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Mapping Cortical Degeneration in ALS with Magnetization Transfer Ratio and Voxel-Based Morphometry

Pathological and imaging data indicate that amyotrophic lateral sclerosis (ALS) is a multisystem disease involving several cerebral cortical areas. Advanced quantitative magnetic resonance imaging (MRI) techniques enable to explore in vivo the volume and microstructure of the cerebral cortex in ALS....

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Autores principales: Cosottini, Mirco, Cecchi, Paolo, Piazza, Selina, Pesaresi, Ilaria, Fabbri, Serena, Diciotti, Stefano, Mascalchi, Mario, Siciliano, Gabriele, Bonuccelli, Ubaldo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706610/
https://www.ncbi.nlm.nih.gov/pubmed/23874570
http://dx.doi.org/10.1371/journal.pone.0068279
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author Cosottini, Mirco
Cecchi, Paolo
Piazza, Selina
Pesaresi, Ilaria
Fabbri, Serena
Diciotti, Stefano
Mascalchi, Mario
Siciliano, Gabriele
Bonuccelli, Ubaldo
author_facet Cosottini, Mirco
Cecchi, Paolo
Piazza, Selina
Pesaresi, Ilaria
Fabbri, Serena
Diciotti, Stefano
Mascalchi, Mario
Siciliano, Gabriele
Bonuccelli, Ubaldo
author_sort Cosottini, Mirco
collection PubMed
description Pathological and imaging data indicate that amyotrophic lateral sclerosis (ALS) is a multisystem disease involving several cerebral cortical areas. Advanced quantitative magnetic resonance imaging (MRI) techniques enable to explore in vivo the volume and microstructure of the cerebral cortex in ALS. We studied with a combined voxel-based morphometry (VBM) and magnetization transfer (MT) imaging approach the capability of MRI to identify the cortical areas affected by neurodegeneration in ALS patients. Eighteen ALS patients and 18 age-matched healthy controls were examined on a 1.5T scanner using a high-resolution 3D T1 weighted spoiled gradient recalled sequence with and without MT saturation pulse. A voxel-based analysis (VBA) was adopted in order to automatically compute the regional atrophy and MT ratio (MTr) changes of the entire cerebral cortex. By using a multimodal image analysis MTr was adjusted for local gray matter (GM) atrophy to investigate if MTr changes can be independent of atrophy of the cerebral cortex. VBA revealed several clusters of combined GM atrophy and MTr decrease in motor-related areas and extra-motor frontotemporal cortex. The multimodal image analysis identified areas of isolated MTr decrease in premotor and extra-motor frontotemporal areas. VBM and MTr are capable to detect the distribution of neurodegenerative alterations in the cortical GM of ALS patients, supporting the hypothesis of a multi-systemic involvement in ALS. MT imaging changes exist beyond volume loss in frontotemporal cortices.
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spelling pubmed-37066102013-07-19 Mapping Cortical Degeneration in ALS with Magnetization Transfer Ratio and Voxel-Based Morphometry Cosottini, Mirco Cecchi, Paolo Piazza, Selina Pesaresi, Ilaria Fabbri, Serena Diciotti, Stefano Mascalchi, Mario Siciliano, Gabriele Bonuccelli, Ubaldo PLoS One Research Article Pathological and imaging data indicate that amyotrophic lateral sclerosis (ALS) is a multisystem disease involving several cerebral cortical areas. Advanced quantitative magnetic resonance imaging (MRI) techniques enable to explore in vivo the volume and microstructure of the cerebral cortex in ALS. We studied with a combined voxel-based morphometry (VBM) and magnetization transfer (MT) imaging approach the capability of MRI to identify the cortical areas affected by neurodegeneration in ALS patients. Eighteen ALS patients and 18 age-matched healthy controls were examined on a 1.5T scanner using a high-resolution 3D T1 weighted spoiled gradient recalled sequence with and without MT saturation pulse. A voxel-based analysis (VBA) was adopted in order to automatically compute the regional atrophy and MT ratio (MTr) changes of the entire cerebral cortex. By using a multimodal image analysis MTr was adjusted for local gray matter (GM) atrophy to investigate if MTr changes can be independent of atrophy of the cerebral cortex. VBA revealed several clusters of combined GM atrophy and MTr decrease in motor-related areas and extra-motor frontotemporal cortex. The multimodal image analysis identified areas of isolated MTr decrease in premotor and extra-motor frontotemporal areas. VBM and MTr are capable to detect the distribution of neurodegenerative alterations in the cortical GM of ALS patients, supporting the hypothesis of a multi-systemic involvement in ALS. MT imaging changes exist beyond volume loss in frontotemporal cortices. Public Library of Science 2013-07-09 /pmc/articles/PMC3706610/ /pubmed/23874570 http://dx.doi.org/10.1371/journal.pone.0068279 Text en © 2013 Cosottini et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Cosottini, Mirco
Cecchi, Paolo
Piazza, Selina
Pesaresi, Ilaria
Fabbri, Serena
Diciotti, Stefano
Mascalchi, Mario
Siciliano, Gabriele
Bonuccelli, Ubaldo
Mapping Cortical Degeneration in ALS with Magnetization Transfer Ratio and Voxel-Based Morphometry
title Mapping Cortical Degeneration in ALS with Magnetization Transfer Ratio and Voxel-Based Morphometry
title_full Mapping Cortical Degeneration in ALS with Magnetization Transfer Ratio and Voxel-Based Morphometry
title_fullStr Mapping Cortical Degeneration in ALS with Magnetization Transfer Ratio and Voxel-Based Morphometry
title_full_unstemmed Mapping Cortical Degeneration in ALS with Magnetization Transfer Ratio and Voxel-Based Morphometry
title_short Mapping Cortical Degeneration in ALS with Magnetization Transfer Ratio and Voxel-Based Morphometry
title_sort mapping cortical degeneration in als with magnetization transfer ratio and voxel-based morphometry
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706610/
https://www.ncbi.nlm.nih.gov/pubmed/23874570
http://dx.doi.org/10.1371/journal.pone.0068279
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