Cargando…

A Comprehensive Approach to Disentangle the Effect of Cerebellar Damage on Physical Disability in Multiple Sclerosis

Cerebellar damage occurs frequently in multiple sclerosis (MS) patients, with a wide exhibition of symptoms particularly as impairments of balance and gait. Recent studies implementing new postprocessing magnetic resonance imaging (MRI) techniques showed how cerebellar subregional atrophy provides a...

Descripción completa

Detalles Bibliográficos
Autores principales: Ruggieri, Serena, Bharti, Komal, Prosperini, Luca, Giannì, Costanza, Petsas, Nikolaos, Tommasin, Silvia, Giglio, Laura De, Pozzilli, Carlo, Pantano, Patrizia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338682/
https://www.ncbi.nlm.nih.gov/pubmed/32695059
http://dx.doi.org/10.3389/fneur.2020.00529
_version_ 1783554735271313408
author Ruggieri, Serena
Bharti, Komal
Prosperini, Luca
Giannì, Costanza
Petsas, Nikolaos
Tommasin, Silvia
Giglio, Laura De
Pozzilli, Carlo
Pantano, Patrizia
author_facet Ruggieri, Serena
Bharti, Komal
Prosperini, Luca
Giannì, Costanza
Petsas, Nikolaos
Tommasin, Silvia
Giglio, Laura De
Pozzilli, Carlo
Pantano, Patrizia
author_sort Ruggieri, Serena
collection PubMed
description Cerebellar damage occurs frequently in multiple sclerosis (MS) patients, with a wide exhibition of symptoms particularly as impairments of balance and gait. Recent studies implementing new postprocessing magnetic resonance imaging (MRI) techniques showed how cerebellar subregional atrophy provides an explanation of disability in MS. The aim of this work was to evaluate the relationship between quantitative measures of physical disability, cerebellar subregional atrophy, and cerebellar peduncle disruption. Forty-nine MS patients and 32 healthy subjects as controls (HS) underwent a 3-Tesla MRI including 3D T1-weighted and diffusion tensor imaging. Patients underwent static posturography to calculate the body's center of pressure (COP) displacement, Expanded Disability Status Scale (EDSS), and 25-ft walking test (25-FWT). Cerebellar lobular volumes were automatically calculated using the Spatially Unbiased Infratentorial Toolbox. Tract-based spatial statistics (TBSS) in FSL was used to process diffusion tensor imaging (DTI) Fit-generated fractional anisotropy (FA) maps to assess structural connectivity of cerebellar peduncles. Stepwise multivariate linear regression analyses were used to explore relationships between variables. Cerebellar volumes (anterior and posterior, as well as lobular volumes from I to X) were significantly lower in patients with MS than HS (p < 0.05). FA in all cerebellar peduncles was lower in MS patients than in HS (p < 0.05). EDSS and 25-FWT showed an association with atrophy of lobule VIIIb (β = −0.37, p < 0.01, and β = −0.45, p < 0.001, respectively) COP measures inversely correlated with volume of lobules I–IV (β = −0.37, p < 0.01, and β = −0.36, p < 0.01). Lower FA in the three cerebellar peduncles of MS patients positively correlated with cerebellar lobular volumes. Our findings show how sensorimotor cerebellum atrophy and disruption of both afferent and efferent cerebellar connections contribute to physical disability in MS patients.
format Online
Article
Text
id pubmed-7338682
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-73386822020-07-20 A Comprehensive Approach to Disentangle the Effect of Cerebellar Damage on Physical Disability in Multiple Sclerosis Ruggieri, Serena Bharti, Komal Prosperini, Luca Giannì, Costanza Petsas, Nikolaos Tommasin, Silvia Giglio, Laura De Pozzilli, Carlo Pantano, Patrizia Front Neurol Neurology Cerebellar damage occurs frequently in multiple sclerosis (MS) patients, with a wide exhibition of symptoms particularly as impairments of balance and gait. Recent studies implementing new postprocessing magnetic resonance imaging (MRI) techniques showed how cerebellar subregional atrophy provides an explanation of disability in MS. The aim of this work was to evaluate the relationship between quantitative measures of physical disability, cerebellar subregional atrophy, and cerebellar peduncle disruption. Forty-nine MS patients and 32 healthy subjects as controls (HS) underwent a 3-Tesla MRI including 3D T1-weighted and diffusion tensor imaging. Patients underwent static posturography to calculate the body's center of pressure (COP) displacement, Expanded Disability Status Scale (EDSS), and 25-ft walking test (25-FWT). Cerebellar lobular volumes were automatically calculated using the Spatially Unbiased Infratentorial Toolbox. Tract-based spatial statistics (TBSS) in FSL was used to process diffusion