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重症进展期新冠患者的基因表达模式与1型糖尿病相关:一项功能注释分析

Gene expression pattern in severely progressing covid-19 patients is related to diabetes mellitus type 1: A functional annotation analysis.

作者信息

Alipour Mohsen, Javeshghani Danesh, Roustazadeh Abazar

机构信息

Department of Biochemistry, Department of Advanced Medical Sciences and Technologies, Jahrom University of Medical Sciences, Jahrom, Iran.

Department of Physiology, Jahrom University of Medical Sciences, Jahrom, Iran.

出版信息

Hum Gene (Amst). 2022 Sep;33:201039. doi: 10.1016/j.humgen.2022.201039. Epub 2022 May 10.

Abstract

AIMS

The aim of this study was to extract the signaling mediators or biological pathways that link covid-19 to other diseases such as type 1 diabetes mellitus (T1DM).

METHODS

Microarray data of covid-19 (GSE164805) was extracted from Gene Expression Omnibus (GEO) and analyses were performed by R package and GEO2R. Functional enrichment analysis was done to extract enriched molecular pathways (MP), biological process (BP) and molecular function (MF). Then commonly up- and down-regulated genes in covid-19 and T1DM were extracted by comparing deferentially expressed genes (DEGs) of GSE164805 and GSE9006.

RESULTS

Down-regulated DEGs in the severely progressing covid-19 patients (SPCP) had a link to T1DM. Major histocompatibility system (MHC) class II, gamma interferon (IFNγ), and IL-1B were enriched in extracted pathway that leads to T1DM. In addition, comparing extracted DEGs from GSE164805 and GSE9006 indicated that MTUS1, EGR1 and EGR3 are the genes that are up-regulated in both SPCP and T1DM.

CONCLUSION

The findings of this study indicate that coincidence of SARS-COV-2 infection and T1DM may increase the severity of both diseases. Although covid-19 reduced the T cell mediated immune response, but increased mediators of T-cell signaling pathway such as IL-1 in both diseases. This could potentiate the inflammation response and worsens the severity of covid-19 cytokine storm or increase the resistance to insulin

摘要

目的

本研究旨在提取将新冠病毒疾病(covid-19)与其他疾病(如1型糖尿病,T1DM)联系起来的信号传导介质或生物学途径。

方法

从基因表达综合数据库(GEO)中提取covid-19的微阵列数据(GSE164805),并通过R包和GEO2R进行分析。进行功能富集分析以提取富集的分子途径(MP)、生物学过程(BP)和分子功能(MF)。然后,通过比较GSE164805和GSE9006的差异表达基因(DEG),提取covid-19和T1DM中共同上调和下调的基因。

结果

病情严重进展的covid-19患者(SPCP)中下调的DEG与T1DM有关。主要组织相容性复合体(MHC)II类、γ干扰素(IFNγ)和IL-1B在导致T1DM的提取途径中富集。此外,比较从GSE164805和GSE9006中提取的DEG表明,MTUS1、EGR1和EGR3是在SPCP和T1DM中均上调的基因。

结论

本研究结果表明,SARS-CoV-2感染与T1DM的同时存在可能会增加两种疾病的严重程度。尽管covid-19降低了T细胞介导的免疫反应,但在两种疾病中均增加了T细胞信号通路的介质,如IL-1。这可能会增强炎症反应,加重covid-19细胞因子风暴的严重程度,或增加对胰岛素的抵抗。

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