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Structural covariance of superficial white matter in mild Alzheimer's disease compared to normal aging

INTRODUCTION: Interindividual variations in regional structural properties covary across the brain, thus forming networks that change as a result of aging and accompanying neurological conditions. The alterations of superficial white matter (SWM) in Alzheimer's disease (AD) are of special inter...

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Autores principales: Carmeli, Cristian, Fornari, Eleonora, Jalili, Mahdi, Meuli, Reto, Knyazeva, Maria G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113976/
https://www.ncbi.nlm.nih.gov/pubmed/25328848
http://dx.doi.org/10.1002/brb3.252
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author Carmeli, Cristian
Fornari, Eleonora
Jalili, Mahdi
Meuli, Reto
Knyazeva, Maria G
author_facet Carmeli, Cristian
Fornari, Eleonora
Jalili, Mahdi
Meuli, Reto
Knyazeva, Maria G
author_sort Carmeli, Cristian
collection PubMed
description INTRODUCTION: Interindividual variations in regional structural properties covary across the brain, thus forming networks that change as a result of aging and accompanying neurological conditions. The alterations of superficial white matter (SWM) in Alzheimer's disease (AD) are of special interest, since they follow the AD-specific pattern characterized by the strongest neurodegeneration of the medial temporal lobe and association cortices. METHODS: Here, we present an SWM network analysis in comparison with SWM topography based on the myelin content quantified with magnetization transfer ratio (MTR) for 39 areas in each hemisphere in 15 AD patients and 15 controls. The networks are represented by graphs, in which nodes correspond to the areas, and edges denote statistical associations between them. RESULTS: In both groups, the networks were characterized by asymmetrically distributed edges (predominantly in the left hemisphere). The AD-related differences were also leftward. The edges lost due to AD tended to connect nodes in the temporal lobe to other lobes or nodes within or between the latter lobes. The newly gained edges were mostly confined to the temporal and paralimbic regions, which manifest demyelination of SWM already in mild AD. CONCLUSION: This pattern suggests that the AD pathological process coordinates SWM demyelination in the temporal and paralimbic regions, but not elsewhere. A comparison of the MTR maps with MTR-based networks shows that although, in general, the changes in network architecture in AD recapitulate the topography of (de)myelination, some aspects of structural covariance (including the interhemispheric asymmetry of networks) have no immediate reflection in the myelination pattern.
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spelling pubmed-41139762014-07-30 Structural covariance of superficial white matter in mild Alzheimer's disease compared to normal aging Carmeli, Cristian Fornari, Eleonora Jalili, Mahdi Meuli, Reto Knyazeva, Maria G Brain Behav Original Research INTRODUCTION: Interindividual variations in regional structural properties covary across the brain, thus forming networks that change as a result of aging and accompanying neurological conditions. The alterations of superficial white matter (SWM) in Alzheimer's disease (AD) are of special interest, since they follow the AD-specific pattern characterized by the strongest neurodegeneration of the medial temporal lobe and association cortices. METHODS: Here, we present an SWM network analysis in comparison with SWM topography based on the myelin content quantified with magnetization transfer ratio (MTR) for 39 areas in each hemisphere in 15 AD patients and 15 controls. The networks are represented by graphs, in which nodes correspond to the areas, and edges denote statistical associations between them. RESULTS: In both groups, the networks were characterized by asymmetrically distributed edges (predominantly in the left hemisphere). The AD-related differences were also leftward. The edges lost due to AD tended to connect nodes in the temporal lobe to other lobes or nodes within or between the latter lobes. The newly gained edges were mostly confined to the temporal and paralimbic regions, which manifest demyelination of SWM already in mild AD. CONCLUSION: This pattern suggests that the AD pathological process coordinates SWM demyelination in the temporal and paralimbic regions, but not elsewhere. A comparison of the MTR maps with MTR-based networks shows that although, in general, the changes in network architecture in AD recapitulate the topography of (de)myelination, some aspects of structural covariance (including the interhemispheric asymmetry of networks) have no immediate reflection in the myelination pattern. Blackwell Publishing Ltd 2014-09 2014-07-28 /pmc/articles/PMC4113976/ /pubmed/25328848 http://dx.doi.org/10.1002/brb3.252 Text en © 2014 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Carmeli, Cristian
Fornari, Eleonora
Jalili, Mahdi
Meuli, Reto
Knyazeva, Maria G
Structural covariance of superficial white matter in mild Alzheimer's disease compared to normal aging
title Structural covariance of superficial white matter in mild Alzheimer's disease compared to normal aging
title_full Structural covariance of superficial white matter in mild Alzheimer's disease compared to normal aging
title_fullStr Structural covariance of superficial white matter in mild Alzheimer's disease compared to normal aging
title_full_unstemmed Structural covariance of superficial white matter in mild Alzheimer's disease compared to normal aging
title_short Structural covariance of superficial white matter in mild Alzheimer's disease compared to normal aging
title_sort structural covariance of superficial white matter in mild alzheimer's disease compared to normal aging
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113976/
https://www.ncbi.nlm.nih.gov/pubmed/25328848
http://dx.doi.org/10.1002/brb3.252
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