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Innovative Experiences at Work Support Hippocampal Maintenance in Late Life

Prior research has demonstrated the positive impact of occupational complexity on cognitive aging, however, neural underpinnings remain unclear. There is emerging evidence linking midlife managerial experience to slower hippocampal atrophy (Suo et al., 2012, 2017), supporting the brain maintenance m...

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Autores principales: Odd, Kaleena, Boron, Julie Blaskewicz, Burzynska, Aga, Santo, Jonathan, Robinson, Paul, Willis, Sherry, Schaie, K Warner
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7742149/
http://dx.doi.org/10.1093/geroni/igaa057.1307
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author Odd, Kaleena
Boron, Julie Blaskewicz
Burzynska, Aga
Santo, Jonathan
Robinson, Paul
Willis, Sherry
Schaie, K Warner
author_facet Odd, Kaleena
Boron, Julie Blaskewicz
Burzynska, Aga
Santo, Jonathan
Robinson, Paul
Willis, Sherry
Schaie, K Warner
author_sort Odd, Kaleena
collection PubMed
description Prior research has demonstrated the positive impact of occupational complexity on cognitive aging, however, neural underpinnings remain unclear. There is emerging evidence linking midlife managerial experience to slower hippocampal atrophy (Suo et al., 2012, 2017), supporting the brain maintenance model (i.e. preservation of young-like brain structure). However, occupational complexity, along with education, is known to be a proxy of cognitive reserve (i.e. mind’s resistance to brain aging). The current study examined the influence of midlife work environment factors (i.e., autonomy, control, and innovation; Work Environment Scale, Moos, 1981) on change in hippocampal thickness, while controlling for education and age. We studied 150 participants (60-78 years, M = 66.27, SD = 5.20, 61% female) from the Seattle Longitudinal Study who had at least one MRI scan and remained cognitively normal between 2006 and 2014. Hypotheses were tested using multilevel modeling in Mplus; gender differences were examined. There was no substantial drop in model fit as a result of adding any of the significant effects. Innovation at work slowed the decrease in hippocampal thickness over time demonstrating the protective effect of more novelty, variety and change in work activities. There was a significant age by gender interaction, such that the decrease in hippocampal thickness was stronger for older women. Together, findings suggest that long-term impact of work environment on the hippocampus extends beyond the effects of education, particularly in men, supporting the brain maintenance hypothesis. Innovation at work should be considered in understanding protective/risk factors in hippocampal atrophy in older age.
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spelling pubmed-77421492020-12-21 Innovative Experiences at Work Support Hippocampal Maintenance in Late Life Odd, Kaleena Boron, Julie Blaskewicz Burzynska, Aga Santo, Jonathan Robinson, Paul Willis, Sherry Schaie, K Warner Innov Aging Abstracts Prior research has demonstrated the positive impact of occupational complexity on cognitive aging, however, neural underpinnings remain unclear. There is emerging evidence linking midlife managerial experience to slower hippocampal atrophy (Suo et al., 2012, 2017), supporting the brain maintenance model (i.e. preservation of young-like brain structure). However, occupational complexity, along with education, is known to be a proxy of cognitive reserve (i.e. mind’s resistance to brain aging). The current study examined the influence of midlife work environment factors (i.e., autonomy, control, and innovation; Work Environment Scale, Moos, 1981) on change in hippocampal thickness, while controlling for education and age. We studied 150 participants (60-78 years, M = 66.27, SD = 5.20, 61% female) from the Seattle Longitudinal Study who had at least one MRI scan and remained cognitively normal between 2006 and 2014. Hypotheses were tested using multilevel modeling in Mplus; gender differences were examined. There was no substantial drop in model fit as a result of adding any of the significant effects. Innovation at work slowed the decrease in hippocampal thickness over time demonstrating the protective effect of more novelty, variety and change in work activities. There was a significant age by gender interaction, such that the decrease in hippocampal thickness was stronger for older women. Together, findings suggest that long-term impact of work environment on the hippocampus extends beyond the effects of education, particularly in men, supporting the brain maintenance hypothesis. Innovation at work should be considered in understanding protective/risk factors in hippocampal atrophy in older age. Oxford University Press 2020-12-16 /pmc/articles/PMC7742149/ http://dx.doi.org/10.1093/geroni/igaa057.1307 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of The Gerontological Society of America. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstracts
Odd, Kaleena
Boron, Julie Blaskewicz
Burzynska, Aga
Santo, Jonathan
Robinson, Paul
Willis, Sherry
Schaie, K Warner
Innovative Experiences at Work Support Hippocampal Maintenance in Late Life
title Innovative Experiences at Work Support Hippocampal Maintenance in Late Life
title_full Innovative Experiences at Work Support Hippocampal Maintenance in Late Life
title_fullStr Innovative Experiences at Work Support Hippocampal Maintenance in Late Life
title_full_unstemmed Innovative Experiences at Work Support Hippocampal Maintenance in Late Life
title_short Innovative Experiences at Work Support Hippocampal Maintenance in Late Life
title_sort innovative experiences at work support hippocampal maintenance in late life
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7742149/
http://dx.doi.org/10.1093/geroni/igaa057.1307
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