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Deep biomarkers of human aging: Application of deep neural networks to biomarker development
One of the major impediments in human aging research is the absence of a comprehensive and actionable set of biomarkers that may be targeted and measured to track the effectiveness of therapeutic interventions. In this study, we designed a modular ensemble of 21 deep neural networks (DNNs) of varyin...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931851/ https://www.ncbi.nlm.nih.gov/pubmed/27191382 http://dx.doi.org/10.18632/aging.100968 |
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author | Putin, Evgeny Mamoshina, Polina Aliper, Alexander Korzinkin, Mikhail Moskalev, Alexey Kolosov, Alexey Ostrovskiy, Alexander Cantor, Charles Vijg, Jan Zhavoronkov, Alex |
author_facet | Putin, Evgeny Mamoshina, Polina Aliper, Alexander Korzinkin, Mikhail Moskalev, Alexey Kolosov, Alexey Ostrovskiy, Alexander Cantor, Charles Vijg, Jan Zhavoronkov, Alex |
author_sort | Putin, Evgeny |
collection | PubMed |
description | One of the major impediments in human aging research is the absence of a comprehensive and actionable set of biomarkers that may be targeted and measured to track the effectiveness of therapeutic interventions. In this study, we designed a modular ensemble of 21 deep neural networks (DNNs) of varying depth, structure and optimization to predict human chronological age using a basic blood test. To train the DNNs, we used over 60,000 samples from common blood biochemistry and cell count tests from routine health exams performed by a single laboratory and linked to chronological age and sex. The best performing DNN in the ensemble demonstrated 81.5 % epsilon-accuracy r = 0.90 with R(2) = 0.80 and MAE = 6.07 years in predicting chronological age within a 10 year frame, while the entire ensemble achieved 83.5% epsilon-accuracy r = 0.91 with R(2) = 0.82 and MAE = 5.55 years. The ensemble also identified the 5 most important markers for predicting human chronological age: albumin, glucose, alkaline phosphatase, urea and erythrocytes. To allow for public testing and evaluate real-life performance of the predictor, we developed an online system available at http://www.aging.ai. The ensemble approach may facilitate integration of multi-modal data linked to chronological age and sex that may lead to simple, minimally invasive, and affordable methods of tracking integrated biomarkers of aging in humans and performing cross-species feature importance analysis. |
format | Online Article Text |
id | pubmed-4931851 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-49318512016-07-18 Deep biomarkers of human aging: Application of deep neural networks to biomarker development Putin, Evgeny Mamoshina, Polina Aliper, Alexander Korzinkin, Mikhail Moskalev, Alexey Kolosov, Alexey Ostrovskiy, Alexander Cantor, Charles Vijg, Jan Zhavoronkov, Alex Aging (Albany NY) Research Paper One of the major impediments in human aging research is the absence of a comprehensive and actionable set of biomarkers that may be targeted and measured to track the effectiveness of therapeutic interventions. In this study, we designed a modular ensemble of 21 deep neural networks (DNNs) of varying depth, structure and optimization to predict human chronological age using a basic blood test. To train the DNNs, we used over 60,000 samples from common blood biochemistry and cell count tests from routine health exams performed by a single laboratory and linked to chronological age and sex. The best performing DNN in the ensemble demonstrated 81.5 % epsilon-accuracy r = 0.90 with R(2) = 0.80 and MAE = 6.07 years in predicting chronological age within a 10 year frame, while the entire ensemble achieved 83.5% epsilon-accuracy r = 0.91 with R(2) = 0.82 and MAE = 5.55 years. The ensemble also identified the 5 most important markers for predicting human chronological age: albumin, glucose, alkaline phosphatase, urea and erythrocytes. To allow for public testing and evaluate real-life performance of the predictor, we developed an online system available at http://www.aging.ai. The ensemble approach may facilitate integration of multi-modal data linked to chronological age and sex that may lead to simple, minimally invasive, and affordable methods of tracking integrated biomarkers of aging in humans and performing cross-species feature importance analysis. Impact Journals LLC 2016-05-18 /pmc/articles/PMC4931851/ /pubmed/27191382 http://dx.doi.org/10.18632/aging.100968 Text en Copyright: © 2016 Putin et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Putin, Evgeny Mamoshina, Polina Aliper, Alexander Korzinkin, Mikhail Moskalev, Alexey Kolosov, Alexey Ostrovskiy, Alexander Cantor, Charles Vijg, Jan Zhavoronkov, Alex Deep biomarkers of human aging: Application of deep neural networks to biomarker development |
title | Deep biomarkers of human aging: Application of deep neural networks to biomarker development |
title_full | Deep biomarkers of human aging: Application of deep neural networks to biomarker development |
title_fullStr | Deep biomarkers of human aging: Application of deep neural networks to biomarker development |
title_full_unstemmed | Deep biomarkers of human aging: Application of deep neural networks to biomarker development |
title_short | Deep biomarkers of human aging: Application of deep neural networks to biomarker development |
title_sort | deep biomarkers of human aging: application of deep neural networks to biomarker development |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4931851/ https://www.ncbi.nlm.nih.gov/pubmed/27191382 http://dx.doi.org/10.18632/aging.100968 |
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