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Decreased myelin content of the fornix predicts poorer memory performance beyond vascular risk, hippocampal volume, and fractional anisotropy in nondemented older adults

Alterations to cerebral white matter tracts have been associated with cognitive decline in aging and Alzheimer’s disease (AD). In particular, the fornix has been implicated as especially vulnerable given that it represents the primary outflow tract of the hippocampus. Despite this, little work has f...

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Autores principales: Bangen, Katherine J., Delano-Wood, Lisa, Deoni, Sean C. L., Clark, Alexandra L., Evangelista, Nicole D., Hoffman, Samantha N., Sorg, Scott F., Holmqvist, Sophia, Osuna, Jessica, Weigand, Alexandra J., Jak, Amy J., Bondi, Mark W., Lamar, Melissa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8500888/
https://www.ncbi.nlm.nih.gov/pubmed/33638111
http://dx.doi.org/10.1007/s11682-021-00458-z
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author Bangen, Katherine J.
Delano-Wood, Lisa
Deoni, Sean C. L.
Clark, Alexandra L.
Evangelista, Nicole D.
Hoffman, Samantha N.
Sorg, Scott F.
Holmqvist, Sophia
Osuna, Jessica
Weigand, Alexandra J.
Jak, Amy J.
Bondi, Mark W.
Lamar, Melissa
author_facet Bangen, Katherine J.
Delano-Wood, Lisa
Deoni, Sean C. L.
Clark, Alexandra L.
Evangelista, Nicole D.
Hoffman, Samantha N.
Sorg, Scott F.
Holmqvist, Sophia
Osuna, Jessica
Weigand, Alexandra J.
Jak, Amy J.
Bondi, Mark W.
Lamar, Melissa
author_sort Bangen, Katherine J.
collection PubMed
description Alterations to cerebral white matter tracts have been associated with cognitive decline in aging and Alzheimer’s disease (AD). In particular, the fornix has been implicated as especially vulnerable given that it represents the primary outflow tract of the hippocampus. Despite this, little work has focused on the fornix using a potential early marker of white matter degeneration—myelin water fraction (MWF; an in vivo marker of myelin content). Therefore, we sought to (1) clarify associations between MWF in the fornix and memory functioning, and (2) examine whether fornix MWF relates to memory performance above and beyond hippocampal volume and conventional imaging measures of white matter that may not be as specific to alterations in myelin content. Forty nondemented older adults (mean age = 72.9 years) underwent an MRI exam and neuropsychological assessment. Multicomponent driven equilibrium single pulse observation of T1 and T2 (mcDESPOT) was used to quantify fornix MWF and diffusion tensor imaging (DTI) was used to measure fornix fractional anisotropy (FA). Adjusting for age, sex, education, and vascular risk factors, linear regression models revealed that, lower fornix MWF was significantly associated with poorer memory functioning (β = 0.405, p = .007) across our sample of older adults. Notably, fornix MWF remained a significant predictor of memory functioning (β = 0.380, p = .015) even after adjusting for fornix DTI FA and hippocampal volume (in addition to the above covariates). Given the observed associations between myelin and memory in older adults without dementia, MWF may be a useful early marker of dementia risk. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11682-021-00458-z.
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spelling pubmed-85008882021-10-19 Decreased myelin content of the fornix predicts poorer memory performance beyond vascular risk, hippocampal volume, and fractional anisotropy in nondemented older adults Bangen, Katherine J. Delano-Wood, Lisa Deoni, Sean C. L. Clark, Alexandra L. Evangelista, Nicole D. Hoffman, Samantha N. Sorg, Scott F. Holmqvist, Sophia Osuna, Jessica Weigand, Alexandra J. Jak, Amy J. Bondi, Mark W. Lamar, Melissa Brain Imaging Behav Original Research Alterations to cerebral white matter tracts have been associated with cognitive decline in aging and Alzheimer’s disease (AD). In particular, the fornix has been implicated as especially vulnerable given that it represents the primary outflow tract of the hippocampus. Despite this, little work has focused on the fornix using a potential early marker of white matter degeneration—myelin water fraction (MWF; an in vivo marker of myelin content). Therefore, we sought to (1) clarify associations between MWF in the fornix and memory functioning, and (2) examine whether fornix MWF relates to memory performance above and beyond hippocampal volume and conventional imaging measures of white matter that may not be as specific to alterations in myelin content. Forty nondemented older adults (mean age = 72.9 years) underwent an MRI exam and neuropsychological assessment. Multicomponent driven equilibrium single pulse observation of T1 and T2 (mcDESPOT) was used to quantify fornix MWF and diffusion tensor imaging (DTI) was used to measure fornix fractional anisotropy (FA). Adjusting for age, sex, education, and vascular risk factors, linear regression models revealed that, lower fornix MWF was significantly associated with poorer memory functioning (β = 0.405, p = .007) across our sample of older adults. Notably, fornix MWF remained a significant predictor of memory functioning (β = 0.380, p = .015) even after adjusting for fornix DTI FA and hippocampal volume (in addition to the above covariates). Given the observed associations between myelin and memory in older adults without dementia, MWF may be a useful early marker of dementia risk. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11682-021-00458-z. Springer US 2021-02-26 2021 /pmc/articles/PMC8500888/ /pubmed/33638111 http://dx.doi.org/10.1007/s11682-021-00458-z Text en © This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Research
Bangen, Katherine J.
Delano-Wood, Lisa
Deoni, Sean C. L.
Clark, Alexandra L.
Evangelista, Nicole D.
Hoffman, Samantha N.
Sorg, Scott F.
Holmqvist, Sophia
Osuna, Jessica
Weigand, Alexandra J.
Jak, Amy J.
Bondi, Mark W.
Lamar, Melissa
Decreased myelin content of the fornix predicts poorer memory performance beyond vascular risk, hippocampal volume, and fractional anisotropy in nondemented older adults
title Decreased myelin content of the fornix predicts poorer memory performance beyond vascular risk, hippocampal volume, and fractional anisotropy in nondemented older adults
title_full Decreased myelin content of the fornix predicts poorer memory performance beyond vascular risk, hippocampal volume, and fractional anisotropy in nondemented older adults
title_fullStr Decreased myelin content of the fornix predicts poorer memory performance beyond vascular risk, hippocampal volume, and fractional anisotropy in nondemented older adults
title_full_unstemmed Decreased myelin content of the fornix predicts poorer memory performance beyond vascular risk, hippocampal volume, and fractional anisotropy in nondemented older adults
title_short Decreased myelin content of the fornix predicts poorer memory performance beyond vascular risk, hippocampal volume, and fractional anisotropy in nondemented older adults
title_sort decreased myelin content of the fornix predicts poorer memory performance beyond vascular risk, hippocampal volume, and fractional anisotropy in nondemented older adults
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8500888/
https://www.ncbi.nlm.nih.gov/pubmed/33638111
http://dx.doi.org/10.1007/s11682-021-00458-z
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