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惊恐障碍中DNA甲基化的全表观基因组关联研究。

Epigenome-wide association study of DNA methylation in panic disorder.

作者信息

Shimada-Sugimoto Mihoko, Otowa Takeshi, Miyagawa Taku, Umekage Tadashi, Kawamura Yoshiya, Bundo Miki, Iwamoto Kazuya, Tochigi Mamoru, Kasai Kiyoto, Kaiya Hisanobu, Tanii Hisashi, Okazaki Yuji, Tokunaga Katsushi, Sasaki Tsukasa

机构信息

Department of Human Genetics, Graduate School of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo Ward, Tokyo, 113-0033 Japan.

Graduate School of Clinical Psychology, Teikyo Heisei University Major of Professional Clinical Psychology, 2-51-4 Higashiikebukuro, Toshima Ward, Tokyo, 171-0014 Japan.

出版信息

Clin Epigenetics. 2017 Jan 21;9:6. doi: 10.1186/s13148-016-0307-1. eCollection 2017.

Abstract

BACKGROUND

Panic disorder (PD) is considered to be a multifactorial disorder emerging from interactions among multiple genetic and environmental factors. To date, although genetic studies reported several susceptibility genes with PD, few of them were replicated and the pathogenesis of PD remains to be clarified. Epigenetics is considered to play an important role in etiology of complex traits and diseases, and DNA methylation is one of the major forms of epigenetic modifications. In this study, we performed an epigenome-wide association study of PD using DNA methylation arrays so as to investigate the possibility that different levels of DNA methylation might be associated with PD.

METHODS

The DNA methylation levels of CpG sites across the genome were examined with genomic DNA samples (PD,  = 48, control,  = 48) extracted from peripheral blood. Methylation arrays were used for the analysis. values, which represent the levels of DNA methylation, were normalized via an appropriate pipeline. Then, values were converted to values via the logit transformation for epigenome-wide association study. The relationship between each DNA methylation site and PD was assessed by linear regression analysis with adjustments for the effects of leukocyte subsets.

RESULTS

Forty CpG sites showed significant association with PD at 5% FDR correction, though the differences of the DNA methylation levels were relatively small. Most of the significant CpG sites (37/40 CpG sites) were located in or around CpG islands. Many of the significant CpG sites (27/40 CpG sites) were located upstream of genes, and all such CpG sites with the exception of two were hypomethylated in PD subjects. A pathway analysis on the genes annotated to the significant CpG sites identified several pathways, including "positive regulation of lymphocyte activation."

CONCLUSIONS

Although future studies with larger number of samples are necessary to confirm the small DNA methylation abnormalities associated with PD, there is a possibility that several CpG sites might be associated, together as a group, with PD.

摘要

背景

惊恐障碍(PD)被认为是一种由多种遗传和环境因素相互作用而产生的多因素疾病。迄今为止,尽管基因研究报告了几个与PD相关的易感基因,但其中很少有得到重复验证的,PD的发病机制仍有待阐明。表观遗传学被认为在复杂性状和疾病的病因学中起重要作用,而DNA甲基化是表观遗传修饰的主要形式之一。在本研究中,我们使用DNA甲基化阵列对PD进行了全表观基因组关联研究,以探讨不同水平的DNA甲基化可能与PD相关的可能性。

方法

用从外周血中提取的基因组DNA样本(PD组,n = 48;对照组,n = 48)检测全基因组中CpG位点的DNA甲基化水平。使用甲基化阵列进行分析。代表DNA甲基化水平的β值通过适当的流程进行标准化。然后,通过逻辑转换将β值转换为M值用于全表观基因组关联研究。通过线性回归分析评估每个DNA甲基化位点与PD之间的关系,并对白细胞亚群的影响进行校正。

结果

在5%的假发现率校正下,40个CpG位点显示与PD有显著关联,尽管DNA甲基化水平的差异相对较小。大多数显著的CpG位点(37/40个CpG位点)位于CpG岛或其周围。许多显著的CpG位点(27/40个CpG位点)位于基因上游,除两个位点外,所有这些CpG位点在PD患者中均为低甲基化。对注释到显著CpG位点的基因进行通路分析,确定了几个通路,包括“淋巴细胞活化的正调控”。

结论

尽管需要更多样本的进一步研究来证实与PD相关的微小DNA甲基化异常,但有几个CpG位点可能作为一个整体与PD相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00a3/5270210/75bb20c36f8a/13148_2016_307_Fig1_HTML.jpg

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