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Objective Physical Function in the Alzheimer’s Disease Continuum: Association with Cerebrospinal Fluid Biomarkers in the ALBION Study

Cognitive and physical decline, both indicators of aging, seem to be associated with each other. The aim of the present study was to investigate whether physical function parameters (walking time and handgrip strength) are related to cerebrospinal fluid (CSF) biomarkers (amyloid-beta Aβ(42), Tau, Ph...

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Autores principales: Sampatakakis, Stefanos N., Mamalaki, Eirini, Ntanasi, Eva, Kalligerou, Faidra, Liampas, Ioannis, Yannakoulia, Mary, Gargalionis, Antonios N., Scarmeas, Nikolaos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531412/
https://www.ncbi.nlm.nih.gov/pubmed/37762384
http://dx.doi.org/10.3390/ijms241814079
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author Sampatakakis, Stefanos N.
Mamalaki, Eirini
Ntanasi, Eva
Kalligerou, Faidra
Liampas, Ioannis
Yannakoulia, Mary
Gargalionis, Antonios N.
Scarmeas, Nikolaos
author_facet Sampatakakis, Stefanos N.
Mamalaki, Eirini
Ntanasi, Eva
Kalligerou, Faidra
Liampas, Ioannis
Yannakoulia, Mary
Gargalionis, Antonios N.
Scarmeas, Nikolaos
author_sort Sampatakakis, Stefanos N.
collection PubMed
description Cognitive and physical decline, both indicators of aging, seem to be associated with each other. The aim of the present study was to investigate whether physical function parameters (walking time and handgrip strength) are related to cerebrospinal fluid (CSF) biomarkers (amyloid-beta Aβ(42), Tau, PhTau) in individuals in the Alzheimer’s disease (AD) continuum. The sample was drawn from the Aiginition Longitudinal Biomarker Investigation of Neurodegeneration study, comprising 163 individuals aged 40–75 years: 112 cognitively normal (CN) and 51 with mild cognitive impairment (MCI). Physical function parameters were measured at baseline, a lumbar puncture was performed the same day and CSF biomarkers were analyzed using automated methods. The association between walking time, handgrip strength and CSF biomarkers was evaluated by linear correlation, followed by multivariate linear regression models adjusted for age, sex, education and APOEe4 genotype. Walking time was inversely related to CSF Aβ(42) (lower CSF values correspond to increased brain deposition) in all participants (p < 0.05). Subgroup analysis showed that this association was stronger in individuals with MCI and participants older than 60 years old, a result which remained statistically significant after adjustment for the aforementioned confounding factors. These findings may open new perspectives regarding the role of mobility in the AD continuum.
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spelling pubmed-105314122023-09-28 Objective Physical Function in the Alzheimer’s Disease Continuum: Association with Cerebrospinal Fluid Biomarkers in the ALBION Study Sampatakakis, Stefanos N. Mamalaki, Eirini Ntanasi, Eva Kalligerou, Faidra Liampas, Ioannis Yannakoulia, Mary Gargalionis, Antonios N. Scarmeas, Nikolaos Int J Mol Sci Article Cognitive and physical decline, both indicators of aging, seem to be associated with each other. The aim of the present study was to investigate whether physical function parameters (walking time and handgrip strength) are related to cerebrospinal fluid (CSF) biomarkers (amyloid-beta Aβ(42), Tau, PhTau) in individuals in the Alzheimer’s disease (AD) continuum. The sample was drawn from the Aiginition Longitudinal Biomarker Investigation of Neurodegeneration study, comprising 163 individuals aged 40–75 years: 112 cognitively normal (CN) and 51 with mild cognitive impairment (MCI). Physical function parameters were measured at baseline, a lumbar puncture was performed the same day and CSF biomarkers were analyzed using automated methods. The association between walking time, handgrip strength and CSF biomarkers was evaluated by linear correlation, followed by multivariate linear regression models adjusted for age, sex, education and APOEe4 genotype. Walking time was inversely related to CSF Aβ(42) (lower CSF values correspond to increased brain deposition) in all participants (p < 0.05). Subgroup analysis showed that this association was stronger in individuals with MCI and participants older than 60 years old, a result which remained statistically significant after adjustment for the aforementioned confounding factors. These findings may open new perspectives regarding the role of mobility in the AD continuum. MDPI 2023-09-14 /pmc/articles/PMC10531412/ /pubmed/37762384 http://dx.doi.org/10.3390/ijms241814079 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sampatakakis, Stefanos N.
Mamalaki, Eirini
Ntanasi, Eva
Kalligerou, Faidra
Liampas, Ioannis
Yannakoulia, Mary
Gargalionis, Antonios N.
Scarmeas, Nikolaos
Objective Physical Function in the Alzheimer’s Disease Continuum: Association with Cerebrospinal Fluid Biomarkers in the ALBION Study
title Objective Physical Function in the Alzheimer’s Disease Continuum: Association with Cerebrospinal Fluid Biomarkers in the ALBION Study
title_full Objective Physical Function in the Alzheimer’s Disease Continuum: Association with Cerebrospinal Fluid Biomarkers in the ALBION Study
title_fullStr Objective Physical Function in the Alzheimer’s Disease Continuum: Association with Cerebrospinal Fluid Biomarkers in the ALBION Study
title_full_unstemmed Objective Physical Function in the Alzheimer’s Disease Continuum: Association with Cerebrospinal Fluid Biomarkers in the ALBION Study
title_short Objective Physical Function in the Alzheimer’s Disease Continuum: Association with Cerebrospinal Fluid Biomarkers in the ALBION Study
title_sort objective physical function in the alzheimer’s disease continuum: association with cerebrospinal fluid biomarkers in the albion study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531412/
https://www.ncbi.nlm.nih.gov/pubmed/37762384
http://dx.doi.org/10.3390/ijms241814079
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