Assessment of DNA methylation from a single genomic region of ELOV2 is sufficient to predict chronological age
Zhu, B.; Li, D.; Han, G.; Yao, X.; Gu, H.; Liu, T.; Liu, L.; Dai, J.; Liu, I. Z.; Liang, Y.; Zheng, J.; Sun, Z.; Lin, H.; Wang, W.; Liu, N.; Yu, H.; Shi, M.; Shen, G.; Qu, L.
Show abstract
Estimation of chronological age is particularly informative in forensic contexts. Assessment of DNA methylation status allows for the prediction of age, though the accuracy and ease of manipulation may vary across different models. In this study, we started with a carefully designed discovery cohort recruiting more elderly subjects than other age categories, to diminish the effect of epigenetic drifting. We analyzed DNA methylation from a single genomic region of ELOV2, which was sufficient to construct an age-prediction model comprising 15 CpG sites. This model is further validated by an independent cohort as well as a multi-center test using trace dried bloodstains. The nature of our analytical pipeline, when combined the assessment of a single genomic locus with high-throughput sequencing, can easily be scaled up with low cost. Taken together, we propose a new age-prediction model featuring accuracy, ease of manipulation, 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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