Smith Rebecca G, Pishva Ehsan, Shireby Gemma, Smith Adam R, Roubroeks Janou A Y, Hannon Eilis, Wheildon Gregory, Mastroeni Diego, Gasparoni Gilles, Riemenschneider Matthias, Giese Armin, Sharp Andrew J, Schalkwyk Leonard, Haroutunian Vahram, Viechtbauer Wolfgang, van den Hove Daniel L A, Weedon Michael, Brokaw Danielle, Francis Paul T, Thomas Alan J, Love Seth, Morgan Kevin, Walter Jörn, Coleman Paul D, Bennett David A, De Jager Philip L, Mill Jonathan, Lunnon Katie
University of Exeter Medical School, College of Medicine and Health, University of Exeter, Exeter, UK.
Department of Psychiatry and Neuropsychology, School for Mental Health and Neuroscience (MHeNS), Maastricht University, Maastricht, The Netherlands.
Nat Commun. 2021 Jun 10;12(1):3517. doi: 10.1038/s41467-021-23243-4.
Epigenome-wide association studies of Alzheimer's disease have highlighted neuropathology-associated DNA methylation differences, although existing studies have been limited in sample size and utilized different brain regions. Here, we combine data from six DNA methylomic studies of Alzheimer's disease (N = 1453 unique individuals) to identify differential methylation associated with Braak stage in different brain regions and across cortex. We identify 236 CpGs in the prefrontal cortex, 95 CpGs in the temporal gyrus and ten CpGs in the entorhinal cortex at Bonferroni significance, with none in the cerebellum. Our cross-cortex meta-analysis (N = 1408 donors) identifies 220 CpGs associated with neuropathology, annotated to 121 genes, of which 84 genes have not been previously reported at this significance threshold. We have replicated our findings using two further DNA methylomic datasets consisting of a further >600 unique donors. The meta-analysis summary statistics are available in our online data resource ( www.epigenomicslab.com/ad-meta-analysis/ ).
阿尔茨海默病的全表观基因组关联研究突出了与神经病理学相关的DNA甲基化差异,尽管现有研究在样本量上存在局限性且使用了不同的脑区。在此,我们整合了六项阿尔茨海默病DNA甲基化组研究的数据(N = 1453名个体),以确定不同脑区和整个皮质中与Braak分期相关的差异甲基化。我们在额叶前皮质中鉴定出236个CpG,在颞回中鉴定出95个CpG,在内嗅皮质中鉴定出10个达到Bonferroni显著性水平的CpG,而在小脑中未发现。我们的跨皮质荟萃分析(N = 1408名供体)鉴定出220个与神经病理学相关的CpG,注释到121个基因,其中84个基因在此显著性阈值下此前未被报道。我们使用另外两个包含超过600名个体的DNA甲基化组数据集重复了我们的研究结果。荟萃分析的汇总统计数据可在我们的在线数据资源(www.epigenomicslab.com/ad-meta-analysis/)中获取。