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Reduced resting-state brain functional network connectivity and poor regional homogeneity in patients with CADASIL

BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) manifests principally as a suite of cognitive impairments, particularly in the executive domain. Executive functioning requires the dynamic coordination of neural activity over large-scal...

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Autores principales: Su, Jingjing, Ban, Shiyu, Wang, Mengxing, Hua, Fengchun, Wang, Liang, Cheng, Xin, Tang, Yuping, Zhou, Houguang, Zhai, Yu, Du, Xiaoxia, Liu, Jianren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Milan 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6849263/
https://www.ncbi.nlm.nih.gov/pubmed/31711415
http://dx.doi.org/10.1186/s10194-019-1052-6
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author Su, Jingjing
Ban, Shiyu
Wang, Mengxing
Hua, Fengchun
Wang, Liang
Cheng, Xin
Tang, Yuping
Zhou, Houguang
Zhai, Yu
Du, Xiaoxia
Liu, Jianren
author_facet Su, Jingjing
Ban, Shiyu
Wang, Mengxing
Hua, Fengchun
Wang, Liang
Cheng, Xin
Tang, Yuping
Zhou, Houguang
Zhai, Yu
Du, Xiaoxia
Liu, Jianren
author_sort Su, Jingjing
collection PubMed
description BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) manifests principally as a suite of cognitive impairments, particularly in the executive domain. Executive functioning requires the dynamic coordination of neural activity over large-scale networks. It remains unclear whether changes in resting-state brain functional network connectivity and regional homogeneities (ReHos) underly the mechanisms of executive dysfunction evident in CADASIL patients. METHODS: In this study, 22 CADASIL patients and 44 matched healthy controls underwent resting-state functional magnetic resonance imaging (fMRI). Independent component analysis (ICA) was used to measure functional brain network connectivity, and ReHos were calculated to evaluate local brain activities. We used seed-based functional connectivity (FC) analyses to determine whether dysfunctional areas (as defined by ReHos) exhibited abnormal FC with other brain areas. Relationships among the mean intra-network connectivity z-scores of dysfunctional areas within functional networks, and cognitive scores were evaluated using Pearson correlation analyses. RESULTS: Compared to the controls, CADASIL patients exhibited decreased intra-network connectivity within the bilateral lingual gyrus (LG) and the right cuneus (CU) (thus within the visual network [VIN)], and within the right precuneus (Pcu), inferior frontal gyrus (IFG), and precentral gyrus (thus within the frontal network [FRN]). Compared to the controls, patients also exhibited significantly lower ReHos in the right precuneus and cuneus (Pcu/CU), visual association cortex, calcarine gyri, posterior cingulate, limbic lobe, and weaker FC between the right Pcu/CU and the bilateral parahippocampal gyrus (PHG), and between the right Pcu/CU and the right postcentral gyrus. Notably, the mean connectivity z-scores of the bilateral LG and the right CU within the VIN were positively associated with compromised attention, calculation and delayed recall as revealed by tests of the various cognitive domains explored by the Mini-Mental State Examination. CONCLUSIONS: The decreases in intra-network connectivity within the VIN and FRN and reduced local brain activity in the posterior parietal area suggest that patients with CADASIL may exhibit dysfunctional visuomotor behaviors (a hallmark of executive function), and that all visual information processing, visuomotor planning, and movement execution may be affected.
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spelling pubmed-68492632019-11-18 Reduced resting-state brain functional network connectivity and poor regional homogeneity in patients with CADASIL Su, Jingjing Ban, Shiyu Wang, Mengxing Hua, Fengchun Wang, Liang Cheng, Xin Tang, Yuping Zhou, Houguang Zhai, Yu Du, Xiaoxia Liu, Jianren J Headache Pain Research Article BACKGROUND: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) manifests principally as a suite of cognitive impairments, particularly in the executive domain. Executive functioning requires the dynamic coordination of neural activity over large-scale networks. It remains unclear whether changes in resting-state brain functional network connectivity and regional homogeneities (ReHos) underly the mechanisms of executive dysfunction evident in CADASIL patients. METHODS: In this study, 22 CADASIL patients and 44 matched healthy controls underwent resting-state functional magnetic resonance imaging (fMRI). Independent component analysis (ICA) was used to measure functional brain network connectivity, and ReHos were calculated to evaluate local brain activities. We used seed-based functional connectivity (FC) analyses to determine whether dysfunctional areas (as defined by ReHos) exhibited abnormal FC with other brain areas. Relationships among the mean intra-network connectivity z-scores of dysfunctional areas within functional networks, and cognitive scores were evaluated using Pearson correlation analyses. RESULTS: Compared to the controls, CADASIL patients exhibited decreased intra-network connectivity within the bilateral lingual gyrus (LG) and the right cuneus (CU) (thus within the visual network [VIN)], and within the right precuneus (Pcu), inferior frontal gyrus (IFG), and precentral gyrus (thus within the frontal network [FRN]). Compared to the controls, patients also exhibited significantly lower ReHos in the right precuneus and cuneus (Pcu/CU), visual association cortex, calcarine gyri, posterior cingulate, limbic lobe, and weaker FC between the right Pcu/CU and the bilateral parahippocampal gyrus (PHG), and between the right Pcu/CU and the right postcentral gyrus. Notably, the mean connectivity z-scores of the bilateral LG and the right CU within the VIN were positively associated with compromised attention, calculation and delayed recall as revealed by tests of the various cognitive domains explored by the Mini-Mental State Examination. CONCLUSIONS: The decreases in intra-network connectivity within the VIN and FRN and reduced local brain activity in the posterior parietal area suggest that patients with CADASIL may exhibit dysfunctional visuomotor behaviors (a hallmark of executive function), and that all visual information processing, visuomotor planning, and movement execution may be affected. Springer Milan 2019-11-11 /pmc/articles/PMC6849263/ /pubmed/31711415 http://dx.doi.org/10.1186/s10194-019-1052-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research Article
Su, Jingjing
Ban, Shiyu
Wang, Mengxing
Hua, Fengchun
Wang, Liang
Cheng, Xin
Tang, Yuping
Zhou, Houguang
Zhai, Yu
Du, Xiaoxia
Liu, Jianren
Reduced resting-state brain functional network connectivity and poor regional homogeneity in patients with CADASIL
title Reduced resting-state brain functional network connectivity and poor regional homogeneity in patients with CADASIL
title_full Reduced resting-state brain functional network connectivity and poor regional homogeneity in patients with CADASIL
title_fullStr Reduced resting-state brain functional network connectivity and poor regional homogeneity in patients with CADASIL
title_full_unstemmed Reduced resting-state brain functional network connectivity and poor regional homogeneity in patients with CADASIL
title_short Reduced resting-state brain functional network connectivity and poor regional homogeneity in patients with CADASIL
title_sort reduced resting-state brain functional network connectivity and poor regional homogeneity in patients with cadasil
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6849263/
https://www.ncbi.nlm.nih.gov/pubmed/31711415
http://dx.doi.org/10.1186/s10194-019-1052-6
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