in Migraine Patients without Aura
title_full_unstemmed Reduced Fractional Anisotropy of Corpus Callosum Modulates Inter-Hemispheric Resting State Functional Connectivity in Migraine Patients without Aura
title_short Reduced Fractional Anisotropy of Corpus Callosum Modulates Inter-Hemispheric Resting State Functional Connectivity in Migraine Patients without Aura
title_sort reduced fractional anisotropy of corpus callosum modulates inter-hemispheric resting state functional connectivity in migraine patients without aura
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3454437/
https://www.ncbi.nlm.nih.gov/pubmed/23029036
http://dx.doi.org/10.1371/journal.pone.0045476
work_keys_str_mv AT yuankai reducedfractionalanisotropyofcorpuscallosummodulatesinterhemisphericrestingstatefunctionalconnectivityinmigrainepatientswithoutaura
AT qinwei reducedfractionalanisotropyofcorpuscallosummodulatesinterhemisphericrestingstatefunctionalconnectivityinmigrainepatientswithoutaura
AT liupeng reducedfractionalanisotropyofcorpuscallosummodulatesinterhemisphericrestingstatefunctionalconnectivityinmigrainepatientswithoutaura
AT zhaoling reducedfractionalanisotropyofcorpuscallosummodulatesinterhemisphericrestingstatefunctionalconnectivityinmigrainepatientswithoutaura
AT yudahua reducedfractionalanisotropyofcorpuscallosummodulatesinterhemisphericrestingstatefunctionalconnectivityinmigrainepatientswithoutaura
AT zhaolimei reducedfractionalanisotropyofcorpuscallosummodulatesinterhemisphericrestingstatefunctionalconnectivityinmigrainepatientswithoutaura
AT dongminghao reducedfractionalanisotropyofcorpuscallosummodulatesinterhemisphericrestingstatefunctionalconnectivityinmigrainepatientswithoutaura
AT liujixin reducedfractionalanisotropyofcorpuscallosummodulatesinterhemisphericrestingstatefunctionalconnectivityinmigrainepatientswithoutaura
AT yangxuejuan reducedfractionalanisotropyofcorpuscallosummodulatesinterhemisphericrestingstatefunctionalconnectivityinmigrainepatientswithoutaura
AT vondeneenkarenm reducedfractionalanisotropyofcorpuscallosummodulatesinterhemisphericrestingstatefunctionalconnectivityinmigrainepatientswithoutaura
AT liangfanrong reducedfractionalanisotropyofcorpuscallosummodulatesinterhemisphericrestingstatefunctionalconnectivityinmigrainepatientswithoutaura
AT tianjie reducedfractionalanisotropyofcorpuscallosummodulatesinterhemisphericrestingstatefunctionalconnectivityinmigrainepatientswithoutaura