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Voxel-based morphometry and task functional magnetic resonance imaging in essential tremor: evidence for a disrupted brain network
The pathophysiology of essential tremor (ET) is controversial and might be further elucidated by advanced neuroimaging. Focusing on homogenous ET patients diagnosed according to the 2018 consensus criteria, this study aimed to: (1) investigate whether task functional MRI (fMRI) can identify networks...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7493988/ https://www.ncbi.nlm.nih.gov/pubmed/32934259 http://dx.doi.org/10.1038/s41598-020-69514-w |
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author | Boscolo Galazzo, Ilaria Magrinelli, Francesca Pizzini, Francesca Benedetta Storti, Silvia Francesca Agosta, Federica Filippi, Massimo Marotta, Angela Mansueto, Giancarlo Menegaz, Gloria Tinazzi, Michele |
author_facet | Boscolo Galazzo, Ilaria Magrinelli, Francesca Pizzini, Francesca Benedetta Storti, Silvia Francesca Agosta, Federica Filippi, Massimo Marotta, Angela Mansueto, Giancarlo Menegaz, Gloria Tinazzi, Michele |
author_sort | Boscolo Galazzo, Ilaria |
collection | PubMed |
description | The pathophysiology of essential tremor (ET) is controversial and might be further elucidated by advanced neuroimaging. Focusing on homogenous ET patients diagnosed according to the 2018 consensus criteria, this study aimed to: (1) investigate whether task functional MRI (fMRI) can identify networks of activated and deactivated brain areas, (2) characterize morphometric and functional modulations, relative to healthy controls (HC). Ten ET patients and ten HC underwent fMRI while performing two motor tasks with their upper limb: (1) maintaining a posture (both groups); (2) simulating tremor (HC only). Activations/deactivations were obtained from General Linear Model and compared across groups/tasks. Voxel-based morphometry and linear regressions between clinical and fMRI data were also performed. Few cerebellar clusters of gray matter loss were found in ET. Conversely, widespread fMRI alterations were shown. Tremor in ET (task 1) was associated with extensive deactivations mainly involving the cerebellum, sensory-motor cortex, and basal ganglia compared to both tasks in HC, and was negatively correlated with clinical tremor scales. Homogeneous ET patients demonstrated deactivation patterns during tasks triggering tremor, encompassing a network of cortical and subcortical regions. Our results point towards a marked cerebellar involvement in ET pathophysiology and the presence of an impaired cerebello-thalamo-cortical tremor network. |
format | Online Article Text |
id | pubmed-7493988 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74939882020-09-16 Voxel-based morphometry and task functional magnetic resonance imaging in essential tremor: evidence for a disrupted brain network Boscolo Galazzo, Ilaria Magrinelli, Francesca Pizzini, Francesca Benedetta Storti, Silvia Francesca Agosta, Federica Filippi, Massimo Marotta, Angela Mansueto, Giancarlo Menegaz, Gloria Tinazzi, Michele Sci Rep Article The pathophysiology of essential tremor (ET) is controversial and might be further elucidated by advanced neuroimaging. Focusing on homogenous ET patients diagnosed according to the 2018 consensus criteria, this study aimed to: (1) investigate whether task functional MRI (fMRI) can identify networks of activated and deactivated brain areas, (2) characterize morphometric and functional modulations, relative to healthy controls (HC). Ten ET patients and ten HC underwent fMRI while performing two motor tasks with their upper limb: (1) maintaining a posture (both groups); (2) simulating tremor (HC only). Activations/deactivations were obtained from General Linear Model and compared across groups/tasks. Voxel-based morphometry and linear regressions between clinical and fMRI data were also performed. Few cerebellar clusters of gray matter loss were found in ET. Conversely, widespread fMRI alterations were shown. Tremor in ET (task 1) was associated with extensive deactivations mainly involving the cerebellum, sensory-motor cortex, and basal ganglia compared to both tasks in HC, and was negatively correlated with clinical tremor scales. Homogeneous ET patients demonstrated deactivation patterns during tasks triggering tremor, encompassing a network of cortical and subcortical regions. Our results point towards a marked cerebellar involvement in ET pathophysiology and the presence of an impaired cerebello-thalamo-cortical tremor network. Nature Publishing Group UK 2020-09-15 /pmc/articles/PMC7493988/ /pubmed/32934259 http://dx.doi.org/10.1038/s41598-020-69514-w Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Boscolo Galazzo, Ilaria Magrinelli, Francesca Pizzini, Francesca Benedetta Storti, Silvia Francesca Agosta, Federica Filippi, Massimo Marotta, Angela Mansueto, Giancarlo Menegaz, Gloria Tinazzi, Michele Voxel-based morphometry and task functional magnetic resonance imaging in essential tremor: evidence for a disrupted brain network |
title | Voxel-based morphometry and task functional magnetic resonance imaging in essential tremor: evidence for a disrupted brain network |
title_full | Voxel-based morphometry and task functional magnetic resonance imaging in essential tremor: evidence for a disrupted brain network |
title_fullStr | Voxel-based morphometry and task functional magnetic resonance imaging in essential tremor: evidence for a disrupted brain network |
title_full_unstemmed | Voxel-based morphometry and task functional magnetic resonance imaging in essential tremor: evidence for a disrupted brain network |
title_short | Voxel-based morphometry and task functional magnetic resonance imaging in essential tremor: evidence for a disrupted brain network |
title_sort | voxel-based morphometry and task functional magnetic resonance imaging in essential tremor: evidence for a disrupted brain network |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7493988/ https://www.ncbi.nlm.nih.gov/pubmed/32934259 http://dx.doi.org/10.1038/s41598-020-69514-w |
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