Cell-free DNA methylation patterns in aging and their association with inflamm-aging
Sijia Li, Xin Gao, Zihui Wang, Jin Li, Lv-Tao Zeng, Ya-Min Dang, Yaqing Ma, Li‐Qun Zhang, Qingyu Wang, Ying-Min Zhang, Honglei Liu, Ruomei Qi, Jianping Cai
Abstract
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.