Frontiers in Aging (Feb 2025)

Multiplexing and massive parallel sequencing of targeted DNA methylation to predict chronological age

  • Bowen Zhu,
  • Bowen Zhu,
  • Dean Li,
  • Dean Li,
  • Guojing Han,
  • Xue Yao,
  • Hongqin Gu,
  • Tao Liu,
  • Linghua Liu,
  • Jie Dai,
  • Isabella Zhaotong Liu,
  • Yanlin Liang,
  • Jian Zheng,
  • Zheming Sun,
  • He Lin,
  • Nan Liu,
  • Haidong Yu,
  • Meifang Shi,
  • Gaofang Shen,
  • Zhaohui Hu,
  • Lefeng Qu

DOI
https://doi.org/10.3389/fragi.2025.1467639
Journal volume & issue
Vol. 6

Abstract

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Estimation of chronological age is particularly informative in forensic contexts. Assessment of DNA methylation status allows for the prediction of age, though the accuracy may vary across models. In this study, we started with a carefully designed discovery cohort with more elderly subjects than other age categories, to diminish the effect of epigenetic drifting. We applied multiplexing and massive parallel sequencing of targeted DNA methylation, which let us to construct a model comprising 25 CpG sites with substantially improved accuracy (MAE = 2.279, R = 0.920). This model is further validated by an independent cohort (MAE = 2.204, 82.7% success (±5 years)). Remarkably, in a multi-center test using trace blood samples from forensic caseworks, the correct predictions (±5 years) are 91.7%. The nature of our analytical pipeline can easily be scaled up with low cost. Taken together, we propose a new age-prediction model featuring accuracy, sensitivity, high-throughput, and low cost. This model can be readily applied in both classic and newly emergent forensic contexts that require age estimation.

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