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Increased posterior default mode network activity and structural connectivity in young adult APOE-ε4 carriers: a multimodal imaging investigation

Young adult APOE-ε4 carriers show increased activity in posterior regions of the default mode network (pDMN), but how this is related to structural connectivity is unknown. Thirty young adults (one half of whom were APOE-ε4 carriers; mean age 20 years) were scanned using both diffusion and functiona...

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Autores principales: Hodgetts, Carl J., Shine, Jonathan P., Williams, Huw, Postans, Mark, Sims, Rebecca, Williams, Julie, Lawrence, Andrew D., Graham, Kim S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6261847/
https://www.ncbi.nlm.nih.gov/pubmed/30339963
http://dx.doi.org/10.1016/j.neurobiolaging.2018.08.026
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author Hodgetts, Carl J.
Shine, Jonathan P.
Williams, Huw
Postans, Mark
Sims, Rebecca
Williams, Julie
Lawrence, Andrew D.
Graham, Kim S.
author_facet Hodgetts, Carl J.
Shine, Jonathan P.
Williams, Huw
Postans, Mark
Sims, Rebecca
Williams, Julie
Lawrence, Andrew D.
Graham, Kim S.
author_sort Hodgetts, Carl J.
collection PubMed
description Young adult APOE-ε4 carriers show increased activity in posterior regions of the default mode network (pDMN), but how this is related to structural connectivity is unknown. Thirty young adults (one half of whom were APOE-ε4 carriers; mean age 20 years) were scanned using both diffusion and functional magnetic resonance imaging. The parahippocampal cingulum bundle (PHCB)—which links the pDMN and the medial temporal lobe—was manually delineated in individual participants using deterministic tractography. Measures of tract microstructure (mean diffusivity and fractional anisotropy) were then extracted from these tract delineations. APOE-ε4 carriers had lower mean diffusivity and higher fractional anisotropy relative to noncarriers in PHCB, but not in a control tract (the inferior longitudinal fasciculus). Furthermore, PHCB microstructure was selectively associated with pDMN (and medial temporal lobe) activity during a scene discrimination task known to be sensitive to Alzheimer's disease. These findings are consistent with a lifespan view of Alzheimer's disease risk, where early-life, connectivity-related changes in specific, vulnerable “hubs” (e.g., pDMN) lead to increased neural activity. Critically, such changes may reflect reduced network efficiency/flexibility in APOE-ε4 carriers, which in itself may portend a faster decline in connectivity over the lifespan and ultimately trigger early amyloid-β deposition in later life.
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spelling pubmed-62618472019-01-01 Increased posterior default mode network activity and structural connectivity in young adult APOE-ε4 carriers: a multimodal imaging investigation Hodgetts, Carl J. Shine, Jonathan P. Williams, Huw Postans, Mark Sims, Rebecca Williams, Julie Lawrence, Andrew D. Graham, Kim S. Neurobiol Aging Article Young adult APOE-ε4 carriers show increased activity in posterior regions of the default mode network (pDMN), but how this is related to structural connectivity is unknown. Thirty young adults (one half of whom were APOE-ε4 carriers; mean age 20 years) were scanned using both diffusion and functional magnetic resonance imaging. The parahippocampal cingulum bundle (PHCB)—which links the pDMN and the medial temporal lobe—was manually delineated in individual participants using deterministic tractography. Measures of tract microstructure (mean diffusivity and fractional anisotropy) were then extracted from these tract delineations. APOE-ε4 carriers had lower mean diffusivity and higher fractional anisotropy relative to noncarriers in PHCB, but not in a control tract (the inferior longitudinal fasciculus). Furthermore, PHCB microstructure was selectively associated with pDMN (and medial temporal lobe) activity during a scene discrimination task known to be sensitive to Alzheimer's disease. These findings are consistent with a lifespan view of Alzheimer's disease risk, where early-life, connectivity-related changes in specific, vulnerable “hubs” (e.g., pDMN) lead to increased neural activity. Critically, such changes may reflect reduced network efficiency/flexibility in APOE-ε4 carriers, which in itself may portend a faster decline in connectivity over the lifespan and ultimately trigger early amyloid-β deposition in later life. Elsevier 2019-01 /pmc/articles/PMC6261847/ /pubmed/30339963 http://dx.doi.org/10.1016/j.neurobiolaging.2018.08.026 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hodgetts, Carl J.
Shine, Jonathan P.
Williams, Huw
Postans, Mark
Sims, Rebecca
Williams, Julie
Lawrence, Andrew D.
Graham, Kim S.
Increased posterior default mode network activity and structural connectivity in young adult APOE-ε4 carriers: a multimodal imaging investigation
title Increased posterior default mode network activity and structural connectivity in young adult APOE-ε4 carriers: a multimodal imaging investigation
title_full Increased posterior default mode network activity and structural connectivity in young adult APOE-ε4 carriers: a multimodal imaging investigation
title_fullStr Increased posterior default mode network activity and structural connectivity in young adult APOE-ε4 carriers: a multimodal imaging investigation
title_full_unstemmed Increased posterior default mode network activity and structural connectivity in young adult APOE-ε4 carriers: a multimodal imaging investigation
title_short Increased posterior default mode network activity and structural connectivity in young adult APOE-ε4 carriers: a multimodal imaging investigation
title_sort increased posterior default mode network activity and structural connectivity in young adult apoe-ε4 carriers: a multimodal imaging investigation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6261847/
https://www.ncbi.nlm.nih.gov/pubmed/30339963
http://dx.doi.org/10.1016/j.neurobiolaging.2018.08.026
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