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Leukoaraiosis and Gray Matter Volume Alteration in Older Adults: The PROOF Study

Background and Purpose: Leukoaraiosis, also called white matter hyperintensities (WMH), is frequently encountered in the brain of older adults. During aging, gray matter structure is also highly affected. WMH or gray matter defects are commonly associated with a higher prevalence of mild cognitive i...

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Autores principales: Celle, Sébastien, Boutet, Claire, Annweiler, Cédric, Ceresetti, Romain, Pichot, Vincent, Barthélémy, Jean-Claude, Roche, Frédéric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8793339/
https://www.ncbi.nlm.nih.gov/pubmed/35095388
http://dx.doi.org/10.3389/fnins.2021.747569
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author Celle, Sébastien
Boutet, Claire
Annweiler, Cédric
Ceresetti, Romain
Pichot, Vincent
Barthélémy, Jean-Claude
Roche, Frédéric
author_facet Celle, Sébastien
Boutet, Claire
Annweiler, Cédric
Ceresetti, Romain
Pichot, Vincent
Barthélémy, Jean-Claude
Roche, Frédéric
author_sort Celle, Sébastien
collection PubMed
description Background and Purpose: Leukoaraiosis, also called white matter hyperintensities (WMH), is frequently encountered in the brain of older adults. During aging, gray matter structure is also highly affected. WMH or gray matter defects are commonly associated with a higher prevalence of mild cognitive impairment. However, little is known about the relationship between WMH and gray matter. Our aim was thus to explore the relationship between leukoaraiosis severity and gray matter volume in a cohort of healthy older adults. Methods: Leukoaraiosis was rated in participants from the PROOF cohort using the Fazekas scale. Voxel-based morphometry was performed on brain scans to examine the potential link between WMH and changes of local brain volume. A neuropsychological evaluation including attentional, executive, and memory tests was also performed to explore cognition. Results: Out of 315 75-year-old subjects, 228 had punctuate foci of leukoaraiosis and 62 had begun the confluence of foci. Leukoaraiosis was associated with a decrease of gray matter in the middle temporal gyrus, in the right medial frontal gyrus, and in the left parahippocampal gyrus. It was also associated with decreased performances in memory recall, executive functioning, and depression. Conclusion: In a population of healthy older adults, leukoaraiosis was associated with gray matter defects and reduced cognitive performance. Controlling vascular risk factors and detecting early cerebrovascular disease may prevent, at least in part, dementia onset and progression.
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spelling pubmed-87933392022-01-28 Leukoaraiosis and Gray Matter Volume Alteration in Older Adults: The PROOF Study Celle, Sébastien Boutet, Claire Annweiler, Cédric Ceresetti, Romain Pichot, Vincent Barthélémy, Jean-Claude Roche, Frédéric Front Neurosci Neuroscience Background and Purpose: Leukoaraiosis, also called white matter hyperintensities (WMH), is frequently encountered in the brain of older adults. During aging, gray matter structure is also highly affected. WMH or gray matter defects are commonly associated with a higher prevalence of mild cognitive impairment. However, little is known about the relationship between WMH and gray matter. Our aim was thus to explore the relationship between leukoaraiosis severity and gray matter volume in a cohort of healthy older adults. Methods: Leukoaraiosis was rated in participants from the PROOF cohort using the Fazekas scale. Voxel-based morphometry was performed on brain scans to examine the potential link between WMH and changes of local brain volume. A neuropsychological evaluation including attentional, executive, and memory tests was also performed to explore cognition. Results: Out of 315 75-year-old subjects, 228 had punctuate foci of leukoaraiosis and 62 had begun the confluence of foci. Leukoaraiosis was associated with a decrease of gray matter in the middle temporal gyrus, in the right medial frontal gyrus, and in the left parahippocampal gyrus. It was also associated with decreased performances in memory recall, executive functioning, and depression. Conclusion: In a population of healthy older adults, leukoaraiosis was associated with gray matter defects and reduced cognitive performance. Controlling vascular risk factors and detecting early cerebrovascular disease may prevent, at least in part, dementia onset and progression. Frontiers Media S.A. 2022-01-13 /pmc/articles/PMC8793339/ /pubmed/35095388 http://dx.doi.org/10.3389/fnins.2021.747569 Text en Copyright © 2022 Celle, Boutet, Annweiler, Ceresetti, Pichot, Barthélémy and Roche. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Celle, Sébastien
Boutet, Claire
Annweiler, Cédric
Ceresetti, Romain
Pichot, Vincent
Barthélémy, Jean-Claude
Roche, Frédéric
Leukoaraiosis and Gray Matter Volume Alteration in Older Adults: The PROOF Study
title Leukoaraiosis and Gray Matter Volume Alteration in Older Adults: The PROOF Study
title_full Leukoaraiosis and Gray Matter Volume Alteration in Older Adults: The PROOF Study
title_fullStr Leukoaraiosis and Gray Matter Volume Alteration in Older Adults: The PROOF Study
title_full_unstemmed Leukoaraiosis and Gray Matter Volume Alteration in Older Adults: The PROOF Study
title_short Leukoaraiosis and Gray Matter Volume Alteration in Older Adults: The PROOF Study
title_sort leukoaraiosis and gray matter volume alteration in older adults: the proof study
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8793339/
https://www.ncbi.nlm.nih.gov/pubmed/35095388
http://dx.doi.org/10.3389/fnins.2021.747569
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