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1
A Systematic Review and Meta-analysis of Environmental, Lifestyle, and Health Factors Associated With DNA Methylation Age.环境、生活方式和健康因素与 DNA 甲基化年龄相关的系统评价和荟萃分析。
J Gerontol A Biol Sci Med Sci. 2020 Feb 14;75(3):481-494. doi: 10.1093/gerona/glz099.
2
The epigenetic clock as a predictor of disease and mortality risk: a systematic review and meta-analysis.表观遗传时钟作为疾病和死亡风险的预测指标:系统评价和荟萃分析。
Clin Epigenetics. 2019 Apr 11;11(1):62. doi: 10.1186/s13148-019-0656-7.
3
Human age prediction based on DNA methylation of non-blood tissues.基于非血液组织 DNA 甲基化的人类年龄预测。
Comput Methods Programs Biomed. 2019 Apr;171:11-18. doi: 10.1016/j.cmpb.2019.02.010. Epub 2019 Feb 19.
4
Telomere Biology and Human Phenotype.端粒生物学与人类表型。
Cells. 2019 Jan 19;8(1):73. doi: 10.3390/cells8010073.
5
DNA methylation GrimAge strongly predicts lifespan and healthspan.DNA甲基化GrimAge能有力地预测寿命和健康跨度。
Aging (Albany NY). 2019 Jan 21;11(2):303-327. doi: 10.18632/aging.101684.
6
Platform-independent models for age prediction using DNA methylation data.基于 DNA 甲基化数据的与平台无关的年龄预测模型。
Forensic Sci Int Genet. 2019 Jan;38:39-47. doi: 10.1016/j.fsigen.2018.10.005. Epub 2018 Oct 9.
7
Epigenetic ageing is distinct from senescence-mediated ageing and is not prevented by telomerase expression.表观遗传衰老不同于衰老介导的衰老,并且不受端粒酶表达的影响。
Aging (Albany NY). 2018 Oct 17;10(10):2800-2815. doi: 10.18632/aging.101588.
8
DNA methylation of the ELOVL2, FHL2, KLF14, C1orf132/MIR29B2C, and TRIM59 genes for age prediction from blood, saliva, and buccal swab samples.从血液、唾液和口腔拭子样本中预测年龄的 ELOVL2、FHL2、KLF14、C1orf132/MIR29B2C 和 TRIM59 基因的 DNA 甲基化。
Forensic Sci Int Genet. 2019 Jan;38:1-8. doi: 10.1016/j.fsigen.2018.09.010. Epub 2018 Sep 29.
9
Effects of Vitamin D3 Supplementation on Epigenetic Aging in Overweight and Obese African Americans With Suboptimal Vitamin D Status: A Randomized Clinical Trial.超重和肥胖且维生素 D 状态不佳的非裔美国人补充维生素 D3 对表观遗传衰老的影响:一项随机临床试验。
J Gerontol A Biol Sci Med Sci. 2019 Jan 1;74(1):91-98. doi: 10.1093/gerona/gly223.
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Horizons in the evolution of aging.衰老演化的新视野
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作为生物老化指标的 DNA 甲基化模式:精准健康促进科学现状与未来方向。

Patterns of DNA methylation as an indicator of biological aging: State of the science and future directions in precision health promotion.

机构信息

Martha S. Pitzer Center for Women, Children, & Youth, College of Nursing, The Ohio State University, Columbus, OH.

Center for Research and Health Analytics, College of Nursing, The Ohio State University, Columbus, OH.

出版信息

Nurs Outlook. 2019 Jul-Aug;67(4):337-344. doi: 10.1016/j.outlook.2019.05.006. Epub 2019 May 17.

DOI:10.1016/j.outlook.2019.05.006
PMID:31248628
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6679732/
Abstract

BACKGROUND

A rapidly expanding literature suggests that individuals of the same chronological age show significant variation in biological age.

PURPOSE

The purpose of this article is to review the literature surrounding epigenetic age as estimated by DNA methylation, involving the addition or removal of methyl groups to DNA that can alter gene expression without changing the DNA sequence.

METHODS

This state of the science literature review summarizes current approaches in epigenetic age determination and applications of aging algorithms.

FINDINGS

A number of algorithms estimate epigenetic age using DNA methylation markers, primarily among adults. Algorithm application has focused on determining predictive value for risk of disease and death and identifying antecedents to age acceleration. Several studies have incorporated epigenetic age to evaluate intervention effectiveness.

DISCUSSION

As the research community continues to refine aging algorithms, there may be opportunity to promote health from a precision health perspective.

摘要

背景

越来越多的文献表明,同一年龄段的个体在生物学年龄上存在显著差异。

目的

本文旨在回顾 DNA 甲基化估算的表观遗传年龄的文献,甲基化是指在 DNA 上添加或去除甲基基团,这种修饰可以改变基因表达而不改变 DNA 序列。

方法

本科学文献综述总结了当前的表观遗传年龄测定方法和衰老算法的应用。

发现

许多算法使用 DNA 甲基化标记来估计表观遗传年龄,主要针对成年人。算法的应用主要集中在确定疾病和死亡风险的预测价值,以及识别年龄加速的前兆上。一些研究已经将表观遗传年龄纳入其中,以评估干预措施的效果。

讨论

随着研究界继续完善衰老算法,从精准健康的角度来看,可能有机会促进健康。