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鉴定 Illumina MethylationEPIC® BeadChip 上与血液相关的年龄相关 DNA 甲基化标记物。

Identifying blood-specific age-related DNA methylation markers on the Illumina MethylationEPIC® BeadChip.

机构信息

Centre for Forensic Science, Department of Pure and Applied Chemistry, University of Strathclyde, Glasgow, Scotland, UK; General Department for Forensic Evidence, State of Kuwait Ministry of Interior, Kuwait.

Centre for Forensic Science, Department of Pure and Applied Chemistry, University of Strathclyde, Glasgow, Scotland, UK.

出版信息

Forensic Sci Int. 2019 Oct;303:109944. doi: 10.1016/j.forsciint.2019.109944. Epub 2019 Sep 12.

Abstract

The past decade has seen rapid development in DNA methylation (DNAm) microarrays, including the Illumina HumanMethylation27 and HumanMethylation450 (450K) chips, which have played an essential role in identifying and evaluating age-related (AR) DNAm markers in different tissues. Recently, a new array, the Illumina MethylationEPIC (EPIC) was introduced, with nearly double the number of probes as the 450K (∼850,000 probes). In this study, we test these newly added probes for age association using a large cohort of 754 DNAm profiles from blood samples assayed on the EPIC BeadChip, for individuals aged 0-88 years old. 52 AR CpG sites (Spearman's abs(rho) >0.6 and P-value <10) were identified, 21 of which were novel sites and mapped to 18 genes, nine of which (LHFPL4, SLC12A8, EGFEM1P, GPR158, TAL1, KIAA1755, LOC730668, DUSP16, and FAM65C) have never previously been reported to be associated with age. The data were subsequently split into a 527-sample training set and a 227-sample testing set to build and validate two age prediction models using elastic net regression and multivariate regression. Elastic net regression selected 425 CpG markers with a mean absolute deviation (MAD) of 2.6 years based on the testing set. To build a multivariate linear regression model, AR CpG sites with R > 0.5 at FDR < 0.05 were input into stepwise regression to select the best subset for age prediction. The resulting six CpG markers were linearly modelled with age and explained 81% of age-correlated variation in DNAm levels. Age estimation accuracy using bootstrap analysis was 4.5 years, with 95% confidence intervals of 4.56 to 4.57 years based on the testing set. These results suggest that EPIC BeadChip probes for age estimation fall within the range of probes found on the previous Illumina HumanMethylation platforms in terms of their age-prediction ability.

摘要

过去十年,DNA 甲基化(DNAm)微阵列技术发展迅速,包括 Illumina HumanMethylation27 和 HumanMethylation450(450K)芯片,这些芯片在识别和评估不同组织中与年龄相关的(AR)DNAm 标志物方面发挥了重要作用。最近,引入了一种新的阵列,即 Illumina MethylationEPIC(EPIC),其探针数量几乎是 450K 的两倍(约 85 万个探针)。在这项研究中,我们使用在 EPIC BeadChip 上进行分析的 754 个血液样本的大型队列,测试这些新添加的探针与年龄的关联,这些个体的年龄在 0 到 88 岁之间。确定了 52 个 AR CpG 位点(Spearman 的 abs(rho)>0.6 和 P 值 <10),其中 21 个是新的位点,映射到 18 个基因,其中 9 个(LHFPL4、SLC12A8、EGFEM1P、GPR158、TAL1、KIAA1755、LOC730668、DUSP16 和 FAM65C)以前从未报道过与年龄有关。随后,将数据分为 527 个样本的训练集和 227 个样本的测试集,使用弹性网络回归和多元回归建立和验证两个年龄预测模型。弹性网络回归根据测试集选择了 425 个 CpG 标记,其平均绝对偏差(MAD)为 2.6 年。为了建立多元线性回归模型,输入 FDR<0.05 且 R>0.5 的 AR CpG 位点进行逐步回归,以选择用于年龄预测的最佳子集。最终选择了 6 个 CpG 标记,并用年龄进行线性建模,解释了 DNAm 水平与年龄相关的 81%的变化。使用自举分析的年龄估计准确性为 4.5 年,测试集的置信区间为 4.56 到 4.57 年。这些结果表明,EPIC BeadChip 探针在年龄预测能力方面,与之前的 Illumina HumanMethylation 平台上的探针范围相当。

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