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Disruption of neurite morphology parallels MS progression
OBJECTIVES: To apply advanced diffusion MRI methods to the study of normal-appearing brain tissue in MS and examine their correlation with measures of clinical disability. METHODS: A multi-compartment model of diffusion MRI called neurite orientation dispersion and density imaging (NODDI) was used t...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Lippincott Williams & Wilkins
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192688/ https://www.ncbi.nlm.nih.gov/pubmed/30345330 http://dx.doi.org/10.1212/NXI.0000000000000502 |
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author | Spanò, Barbara Giulietti, Giovanni Pisani, Valerio Morreale, Manuela Tuzzi, Elisa Nocentini, Ugo Francia, Ada Caltagirone, Carlo Bozzali, Marco Cercignani, Mara |
author_facet | Spanò, Barbara Giulietti, Giovanni Pisani, Valerio Morreale, Manuela Tuzzi, Elisa Nocentini, Ugo Francia, Ada Caltagirone, Carlo Bozzali, Marco Cercignani, Mara |
author_sort | Spanò, Barbara |
collection | PubMed |
description | OBJECTIVES: To apply advanced diffusion MRI methods to the study of normal-appearing brain tissue in MS and examine their correlation with measures of clinical disability. METHODS: A multi-compartment model of diffusion MRI called neurite orientation dispersion and density imaging (NODDI) was used to study 20 patients with relapsing-remitting MS (RRMS), 15 with secondary progressive MS (SPMS), and 20 healthy controls. Maps of NODDI were analyzed voxel-wise to assess the presence of abnormalities within the normal-appearing brain tissue and the association with disease severity. Standard diffusion tensor imaging (DTI) parameters were also computed for comparing the 2 techniques. RESULTS: Patients with MS showed reduced neurite density index (NDI) and increased orientation dispersion index (ODI) compared with controls in several brain areas (p < 0.05), with patients with SPMS having more widespread abnormalities. DTI indices were also sensitive to some changes. In addition, patients with SPMS showed reduced ODI in the thalamus and caudate nucleus. These abnormalities were associated with scores of disease severity (p < 0.05). The association with the MS functional composite score was higher in patients with SPMS compared with patients with RRMS. CONCLUSIONS: NODDI and DTI findings are largely overlapping. Nevertheless, NODDI helps interpret previous findings of increased anisotropy in the thalamus of patients with MS and are consistent with the degeneration of selective axon populations. |
format | Online Article Text |
id | pubmed-6192688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
spelling | pubmed-61926882018-10-19 Disruption of neurite morphology parallels MS progression Spanò, Barbara Giulietti, Giovanni Pisani, Valerio Morreale, Manuela Tuzzi, Elisa Nocentini, Ugo Francia, Ada Caltagirone, Carlo Bozzali, Marco Cercignani, Mara Neurol Neuroimmunol Neuroinflamm Article OBJECTIVES: To apply advanced diffusion MRI methods to the study of normal-appearing brain tissue in MS and examine their correlation with measures of clinical disability. METHODS: A multi-compartment model of diffusion MRI called neurite orientation dispersion and density imaging (NODDI) was used to study 20 patients with relapsing-remitting MS (RRMS), 15 with secondary progressive MS (SPMS), and 20 healthy controls. Maps of NODDI were analyzed voxel-wise to assess the presence of abnormalities within the normal-appearing brain tissue and the association with disease severity. Standard diffusion tensor imaging (DTI) parameters were also computed for comparing the 2 techniques. RESULTS: Patients with MS showed reduced neurite density index (NDI) and increased orientation dispersion index (ODI) compared with controls in several brain areas (p < 0.05), with patients with SPMS having more widespread abnormalities. DTI indices were also sensitive to some changes. In addition, patients with SPMS showed reduced ODI in the thalamus and caudate nucleus. These abnormalities were associated with scores of disease severity (p < 0.05). The association with the MS functional composite score was higher in patients with SPMS compared with patients with RRMS. CONCLUSIONS: NODDI and DTI findings are largely overlapping. Nevertheless, NODDI helps interpret previous findings of increased anisotropy in the thalamus of patients with MS and are consistent with the degeneration of selective axon populations. Lippincott Williams & Wilkins 2018-09-26 /pmc/articles/PMC6192688/ /pubmed/30345330 http://dx.doi.org/10.1212/NXI.0000000000000502 Text en Copyright © 2018 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (http://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits downloading and sharing the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. |
spellingShingle | Article Spanò, Barbara Giulietti, Giovanni Pisani, Valerio Morreale, Manuela Tuzzi, Elisa Nocentini, Ugo Francia, Ada Caltagirone, Carlo Bozzali, Marco Cercignani, Mara Disruption of neurite morphology parallels MS progression |
title | Disruption of neurite morphology parallels MS progression |
title_full | Disruption of neurite morphology parallels MS progression |
title_fullStr | Disruption of neurite morphology parallels MS progression |
title_full_unstemmed | Disruption of neurite morphology parallels MS progression |
title_short | Disruption of neurite morphology parallels MS progression |
title_sort | disruption of neurite morphology parallels ms progression |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6192688/ https://www.ncbi.nlm.nih.gov/pubmed/30345330 http://dx.doi.org/10.1212/NXI.0000000000000502 |
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