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新型冠状病毒肺炎重症病例关键生物标志物识别的综合生物信息学探索与初步临床验证

Integrated Bioinformatics Exploration and Preliminary Clinical Verification for the Identification of Crucial Biomarkers in Severe Cases of COVID-19.

作者信息

Huang Zhisheng, Cheng Zuowang, Deng Xia, Yang Ying, Sun Na, Hou Peibin, Fan Ruyue, Liu Shuai

机构信息

Department of Pulmonary and Critical Care Medicine, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, People's Republic of China.

Department of Pulmonary and Critical Care Medicine, National Regional Center for Respiratory Medicine, Jiangxi Hospital of China-Japan Friendship Hospital, Nanchang, Jiangxi, People's Republic of China.

出版信息

J Inflamm Res. 2024 Mar 11;17:1561-1576. doi: 10.2147/JIR.S454284. eCollection 2024.

Abstract

BACKGROUND

Coronavirus disease 2019 (COVID-19) is a respiratory infectious illness caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The objective of this study is to identify reliable and accurate biomarkers for the early stratification of disease severity, a crucial aspect that is currently lacking for the impending phases of the next COVID-19 pandemic.

METHODS

In this study, we identified important module and hub genes related to clinical severe COVID-19 using differentially expressed genes (DEGs) screening combing weighted gene co-expression network analysis (WGCNA) in dataset GSE213313. We further screened and confirmed these hub genes in another two new independent datasets (GSE172114 and GSE157103). In order to evaluate these key genes' stability and robustness for diagnosing or predicting the progression of illness, we used RT-PCR validation of selected genes in blood samples obtained from hospitalized COVID-19 patients.

RESULTS

A total of 968 and 52 DEGs were identified between COVID-19 patients and normal people, critical and non-critical patients, respectively. Then, using WGCNA, 10 modules were constructed. Among them, the blue module positively associated with clinic disease severity of COVID-19. From overlapped section between DEGs and blue module, 12 intersected common differential genes were obtained. Subsequently, these hub genes were validated in another two new independent datasets as well and 9 genes that overlapped showed a highly correlation with disease severity. Finally, the mRNA expression levels of these hub genes were tested in blood samples from COVID-19 patients. In severe cases, there was increased expression of , and . In particular, increased with disease severity, which suggested an unfavorable development and a frustrating prognosis.

CONCLUSION

Using comprehensive bioinformatical analysis and the validation of clinical samples, we identified four major candidate genes, , and , which are essential for diagnosis or development of COVID-19.

摘要

背景

2019冠状病毒病(COVID-19)是由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的一种呼吸道传染病。本研究的目的是确定可靠且准确的生物标志物,用于疾病严重程度的早期分层,这是即将到来的下一波COVID-19大流行阶段目前所缺乏的一个关键方面。

方法

在本研究中,我们在数据集GSE213313中使用差异表达基因(DEG)筛选结合加权基因共表达网络分析(WGCNA),确定了与临床严重COVID-19相关的重要模块和枢纽基因。我们在另外两个新的独立数据集(GSE172114和GSE157103)中进一步筛选并确认了这些枢纽基因。为了评估这些关键基因在诊断或预测疾病进展方面的稳定性和稳健性,我们对从住院COVID-19患者获得的血液样本中的选定基因进行了RT-PCR验证。

结果

分别在COVID-19患者与正常人、重症与非重症患者之间鉴定出总共968个和52个差异表达基因。然后,使用WGCNA构建了10个模块。其中,蓝色模块与COVID-19的临床疾病严重程度呈正相关。从差异表达基因与蓝色模块的重叠部分,获得了12个相交的共同差异基因。随后,这些枢纽基因也在另外两个新的独立数据集中得到验证,9个重叠的基因与疾病严重程度高度相关。最后,在COVID-19患者的血液样本中检测了这些枢纽基因的mRNA表达水平。在重症病例中,[具体基因1]、[具体基因2]和[具体基因3]的表达增加。特别是,[具体基因4]随着疾病严重程度增加,这表明病情发展不利且预后不佳。

结论

通过综合生物信息学分析和临床样本验证,我们确定了四个主要候选基因,[具体基因1]、[具体基因2]、[具体基因3]和[具体基因4],它们对于COVID-19的诊断或病情发展至关重要。

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