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Functional connectivity changes resemble patterns of pTDP-43 pathology in amyotrophic lateral sclerosis
‘Resting-state’ fMRI allows investigation of alterations in functional brain organization that are associated with an underlying pathological process. We determine whether abnormal connectivity in amyotrophic lateral sclerosis (ALS) in a priori-defined intrinsic functional connectivity networks, acc...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5144012/ https://www.ncbi.nlm.nih.gov/pubmed/27929102 http://dx.doi.org/10.1038/srep38391 |
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author | Schulthess, Ines Gorges, Martin Müller, Hans-Peter Lulé, Dorothée Del Tredici, Kelly Ludolph, Albert C. Kassubek, Jan |
author_facet | Schulthess, Ines Gorges, Martin Müller, Hans-Peter Lulé, Dorothée Del Tredici, Kelly Ludolph, Albert C. Kassubek, Jan |
author_sort | Schulthess, Ines |
collection | PubMed |
description | ‘Resting-state’ fMRI allows investigation of alterations in functional brain organization that are associated with an underlying pathological process. We determine whether abnormal connectivity in amyotrophic lateral sclerosis (ALS) in a priori-defined intrinsic functional connectivity networks, according to a neuropathological staging scheme and its DTI-based tract correlates, permits recognition of a sequential involvement of functional networks. ‘Resting-state’ fMRI data from 135 ALS patients and 56 matched healthy controls were investigated for the motor network (corresponding to neuropathological stage 1), brainstem (stage 2), ventral attention (stage 3), default mode/hippocampal network (stage 4), and primary visual network (as the control network) in a cross-sectional analysis and longitudinally in a subgroup of 27 patients after 6 months. Group comparison from cross-sectional and longitudinal data revealed significantly increased functional connectivity (p < 0.05, corrected) in all four investigated networks (but not in the control network), presenting as a network expansion that was correlated with physical disability. Increased connectivity of functional networks, as investigated in a hypothesis-driven approach, is characterized by network expansions and resembled the pattern of pTDP-43 pathology in ALS. However, our data did not allow for the recognition of a sequential involvement of functional connectivity networks at the individual level. |
format | Online Article Text |
id | pubmed-5144012 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-51440122016-12-16 Functional connectivity changes resemble patterns of pTDP-43 pathology in amyotrophic lateral sclerosis Schulthess, Ines Gorges, Martin Müller, Hans-Peter Lulé, Dorothée Del Tredici, Kelly Ludolph, Albert C. Kassubek, Jan Sci Rep Article ‘Resting-state’ fMRI allows investigation of alterations in functional brain organization that are associated with an underlying pathological process. We determine whether abnormal connectivity in amyotrophic lateral sclerosis (ALS) in a priori-defined intrinsic functional connectivity networks, according to a neuropathological staging scheme and its DTI-based tract correlates, permits recognition of a sequential involvement of functional networks. ‘Resting-state’ fMRI data from 135 ALS patients and 56 matched healthy controls were investigated for the motor network (corresponding to neuropathological stage 1), brainstem (stage 2), ventral attention (stage 3), default mode/hippocampal network (stage 4), and primary visual network (as the control network) in a cross-sectional analysis and longitudinally in a subgroup of 27 patients after 6 months. Group comparison from cross-sectional and longitudinal data revealed significantly increased functional connectivity (p < 0.05, corrected) in all four investigated networks (but not in the control network), presenting as a network expansion that was correlated with physical disability. Increased connectivity of functional networks, as investigated in a hypothesis-driven approach, is characterized by network expansions and resembled the pattern of pTDP-43 pathology in ALS. However, our data did not allow for the recognition of a sequential involvement of functional connectivity networks at the individual level. Nature Publishing Group 2016-12-08 /pmc/articles/PMC5144012/ /pubmed/27929102 http://dx.doi.org/10.1038/srep38391 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Schulthess, Ines Gorges, Martin Müller, Hans-Peter Lulé, Dorothée Del Tredici, Kelly Ludolph, Albert C. Kassubek, Jan Functional connectivity changes resemble patterns of pTDP-43 pathology in amyotrophic lateral sclerosis |
title | Functional connectivity changes resemble patterns of pTDP-43 pathology in amyotrophic lateral sclerosis |
title_full | Functional connectivity changes resemble patterns of pTDP-43 pathology in amyotrophic lateral sclerosis |
title_fullStr | Functional connectivity changes resemble patterns of pTDP-43 pathology in amyotrophic lateral sclerosis |
title_full_unstemmed | Functional connectivity changes resemble patterns of pTDP-43 pathology in amyotrophic lateral sclerosis |
title_short | Functional connectivity changes resemble patterns of pTDP-43 pathology in amyotrophic lateral sclerosis |
title_sort | functional connectivity changes resemble patterns of ptdp-43 pathology in amyotrophic lateral sclerosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5144012/ https://www.ncbi.nlm.nih.gov/pubmed/27929102 http://dx.doi.org/10.1038/srep38391 |
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