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Apathy and the Risk of Predementia Syndromes in Community-Dwelling Older Adults

OBJECTIVES: Apathy is a potential predictor of dementia in older adults, but this investigation has been limited to older adults with a preexisting neurological illness like mild cognitive impairment (MCI), stroke or Parkinson’s disease. The objective of this study was to investigate the association...

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Autores principales: Ceïde, Mirnova E, Warhit, Alana, Ayers, Emmeline I, Kennedy, Gary, Verghese, Joe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7424283/
https://www.ncbi.nlm.nih.gov/pubmed/32374839
http://dx.doi.org/10.1093/geronb/gbaa063
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author Ceïde, Mirnova E
Warhit, Alana
Ayers, Emmeline I
Kennedy, Gary
Verghese, Joe
author_facet Ceïde, Mirnova E
Warhit, Alana
Ayers, Emmeline I
Kennedy, Gary
Verghese, Joe
author_sort Ceïde, Mirnova E
collection PubMed
description OBJECTIVES: Apathy is a potential predictor of dementia in older adults, but this investigation has been limited to older adults with a preexisting neurological illness like mild cognitive impairment (MCI), stroke or Parkinson’s disease. The objective of this study was to investigate the association between apathy at baseline and incident predementia syndromes, including MCI and motoric cognitive risk syndrome (MCR), subjective cognitive complaints and slow gait, in community-dwelling older adults. METHOD: We prospectively studied the association between apathy (using the 3-item subscale of the Geriatric Depression Scale [GDS3A]) and incident cognitive disorders in 542 community-dwelling older adults enrolled in the Central Control of Mobility in Aging study using Cox proportional hazard models. Associations were reported as hazard ratio (HR) with 95% confidence intervals (CIs), adjusting for age, education, baseline cognitive performance, and depressive symptoms. RESULTS: Apathy was associated with incident MCR (HR 2.39, 95% CI: 1.10–5.20), but not predementia syndromes overall nor MCI. In sensitivity analyses of MCI subtypes, apathy was associated with nonamnestic MCI (HR 2.44, 95% CI: 1.14–5.22), but not amnestic MCI. Our study was limited by a short follow-up time (median 13.6 months; interquartile range 29.8) and a brief subscale measurement of apathy, GDS3A. DISCUSSION: In our study, apathy predicted MCR but not MCI in community-dwelling older adults. These results and the current literature suggest that apathy is an early risk factor for dementia. Additionally, apathy may be a novel treatment target that could forestall the disability of dementia.
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spelling pubmed-74242832020-08-17 Apathy and the Risk of Predementia Syndromes in Community-Dwelling Older Adults Ceïde, Mirnova E Warhit, Alana Ayers, Emmeline I Kennedy, Gary Verghese, Joe J Gerontol B Psychol Sci Soc Sci The Journal of Gerontology: Psychological Sciences OBJECTIVES: Apathy is a potential predictor of dementia in older adults, but this investigation has been limited to older adults with a preexisting neurological illness like mild cognitive impairment (MCI), stroke or Parkinson’s disease. The objective of this study was to investigate the association between apathy at baseline and incident predementia syndromes, including MCI and motoric cognitive risk syndrome (MCR), subjective cognitive complaints and slow gait, in community-dwelling older adults. METHOD: We prospectively studied the association between apathy (using the 3-item subscale of the Geriatric Depression Scale [GDS3A]) and incident cognitive disorders in 542 community-dwelling older adults enrolled in the Central Control of Mobility in Aging study using Cox proportional hazard models. Associations were reported as hazard ratio (HR) with 95% confidence intervals (CIs), adjusting for age, education, baseline cognitive performance, and depressive symptoms. RESULTS: Apathy was associated with incident MCR (HR 2.39, 95% CI: 1.10–5.20), but not predementia syndromes overall nor MCI. In sensitivity analyses of MCI subtypes, apathy was associated with nonamnestic MCI (HR 2.44, 95% CI: 1.14–5.22), but not amnestic MCI. Our study was limited by a short follow-up time (median 13.6 months; interquartile range 29.8) and a brief subscale measurement of apathy, GDS3A. DISCUSSION: In our study, apathy predicted MCR but not MCI in community-dwelling older adults. These results and the current literature suggest that apathy is an early risk factor for dementia. Additionally, apathy may be a novel treatment target that could forestall the disability of dementia. Oxford University Press 2020-08 2020-05-06 /pmc/articles/PMC7424283/ /pubmed/32374839 http://dx.doi.org/10.1093/geronb/gbaa063 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of The Gerontological Society of America. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle The Journal of Gerontology: Psychological Sciences
Ceïde, Mirnova E
Warhit, Alana
Ayers, Emmeline I
Kennedy, Gary
Verghese, Joe
Apathy and the Risk of Predementia Syndromes in Community-Dwelling Older Adults
title Apathy and the Risk of Predementia Syndromes in Community-Dwelling Older Adults
title_full Apathy and the Risk of Predementia Syndromes in Community-Dwelling Older Adults
title_fullStr Apathy and the Risk of Predementia Syndromes in Community-Dwelling Older Adults
title_full_unstemmed Apathy and the Risk of Predementia Syndromes in Community-Dwelling Older Adults
title_short Apathy and the Risk of Predementia Syndromes in Community-Dwelling Older Adults
title_sort apathy and the risk of predementia syndromes in community-dwelling older adults
topic The Journal of Gerontology: Psychological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7424283/
https://www.ncbi.nlm.nih.gov/pubmed/32374839
http://dx.doi.org/10.1093/geronb/gbaa063
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