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Low expression of miR-126 constitutes a risk factor for perioperative respiratory adverse events among pediatric
Wenjuan Luo1, Kaili Lv2, Jun Liu3
1Department of General Surgery, Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Children and Adolescents' Health and Diseases, Hangzhou, 310052, China.
Insights
MicroRNA-126 (miR-126) is downregulated in children experiencing perioperative respiratory adverse events (PRAEs). Low miR-126 levels are a risk factor, suggesting its potential as a diagnostic biomarker for PRAEs.
Area of Science:
- Biochemistry
- Molecular Biology
- Pediatric Medicine
Background:
- Perioperative respiratory adverse events (PRAEs) are common in pediatric surgery.
- Identifying reliable biomarkers for PRAEs is crucial for early diagnosis and management.
Purpose of the Study:
- To investigate the diagnostic value of microRNA-126 (miR-126) in pediatric patients experiencing PRAEs.
- To explore the correlation between miR-126 levels and inflammatory markers.
Main Methods:
- Serum miR-126 levels were quantified using RT-qPCR in 228 pediatric patients.
- Cell proliferation was assessed via CCK-8 assay.
- Inflammatory cytokines (TNF-α, IL-6, IL-13) were measured using ELISA.
- Diagnostic accuracy was evaluated using receiver operating characteristic (ROC) curve analysis.
Main Results:
- miR-126 was significantly downregulated in children with PRAEs compared to controls.
- Lower miR-126 expression was identified as a risk factor for PRAEs.
- miR-126 levels negatively correlated with serum inflammatory markers.
- Overexpression of miR-126 enhanced cell proliferation in vitro.
Conclusions:
- miR-126 may serve as a valuable diagnostic biomarker for PRAEs in pediatric patients.
- miR-126 may play a role in suppressing PRAEs by modulating proliferation and inflammatory responses.
Aim:
This study aims to investigate the diagnostic value of miR-126 in Perioperative respiratory adverse events (PRAEs).
Methods:
This study included 228 pediatric patients undergoing anesthesia and surgery, who were divided into two groups based on the occurrence of PRAEs. RT-qPCR was used to detect miR-126 levels, the CCK-8 assay was employed to evaluate cell proliferation capacity, and ELISA kits were utilized to measure TNF-α, IL-6, and IL-13 concentrations. The diagnostic value of miR-126 was assessed through receiver operating characteristic curve analysis.
Results:
miR-126 is significantly downregulated in the serum of children with PAREs. Low expression of miR-126 is one of the risk factors for PRAEs occurrence. miR-126 level shows a negative correlation with the inflammatory levels in children with PRAEs. Overexpression of miR-126 promotes cell proliferation activity.
Conclusion:
miR-126 may contribute to the suppression of PRAEs by regulating proliferation and inflammatory responses in BEAS-2B cells and may serve as a diagnostic biomarker.
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