tensor imaging (DTI) Fit-generated fractional anisotropy (FA) maps to assess structural connectivity of cerebellar peduncles. Stepwise multivariate linear regression analyses were used to explore relationships between variables. Cerebellar volumes (anterior and posterior, as well as lobular volumes from I to X) were significantly lower in patients with MS than HS (p < 0.05). FA in all cerebellar peduncles was lower in MS patients than in HS (p < 0.05). EDSS and 25-FWT showed an association with atrophy of lobule VIIIb (β = −0.37, p < 0.01, and β = −0.45, p < 0.001, respectively) COP measures inversely correlated with volume of lobules I–IV (β = −0.37, p < 0.01, and β = −0.36, p < 0.01). Lower FA in the three cerebellar peduncles of MS patients positively correlated with cerebellar lobular volumes. Our findings show how sensorimotor cerebellum atrophy and disruption of both afferent and efferent cerebellar connections contribute to physical disability in MS patients. Frontiers Media S.A. 2020-06-30 /pmc/articles/PMC7338682/ /pubmed/32695059 http://dx.doi.org/10.3389/fneur.2020.00529 Text en Copyright © 2020 Ruggieri, Bharti, Prosperini, Giannì, Petsas, Tommasin, Giglio, Pozzilli and Pantano. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neurology
Ruggieri, Serena
Bharti, Komal
Prosperini, Luca
Giannì, Costanza
Petsas, Nikolaos
Tommasin, Silvia
Giglio, Laura De
Pozzilli, Carlo
Pantano, Patrizia
A Comprehensive Approach to Disentangle the Effect of Cerebellar Damage on Physical Disability in Multiple Sclerosis
title A Comprehensive Approach to Disentangle the Effect of Cerebellar Damage on Physical Disability in Multiple Sclerosis
title_full A Comprehensive Approach to Disentangle the Effect of Cerebellar Damage on Physical Disability in Multiple Sclerosis
title_fullStr A Comprehensive Approach to Disentangle the Effect of Cerebellar Damage on Physical Disability in Multiple Sclerosis
title_full_unstemmed A Comprehensive Approach to Disentangle the Effect of Cerebellar Damage on Physical Disability in Multiple Sclerosis
title_short A Comprehensive Approach to Disentangle the Effect of Cerebellar Damage on Physical Disability in Multiple Sclerosis
title_sort comprehensive approach to disentangle the effect of cerebellar damage on physical disability in multiple sclerosis
topic Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7338682/
https://www.ncbi.nlm.nih.gov/pubmed/32695059
http://dx.doi.org/10.3389/fneur.2020.00529
work_keys_str_mv AT ruggieriserena acomprehensiveapproachtodisentangletheeffectofcerebellardamageonphysicaldisabilityinmultiplesclerosis
AT bhartikomal acomprehensiveapproachtodisentangletheeffectofcerebellardamageonphysicaldisabilityinmultiplesclerosis
AT prosperiniluca acomprehensiveapproachtodisentangletheeffectofcerebellardamageonphysicaldisabilityinmultiplesclerosis
AT giannicostanza acomprehensiveapproachtodisentangletheeffectofcerebellardamageonphysicaldisabilityinmultiplesclerosis
AT petsasnikolaos acomprehensiveapproachtodisentangletheeffectofcerebellardamageonphysicaldisabilityinmultiplesclerosis
AT tommasinsilvia acomprehensiveapproachtodisentangletheeffectofcerebellardamageonphysicaldisabilityinmultiplesclerosis
AT gigliolaurade acomprehensiveapproachtodisentangletheeffectofcerebellardamageonphysicaldisabilityinmultiplesclerosis
AT pozzillicarlo acomprehensiveapproachtodisentangletheeffectofcerebellardamageonphysicaldisabilityinmultiplesclerosis
AT pantanopatrizia acomprehensiveapproachtodisentangletheeffectofcerebellardamageonphysicaldisabilityinmultiplesclerosis
AT ruggieriserena comprehensiveapproachtodisentangletheeffectofcerebellardamageonphysicaldisabilityinmultiplesclerosis
AT bhartikomal comprehensiveapproachtodisentangletheeffectofcerebellardamageonphysicaldisabilityinmultiplesclerosis
AT prosperiniluca comprehensiveapproachtodisentangletheeffectofcerebellardamageonphysicaldisabilityinmultiplesclerosis
AT giannicostanza comprehensiveapproachtodisentangletheeffectofcerebellardamageonphysicaldisabilityinmultiplesclerosis
AT petsasnikolaos comprehensiveapproachtodisentangletheeffectofcerebellardamageonphysicaldisabilityinmultiplesclerosis
AT tommasinsilvia comprehensiveapproachtodisentangletheeffectofcerebellardamageonphysicaldisabilityinmultiplesclerosis
AT gigliolaurade comprehensiveapproachtodisentangletheeffectofcerebellardamageonphysicaldisabilityinmultiplesclerosis
AT pozzillicarlo comprehensiveapproachtodisentangletheeffectofcerebellardamageonphysicaldisabilityinmultiplesclerosis
AT pantanopatrizia comprehensiveapproachtodisentangletheeffectofcerebellardamageonphysicaldisabilityinmultiplesclerosis