Cargando…
Tract-specific white matter hyperintensities disrupt neural network function in Alzheimer's disease
INTRODUCTION: White matter hyperintensities (WMHs) increase the risk of Alzheimer's disease (AD). Whether WMHs are associated with the decline of functional neural networks in AD is debated. METHOD: Resting-state functional magnetic resonance imaging and WMH were assessed in 78 subjects with in...
Autores principales: | , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier, Inc
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319922/ https://www.ncbi.nlm.nih.gov/pubmed/27432800 http://dx.doi.org/10.1016/j.jalz.2016.06.2358 |
_version_ | 1782509437819289600 |
---|---|
author | Taylor, Alexander N.W. Kambeitz-Ilankovic, Lana Gesierich, Benno Simon-Vermot, Lee Franzmeier, Nicolai Araque Caballero, Miguel Á. Müller, Sophia Hesheng, Liu Ertl-Wagner, Birgit Bürger, Katharina Weiner, Michael W. Dichgans, Martin Duering, Marco Ewers, Michael |
author_facet | Taylor, Alexander N.W. Kambeitz-Ilankovic, Lana Gesierich, Benno Simon-Vermot, Lee Franzmeier, Nicolai Araque Caballero, Miguel Á. Müller, Sophia Hesheng, Liu Ertl-Wagner, Birgit Bürger, Katharina Weiner, Michael W. Dichgans, Martin Duering, Marco Ewers, Michael |
author_sort | Taylor, Alexander N.W. |
collection | PubMed |
description | INTRODUCTION: White matter hyperintensities (WMHs) increase the risk of Alzheimer's disease (AD). Whether WMHs are associated with the decline of functional neural networks in AD is debated. METHOD: Resting-state functional magnetic resonance imaging and WMH were assessed in 78 subjects with increased amyloid levels on AV-45 positron emission tomography (PET) in different clinical stages of AD. We tested the association between WMH volume in major atlas-based fiber tract regions of interest (ROIs) and changes in functional connectivity (FC) between the tracts' projection areas within the default mode network (DMN). RESULTS: WMH volume within the inferior fronto-occipital fasciculus (IFOF) was the highest among all tract ROIs and associated with reduced FC in IFOF-connected DMN areas, independently of global AV-45 PET. Higher AV-45 PET contributed to reduced FC in IFOF-connected, temporal, and parietal DMN areas. CONCLUSIONS: High fiber tract WMH burden is associated with reduced FC in connected areas, thus adding to the effects of amyloid pathology on neuronal network function. |
format | Online Article Text |
id | pubmed-5319922 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier, Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-53199222018-01-10 Tract-specific white matter hyperintensities disrupt neural network function in Alzheimer's disease Taylor, Alexander N.W. Kambeitz-Ilankovic, Lana Gesierich, Benno Simon-Vermot, Lee Franzmeier, Nicolai Araque Caballero, Miguel Á. Müller, Sophia Hesheng, Liu Ertl-Wagner, Birgit Bürger, Katharina Weiner, Michael W. Dichgans, Martin Duering, Marco Ewers, Michael Alzheimers Dement Article INTRODUCTION: White matter hyperintensities (WMHs) increase the risk of Alzheimer's disease (AD). Whether WMHs are associated with the decline of functional neural networks in AD is debated. METHOD: Resting-state functional magnetic resonance imaging and WMH were assessed in 78 subjects with increased amyloid levels on AV-45 positron emission tomography (PET) in different clinical stages of AD. We tested the association between WMH volume in major atlas-based fiber tract regions of interest (ROIs) and changes in functional connectivity (FC) between the tracts' projection areas within the default mode network (DMN). RESULTS: WMH volume within the inferior fronto-occipital fasciculus (IFOF) was the highest among all tract ROIs and associated with reduced FC in IFOF-connected DMN areas, independently of global AV-45 PET. Higher AV-45 PET contributed to reduced FC in IFOF-connected, temporal, and parietal DMN areas. CONCLUSIONS: High fiber tract WMH burden is associated with reduced FC in connected areas, thus adding to the effects of amyloid pathology on neuronal network function. Elsevier, Inc 2017-03 /pmc/articles/PMC5319922/ /pubmed/27432800 http://dx.doi.org/10.1016/j.jalz.2016.06.2358 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Taylor, Alexander N.W. Kambeitz-Ilankovic, Lana Gesierich, Benno Simon-Vermot, Lee Franzmeier, Nicolai Araque Caballero, Miguel Á. Müller, Sophia Hesheng, Liu Ertl-Wagner, Birgit Bürger, Katharina Weiner, Michael W. Dichgans, Martin Duering, Marco Ewers, Michael Tract-specific white matter hyperintensities disrupt neural network function in Alzheimer's disease |
title | Tract-specific white matter hyperintensities disrupt neural network function in Alzheimer's disease |
title_full | Tract-specific white matter hyperintensities disrupt neural network function in Alzheimer's disease |
title_fullStr | Tract-specific white matter hyperintensities disrupt neural network function in Alzheimer's disease |
title_full_unstemmed | Tract-specific white matter hyperintensities disrupt neural network function in Alzheimer's disease |
title_short | Tract-specific white matter hyperintensities disrupt neural network function in Alzheimer's disease |
title_sort | tract-specific white matter hyperintensities disrupt neural network function in alzheimer's disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319922/ https://www.ncbi.nlm.nih.gov/pubmed/27432800 http://dx.doi.org/10.1016/j.jalz.2016.06.2358 |
work_keys_str_mv | AT tayloralexandernw tractspecificwhitematterhyperintensitiesdisruptneuralnetworkfunctioninalzheimersdisease AT kambeitzilankoviclana tractspecificwhitematterhyperintensitiesdisruptneuralnetworkfunctioninalzheimersdisease AT gesierichbenno tractspecificwhitematterhyperintensitiesdisruptneuralnetworkfunctioninalzheimersdisease AT simonvermotlee tractspecificwhitematterhyperintensitiesdisruptneuralnetworkfunctioninalzheimersdisease AT franzmeiernicolai tractspecificwhitematterhyperintensitiesdisruptneuralnetworkfunctioninalzheimersdisease AT araquecaballeromiguela tractspecificwhitematterhyperintensitiesdisruptneuralnetworkfunctioninalzheimersdisease AT mullersophia tractspecificwhitematterhyperintensitiesdisruptneuralnetworkfunctioninalzheimersdisease AT heshengliu tractspecificwhitematterhyperintensitiesdisruptneuralnetworkfunctioninalzheimersdisease AT ertlwagnerbirgit tractspecificwhitematterhyperintensitiesdisruptneuralnetworkfunctioninalzheimersdisease AT burgerkatharina tractspecificwhitematterhyperintensitiesdisruptneuralnetworkfunctioninalzheimersdisease AT weinermichaelw tractspecificwhitematterhyperintensitiesdisruptneuralnetworkfunctioninalzheimersdisease AT dichgansmartin tractspecificwhitematterhyperintensitiesdisruptneuralnetworkfunctioninalzheimersdisease AT dueringmarco tractspecificwhitematterhyperintensitiesdisruptneuralnetworkfunctioninalzheimersdisease AT ewersmichael tractspecificwhitematterhyperintensitiesdisruptneuralnetworkfunctioninalzheimersdisease |