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Frailty effects on non-demented cognitive trajectories are moderated by sex and Alzheimer’s genetic risk
BACKGROUND: Age-related frailty reflects cumulative multisystem physiological and health decline. Frailty increases the risk of adverse brain and cognitive outcomes, including differential decline and dementia. In a longitudinal sample of non-demented older adults, we examine whether (a) the level a...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587247/ https://www.ncbi.nlm.nih.gov/pubmed/31221191 http://dx.doi.org/10.1186/s13195-019-0509-9 |
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author | Thibeau, Sherilyn McDermott, Kirstie McFall, G. Peggy Rockwood, Kenneth Dixon, Roger A. |
author_facet | Thibeau, Sherilyn McDermott, Kirstie McFall, G. Peggy Rockwood, Kenneth Dixon, Roger A. |
author_sort | Thibeau, Sherilyn |
collection | PubMed |
description | BACKGROUND: Age-related frailty reflects cumulative multisystem physiological and health decline. Frailty increases the risk of adverse brain and cognitive outcomes, including differential decline and dementia. In a longitudinal sample of non-demented older adults, we examine whether (a) the level and/or change in frailty predicts trajectories across three cognitive domains (memory, speed, and executive function (EF)) and (b) prediction patterns are modified by sex or Alzheimer’s genetic risk (Apolipoprotein E (APOE)). METHODS: Participants (n = 632; M age = 70.7, range 53–95; 3 waves) were from the Victoria Longitudinal Study. After computing a frailty index, we used latent growth modeling and path analysis to test the frailty effects on level and change in three latent variables of cognition. We tested two potential moderators by stratifying by sex and APOE risk (ε4+, ε4-). RESULTS: First, frailty levels predicted speed and EF performance (level) and differential memory change slopes. Second, change in frailty predicted the rate of decline for both speed and EF. Third, sex moderation analyses showed that females were selectively sensitive to (a) frailty effects on memory change and (b) frailty change effects on speed change. In contrast, the frailty effects on EF change were stronger in males. Fourth, genetic moderation analyses showed that APOE risk (e4+) carriers were selectively sensitive to frailty effects on memory change. CONCLUSION: In non-demented older adults, increasing frailty is strongly associated with the differential decline in cognitive trajectories. For example, higher (worse) frailty was associated with more rapid memory decline than was lower (better) frailty. These effects, however, are moderated by both genetic risk and sex. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13195-019-0509-9) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6587247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65872472019-06-27 Frailty effects on non-demented cognitive trajectories are moderated by sex and Alzheimer’s genetic risk Thibeau, Sherilyn McDermott, Kirstie McFall, G. Peggy Rockwood, Kenneth Dixon, Roger A. Alzheimers Res Ther Research BACKGROUND: Age-related frailty reflects cumulative multisystem physiological and health decline. Frailty increases the risk of adverse brain and cognitive outcomes, including differential decline and dementia. In a longitudinal sample of non-demented older adults, we examine whether (a) the level and/or change in frailty predicts trajectories across three cognitive domains (memory, speed, and executive function (EF)) and (b) prediction patterns are modified by sex or Alzheimer’s genetic risk (Apolipoprotein E (APOE)). METHODS: Participants (n = 632; M age = 70.7, range 53–95; 3 waves) were from the Victoria Longitudinal Study. After computing a frailty index, we used latent growth modeling and path analysis to test the frailty effects on level and change in three latent variables of cognition. We tested two potential moderators by stratifying by sex and APOE risk (ε4+, ε4-). RESULTS: First, frailty levels predicted speed and EF performance (level) and differential memory change slopes. Second, change in frailty predicted the rate of decline for both speed and EF. Third, sex moderation analyses showed that females were selectively sensitive to (a) frailty effects on memory change and (b) frailty change effects on speed change. In contrast, the frailty effects on EF change were stronger in males. Fourth, genetic moderation analyses showed that APOE risk (e4+) carriers were selectively sensitive to frailty effects on memory change. CONCLUSION: In non-demented older adults, increasing frailty is strongly associated with the differential decline in cognitive trajectories. For example, higher (worse) frailty was associated with more rapid memory decline than was lower (better) frailty. These effects, however, are moderated by both genetic risk and sex. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13195-019-0509-9) contains supplementary material, which is available to authorized users. BioMed Central 2019-06-21 /pmc/articles/PMC6587247/ /pubmed/31221191 http://dx.doi.org/10.1186/s13195-019-0509-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Thibeau, Sherilyn McDermott, Kirstie McFall, G. Peggy Rockwood, Kenneth Dixon, Roger A. Frailty effects on non-demented cognitive trajectories are moderated by sex and Alzheimer’s genetic risk |
title | Frailty effects on non-demented cognitive trajectories are moderated by sex and Alzheimer’s genetic risk |
title_full | Frailty effects on non-demented cognitive trajectories are moderated by sex and Alzheimer’s genetic risk |
title_fullStr | Frailty effects on non-demented cognitive trajectories are moderated by sex and Alzheimer’s genetic risk |
title_full_unstemmed | Frailty effects on non-demented cognitive trajectories are moderated by sex and Alzheimer’s genetic risk |
title_short | Frailty effects on non-demented cognitive trajectories are moderated by sex and Alzheimer’s genetic risk |
title_sort | frailty effects on non-demented cognitive trajectories are moderated by sex and alzheimer’s genetic risk |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6587247/ https://www.ncbi.nlm.nih.gov/pubmed/31221191 http://dx.doi.org/10.1186/s13195-019-0509-9 |
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