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Potential Predictive Value of MiR-125b-5p, MiR-155-5p and Their Target Genes in the Course of COVID-19

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Publisher Dove Medical Press
Date 2022 Aug 8
PMID 35937783
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Abstract

Purpose: This study aimed to provide new biomarkers for predicting the disease course of COVID-19 by analyzing the dynamic changes of microRNA (miRNA) and its target gene expression in the serum of COVID-19 patients at different stages.

Methods: Serum samples were collected from all COVID-19 patients at three time points: the acute stage, the turn-negative stage, and the recovery stage. The expression level of miRNA and the target mRNA was measured by Quantitative Real-Time Polymerase Chain Reaction (RT-qPCR). The classification tree model was established to predict the disease course, and the prediction efficiency of independent variables in the model was analyzed using the receiver operating characteristic (ROC) curve.

Results: The expression of miR-125b-5p and miR-155-5p was significantly up-regulated in the acute stage and gradually decreased in the turn-negative and recovery stages. The expression of the target genes CDH5, STAT3, and TRIM32 gradually down-regulated in the acute, turn-negative, and recovery stages. MiR-125b-5p, miR-155-5p, STAT3, and TRIM32 constituted a classification tree model with 100% accuracy of prediction and AUC >0.7 for identification and prediction in all stages.

Conclusion: MiR-125b-5p, miR-155-5p, STAT3, and TRIM32 could be useful biomarkers to predict the time nodes of the acute, turn-negative, and recovery stages of COVID-19.

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References
1.
Visacri M, Nicoletti A, Pincinato E, Loren P, Saavedra N, Saavedra K . Role of miRNAs as biomarkers of COVID-19: a scoping review of the status and future directions for research in this field. Biomark Med. 2021; 15(18):1785-1795. PMC: 8601154. DOI: 10.2217/bmm-2021-0348. View

2.
Garcia-Hidalgo M, Gonzalez J, Benitez I, Carmona P, Santisteve S, Perez-Pons M . Identification of circulating microRNA profiles associated with pulmonary function and radiologic features in survivors of SARS-CoV-2-induced ARDS. Emerg Microbes Infect. 2022; 11(1):1537-1549. PMC: 9176679. DOI: 10.1080/22221751.2022.2081615. View

3.
Kudose S, Batal I, Santoriello D, Xu K, Barasch J, Peleg Y . Kidney Biopsy Findings in Patients with COVID-19. J Am Soc Nephrol. 2020; 31(9):1959-1968. PMC: 7461665. DOI: 10.1681/ASN.2020060802. View

4.
Bonilla-Muro M, Hernandez de la Cruz O, Gonzalez-Barrios J, Alcaraz-Estrada S, Castanon-Arreola M . EsxA mainly contributes to the miR-155 overexpression in human monocyte-derived macrophages and potentially affect the immune mechanism of macrophages through miRNA dysregulation. J Microbiol Immunol Infect. 2019; 54(2):185-192. DOI: 10.1016/j.jmii.2019.07.007. View

5.
Schmittgen T, Livak K . Analyzing real-time PCR data by the comparative C(T) method. Nat Protoc. 2008; 3(6):1101-8. DOI: 10.1038/nprot.2008.73. View