DNA甲基化
生物
甲基化
表观遗传学
DNA
遗传学
基因
基因表达
作者
Sijia Li,Xin Gao,Zihui Wang,Jin Li,Lv-Tao Zeng,Ya-Min Dang,Yaqing Ma,L.‐Q. Zhang,Qingyu Wang,Ying-Min Zhang,Honglei Liu,Ruomei Qi,Jianping Cai
出处
期刊:Epigenomics
[Future Medicine]
日期:2024-05-15
卷期号:16 (10): 715-731
被引量:2
标识
DOI:10.1080/17501911.2024.2340958
摘要
Aim: Liquid biopsies analyzing cell-free DNA (cfDNA) methylation in plasma offer a noninvasive diagnostic for diseases, with the potential of aging biomarkers underexplored. Methods: Utilizing enzymatic methyl-seq (EM-seq), this study assessed cfDNA methylation patterns in aging with blood from 35 healthy individuals. Results: It found aging signatures, including higher cfDNA levels and variations in fragment sizes, plus approximately 2000 age-related differentially methylated CpG sites. A biological age predictive model based on 48 CpG sites showed a strong correlation with chronological age, verified by two datasets. Age-specific epigenetic shifts linked to inflammation were revealed through differentially methylated regions profiling and Olink proteomics. Conclusion: These findings suggest cfDNA methylation as a potential aging biomarker and might exacerbate immunoinflammatory reactivity in older individuals.
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