Differential expression of serum extracellular vesicle microRNAs and analysis of target-gene pathways in major depressive disorder

Q2 Medicine
Nagiua Cuomo-Haymour , Stefan Kaiser , Matthias Hartmann-Riemer , Karoline Guetter , Federica Klaus , Flurin Cathomas , Erich Seifritz , Giorgio Bergamini , Giancarlo Russo , Christopher R. Pryce
{"title":"Differential expression of serum extracellular vesicle microRNAs and analysis of target-gene pathways in major depressive disorder","authors":"Nagiua Cuomo-Haymour ,&nbsp;Stefan Kaiser ,&nbsp;Matthias Hartmann-Riemer ,&nbsp;Karoline Guetter ,&nbsp;Federica Klaus ,&nbsp;Flurin Cathomas ,&nbsp;Erich Seifritz ,&nbsp;Giorgio Bergamini ,&nbsp;Giancarlo Russo ,&nbsp;Christopher R. Pryce","doi":"10.1016/j.bionps.2022.100049","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Major depressive disorder (MDD) presents with both peripheral and central alterations, such that crosstalk between the periphery and the central nervous system could contribute to its aetio-pathophysiology. One putative mediating mechanism is circulating extracellular vesicles (EVs) and their microRNA (miRNA) cargo. In this study, we investigated differential expression of the serum EV miRNome in MDD patients versus controls with the aims of identifying potential EV miRNA biomarkers and downstream target gene pathways.</p></div><div><h3>Methods</h3><p>miRNA-Sequencing was performed on serum EVs isolated from MDD patients (n = 42) and matched healthy Controls (n = 18). Differential expression analysis was conducted, followed by diagnostic power analysis of dysregulated EV miRNAs, and pathway analysis of their target genes.</p></div><div><h3>Results</h3><p>Of 1800 serum EV miRNAs detected consistently, 33 were differentially expressed in MDD and Control subjects, 17 up-regulated and 16 down-regulated. Receiver-operating characteristic analysis identified an up-regulated and a down-regulated panel of EV miRNAs, each with additive diagnostic power as a differential biomarker for MDD. Predicted target gene-pathways were significantly enriched with respect to brain function, signal transduction and substance dependence ontology.</p></div><div><h3>Conclusions</h3><p>This study provides one of the first reports of dysregulation of the peripheral EV miRNome in MDD, including evidence for EV miRNAs as potential MDD biomarkers and identification of pathways via which they may contribute to MDD pathophysiology. Large-scale studies are required to confirm EV miRNome biomarker potential in MDD. Empirical evidence for involvement of the dysregulated EV miRNAs in the predicted target-gene pathways relevant to MDD pathophysiology is required.</p></div>","PeriodicalId":52767,"journal":{"name":"Biomarkers in Neuropsychiatry","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2022-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666144622000041/pdfft?md5=fa7c10a0745f823a352b107bccf40bd4&pid=1-s2.0-S2666144622000041-main.pdf","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomarkers in Neuropsychiatry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666144622000041","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 4

Abstract

Background

Major depressive disorder (MDD) presents with both peripheral and central alterations, such that crosstalk between the periphery and the central nervous system could contribute to its aetio-pathophysiology. One putative mediating mechanism is circulating extracellular vesicles (EVs) and their microRNA (miRNA) cargo. In this study, we investigated differential expression of the serum EV miRNome in MDD patients versus controls with the aims of identifying potential EV miRNA biomarkers and downstream target gene pathways.

Methods

miRNA-Sequencing was performed on serum EVs isolated from MDD patients (n = 42) and matched healthy Controls (n = 18). Differential expression analysis was conducted, followed by diagnostic power analysis of dysregulated EV miRNAs, and pathway analysis of their target genes.

Results

Of 1800 serum EV miRNAs detected consistently, 33 were differentially expressed in MDD and Control subjects, 17 up-regulated and 16 down-regulated. Receiver-operating characteristic analysis identified an up-regulated and a down-regulated panel of EV miRNAs, each with additive diagnostic power as a differential biomarker for MDD. Predicted target gene-pathways were significantly enriched with respect to brain function, signal transduction and substance dependence ontology.

Conclusions

This study provides one of the first reports of dysregulation of the peripheral EV miRNome in MDD, including evidence for EV miRNAs as potential MDD biomarkers and identification of pathways via which they may contribute to MDD pathophysiology. Large-scale studies are required to confirm EV miRNome biomarker potential in MDD. Empirical evidence for involvement of the dysregulated EV miRNAs in the predicted target-gene pathways relevant to MDD pathophysiology is required.

重度抑郁症患者血清细胞外囊泡microrna的差异表达及靶基因通路分析
重度抑郁症(MDD)表现为外周和中枢神经系统的改变,因此外周和中枢神经系统之间的串扰可能有助于其运动病理生理。一种推测的介导机制是循环细胞外囊泡(EVs)及其microRNA (miRNA)货物。在这项研究中,我们研究了MDD患者与对照组血清EV miRNA的差异表达,目的是确定潜在的EV miRNA生物标志物和下游靶基因途径。方法对MDD患者(n = 42)和健康对照(n = 18)分离的血清EVs进行smirna测序。进行差异表达分析,随后进行EV mirna异常的诊断能力分析,并对其靶基因进行通路分析。结果一致检测到的1800个血清EV mirna中,MDD组与对照组差异表达的有33个,其中上调17个,下调16个。受体操作特征分析确定了一个上调和下调的EV mirna面板,每个mirna都具有附加诊断能力,作为MDD的差异生物标志物。在脑功能、信号转导和物质依赖本体论方面,预测的靶基因通路显著丰富。本研究提供了MDD中外周EV mirna失调的首批报告之一,包括EV mirna作为潜在的MDD生物标志物的证据,以及它们可能参与MDD病理生理的途径的鉴定。需要大规模的研究来证实EV miRNome生物标志物在MDD中的潜力。需要经验证据来证明失调的EV mirna参与了与MDD病理生理相关的预测靶基因通路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Biomarkers in Neuropsychiatry
Biomarkers in Neuropsychiatry Medicine-Psychiatry and Mental Health
CiteScore
4.00
自引率
0.00%
发文量
12
审稿时长
7 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信