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Author Spotlight: Advancing Allergic Rhinitis Research with Multicolor Immunofluorescence
Published on: September 22, 2023
Expression Profile of miR-92a-3p in Combined Allergic Rhinitis and Asthma Syndrome Patients and Its Correlation with
Lina Kang1, Lijing Kang2, Lijing Sun3
1Department of Pediatrics, Xingtai People's Hospital, Xingtai, China, kanglinaxt@163.com.
Introduction:
The study aimed to investigate the expression level of miR-92a-3p in combined allergic rhinitis and asthma syndrome (CARAS) and its predictive value for CARAS combined with small airway dysfunction (SAD).
Methods:
This study included 85 children with allergic rhinitis and 85 children with CARAS. According to whether SAD occurred, children with CARAS were divided into 35 cases of CARAS-SAD and 50 cases of simple CARAS. The expressions of miR-92a-3p in the blood sample were detected by RT-qPCR. The pulmonary function of children with CARAS was detected by a pulmonary function tester. ROC curve was constructed to evaluate the diagnostic value of miR-92a-3p for CARAS-SAD. Logistic regression analysis was conducted to evaluate the risk factors for the occurrence of CARAS-SAD. The target genes of miR-92a-3p were predicted using the online database and GO functional annotation and KEGG pathway enrichment analysis were performed on these target genes.
Results:
The expression of miR-92a-3p is increased in patients with CARAS, and the elevation in CARAS-SAD is higher than that in simple CARAS. MiR-92a-3p demonstrated excellent efficacy in differentiating CARAS-SAD from simple CARAS, with an AUC of 0.903. MiR-92a-3p, history of secondhand smoke exposure and childhood asthma control test score are independent risk factors for the occurrence of CARAS-SAD. The database predicted 403 overlapping target genes, and the pathways enriched by these target genes involved the FoxO signaling pathway and the cAMP signaling pathway.
Conclusions:
Within the CARAS population, miR-92a-3p demonstrates relatively high diagnostic efficacy for CARAS-SAD, suggesting its potential as a diagnostic biomarker for CARAS-SAD. This finding indicated that miR-92a-3p has significant discriminative value for CARAS-SAD in CARAS patients.
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