White Matter Hyperintensity Load Modulates Brain Morphometry and Brain Connectivity in Healthy Adults: A Neuroplastic Mechanism?
White matter hyperintensities (WMHs) are acquired lesions that accumulate and disrupt neuron-to-neuron connectivity. We tested the associations between WMH load and (1) regional grey matter volumes and (2) functional connectivity of resting-state networks, in a sample of 51 healthy adults. Specifica...
Saved in:
Main Authors: | , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2017-01-01
|
Series: | Neural Plasticity |
Online Access: | http://dx.doi.org/10.1155/2017/4050536 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1832563669738717184 |
---|---|
author | Matteo De Marco Riccardo Manca Micaela Mitolo Annalena Venneri |
author_facet | Matteo De Marco Riccardo Manca Micaela Mitolo Annalena Venneri |
author_sort | Matteo De Marco |
collection | DOAJ |
description | White matter hyperintensities (WMHs) are acquired lesions that accumulate and disrupt neuron-to-neuron connectivity. We tested the associations between WMH load and (1) regional grey matter volumes and (2) functional connectivity of resting-state networks, in a sample of 51 healthy adults. Specifically, we focused on the positive associations (more damage, more volume/connectivity) to investigate a potential route of adaptive plasticity. WMHs were quantified with an automated procedure. Voxel-based morphometry was carried out to model grey matter. An independent component analysis was run to extract the anterior and posterior default-mode network, the salience network, the left and right frontoparietal networks, and the visual network. Each model was corrected for age, global levels of atrophy, and indices of brain and cognitive reserve. Positive associations were found with morphometry and functional connectivity of the anterior default-mode network and salience network. Within the anterior default-mode network, an association was found in the left mediotemporal-limbic complex. Within the salience network, an association was found in the right parietal cortex. The findings support the suggestion that, even in the absence of overt disease, the brain actuates a compensatory (neuroplastic) response to the accumulation of WMH, leading to increases in regional grey matter and modified functional connectivity. |
format | Article |
id | doaj-art-ea8412cc4e104575b5aa91ee1cc75bfa |
institution | Kabale University |
issn | 2090-5904 1687-5443 |
language | English |
publishDate | 2017-01-01 |
publisher | Wiley |
record_format | Article |
series | Neural Plasticity |
spelling | doaj-art-ea8412cc4e104575b5aa91ee1cc75bfa2025-02-03T01:12:58ZengWileyNeural Plasticity2090-59041687-54432017-01-01201710.1155/2017/40505364050536White Matter Hyperintensity Load Modulates Brain Morphometry and Brain Connectivity in Healthy Adults: A Neuroplastic Mechanism?Matteo De Marco0Riccardo Manca1Micaela Mitolo2Annalena Venneri3Department of Neuroscience, University of Sheffield, Sheffield, UKDepartment of Neuroscience, University of Sheffield, Sheffield, UKFunctional MR, S.Orsola-Malpighi Hospital, Department of Biomedical and Neuromotor Science (DIBINEM), Bologna, ItalyDepartment of Neuroscience, University of Sheffield, Sheffield, UKWhite matter hyperintensities (WMHs) are acquired lesions that accumulate and disrupt neuron-to-neuron connectivity. We tested the associations between WMH load and (1) regional grey matter volumes and (2) functional connectivity of resting-state networks, in a sample of 51 healthy adults. Specifically, we focused on the positive associations (more damage, more volume/connectivity) to investigate a potential route of adaptive plasticity. WMHs were quantified with an automated procedure. Voxel-based morphometry was carried out to model grey matter. An independent component analysis was run to extract the anterior and posterior default-mode network, the salience network, the left and right frontoparietal networks, and the visual network. Each model was corrected for age, global levels of atrophy, and indices of brain and cognitive reserve. Positive associations were found with morphometry and functional connectivity of the anterior default-mode network and salience network. Within the anterior default-mode network, an association was found in the left mediotemporal-limbic complex. Within the salience network, an association was found in the right parietal cortex. The findings support the suggestion that, even in the absence of overt disease, the brain actuates a compensatory (neuroplastic) response to the accumulation of WMH, leading to increases in regional grey matter and modified functional connectivity.http://dx.doi.org/10.1155/2017/4050536 |
spellingShingle | Matteo De Marco Riccardo Manca Micaela Mitolo Annalena Venneri White Matter Hyperintensity Load Modulates Brain Morphometry and Brain Connectivity in Healthy Adults: A Neuroplastic Mechanism? Neural Plasticity |
title | White Matter Hyperintensity Load Modulates Brain Morphometry and Brain Connectivity in Healthy Adults: A Neuroplastic Mechanism? |
title_full | White Matter Hyperintensity Load Modulates Brain Morphometry and Brain Connectivity in Healthy Adults: A Neuroplastic Mechanism? |
title_fullStr | White Matter Hyperintensity Load Modulates Brain Morphometry and Brain Connectivity in Healthy Adults: A Neuroplastic Mechanism? |
title_full_unstemmed | White Matter Hyperintensity Load Modulates Brain Morphometry and Brain Connectivity in Healthy Adults: A Neuroplastic Mechanism? |
title_short | White Matter Hyperintensity Load Modulates Brain Morphometry and Brain Connectivity in Healthy Adults: A Neuroplastic Mechanism? |
title_sort | white matter hyperintensity load modulates brain morphometry and brain connectivity in healthy adults a neuroplastic mechanism |
url | http://dx.doi.org/10.1155/2017/4050536 |
work_keys_str_mv | AT matteodemarco whitematterhyperintensityloadmodulatesbrainmorphometryandbrainconnectivityinhealthyadultsaneuroplasticmechanism AT riccardomanca whitematterhyperintensityloadmodulatesbrainmorphometryandbrainconnectivityinhealthyadultsaneuroplasticmechanism AT micaelamitolo whitematterhyperintensityloadmodulatesbrainmorphometryandbrainconnectivityinhealthyadultsaneuroplasticmechanism AT annalenavenneri whitematterhyperintensityloadmodulatesbrainmorphometryandbrainconnectivityinhealthyadultsaneuroplasticmechanism |