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10‐year frailty trajectory is associated with Alzheimer’s dementia after considering neuropathological burden

MAIN PROBLEM: Frailty is an established risk factor for cognitive decline and Alzheimer's disease. Few studies have examined the longitudinal relationship between frailty and cognition. METHODS: Participants of Rush Memory and Aging project (n = 625, 67.5% female, 83.2 ± 5.9 years at baseline)...

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Autores principales: Wallace, Lindsay M. K., Theou, Olga, Godin, Judith, Ward, David D., Andrew, Melissa K., Bennett, David A., Rockwood, Kenneth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8711220/
https://www.ncbi.nlm.nih.gov/pubmed/34964005
http://dx.doi.org/10.1002/agm2.12187
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author Wallace, Lindsay M. K.
Theou, Olga
Godin, Judith
Ward, David D.
Andrew, Melissa K.
Bennett, David A.
Rockwood, Kenneth
author_facet Wallace, Lindsay M. K.
Theou, Olga
Godin, Judith
Ward, David D.
Andrew, Melissa K.
Bennett, David A.
Rockwood, Kenneth
author_sort Wallace, Lindsay M. K.
collection PubMed
description MAIN PROBLEM: Frailty is an established risk factor for cognitive decline and Alzheimer's disease. Few studies have examined the longitudinal relationship between frailty and cognition. METHODS: Participants of Rush Memory and Aging project (n = 625, 67.5% female, 83.2 ± 5.9 years at baseline) underwent annual clinical evaluations (average follow‐up 5.6 ± 3.7 years) followed by neuropathologic assessment after death. A frailty index was calculated from 41 health variables at each evaluation. Clinical diagnosis of MCI and/or dementia was ascertained by clinical data review (blinded to neuropathological data) after death. Age, sex, education, and neuropathological burden (10‐item index) were evaluated as covariates. Frailty trajectories were calculated using a mixed effects model. RESULTS: At baseline the mean frailty index = 0.24 ± 0.12 and increased at rate of 0.026 or ~1 deficit per year. At death, 27.7% of the sample had MCI, and 38.6% had dementia. Frailty trajectories were significantly steeper among those individuals who were ultimately diagnosed as clinically impaired prior to death, even after controlling for age, sex, education, and neuropathological index. CONCLUSIONS: Findings suggest a strong link between health status (frailty index) and dementia, even after considering neuropathology. Frailty trajectories were associated with risk for MCI and dementia, underscoring the importance of addressing frailty to manage dementia risk.
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spelling pubmed-87112202021-12-27 10‐year frailty trajectory is associated with Alzheimer’s dementia after considering neuropathological burden Wallace, Lindsay M. K. Theou, Olga Godin, Judith Ward, David D. Andrew, Melissa K. Bennett, David A. Rockwood, Kenneth Aging Med (Milton) SPECIAL ISSUE FOR FRAILTY AND SARCOPENIA IN THE ELDERLY MAIN PROBLEM: Frailty is an established risk factor for cognitive decline and Alzheimer's disease. Few studies have examined the longitudinal relationship between frailty and cognition. METHODS: Participants of Rush Memory and Aging project (n = 625, 67.5% female, 83.2 ± 5.9 years at baseline) underwent annual clinical evaluations (average follow‐up 5.6 ± 3.7 years) followed by neuropathologic assessment after death. A frailty index was calculated from 41 health variables at each evaluation. Clinical diagnosis of MCI and/or dementia was ascertained by clinical data review (blinded to neuropathological data) after death. Age, sex, education, and neuropathological burden (10‐item index) were evaluated as covariates. Frailty trajectories were calculated using a mixed effects model. RESULTS: At baseline the mean frailty index = 0.24 ± 0.12 and increased at rate of 0.026 or ~1 deficit per year. At death, 27.7% of the sample had MCI, and 38.6% had dementia. Frailty trajectories were significantly steeper among those individuals who were ultimately diagnosed as clinically impaired prior to death, even after controlling for age, sex, education, and neuropathological index. CONCLUSIONS: Findings suggest a strong link between health status (frailty index) and dementia, even after considering neuropathology. Frailty trajectories were associated with risk for MCI and dementia, underscoring the importance of addressing frailty to manage dementia risk. John Wiley and Sons Inc. 2021-12-15 /pmc/articles/PMC8711220/ /pubmed/34964005 http://dx.doi.org/10.1002/agm2.12187 Text en © 2021 The Authors. Aging Medicine published by Beijing Hospital and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle SPECIAL ISSUE FOR FRAILTY AND SARCOPENIA IN THE ELDERLY
Wallace, Lindsay M. K.
Theou, Olga
Godin, Judith
Ward, David D.
Andrew, Melissa K.
Bennett, David A.
Rockwood, Kenneth
10‐year frailty trajectory is associated with Alzheimer’s dementia after considering neuropathological burden
title 10‐year frailty trajectory is associated with Alzheimer’s dementia after considering neuropathological burden
title_full 10‐year frailty trajectory is associated with Alzheimer’s dementia after considering neuropathological burden
title_fullStr 10‐year frailty trajectory is associated with Alzheimer’s dementia after considering neuropathological burden
title_full_unstemmed 10‐year frailty trajectory is associated with Alzheimer’s dementia after considering neuropathological burden
title_short 10‐year frailty trajectory is associated with Alzheimer’s dementia after considering neuropathological burden
title_sort 10‐year frailty trajectory is associated with alzheimer’s dementia after considering neuropathological burden
topic SPECIAL ISSUE FOR FRAILTY AND SARCOPENIA IN THE ELDERLY
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8711220/
https://www.ncbi.nlm.nih.gov/pubmed/34964005
http://dx.doi.org/10.1002/agm2.12187
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