Age-Modulated Associations between KIBRA, Brain Volume, and Verbal Memory among Healthy Older Adults
The resource modulation hypothesis suggests that the influence of genes on cognitive functioning increases with age. The KIBRA single nucleotide polymorphism rs17070145, associated with episodic memory and working memory, has been suggested to follow such a pattern, but few studies have tested this...
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ndltd-arizona.edu-oai-arizona.openrepository.com-10150-6265502018-02-14T03:00:32Z Age-Modulated Associations between KIBRA, Brain Volume, and Verbal Memory among Healthy Older Adults Stickel, Ariana Kawa, Kevin Walther, Katrin Glisky, Elizabeth Richholt, Ryan Huentelman, Matt Ryan, Lee Univ Arizona, Dept Psychol, Cognit & Neuroimaging Lab Univ Arizona, Dept Psychol, Aging & Cognit Lab KIBRA brain volumes age-interactions cognition resource modulation The resource modulation hypothesis suggests that the influence of genes on cognitive functioning increases with age. The KIBRA single nucleotide polymorphism rs17070145, associated with episodic memory and working memory, has been suggested to follow such a pattern, but few studies have tested this assertion directly. The present study investigated the relationship between KIBRA alleles (T carriers vs. CC homozygotes), cognitive performance, and brain volumes in three groups of cognitively healthy adults-middle aged (ages 52-64, n = 38), young old (ages 65-72, n = 45), and older old (ages 73-92, n = 62)-who were carefully matched on potentially confounding variables including apolipoprotein epsilon 4 status and hypertension. Consistent with our prediction, T carriers maintained verbal memory performance with increasing age while CC homozygotes declined. Voxel-based morphometric analysis of magnetic resonance images showed an advantage for T carriers in frontal white matter volume that increased with age. Focusing on the older old group, this advantage for T carriers was also evident in left lingual gyrus gray matter and several additional frontal white matter regions. Contrary to expectations, neither KIBRA nor the interaction between KIBRA and age predicted hippocampal volumes. None of the brain regions investigated showed a CC homozygote advantage. Taken together, these data suggest that KIBRA results in decreased verbal memory performance and lower brain volumes in CC homozygotes compared to T carriers, particularly among the oldest old, consistent with the resource modulation hypothesis. 2018-01-10 Article Age-Modulated Associations between KIBRA, Brain Volume, and Verbal Memory among Healthy Older Adults 2018, 9 Frontiers in Aging Neuroscience 1663-4365 10.3389/fnagi.2017.00431 http://hdl.handle.net/10150/626550 http://arizona.openrepository.com/arizona/handle/10150/626550 Frontiers in Aging Neuroscience en http://journal.frontiersin.org/article/10.3389/fnagi.2017.00431/full © 2018 Stickel, Kawa, Walther, Glisky, Richholt, Huentelman and Ryan. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). FRONTIERS MEDIA SA |
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en |
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KIBRA brain volumes age-interactions cognition resource modulation |
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KIBRA brain volumes age-interactions cognition resource modulation Stickel, Ariana Kawa, Kevin Walther, Katrin Glisky, Elizabeth Richholt, Ryan Huentelman, Matt Ryan, Lee Age-Modulated Associations between KIBRA, Brain Volume, and Verbal Memory among Healthy Older Adults |
description |
The resource modulation hypothesis suggests that the influence of genes on cognitive functioning increases with age. The KIBRA single nucleotide polymorphism rs17070145, associated with episodic memory and working memory, has been suggested to follow such a pattern, but few studies have tested this assertion directly. The present study investigated the relationship between KIBRA alleles (T carriers vs. CC homozygotes), cognitive performance, and brain volumes in three groups of cognitively healthy adults-middle aged (ages 52-64, n = 38), young old (ages 65-72, n = 45), and older old (ages 73-92, n = 62)-who were carefully matched on potentially confounding variables including apolipoprotein epsilon 4 status and hypertension. Consistent with our prediction, T carriers maintained verbal memory performance with increasing age while CC homozygotes declined. Voxel-based morphometric analysis of magnetic resonance images showed an advantage for T carriers in frontal white matter volume that increased with age. Focusing on the older old group, this advantage for T carriers was also evident in left lingual gyrus gray matter and several additional frontal white matter regions. Contrary to expectations, neither KIBRA nor the interaction between KIBRA and age predicted hippocampal volumes. None of the brain regions investigated showed a CC homozygote advantage. Taken together, these data suggest that KIBRA results in decreased verbal memory performance and lower brain volumes in CC homozygotes compared to T carriers, particularly among the oldest old, consistent with the resource modulation hypothesis. |
author2 |
Univ Arizona, Dept Psychol, Cognit & Neuroimaging Lab |
author_facet |
Univ Arizona, Dept Psychol, Cognit & Neuroimaging Lab Stickel, Ariana Kawa, Kevin Walther, Katrin Glisky, Elizabeth Richholt, Ryan Huentelman, Matt Ryan, Lee |
author |
Stickel, Ariana Kawa, Kevin Walther, Katrin Glisky, Elizabeth Richholt, Ryan Huentelman, Matt Ryan, Lee |
author_sort |
Stickel, Ariana |
title |
Age-Modulated Associations between KIBRA, Brain Volume, and Verbal Memory among Healthy Older Adults |
title_short |
Age-Modulated Associations between KIBRA, Brain Volume, and Verbal Memory among Healthy Older Adults |
title_full |
Age-Modulated Associations between KIBRA, Brain Volume, and Verbal Memory among Healthy Older Adults |
title_fullStr |
Age-Modulated Associations between KIBRA, Brain Volume, and Verbal Memory among Healthy Older Adults |
title_full_unstemmed |
Age-Modulated Associations between KIBRA, Brain Volume, and Verbal Memory among Healthy Older Adults |
title_sort |
age-modulated associations between kibra, brain volume, and verbal memory among healthy older adults |
publisher |
FRONTIERS MEDIA SA |
publishDate |
2018 |
url |
http://hdl.handle.net/10150/626550 http://arizona.openrepository.com/arizona/handle/10150/626550 |
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