Cargando…

Precommissural and postcommissural fornix microstructure in healthy aging and cognition

The fornix is a key tract of the hippocampal formation, whose status is presumed to contribute to age-related cognitive decline. The precommissural and postcommissural fornix subdivisions form respective basal forebrain/frontal and diencephalic networks that may differentially affect aging and cogni...

Descripción completa

Detalles Bibliográficos
Autores principales: Coad, Bethany M., Craig, Emma, Louch, Rebecca, Aggleton, John P., Vann, Seralynne D., Metzler-Baddeley, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7085915/
https://www.ncbi.nlm.nih.gov/pubmed/32219177
http://dx.doi.org/10.1177/2398212819899316
_version_ 1783509039867494400
author Coad, Bethany M.
Craig, Emma
Louch, Rebecca
Aggleton, John P.
Vann, Seralynne D.
Metzler-Baddeley, Claudia
author_facet Coad, Bethany M.
Craig, Emma
Louch, Rebecca
Aggleton, John P.
Vann, Seralynne D.
Metzler-Baddeley, Claudia
author_sort Coad, Bethany M.
collection PubMed
description The fornix is a key tract of the hippocampal formation, whose status is presumed to contribute to age-related cognitive decline. The precommissural and postcommissural fornix subdivisions form respective basal forebrain/frontal and diencephalic networks that may differentially affect aging and cognition. We employed multi-parametric magnetic resonance imaging (MRI) including neurite orientation density and dispersion imaging, quantitative magnetization transfer (qMT), and T(1)-relaxometry MRI to investigate the microstructural properties of these fornix subdivisions and their relationship with aging and cognition in 149 asymptomatic participants (38–71 years). Aging was associated with increased free water signal and reductions in myelin-sensitive R(1) and qMT indices but no apparent axon density differences in both precommissural and postcommissural fibers. Precommissural relative to postcommissural fibers showed a distinct microstructural pattern characterised by larger free water signal and axon orientation dispersion, with lower apparent myelin and axon density. Furthermore, differences in postcommissural microstructure were related to performance differences in object-location paired-associate learning. These results provide novel in vivo neuroimaging evidence for distinct microstructural properties of precommissural and postcommissural fibers that are consistent with their anatomy as found in axonal tracer studies, as well as for a contribution of postcommissural fibers to the learning of spatial configurations.
format Online
Article
Text
id pubmed-7085915
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher SAGE Publications
record_format MEDLINE/PubMed
spelling pubmed-70859152020-03-26 Precommissural and postcommissural fornix microstructure in healthy aging and cognition Coad, Bethany M. Craig, Emma Louch, Rebecca Aggleton, John P. Vann, Seralynne D. Metzler-Baddeley, Claudia Brain Neurosci Adv Research Paper The fornix is a key tract of the hippocampal formation, whose status is presumed to contribute to age-related cognitive decline. The precommissural and postcommissural fornix subdivisions form respective basal forebrain/frontal and diencephalic networks that may differentially affect aging and cognition. We employed multi-parametric magnetic resonance imaging (MRI) including neurite orientation density and dispersion imaging, quantitative magnetization transfer (qMT), and T(1)-relaxometry MRI to investigate the microstructural properties of these fornix subdivisions and their relationship with aging and cognition in 149 asymptomatic participants (38–71 years). Aging was associated with increased free water signal and reductions in myelin-sensitive R(1) and qMT indices but no apparent axon density differences in both precommissural and postcommissural fibers. Precommissural relative to postcommissural fibers showed a distinct microstructural pattern characterised by larger free water signal and axon orientation dispersion, with lower apparent myelin and axon density. Furthermore, differences in postcommissural microstructure were related to performance differences in object-location paired-associate learning. These results provide novel in vivo neuroimaging evidence for distinct microstructural properties of precommissural and postcommissural fibers that are consistent with their anatomy as found in axonal tracer studies, as well as for a contribution of postcommissural fibers to the learning of spatial configurations. SAGE Publications 2020-01-22 /pmc/articles/PMC7085915/ /pubmed/32219177 http://dx.doi.org/10.1177/2398212819899316 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Research Paper
Coad, Bethany M.
Craig, Emma
Louch, Rebecca
Aggleton, John P.
Vann, Seralynne D.
Metzler-Baddeley, Claudia
Precommissural and postcommissural fornix microstructure in healthy aging and cognition
title Precommissural and postcommissural fornix microstructure in healthy aging and cognition
title_full Precommissural and postcommissural fornix microstructure in healthy aging and cognition
title_fullStr Precommissural and postcommissural fornix microstructure in healthy aging and cognition
title_full_unstemmed Precommissural and postcommissural fornix microstructure in healthy aging and cognition
title_short Precommissural and postcommissural fornix microstructure in healthy aging and cognition
title_sort precommissural and postcommissural fornix microstructure in healthy aging and cognition
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7085915/
https://www.ncbi.nlm.nih.gov/pubmed/32219177
http://dx.doi.org/10.1177/2398212819899316
work_keys_str_mv AT coadbethanym precommissuralandpostcommissuralfornixmicrostructureinhealthyagingandcognition
AT craigemma precommissuralandpostcommissuralfornixmicrostructureinhealthyagingandcognition
AT louchrebecca precommissuralandpostcommissuralfornixmicrostructureinhealthyagingandcognition
AT aggletonjohnp precommissuralandpostcommissuralfornixmicrostructureinhealthyagingandcognition
AT vannseralynned precommissuralandpostcommissuralfornixmicrostructureinhealthyagingandcognition
AT metzlerbaddeleyclaudia precommissuralandpostcommissuralfornixmicrostructureinhealthyagingandcognition