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基于 Y 染色体 DNA 甲基化的男性特异性年龄估计。

Male-specific age estimation based on Y-chromosomal DNA methylation.

机构信息

Department of Genetic Identification, Erasmus University Medical Center Rotterdam, Rotterdam 3000, CA, The Netherlands.

出版信息

Aging (Albany NY). 2021 Mar 11;13(5):6442-6458. doi: 10.18632/aging.202775.

DOI:10.18632/aging.202775
PMID:33744870
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7993701/
Abstract

Although DNA methylation variation of autosomal CpGs provides robust age predictive biomarkers, no male-specific age predictor exists based on Y-CpGs yet. Since sex chromosomes play an important role in aging, a Y-chromosome-based age predictor would allow studying male-specific aging effects and would also be useful in forensics. Here, we used blood-based DNA methylation microarray data of 1,057 males from six cohorts aged 15-87 and identified 75 Y-CpGs with an interquartile range of ≥0.1. Of these, 22 and six were significantly hyper- and hypomethylated with age (p(cor)<0.05, Bonferroni), respectively. Amongst several machine learning algorithms, a model based on support vector machines with radial kernel performed best in male-specific age prediction. We achieved a mean absolute deviation (MAD) between true and predicted age of 7.54 years (cor=0.81, validation) when using all 75 Y-CpGs, and a MAD of 8.46 years (cor=0.73, validation) based on the most predictive 19 Y-CpGs. The accuracies of both age predictors did not worsen with increased age, in contrast to autosomal CpG-based age predictors that are known to predict age with reduced accuracy in the elderly. Overall, we introduce the first-of-its-kind male-specific epigenetic age predictor for future applications in aging research and forensics.

摘要

虽然常染色体 CpG 的 DNA 甲基化变化提供了强大的年龄预测生物标志物,但目前尚未基于 Y-CpG 开发出男性特异性年龄预测器。由于性染色体在衰老中起着重要作用,基于 Y 染色体的年龄预测器可以研究男性特异性衰老效应,在法医学中也很有用。在这里,我们使用了来自六个年龄在 15-87 岁的男性队列的基于血液的 DNA 甲基化微阵列数据,鉴定了 75 个 Y-CpG,其四分位间距(IQR)≥0.1。其中,22 个和 6 个 Y-CpG 分别与年龄呈显著的高甲基化和低甲基化(p(cor)<0.05,Bonferroni)。在几种机器学习算法中,基于支持向量机和径向核的模型在男性特异性年龄预测方面表现最佳。当使用所有 75 个 Y-CpG 时,我们在男性特异性年龄预测中获得了真实年龄和预测年龄之间的平均绝对偏差(MAD)为 7.54 岁(cor=0.81,验证),而基于最具预测性的 19 个 Y-CpG 的 MAD 为 8.46 岁(cor=0.73,验证)。与已知在老年人中预测年龄准确性降低的基于常染色体 CpG 的年龄预测器不同,这两种年龄预测器的准确性不会随年龄增加而恶化。总的来说,我们引入了首例男性特异性表观遗传年龄预测器,用于未来的衰老研究和法医学应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2ec/7993701/ecd9578c722e/aging-13-202775-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2ec/7993701/134b296d9145/aging-13-202775-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2ec/7993701/6865439a6f55/aging-13-202775-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2ec/7993701/fcbffa0c7968/aging-13-202775-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2ec/7993701/ecd9578c722e/aging-13-202775-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2ec/7993701/134b296d9145/aging-13-202775-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2ec/7993701/6865439a6f55/aging-13-202775-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2ec/7993701/fcbffa0c7968/aging-13-202775-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2ec/7993701/ecd9578c722e/aging-13-202775-g004.jpg

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