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Age-related iron accumulation and demyelination in the basal ganglia are closely related to verbal memory and executive functioning

Age-related cognitive decline has been linked to alterations of the dopaminergic system and its subcortical trajectories. Recent work suggests a critical role of iron accumulation within the basal ganglia (BG) in verbal memory performance, and increased iron levels have been related to demyelination...

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Autores principales: Biel, Davina, Steiger, Tineke K., Bunzeck, Nico
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8093241/
https://www.ncbi.nlm.nih.gov/pubmed/33941809
http://dx.doi.org/10.1038/s41598-021-88840-1
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author Biel, Davina
Steiger, Tineke K.
Bunzeck, Nico
author_facet Biel, Davina
Steiger, Tineke K.
Bunzeck, Nico
author_sort Biel, Davina
collection PubMed
description Age-related cognitive decline has been linked to alterations of the dopaminergic system and its subcortical trajectories. Recent work suggests a critical role of iron accumulation within the basal ganglia (BG) in verbal memory performance, and increased iron levels have been related to demyelination. However, the specificity of age-related iron increases with respect to cognitive functions remains unclear. Therefore, we investigated the interplay of age, cognitive performance, and structural integrity of the BG. In total, 79 healthy older participants underwent a broad cognitive assessment (fluid and crystallized intelligence, verbal and numeric memory, processing speed, executive functions) and structural MRI. As expected, performance in most cognitive tests had a negative relationship with age. Moreover, BG grey matter volume and magnetization transfer (MT, indicative of myelin) decreased, and R2* (indicative of iron) increased with age. Importantly, R2* and demyelination negatively correlated with verbal memory and executive functions. Within the SN/VTA, age correlated negatively with MT, but there was no clear evidence in favor of a relationship between behavior and R2* or MT. Our results suggest that age-related increases in iron and demyelination within the BG, which are part of a fronto-striatal network, not only impact on verbal memory but also executive functions.
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spelling pubmed-80932412021-05-05 Age-related iron accumulation and demyelination in the basal ganglia are closely related to verbal memory and executive functioning Biel, Davina Steiger, Tineke K. Bunzeck, Nico Sci Rep Article Age-related cognitive decline has been linked to alterations of the dopaminergic system and its subcortical trajectories. Recent work suggests a critical role of iron accumulation within the basal ganglia (BG) in verbal memory performance, and increased iron levels have been related to demyelination. However, the specificity of age-related iron increases with respect to cognitive functions remains unclear. Therefore, we investigated the interplay of age, cognitive performance, and structural integrity of the BG. In total, 79 healthy older participants underwent a broad cognitive assessment (fluid and crystallized intelligence, verbal and numeric memory, processing speed, executive functions) and structural MRI. As expected, performance in most cognitive tests had a negative relationship with age. Moreover, BG grey matter volume and magnetization transfer (MT, indicative of myelin) decreased, and R2* (indicative of iron) increased with age. Importantly, R2* and demyelination negatively correlated with verbal memory and executive functions. Within the SN/VTA, age correlated negatively with MT, but there was no clear evidence in favor of a relationship between behavior and R2* or MT. Our results suggest that age-related increases in iron and demyelination within the BG, which are part of a fronto-striatal network, not only impact on verbal memory but also executive functions. Nature Publishing Group UK 2021-05-03 /pmc/articles/PMC8093241/ /pubmed/33941809 http://dx.doi.org/10.1038/s41598-021-88840-1 Text en © The Author(s) 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 Article
Biel, Davina
Steiger, Tineke K.
Bunzeck, Nico
Age-related iron accumulation and demyelination in the basal ganglia are closely related to verbal memory and executive functioning
title Age-related iron accumulation and demyelination in the basal ganglia are closely related to verbal memory and executive functioning
title_full Age-related iron accumulation and demyelination in the basal ganglia are closely related to verbal memory and executive functioning
title_fullStr Age-related iron accumulation and demyelination in the basal ganglia are closely related to verbal memory and executive functioning
title_full_unstemmed Age-related iron accumulation and demyelination in the basal ganglia are closely related to verbal memory and executive functioning
title_short Age-related iron accumulation and demyelination in the basal ganglia are closely related to verbal memory and executive functioning
title_sort age-related iron accumulation and demyelination in the basal ganglia are closely related to verbal memory and executive functioning
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8093241/
https://www.ncbi.nlm.nih.gov/pubmed/33941809
http://dx.doi.org/10.1038/s41598-021-88840-1
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