Cargando…

Altered Functional Connectivity in Essential Tremor: A Resting-State fMRI Study

Essential tremor (ET) has been associated with a spectrum of clinical features, with both motor and nonmotor elements, including cognitive deficits. We employed resting-state functional magnetic resonance imaging (fMRI) to assess whether brain networks that might be involved in the pathogenesis of n...

Descripción completa

Detalles Bibliográficos
Autores principales: Benito-León, Julián, Louis, Elan D., Romero, Juan Pablo, Hernández-Tamames, Juan Antonio, Manzanedo, Eva, Álvarez-Linera, Juan, Bermejo-Pareja, Félix, Posada, Ignacio, Rocon, Eduardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008470/
https://www.ncbi.nlm.nih.gov/pubmed/26656325
http://dx.doi.org/10.1097/MD.0000000000001936
_version_ 1782451375412609024
author Benito-León, Julián
Louis, Elan D.
Romero, Juan Pablo
Hernández-Tamames, Juan Antonio
Manzanedo, Eva
Álvarez-Linera, Juan
Bermejo-Pareja, Félix
Posada, Ignacio
Rocon, Eduardo
author_facet Benito-León, Julián
Louis, Elan D.
Romero, Juan Pablo
Hernández-Tamames, Juan Antonio
Manzanedo, Eva
Álvarez-Linera, Juan
Bermejo-Pareja, Félix
Posada, Ignacio
Rocon, Eduardo
author_sort Benito-León, Julián
collection PubMed
description Essential tremor (ET) has been associated with a spectrum of clinical features, with both motor and nonmotor elements, including cognitive deficits. We employed resting-state functional magnetic resonance imaging (fMRI) to assess whether brain networks that might be involved in the pathogenesis of nonmotor manifestations associated with ET are altered, and the relationship between abnormal connectivity and ET severity and neuropsychological function. Resting-state fMRI data in 23 ET patients (12 women and 11 men) and 22 healthy controls (HC) (12 women and 10 men) were analyzed using independent component analysis, in combination with a “dual-regression” technique, to identify the group differences of resting-state networks (RSNs) (default mode network [DMN] and executive, frontoparietal, sensorimotor, cerebellar, auditory/language, and visual networks). All participants underwent a neuropsychological and neuroimaging session, where resting-state data were collected. Relative to HC, ET patients showed increased connectivity in RSNs involved in cognitive processes (DMN and frontoparietal networks) and decreased connectivity in the cerebellum and visual networks. Changes in network integrity were associated not only with ET severity (DMN) and ET duration (DMN and left frontoparietal network), but also with cognitive ability. Moreover, in at least 3 networks (DMN and frontoparietal networks), increased connectivity was associated with worse performance on different cognitive domains (attention, executive function, visuospatial ability, verbal memory, visual memory, and language) and depressive symptoms. Further, in the visual network, decreased connectivity was associated with worse performance on visuospatial ability. ET was associated with abnormal brain connectivity in major RSNs that might be involved in both motor and nonmotor symptoms. Our findings underscore the importance of examining RSNs in this population as a biomarker of disease.
format Online
Article
Text
id pubmed-5008470
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Wolters Kluwer Health
record_format MEDLINE/PubMed
spelling pubmed-50084702016-09-09 Altered Functional Connectivity in Essential Tremor: A Resting-State fMRI Study Benito-León, Julián Louis, Elan D. Romero, Juan Pablo Hernández-Tamames, Juan Antonio Manzanedo, Eva Álvarez-Linera, Juan Bermejo-Pareja, Félix Posada, Ignacio Rocon, Eduardo Medicine (Baltimore) 5300 Essential tremor (ET) has been associated with a spectrum of clinical features, with both motor and nonmotor elements, including cognitive deficits. We employed resting-state functional magnetic resonance imaging (fMRI) to assess whether brain networks that might be involved in the pathogenesis of nonmotor manifestations associated with ET are altered, and the relationship between abnormal connectivity and ET severity and neuropsychological function. Resting-state fMRI data in 23 ET patients (12 women and 11 men) and 22 healthy controls (HC) (12 women and 10 men) were analyzed using independent component analysis, in combination with a “dual-regression” technique, to identify the group differences of resting-state networks (RSNs) (default mode network [DMN] and executive, frontoparietal, sensorimotor, cerebellar, auditory/language, and visual networks). All participants underwent a neuropsychological and neuroimaging session, where resting-state data were collected. Relative to HC, ET patients showed increased connectivity in RSNs involved in cognitive processes (DMN and frontoparietal networks) and decreased connectivity in the cerebellum and visual networks. Changes in network integrity were associated not only with ET severity (DMN) and ET duration (DMN and left frontoparietal network), but also with cognitive ability. Moreover, in at least 3 networks (DMN and frontoparietal networks), increased connectivity was associated with worse performance on different cognitive domains (attention, executive function, visuospatial ability, verbal memory, visual memory, and language) and depressive symptoms. Further, in the visual network, decreased connectivity was associated with worse performance on visuospatial ability. ET was associated with abnormal brain connectivity in major RSNs that might be involved in both motor and nonmotor symptoms. Our findings underscore the importance of examining RSNs in this population as a biomarker of disease. Wolters Kluwer Health 2015-12-11 /pmc/articles/PMC5008470/ /pubmed/26656325 http://dx.doi.org/10.1097/MD.0000000000001936 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0
spellingShingle 5300
Benito-León, Julián
Louis, Elan D.
Romero, Juan Pablo
Hernández-Tamames, Juan Antonio
Manzanedo, Eva
Álvarez-Linera, Juan
Bermejo-Pareja, Félix
Posada, Ignacio
Rocon, Eduardo
Altered Functional Connectivity in Essential Tremor: A Resting-State fMRI Study
title Altered Functional Connectivity in Essential Tremor: A Resting-State fMRI Study
title_full Altered Functional Connectivity in Essential Tremor: A Resting-State fMRI Study
title_fullStr Altered Functional Connectivity in Essential Tremor: A Resting-State fMRI Study
title_full_unstemmed Altered Functional Connectivity in Essential Tremor: A Resting-State fMRI Study
title_short Altered Functional Connectivity in Essential Tremor: A Resting-State fMRI Study
title_sort altered functional connectivity in essential tremor: a resting-state fmri study
topic 5300
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008470/
https://www.ncbi.nlm.nih.gov/pubmed/26656325
http://dx.doi.org/10.1097/MD.0000000000001936
work_keys_str_mv AT benitoleonjulian alteredfunctionalconnectivityinessentialtremorarestingstatefmristudy
AT louiseland alteredfunctionalconnectivityinessentialtremorarestingstatefmristudy
AT romerojuanpablo alteredfunctionalconnectivityinessentialtremorarestingstatefmristudy
AT hernandeztamamesjuanantonio alteredfunctionalconnectivityinessentialtremorarestingstatefmristudy
AT manzanedoeva alteredfunctionalconnectivityinessentialtremorarestingstatefmristudy
AT alvarezlinerajuan alteredfunctionalconnectivityinessentialtremorarestingstatefmristudy
AT bermejoparejafelix alteredfunctionalconnectivityinessentialtremorarestingstatefmristudy
AT posadaignacio alteredfunctionalconnectivityinessentialtremorarestingstatefmristudy
AT roconeduardo alteredfunctionalconnectivityinessentialtremorarestingstatefmristudy