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Assessment of disrupted brain functional connectome in tuberous sclerosis complex using resting-state fMRI

Tuberous sclerosis complex (TSC) is a rare genetic disorder with multisystem involvement. TSC is characterized by benign hamartomas in multiple organs, including the brain, and its clinical phenotypes may be associated with abnormal functional connections. We aimed to use resting-state functional co...

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Autores principales: Tsai, Jeng-Dau, Ho, Ming-Chou, Shen, Chao-Yu, Weng, Jun-Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10684191/
https://www.ncbi.nlm.nih.gov/pubmed/35356911
http://dx.doi.org/10.1097/MD.0000000000029024
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author Tsai, Jeng-Dau
Ho, Ming-Chou
Shen, Chao-Yu
Weng, Jun-Cheng
author_facet Tsai, Jeng-Dau
Ho, Ming-Chou
Shen, Chao-Yu
Weng, Jun-Cheng
author_sort Tsai, Jeng-Dau
collection PubMed
description Tuberous sclerosis complex (TSC) is a rare genetic disorder with multisystem involvement. TSC is characterized by benign hamartomas in multiple organs, including the brain, and its clinical phenotypes may be associated with abnormal functional connections. We aimed to use resting-state functional connectivity to provide findings of disrupted functional brain networks in TSC patients using graph theoretical analysis (GTA) and network-based statistic (NBS) analysis. Forty TSC patients (age = 24.11+/-11.44 years old) and 18 age-matched (25.13+/- 10.01 years old) healthy controls were recruited; they underwent resting-state functional magnetic resonance imaging using a 3T magnetic resonance imaging scanner. After image preprocessing and removing physiological noises, GTA was used to calculate the topological parameters of the brain network. NBS analysis was then used to determine the differences in cerebrum functional connectivity between the 2 groups. In GTA, several topological parameters, including the clustering coefficient, local efficiency, transitivity, and modularity, were better in controls than in TSC patients (P < .05). In NBS analysis, the edges of the brain networks between the groups were compared. One subnetwork showed more edges in controls than in TSC patients (P < .05), including the connections from the frontal lobe to the temporal and parietal lobe. The study results provide the findings on disrupted functional connectivity and organization in TSC patients compared with controls. The findings may help better understand the underlying physiological mechanisms of brain connection in TSC.
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spelling pubmed-106841912023-11-30 Assessment of disrupted brain functional connectome in tuberous sclerosis complex using resting-state fMRI Tsai, Jeng-Dau Ho, Ming-Chou Shen, Chao-Yu Weng, Jun-Cheng Medicine (Baltimore) Observational Study Tuberous sclerosis complex (TSC) is a rare genetic disorder with multisystem involvement. TSC is characterized by benign hamartomas in multiple organs, including the brain, and its clinical phenotypes may be associated with abnormal functional connections. We aimed to use resting-state functional connectivity to provide findings of disrupted functional brain networks in TSC patients using graph theoretical analysis (GTA) and network-based statistic (NBS) analysis. Forty TSC patients (age = 24.11+/-11.44 years old) and 18 age-matched (25.13+/- 10.01 years old) healthy controls were recruited; they underwent resting-state functional magnetic resonance imaging using a 3T magnetic resonance imaging scanner. After image preprocessing and removing physiological noises, GTA was used to calculate the topological parameters of the brain network. NBS analysis was then used to determine the differences in cerebrum functional connectivity between the 2 groups. In GTA, several topological parameters, including the clustering coefficient, local efficiency, transitivity, and modularity, were better in controls than in TSC patients (P < .05). In NBS analysis, the edges of the brain networks between the groups were compared. One subnetwork showed more edges in controls than in TSC patients (P < .05), including the connections from the frontal lobe to the temporal and parietal lobe. The study results provide the findings on disrupted functional connectivity and organization in TSC patients compared with controls. The findings may help better understand the underlying physiological mechanisms of brain connection in TSC. Lippincott Williams & Wilkins 2022-03-18 /pmc/articles/PMC10684191/ /pubmed/35356911 http://dx.doi.org/10.1097/MD.0000000000029024 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC) (https://creativecommons.org/licenses/by-nc/4.0/) , where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal.
spellingShingle Observational Study
Tsai, Jeng-Dau
Ho, Ming-Chou
Shen, Chao-Yu
Weng, Jun-Cheng
Assessment of disrupted brain functional connectome in tuberous sclerosis complex using resting-state fMRI
title Assessment of disrupted brain functional connectome in tuberous sclerosis complex using resting-state fMRI
title_full Assessment of disrupted brain functional connectome in tuberous sclerosis complex using resting-state fMRI
title_fullStr Assessment of disrupted brain functional connectome in tuberous sclerosis complex using resting-state fMRI
title_full_unstemmed Assessment of disrupted brain functional connectome in tuberous sclerosis complex using resting-state fMRI
title_short Assessment of disrupted brain functional connectome in tuberous sclerosis complex using resting-state fMRI
title_sort assessment of disrupted brain functional connectome in tuberous sclerosis complex using resting-state fmri
topic Observational Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10684191/
https://www.ncbi.nlm.nih.gov/pubmed/35356911
http://dx.doi.org/10.1097/MD.0000000000029024
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