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Individual Differences in Cognitive Function in Older Adults Predicted by Neuronal Selectivity at Corresponding Brain Regions

Relating individual differences in cognitive abilities to neural substrates in older adults is of significant scientific and clinical interest, but remains a major challenge. Previous functional magnetic resonance imaging (fMRI) studies of cognitive aging have mainly focused on the amplitude of fMRI...

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Autores principales: Jiang, Xiong, Petok, Jessica R., Howard, Darlene V., Howard, James H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394166/
https://www.ncbi.nlm.nih.gov/pubmed/28458636
http://dx.doi.org/10.3389/fnagi.2017.00103
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author Jiang, Xiong
Petok, Jessica R.
Howard, Darlene V.
Howard, James H.
author_facet Jiang, Xiong
Petok, Jessica R.
Howard, Darlene V.
Howard, James H.
author_sort Jiang, Xiong
collection PubMed
description Relating individual differences in cognitive abilities to neural substrates in older adults is of significant scientific and clinical interest, but remains a major challenge. Previous functional magnetic resonance imaging (fMRI) studies of cognitive aging have mainly focused on the amplitude of fMRI response, which does not measure neuronal selectivity and has led to some conflicting findings. Here, using local regional heterogeneity analysis, or H(corr), a novel fMRI analysis technique developed to probe the sparseness of neuronal activations as an indirect measure of neuronal selectivity, we found that individual differences in two different cognitive functions, episodic memory and letter verbal fluency, are selectively related to H(corr)-estimated neuronal selectivity at their corresponding brain regions (hippocampus and visual-word form area, respectively). This suggests a direct relationship between cognitive function and neuronal selectivity at the corresponding brain regions in healthy older adults, which in turn suggests that age-related neural dedifferentiation might contribute to rather than compensate for cognitive decline in healthy older adults. Additionally, the capability to estimate neuronal selectivity across brain regions with a single data set and link them to cognitive performance suggests that, compared to fMRI-adaptation—the established fMRI technique to assess neuronal selectivity, H(corr) might be a better alternative in studying normal aging and neurodegenerative diseases, both of which are associated with widespread changes across the brain.
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spelling pubmed-53941662017-04-28 Individual Differences in Cognitive Function in Older Adults Predicted by Neuronal Selectivity at Corresponding Brain Regions Jiang, Xiong Petok, Jessica R. Howard, Darlene V. Howard, James H. Front Aging Neurosci Neuroscience Relating individual differences in cognitive abilities to neural substrates in older adults is of significant scientific and clinical interest, but remains a major challenge. Previous functional magnetic resonance imaging (fMRI) studies of cognitive aging have mainly focused on the amplitude of fMRI response, which does not measure neuronal selectivity and has led to some conflicting findings. Here, using local regional heterogeneity analysis, or H(corr), a novel fMRI analysis technique developed to probe the sparseness of neuronal activations as an indirect measure of neuronal selectivity, we found that individual differences in two different cognitive functions, episodic memory and letter verbal fluency, are selectively related to H(corr)-estimated neuronal selectivity at their corresponding brain regions (hippocampus and visual-word form area, respectively). This suggests a direct relationship between cognitive function and neuronal selectivity at the corresponding brain regions in healthy older adults, which in turn suggests that age-related neural dedifferentiation might contribute to rather than compensate for cognitive decline in healthy older adults. Additionally, the capability to estimate neuronal selectivity across brain regions with a single data set and link them to cognitive performance suggests that, compared to fMRI-adaptation—the established fMRI technique to assess neuronal selectivity, H(corr) might be a better alternative in studying normal aging and neurodegenerative diseases, both of which are associated with widespread changes across the brain. Frontiers Media S.A. 2017-04-18 /pmc/articles/PMC5394166/ /pubmed/28458636 http://dx.doi.org/10.3389/fnagi.2017.00103 Text en Copyright © 2017 Jiang, Petok, Howard and Howard. http://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) or licensor 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
Jiang, Xiong
Petok, Jessica R.
Howard, Darlene V.
Howard, James H.
Individual Differences in Cognitive Function in Older Adults Predicted by Neuronal Selectivity at Corresponding Brain Regions
title Individual Differences in Cognitive Function in Older Adults Predicted by Neuronal Selectivity at Corresponding Brain Regions
title_full Individual Differences in Cognitive Function in Older Adults Predicted by Neuronal Selectivity at Corresponding Brain Regions
title_fullStr Individual Differences in Cognitive Function in Older Adults Predicted by Neuronal Selectivity at Corresponding Brain Regions
title_full_unstemmed Individual Differences in Cognitive Function in Older Adults Predicted by Neuronal Selectivity at Corresponding Brain Regions
title_short Individual Differences in Cognitive Function in Older Adults Predicted by Neuronal Selectivity at Corresponding Brain Regions
title_sort individual differences in cognitive function in older adults predicted by neuronal selectivity at corresponding brain regions
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5394166/
https://www.ncbi.nlm.nih.gov/pubmed/28458636
http://dx.doi.org/10.3389/fnagi.2017.00103
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