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Spatial pattern completion deficits in older adults

Aging may have an impact on the CA3 autoassociative network of the hippocampus, posited by computational models as supporting pattern completion. Twenty-five young (YAs) and 25 older adults (OAs) performed a spatial pattern completion task using a computerized navigational paradigm analogous to a ro...

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Autores principales: Paleja, Meera, Spaniol, Julia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3571199/
https://www.ncbi.nlm.nih.gov/pubmed/23407761
http://dx.doi.org/10.3389/fnagi.2013.00003
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author Paleja, Meera
Spaniol, Julia
author_facet Paleja, Meera
Spaniol, Julia
author_sort Paleja, Meera
collection PubMed
description Aging may have an impact on the CA3 autoassociative network of the hippocampus, posited by computational models as supporting pattern completion. Twenty-five young (YAs) and 25 older adults (OAs) performed a spatial pattern completion task using a computerized navigational paradigm analogous to a rodent pattern completion task reliant on the CA3. Participants identified a previously seen goal location, and the availability of distal cues in the environment was manipulated such that 0, 2, or 4 cues were missing. Performance in both groups declined as a function of decreased cue availability. However, controlling for age differences in task performance during a pre-experimental baseline task, OAs performed equivalently to YAs when all cues were available, but worse than YAs as the number of cues decreased. These findings suggest spatial pattern completion may be impaired in OAs. We discuss these findings in the context of a growing body of literature suggesting age-related imbalances in pattern separation vs. pattern completion.
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spelling pubmed-35711992013-02-13 Spatial pattern completion deficits in older adults Paleja, Meera Spaniol, Julia Front Aging Neurosci Neuroscience Aging may have an impact on the CA3 autoassociative network of the hippocampus, posited by computational models as supporting pattern completion. Twenty-five young (YAs) and 25 older adults (OAs) performed a spatial pattern completion task using a computerized navigational paradigm analogous to a rodent pattern completion task reliant on the CA3. Participants identified a previously seen goal location, and the availability of distal cues in the environment was manipulated such that 0, 2, or 4 cues were missing. Performance in both groups declined as a function of decreased cue availability. However, controlling for age differences in task performance during a pre-experimental baseline task, OAs performed equivalently to YAs when all cues were available, but worse than YAs as the number of cues decreased. These findings suggest spatial pattern completion may be impaired in OAs. We discuss these findings in the context of a growing body of literature suggesting age-related imbalances in pattern separation vs. pattern completion. Frontiers Media S.A. 2013-02-13 /pmc/articles/PMC3571199/ /pubmed/23407761 http://dx.doi.org/10.3389/fnagi.2013.00003 Text en Copyright © 2013 Paleja and Spaniol. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Paleja, Meera
Spaniol, Julia
Spatial pattern completion deficits in older adults
title Spatial pattern completion deficits in older adults
title_full Spatial pattern completion deficits in older adults
title_fullStr Spatial pattern completion deficits in older adults
title_full_unstemmed Spatial pattern completion deficits in older adults
title_short Spatial pattern completion deficits in older adults
title_sort spatial pattern completion deficits in older adults
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3571199/
https://www.ncbi.nlm.nih.gov/pubmed/23407761
http://dx.doi.org/10.3389/fnagi.2013.00003
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