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Trajectories of physical function prior to death and brain neuropathology in a community-based cohort: the act study

BACKGROUND: Mechanisms linking cognitive and physical functioning in older adults are unclear. We sought to determine whether brain pathological changes relate to the level or rate of physical performance decline. METHODS: This study analyzed data from 305 participants in the autopsy subcohort of th...

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Autores principales: LaCroix, Andrea Z., Hubbard, Rebecca A., Gray, Shelly L., Anderson, Melissa L., Crane, Paul K., Sonnen, Joshua A., Zaslavsky, Oleg, Larson, Eric B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5667523/
https://www.ncbi.nlm.nih.gov/pubmed/29096630
http://dx.doi.org/10.1186/s12877-017-0637-7
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author LaCroix, Andrea Z.
Hubbard, Rebecca A.
Gray, Shelly L.
Anderson, Melissa L.
Crane, Paul K.
Sonnen, Joshua A.
Zaslavsky, Oleg
Larson, Eric B.
author_facet LaCroix, Andrea Z.
Hubbard, Rebecca A.
Gray, Shelly L.
Anderson, Melissa L.
Crane, Paul K.
Sonnen, Joshua A.
Zaslavsky, Oleg
Larson, Eric B.
author_sort LaCroix, Andrea Z.
collection PubMed
description BACKGROUND: Mechanisms linking cognitive and physical functioning in older adults are unclear. We sought to determine whether brain pathological changes relate to the level or rate of physical performance decline. METHODS: This study analyzed data from 305 participants in the autopsy subcohort of the prospective Adult Changes in Thought (ACT) study. Participants were aged 65+ and free of dementia at enrollment. Physical performance was measured at baseline and every two years using the Short Physical Performance Battery (SPPB). Data from 3174 ACT participants with ≥2 SPPB measurements were used to estimate two physical function measures: 1) rate of SPPB decline defined by intercept and slope; and 2) estimated SPPB 5 years prior to death. Neuropathology findings at autopsy included neurofibrillary tangles (Braak stage), neuritic plaques (CERAD level), presence of amyloid angiopathy, microinfarcts, cystic infarcts, and Lewy bodies. Associations (adjusted for sex, age, body mass index and education) between dichotomized neuropathologic outcomes and SPPB measures were estimated using modified Poisson regression with inverse probability weights (IPW) estimated via Generalized Estimating Equations (GEE). Relative risks for the 20(th), 40(th), and 60(th) percentiles (lowest levels and highest rates of decline) relative to the 80th percentile (highest level and lowest rate of decline) were calculated. RESULTS: Decedents with the least vs. most SPPB decline (slope > 75(th) vs. < 25(th) percentiles) had higher SPPB scores, and were more likely to be male, older, have higher education, and exercise regularly at baseline. No significant associations were observed between neuropathology findings and rate of SPPB decline. Lower predicted SPPB scores 5 years prior to death were associated with higher risk of microinfarcts (RR = 3.08, 95% confidence interval (CI) 0.93–1.07 for the 20(th) vs. 80(th) percentiles of SPPB) and significantly higher risk of cystic infarcts (RR = 2.72, 95% CI 1.45–5.57 for 20(th) vs. 80(th) percentiles of SPPB). CONCLUSION: Cystic infarcts and microinfarcts, but not neuropathology findings of Alzheimer’s disease, were related to physical performance levels five years before death. No pathology findings were associated with rates of physical performance decline. Physical function levels in the years prior to death may be affected by vascular brain pathologies.
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spelling pubmed-56675232017-11-08 Trajectories of physical function prior to death and brain neuropathology in a community-based cohort: the act study LaCroix, Andrea Z. Hubbard, Rebecca A. Gray, Shelly L. Anderson, Melissa L. Crane, Paul K. Sonnen, Joshua A. Zaslavsky, Oleg Larson, Eric B. BMC Geriatr Research Article BACKGROUND: Mechanisms linking cognitive and physical functioning in older adults are unclear. We sought to determine whether brain pathological changes relate to the level or rate of physical performance decline. METHODS: This study analyzed data from 305 participants in the autopsy subcohort of the prospective Adult Changes in Thought (ACT) study. Participants were aged 65+ and free of dementia at enrollment. Physical performance was measured at baseline and every two years using the Short Physical Performance Battery (SPPB). Data from 3174 ACT participants with ≥2 SPPB measurements were used to estimate two physical function measures: 1) rate of SPPB decline defined by intercept and slope; and 2) estimated SPPB 5 years prior to death. Neuropathology findings at autopsy included neurofibrillary tangles (Braak stage), neuritic plaques (CERAD level), presence of amyloid angiopathy, microinfarcts, cystic infarcts, and Lewy bodies. Associations (adjusted for sex, age, body mass index and education) between dichotomized neuropathologic outcomes and SPPB measures were estimated using modified Poisson regression with inverse probability weights (IPW) estimated via Generalized Estimating Equations (GEE). Relative risks for the 20(th), 40(th), and 60(th) percentiles (lowest levels and highest rates of decline) relative to the 80th percentile (highest level and lowest rate of decline) were calculated. RESULTS: Decedents with the least vs. most SPPB decline (slope > 75(th) vs. < 25(th) percentiles) had higher SPPB scores, and were more likely to be male, older, have higher education, and exercise regularly at baseline. No significant associations were observed between neuropathology findings and rate of SPPB decline. Lower predicted SPPB scores 5 years prior to death were associated with higher risk of microinfarcts (RR = 3.08, 95% confidence interval (CI) 0.93–1.07 for the 20(th) vs. 80(th) percentiles of SPPB) and significantly higher risk of cystic infarcts (RR = 2.72, 95% CI 1.45–5.57 for 20(th) vs. 80(th) percentiles of SPPB). CONCLUSION: Cystic infarcts and microinfarcts, but not neuropathology findings of Alzheimer’s disease, were related to physical performance levels five years before death. No pathology findings were associated with rates of physical performance decline. Physical function levels in the years prior to death may be affected by vascular brain pathologies. BioMed Central 2017-11-02 /pmc/articles/PMC5667523/ /pubmed/29096630 http://dx.doi.org/10.1186/s12877-017-0637-7 Text en © The Author(s). 2017 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 Article
LaCroix, Andrea Z.
Hubbard, Rebecca A.
Gray, Shelly L.
Anderson, Melissa L.
Crane, Paul K.
Sonnen, Joshua A.
Zaslavsky, Oleg
Larson, Eric B.
Trajectories of physical function prior to death and brain neuropathology in a community-based cohort: the act study
title Trajectories of physical function prior to death and brain neuropathology in a community-based cohort: the act study
title_full Trajectories of physical function prior to death and brain neuropathology in a community-based cohort: the act study
title_fullStr Trajectories of physical function prior to death and brain neuropathology in a community-based cohort: the act study
title_full_unstemmed Trajectories of physical function prior to death and brain neuropathology in a community-based cohort: the act study
title_short Trajectories of physical function prior to death and brain neuropathology in a community-based cohort: the act study
title_sort trajectories of physical function prior to death and brain neuropathology in a community-based cohort: the act study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5667523/
https://www.ncbi.nlm.nih.gov/pubmed/29096630
http://dx.doi.org/10.1186/s12877-017-0637-7
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