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本文引用的文献

1
Prospective Study of Epigenetic Age Acceleration and Incidence of Cardiovascular Disease Outcomes in the ARIC Study (Atherosclerosis Risk in Communities).前瞻性研究表观遗传年龄加速与心血管疾病结局在 ARIC 研究中的发生(社区动脉粥样硬化风险)。
Circ Genom Precis Med. 2018 Mar;11(3):e001937. doi: 10.1161/CIRCGEN.117.001937.
2
Cadmium exposure and age-associated DNA methylation changes in non-smoking women from northern Thailand.泰国北部非吸烟女性的镉暴露与年龄相关的DNA甲基化变化
Environ Epigenet. 2017 Jul 18;3(2):dvx006. doi: 10.1093/eep/dvx006. eCollection 2017 May.
3
High plasma organochlorine pesticide levels are related to increased biological age as calculated by DNA methylation analysis.血浆中有机氯农药水平较高与通过 DNA 甲基化分析计算得出的生物年龄增加有关。
Environ Int. 2018 Apr;113:109-113. doi: 10.1016/j.envint.2018.01.019. Epub 2018 Feb 6.
4
GWAS of epigenetic aging rates in blood reveals a critical role for TERT.血液表观遗传衰老速度的全基因组关联研究揭示了 TERT 的关键作用。
Nat Commun. 2018 Jan 26;9(1):387. doi: 10.1038/s41467-017-02697-5.
5
Faster ticking rate of the epigenetic clock is associated with faster pubertal development in girls.表观遗传时钟的更快摆动速度与女孩青春期发育的更快速度相关。
Epigenetics. 2018;13(1):85-94. doi: 10.1080/15592294.2017.1414127. Epub 2018 Feb 15.
6
Accelerated epigenetic aging and mitochondrial DNA copy number in bipolar disorder.双相情感障碍中的加速表观遗传衰老和线粒体 DNA 拷贝数。
Transl Psychiatry. 2017 Dec 11;7(12):1283. doi: 10.1038/s41398-017-0048-8.
7
Eleven Telomere, Epigenetic Clock, and Biomarker-Composite Quantifications of Biological Aging: Do They Measure the Same Thing?端粒、表观遗传时钟和生物老化生物标志物综合定量:它们测量的是同一件事吗?
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J Cell Biol. 2018 Jan 2;217(1):65-77. doi: 10.1083/jcb.201708092. Epub 2017 Nov 7.
9
miRNA processing gene polymorphisms, blood DNA methylation age and long-term ambient PM exposure in elderly men.miRNA 加工基因多态性、血液 DNA 甲基化年龄与老年男性长期环境 PM 暴露
Epigenomics. 2017 Dec;9(12):1529-1542. doi: 10.2217/epi-2017-0094. Epub 2017 Nov 6.
10
Erythrocyte Sedimentation Rate and C-reactive Protein Measurements and Their Relevance in Clinical Medicine.红细胞沉降率和C反应蛋白检测及其在临床医学中的相关性。
WMJ. 2016 Dec;115(6):317-21.

多组织 DNA 甲基化年龄:推进生物标志物应用的分子关系和展望。

Multi-tissue DNA methylation age: Molecular relationships and perspectives for advancing biomarker utility.

机构信息

Department of Environmental Health, Harvard T.H. Chan School of Public Health and MD-PhD Program, Harvard Medical School, Boston, MA, USA.

Department of Environmental Health and Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, MA, USA.

出版信息

Ageing Res Rev. 2018 Aug;45:15-23. doi: 10.1016/j.arr.2018.04.005. Epub 2018 Apr 23.

DOI:10.1016/j.arr.2018.04.005
PMID:29698722
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6047923/
Abstract

The multi-tissue DNA methylation estimator of chronological age (DNAm-age) has been associated with a wide range of exposures and health outcomes. Still, it is unclear how DNAm-age can have such broad relationships and how it can be best utilized as a biomarker. Understanding DNAm-age's molecular relationships is a promising approach to address this critical knowledge gap. In this review, we discuss the existing literature regarding DNAm-age's molecular relationships in six major categories: animal model systems, cancer processes, cellular aging processes, immune system processes, metabolic processes, and nucleic acid processes. We also present perspectives regarding the future of DNAm-age research, including the need to translate a greater number of ongoing research efforts to experimental and animal model systems.

摘要

多组织 DNA 甲基化估计的生物钟 (DNAm-age) 与广泛的暴露和健康结果有关。尽管如此,目前尚不清楚 DNAm-age 如何具有如此广泛的关系,以及如何将其作为生物标志物最佳利用。了解 DNAm-age 的分子关系是解决这一关键知识空白的有前途的方法。在这篇综述中,我们讨论了关于 DNAm-age 在六个主要类别中的分子关系的现有文献:动物模型系统、癌症过程、细胞衰老过程、免疫系统过程、代谢过程和核酸过程。我们还提出了关于 DNAm-age 研究未来的观点,包括需要将更多正在进行的研究工作转化为实验和动物模型系统。