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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals
2019
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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. |
format | Online Article Text |
id | pubmed-6914436 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Impact Journals |
record_format | MEDLINE/PubMed |
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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