Correlating continuously captured home-based digital biomarkers of daily function with postmortem neurodegenerative neuropathology

<h4>Background</h4> Outcome measures available for use in Alzheimer’s disease (AD) clinical trials are limited in ability to detect gradual changes. Measures of everyday function and cognition assessed unobtrusively at home using embedded sensing and computing generated “digital biomarke...

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Main Authors: Nathan C. Hantke, Jeffrey Kaye, Nora Mattek, Chao-Yi Wu, Hiroko H. Dodge, Zachary Beattie, Randy Woltjer
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10249904/?tool=EBI
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author Nathan C. Hantke
Jeffrey Kaye
Nora Mattek
Chao-Yi Wu
Hiroko H. Dodge
Zachary Beattie
Randy Woltjer
author_facet Nathan C. Hantke
Jeffrey Kaye
Nora Mattek
Chao-Yi Wu
Hiroko H. Dodge
Zachary Beattie
Randy Woltjer
author_sort Nathan C. Hantke
collection DOAJ
description <h4>Background</h4> Outcome measures available for use in Alzheimer’s disease (AD) clinical trials are limited in ability to detect gradual changes. Measures of everyday function and cognition assessed unobtrusively at home using embedded sensing and computing generated “digital biomarkers” (DBs) have been shown to be ecologically valid and to improve efficiency of clinical trials. However, DBs have not been assessed for their relationship to AD neuropathology. <h4>Objectives</h4> The goal of the current study is to perform an exploratory examination of possible associations between DBs and AD neuropathology in an initially cognitively intact community-based cohort. <h4>Methods</h4> Participants included in this study were ≥65 years of age, living independently, of average health for age, and followed until death. Algorithms, run on the continuously-collected passive sensor data, generated daily metrics for each DB: cognitive function, mobility, socialization, and sleep. Fixed postmortem brains were evaluated for neurofibrillary tangles (NFTs) and neuritic plaque (NP) pathology and staged by Braak and CERAD systems in the context of the “ABC” assessment of AD-associated changes. <h4>Results</h4> The analysis included a total of 41 participants (M±SD age at death = 92.2±5.1 years). The four DBs showed consistent patterns relative to both Braak stage and NP score severity. Greater NP severity was correlated with the DB composite and reduced walking speed. Braak stage was associated with reduced computer use time and increased total time in bed. <h4>Discussion</h4> This study provides the first data showing correlations between DBs and neuropathological markers in an aging cohort. The findings suggest continuous, home-based DBs may hold potential to serve as behavioral proxies that index neurodegenerative processes.
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spelling doaj.art-c658683b45d64d44b6c4d911d66b73752023-06-11T05:31:25ZengPublic Library of Science (PLoS)PLoS ONE1932-62032023-01-01186Correlating continuously captured home-based digital biomarkers of daily function with postmortem neurodegenerative neuropathologyNathan C. HantkeJeffrey KayeNora MattekChao-Yi WuHiroko H. DodgeZachary BeattieRandy Woltjer<h4>Background</h4> Outcome measures available for use in Alzheimer’s disease (AD) clinical trials are limited in ability to detect gradual changes. Measures of everyday function and cognition assessed unobtrusively at home using embedded sensing and computing generated “digital biomarkers” (DBs) have been shown to be ecologically valid and to improve efficiency of clinical trials. However, DBs have not been assessed for their relationship to AD neuropathology. <h4>Objectives</h4> The goal of the current study is to perform an exploratory examination of possible associations between DBs and AD neuropathology in an initially cognitively intact community-based cohort. <h4>Methods</h4> Participants included in this study were ≥65 years of age, living independently, of average health for age, and followed until death. Algorithms, run on the continuously-collected passive sensor data, generated daily metrics for each DB: cognitive function, mobility, socialization, and sleep. Fixed postmortem brains were evaluated for neurofibrillary tangles (NFTs) and neuritic plaque (NP) pathology and staged by Braak and CERAD systems in the context of the “ABC” assessment of AD-associated changes. <h4>Results</h4> The analysis included a total of 41 participants (M±SD age at death = 92.2±5.1 years). The four DBs showed consistent patterns relative to both Braak stage and NP score severity. Greater NP severity was correlated with the DB composite and reduced walking speed. Braak stage was associated with reduced computer use time and increased total time in bed. <h4>Discussion</h4> This study provides the first data showing correlations between DBs and neuropathological markers in an aging cohort. The findings suggest continuous, home-based DBs may hold potential to serve as behavioral proxies that index neurodegenerative processes.https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10249904/?tool=EBI
spellingShingle Nathan C. Hantke
Jeffrey Kaye
Nora Mattek
Chao-Yi Wu
Hiroko H. Dodge
Zachary Beattie
Randy Woltjer
Correlating continuously captured home-based digital biomarkers of daily function with postmortem neurodegenerative neuropathology
PLoS ONE
title Correlating continuously captured home-based digital biomarkers of daily function with postmortem neurodegenerative neuropathology
title_full Correlating continuously captured home-based digital biomarkers of daily function with postmortem neurodegenerative neuropathology
title_fullStr Correlating continuously captured home-based digital biomarkers of daily function with postmortem neurodegenerative neuropathology
title_full_unstemmed Correlating continuously captured home-based digital biomarkers of daily function with postmortem neurodegenerative neuropathology
title_short Correlating continuously captured home-based digital biomarkers of daily function with postmortem neurodegenerative neuropathology
title_sort correlating continuously captured home based digital biomarkers of daily function with postmortem neurodegenerative neuropathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10249904/?tool=EBI
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