University of Iowa Carver College of Medicine, Department of Psychiatry, Iowa City, IA, USA; Oregon Health & Science University, School of Medicine, Department of Psychiatry, Portland, OR, USA.
Stanford University School of Medicine, Department of Psychiatry and Behavioral Sciences, Palo Alto, CA, USA; Osaka Medical and Pharmaceutical University, Faculty of Medicine, Department of Neuropsychiatry, Takatsuki, Osaka, Japan.
J Psychiatr Res. 2022 Dec;156:245-251. doi: 10.1016/j.jpsychires.2022.10.023. Epub 2022 Oct 9.
No previous study demonstrates the difference in the genome-wide DNA methylation status of post-operative delirium (POD) using human brain tissue obtained from neurosurgery and multiple peripheral tissues such as blood, saliva, and buccal samples from the same individuals. We aimed to identify epigenetic marks of DNA methylation in the brain and peripheral tissues to elucidate the potential pathophysiological mechanism of POD.
The four tissue types (brain, blood, saliva, buccal) of DNA samples from up to 40 patients, including 11 POD cases, were analyzed using Illumina EPIC array. DNAm differences between patients with and without POD were examined. We also conducted enrichment analysis based on the top DNAm signals.
The most different CpG site between control and POD was found at cg16526133 near the ADAMTS9 gene from the brain tissue(p = 8.66E-08). However, there are no CpG sites to reach the genome-wide significant level. The enrichment analysis based on the 1000 top hit CpG site (p < 0.05) on the four tissues showed several intriguing pathways. In the brain, there are pathways including "positive regulation of glial cell differentiation". Blood samples showed also pathways related to immune function. Besides, both saliva and the buccal sample showed pathways related to circadian rhythm, although these findings were not FDR significant.
Enrichment analysis found several intriguing pathways related to potential delirium pathophysiology. Present data may further support the role of epigenetics, especially DNA methylation, in the molecular mechanisms of delirium pathogenesis.
以前没有研究使用从神经外科获得的人脑组织和来自同一个体的血液、唾液和颊拭子等多种外周组织来展示术后谵妄(POD)的全基因组 DNA 甲基化状态的差异。我们旨在确定大脑和外周组织中 DNA 甲基化的表观遗传标记,以阐明 POD 的潜在病理生理机制。
对多达 40 名患者的四种组织类型(大脑、血液、唾液、颊拭子)的 DNA 样本进行了 Illumina EPIC 芯片分析。检查了 POD 患者与无 POD 患者之间的 DNAm 差异。我们还根据顶级 DNAm 信号进行了富集分析。
在脑组织中,在 ADAMTS9 基因附近的 cg16526133 处发现了控制与 POD 之间差异最大的 CpG 位点(p = 8.66E-08)。但是,没有 CpG 位点达到全基因组显著水平。基于四个组织中前 1000 个命中 CpG 位点(p < 0.05)的富集分析显示了几个有趣的途径。在大脑中,存在包括“胶质细胞分化的正调节”在内的途径。血液样本也显示了与免疫功能相关的途径。此外,唾液和颊拭子样本都显示了与昼夜节律相关的途径,尽管这些发现没有 FDR 意义。
富集分析发现了几个与潜在谵妄病理生理学相关的有趣途径。目前的数据可能进一步支持表观遗传学,特别是 DNA 甲基化,在谵妄发病机制的分子机制中的作用。