DNA甲基化
表观遗传学
生物
甲基化
生命银行
遗传学
DNA
计算生物学
基因
生物信息学
基因表达
作者
Meiqi Yang,Mei Wang,Xiaoyu Zhao,Furong Xu,Sen Liang,Yifan Wang,N Wang,Muhammed Lamin Sambou,Hongbing Shen,Juncheng Dai
出处
期刊:Epigenomics
[Future Medicine]
日期:2024-04-01
卷期号:16 (7): 461-472
标识
DOI:10.2217/epi-2023-0343
摘要
Aim: To elucidate the epigenetic consequences of DNA methylation in healthspan termination (HST), considering the current limited understanding. Materials & methods: Genetically predicted DNA methylation models were established (n = 2478). These models were applied to genome-wide association study data on HST. Then, a poly-methylation risk score (PMRS) was established in 241,008 individuals from the UK Biobank. Results: Of the 63,046 CpGs from the prediction models, 13 novel CpGs were associated with HST. Furthermore, people with high PMRSs showed higher HST risk (hazard ratio: 1.18; 95% CI: 1.13-1.25). Conclusion: The study indicates that DNA methylation may influence HST by regulating the expression of genes (e.g., PRMT6, CTSK). PMRSs have a promising application in discriminating subpopulations to facilitate early prevention.
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