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DNA methylation profile is a quantitative measure of biological aging in children

DNA methylation changes within the genome can be used to predict human age. However, the existing biological age prediction models based on DNA methylation are predominantly adult-oriented. We established a methylation-based age prediction model for children (9-212 months old) using data from 716 bl...

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Autores principales: Wu, Xiaohui, Chen, Weidan, Lin, Fangqin, Huang, Qingsheng, Zhong, Jiayong, Gao, Huan, Song, Yanyan, Liang, Huiying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6914436/
https://www.ncbi.nlm.nih.gov/pubmed/31756171
http://dx.doi.org/10.18632/aging.102399
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author Wu, Xiaohui
Chen, Weidan
Lin, Fangqin
Huang, Qingsheng
Zhong, Jiayong
Gao, Huan
Song, Yanyan
Liang, Huiying
author_facet Wu, Xiaohui
Chen, Weidan
Lin, Fangqin
Huang, Qingsheng
Zhong, Jiayong
Gao, Huan
Song, Yanyan
Liang, Huiying
author_sort Wu, Xiaohui
collection PubMed
description DNA methylation changes within the genome can be used to predict human age. However, the existing biological age prediction models based on DNA methylation are predominantly adult-oriented. We established a methylation-based age prediction model for children (9-212 months old) using data from 716 blood samples in 11 DNA methylation datasets. Our elastic net model includes 111 CpG sites, mostly in genes associated with development and aging. The model performed well and exhibited high precision, yielding a 98% correlation between the DNA methylation age and the chronological age, with an error of only 6.7 months. When we used the model to assess age acceleration in children based on their methylation data, we observed the following: first, the aging rate appears to be fastest in mid-childhood, and this acceleration is more pronounced in autistic children; second, lead exposure early in life increases the aging rate in boys, but not in girls; third, short-term recombinant human growth hormone treatment has little effect on the aging rate of children. Our child-specific methylation-based age prediction model can effectively detect epigenetic changes and health imbalances early in life. This may thus be a useful model for future studies of epigenetic interventions for age-related diseases.
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spelling pubmed-69144362019-12-19 DNA methylation profile is a quantitative measure of biological aging in children Wu, Xiaohui Chen, Weidan Lin, Fangqin Huang, Qingsheng Zhong, Jiayong Gao, Huan Song, Yanyan Liang, Huiying Aging (Albany NY) Research Paper DNA methylation changes within the genome can be used to predict human age. However, the existing biological age prediction models based on DNA methylation are predominantly adult-oriented. We established a methylation-based age prediction model for children (9-212 months old) using data from 716 blood samples in 11 DNA methylation datasets. Our elastic net model includes 111 CpG sites, mostly in genes associated with development and aging. The model performed well and exhibited high precision, yielding a 98% correlation between the DNA methylation age and the chronological age, with an error of only 6.7 months. When we used the model to assess age acceleration in children based on their methylation data, we observed the following: first, the aging rate appears to be fastest in mid-childhood, and this acceleration is more pronounced in autistic children; second, lead exposure early in life increases the aging rate in boys, but not in girls; third, short-term recombinant human growth hormone treatment has little effect on the aging rate of children. Our child-specific methylation-based age prediction model can effectively detect epigenetic changes and health imbalances early in life. This may thus be a useful model for future studies of epigenetic interventions for age-related diseases. Impact Journals 2019-11-22 /pmc/articles/PMC6914436/ /pubmed/31756171 http://dx.doi.org/10.18632/aging.102399 Text en Copyright © 2019 Wu et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Wu, Xiaohui
Chen, Weidan
Lin, Fangqin
Huang, Qingsheng
Zhong, Jiayong
Gao, Huan
Song, Yanyan
Liang, Huiying
DNA methylation profile is a quantitative measure of biological aging in children
title DNA methylation profile is a quantitative measure of biological aging in children
title_full DNA methylation profile is a quantitative measure of biological aging in children
title_fullStr DNA methylation profile is a quantitative measure of biological aging in children
title_full_unstemmed DNA methylation profile is a quantitative measure of biological aging in children
title_short DNA methylation profile is a quantitative measure of biological aging in children
title_sort dna methylation profile is a quantitative measure of biological aging in children
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6914436/
https://www.ncbi.nlm.nih.gov/pubmed/31756171
http://dx.doi.org/10.18632/aging.102399
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