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与谵妄相关的表观遗传信号在四个独立队列中得到复制。

Epigenetic signals associated with delirium replicated across four independent cohorts.

机构信息

Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, CA, USA.

Department of Psychiatry, Osaka Medical and Pharmaceutical University School of Medicine, Osaka, Japan.

出版信息

Transl Psychiatry. 2024 Jul 4;14(1):275. doi: 10.1038/s41398-024-02986-w.

DOI:10.1038/s41398-024-02986-w
PMID:38965205
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11224347/
Abstract

Delirium is risky and indicates poor outcomes for patients. Therefore, it is crucial to create an effective delirium detection method. However, the epigenetic pathophysiology of delirium remains largely unknown. We aimed to discover reliable and replicable epigenetic (DNA methylation: DNAm) markers that are associated with delirium including post-operative delirium (POD) in blood obtained from patients among four independent cohorts. Blood DNA from four independent cohorts (two inpatient cohorts and two surgery cohorts; 16 to 88 patients each) were analyzed using the Illumina EPIC array platform for genome-wide DNAm analysis. We examined DNAm differences in blood between patients with and without delirium including POD. When we compared top CpG sites previously identified from the initial inpatient cohort with three additional cohorts (one inpatient and two surgery cohorts), 11 of the top 13 CpG sites showed statistically significant differences in DNAm values between the delirium group and non-delirium group in the same directions as found in the initial cohort. This study demonstrated the potential value of epigenetic biomarkers as future diagnostic tools. Furthermore, our findings provide additional evidence of the potential role of epigenetics in the pathophysiology of delirium including POD.

摘要

谵妄具有风险,并预示着患者预后不良。因此,创建一种有效的谵妄检测方法至关重要。然而,谵妄的表观病理生理学在很大程度上仍然未知。我们旨在发现与谵妄相关的可靠且可重复的表观遗传(DNA 甲基化:DNAm)标志物,包括来自四个独立队列的患者血液中的术后谵妄(POD)。使用 Illumina EPIC 阵列平台对来自四个独立队列(两个住院患者队列和两个手术队列;每个队列 16 至 88 名患者)的血液 DNA 进行全基因组 DNAm 分析。我们研究了谵妄(包括 POD)患者与无谵妄患者之间血液中的 DNAm 差异。当我们将最初住院患者队列中鉴定出的前 topCpG 位点与另外三个队列(一个住院患者队列和两个手术队列)进行比较时,在最初队列中发现的 top13CpG 位点中有 11 个在谵妄组和非谵妄组之间的 DNAm 值存在统计学显著差异,其变化方向与最初队列相同。这项研究表明了表观遗传生物标志物作为未来诊断工具的潜在价值。此外,我们的发现提供了更多证据表明,表观遗传学在谵妄(包括 POD)的病理生理学中具有潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/891a/11224347/8944fd3c9123/41398_2024_2986_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/891a/11224347/8944fd3c9123/41398_2024_2986_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/891a/11224347/8944fd3c9123/41398_2024_2986_Fig1_HTML.jpg

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