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Predicting Age From Behavioral Test Performance for Screening Early Onset of Cognitive Decline

Background: Neuronal reactions and cognitive processes slow down during aging. The onset, rate, and extent of changes vary considerably from individual to individual. Assessing the changes throughout the lifespan is a challenging task. No existing test covers all domains, and batteries of tests are...

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Autores principales: Statsenko, Yauhen, Habuza, Tetiana, Charykova, Inna, Gorkom, Klaus Neidl-Van, Zaki, Nazar, Almansoori, Taleb M., Baylis, Gordon, Ljubisavljevic, Milos, Belghali, Maroua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8312225/
https://www.ncbi.nlm.nih.gov/pubmed/34322006
http://dx.doi.org/10.3389/fnagi.2021.661514
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author Statsenko, Yauhen
Habuza, Tetiana
Charykova, Inna
Gorkom, Klaus Neidl-Van
Zaki, Nazar
Almansoori, Taleb M.
Baylis, Gordon
Ljubisavljevic, Milos
Belghali, Maroua
author_facet Statsenko, Yauhen
Habuza, Tetiana
Charykova, Inna
Gorkom, Klaus Neidl-Van
Zaki, Nazar
Almansoori, Taleb M.
Baylis, Gordon
Ljubisavljevic, Milos
Belghali, Maroua
author_sort Statsenko, Yauhen
collection PubMed
description Background: Neuronal reactions and cognitive processes slow down during aging. The onset, rate, and extent of changes vary considerably from individual to individual. Assessing the changes throughout the lifespan is a challenging task. No existing test covers all domains, and batteries of tests are administered. The best strategy is to study each functional domain separately by applying different behavioral tasks whereby the tests reflect the conceptual structure of cognition. Such an approach has limitations that are described in the article. Objective: Our aim was to improve the diagnosis of early cognitive decline. We estimated the onset of cognitive decline in a healthy population, using behavioral tests, and predicted the age group of an individual. The comparison between the predicted (“cognitive”) and chronological age will contribute to the early diagnosis of accelerated aging. Materials and Methods: We used publicly available datasets (POBA, SSCT) and Pearson correlation coefficients to assess the relationship between age and tests results, Kruskal-Wallis test to compare distribution, clustering methods to find an onset of cognitive decline, feature selection to enhance performance of the clustering algorithms, and classification methods to predict an age group from cognitive tests results. Results: The major results of the psychophysiological tests followed a U-shape function across the lifespan, which reflected the known inverted function of white matter volume changes. Optimal values were observed in those aged over 35 years, with a period of stability and accelerated decline after 55–60 years of age. The shape of the age-related variance of the performance of major cognitive tests was linear, which followed the trend of lifespan gray matter volume changes starting from adolescence. There was no significant sex difference in lifelong dynamics of major tests estimates. The performance of the classification model for identifying subject age groups was high. Conclusions: ML models can be designed and utilized as computer-aided detectors of neurocognitive decline. Our study demonstrated great promise for the utility of classification models to predict age-related changes. These findings encourage further explorations combining several tests from the cognitive and psychophysiological test battery to derive the most reliable set of tests toward the development of a highly-accurate ML model.
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spelling pubmed-83122252021-07-27 Predicting Age From Behavioral Test Performance for Screening Early Onset of Cognitive Decline Statsenko, Yauhen Habuza, Tetiana Charykova, Inna Gorkom, Klaus Neidl-Van Zaki, Nazar Almansoori, Taleb M. Baylis, Gordon Ljubisavljevic, Milos Belghali, Maroua Front Aging Neurosci Neuroscience Background: Neuronal reactions and cognitive processes slow down during aging. The onset, rate, and extent of changes vary considerably from individual to individual. Assessing the changes throughout the lifespan is a challenging task. No existing test covers all domains, and batteries of tests are administered. The best strategy is to study each functional domain separately by applying different behavioral tasks whereby the tests reflect the conceptual structure of cognition. Such an approach has limitations that are described in the article. Objective: Our aim was to improve the diagnosis of early cognitive decline. We estimated the onset of cognitive decline in a healthy population, using behavioral tests, and predicted the age group of an individual. The comparison between the predicted (“cognitive”) and chronological age will contribute to the early diagnosis of accelerated aging. Materials and Methods: We used publicly available datasets (POBA, SSCT) and Pearson correlation coefficients to assess the relationship between age and tests results, Kruskal-Wallis test to compare distribution, clustering methods to find an onset of cognitive decline, feature selection to enhance performance of the clustering algorithms, and classification methods to predict an age group from cognitive tests results. Results: The major results of the psychophysiological tests followed a U-shape function across the lifespan, which reflected the known inverted function of white matter volume changes. Optimal values were observed in those aged over 35 years, with a period of stability and accelerated decline after 55–60 years of age. The shape of the age-related variance of the performance of major cognitive tests was linear, which followed the trend of lifespan gray matter volume changes starting from adolescence. There was no significant sex difference in lifelong dynamics of major tests estimates. The performance of the classification model for identifying subject age groups was high. Conclusions: ML models can be designed and utilized as computer-aided detectors of neurocognitive decline. Our study demonstrated great promise for the utility of classification models to predict age-related changes. These findings encourage further explorations combining several tests from the cognitive and psychophysiological test battery to derive the most reliable set of tests toward the development of a highly-accurate ML model. Frontiers Media S.A. 2021-07-12 /pmc/articles/PMC8312225/ /pubmed/34322006 http://dx.doi.org/10.3389/fnagi.2021.661514 Text en Copyright © 2021 Statsenko, Habuza, Charykova, Gorkom, Zaki, Almansoori, Baylis, Ljubisavljevic and Belghali. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Statsenko, Yauhen
Habuza, Tetiana
Charykova, Inna
Gorkom, Klaus Neidl-Van
Zaki, Nazar
Almansoori, Taleb M.
Baylis, Gordon
Ljubisavljevic, Milos
Belghali, Maroua
Predicting Age From Behavioral Test Performance for Screening Early Onset of Cognitive Decline
title Predicting Age From Behavioral Test Performance for Screening Early Onset of Cognitive Decline
title_full Predicting Age From Behavioral Test Performance for Screening Early Onset of Cognitive Decline
title_fullStr Predicting Age From Behavioral Test Performance for Screening Early Onset of Cognitive Decline
title_full_unstemmed Predicting Age From Behavioral Test Performance for Screening Early Onset of Cognitive Decline
title_short Predicting Age From Behavioral Test Performance for Screening Early Onset of Cognitive Decline
title_sort predicting age from behavioral test performance for screening early onset of cognitive decline
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8312225/
https://www.ncbi.nlm.nih.gov/pubmed/34322006
http://dx.doi.org/10.3389/fnagi.2021.661514
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