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HETEROGENEITY OF AGING IN HUMAN POPULATIONS

Recently by analyzing the 3D facial images, we generated the first comprehensive mapping of the aging human facial phenome. We constructed a robust age predictor and found that on average people of the same chronological age differ by +/-6 years in facial age, with the deviations increasing after ag...

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Autor principal: Jackie Han, Jing-Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6845089/
http://dx.doi.org/10.1093/geroni/igz038.870
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author Jackie Han, Jing-Dong
author_facet Jackie Han, Jing-Dong
author_sort Jackie Han, Jing-Dong
collection PubMed
description Recently by analyzing the 3D facial images, we generated the first comprehensive mapping of the aging human facial phenome. We constructed a robust age predictor and found that on average people of the same chronological age differ by +/-6 years in facial age, with the deviations increasing after age 40. Using this predictor we identified slow- and fast-agers that are significantly supported by health indicators. We further profiled blood cell mRNA and lncRNA expression by RNA-seq of this cohort and computationally predict their regulatory networks and their contributions to the variation in aging rate among different individuals, and those that are modifiable by their lifestyles. By extending the study to a large Northern Chinese cohort of 10,000 people we can now use deep learning AI approaches to precisely estimate aging status based on 3D facial images and their associations with individuals’ health and medical history.
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spelling pubmed-68450892019-11-18 HETEROGENEITY OF AGING IN HUMAN POPULATIONS Jackie Han, Jing-Dong Innov Aging Session 1245 (Symposium) Recently by analyzing the 3D facial images, we generated the first comprehensive mapping of the aging human facial phenome. We constructed a robust age predictor and found that on average people of the same chronological age differ by +/-6 years in facial age, with the deviations increasing after age 40. Using this predictor we identified slow- and fast-agers that are significantly supported by health indicators. We further profiled blood cell mRNA and lncRNA expression by RNA-seq of this cohort and computationally predict their regulatory networks and their contributions to the variation in aging rate among different individuals, and those that are modifiable by their lifestyles. By extending the study to a large Northern Chinese cohort of 10,000 people we can now use deep learning AI approaches to precisely estimate aging status based on 3D facial images and their associations with individuals’ health and medical history. Oxford University Press 2019-11-08 /pmc/articles/PMC6845089/ http://dx.doi.org/10.1093/geroni/igz038.870 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of The Gerontological Society of America. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Session 1245 (Symposium)
Jackie Han, Jing-Dong
HETEROGENEITY OF AGING IN HUMAN POPULATIONS
title HETEROGENEITY OF AGING IN HUMAN POPULATIONS
title_full HETEROGENEITY OF AGING IN HUMAN POPULATIONS
title_fullStr HETEROGENEITY OF AGING IN HUMAN POPULATIONS
title_full_unstemmed HETEROGENEITY OF AGING IN HUMAN POPULATIONS
title_short HETEROGENEITY OF AGING IN HUMAN POPULATIONS
title_sort heterogeneity of aging in human populations
topic Session 1245 (Symposium)
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6845089/
http://dx.doi.org/10.1093/geroni/igz038.870
work_keys_str_mv AT jackiehanjingdong heterogeneityofaginginhumanpopulations