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The expression of circulating hsa-miR-126-3p in dengue-infected Thai pediatric patients
Methee Sriprapun1, Jittraporn Rattanamahaphoom2,3, Pimolpachr Sriburin2,3
1Department of Microbiology, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand.
Abstract:
Circulating hsa-miRNA-126 (CmiR-126) has been reported to involve in the pathogenesis of many infectious diseases including dengue virus infection. However, no prior study has been conducted to describe more details in dengue-infected pediatric patients. This study aimed to describe CmiR-126-3p in dengue-infected pediatric patients during the febrile and convalescent phases. Additionally, the correlations between CmiR-126-3p and other relevant clinical laboratory factors were investigated. Sixty paired-serum specimens collected during febrile and convalescent phases were retrieved from patients with dengue fever (DF) (n = 30) and dengue hemorrhagic fever (DHF) (n = 30). Thirty paired-serum specimens collected from non-dengue acute febrile illness patients (AFI) were included as the control group. CmiR-126-3p was determined using reverse transcription quantitative real-time polymerase-chain reaction (RT-qPCR). Relative miRNA expression was calculated as 2-ΔCt using CmiR-16-5p for data normalization. CmiR-126-3p expression during febrile and convalescent phases in dengue-infected patients was significantly lower than AFI (p < 0.05). However, miRNA levels were not different (p > 0.05) compared between DF and DHF and between primary and secondary infection. CmiR-126-3p levels in DF in the convalescent were significantly higher than in the febrile phase (p = 0.025). No association between CmiR-126-3p and hematocrit, WBC level, platelet count, WBC differential count or dengue viral load was observed (p > 0.05). The data suggest that hsa-miR-126-3p involved in pathogenesis of dengue infection and may be a promising early and late biomarker for DENV infection. However, hsa-miR-126-3p alone cannot be used as a predictor for dengue severity.
Insights
Circulating hsa-miR-126-3p levels are lower in pediatric dengue patients compared to controls. While not predicting severity, it shows potential as an early and late biomarker for dengue virus infection.
Area of Science:
- Molecular biology
- Virology
- Pediatrics
Background:
- Circulating microRNAs (miRNAs) are implicated in infectious disease pathogenesis.
- Hsa-miRNA-126 (CmiR-126) is involved in dengue virus infection.
- Pediatric dengue patients require further investigation regarding CmiR-126.
Purpose of the Study:
- To describe CmiR-126-3p levels in pediatric dengue patients during febrile and convalescent phases.
- To investigate correlations between CmiR-126-3p and clinical laboratory factors.
- To assess CmiR-126-3p as a potential biomarker for dengue virus infection.
Main Methods:
- Serum samples from dengue fever (DF), dengue hemorrhagic fever (DHF), and acute febrile illness (AFI) pediatric patients were analyzed.
- CmiR-126-3p expression was quantified using reverse transcription quantitative real-time polymerase-chain reaction (RT-qPCR).
- Data normalization was performed using CmiR-16-5p, and relative expression was calculated via the 2^-ΔCt method.
Main Results:
- CmiR-126-3p expression was significantly lower in dengue patients (DF and DHF) compared to AFI controls during both febrile and convalescent phases (p < 0.05).
- No significant differences in CmiR-126-3p levels were observed between DF and DHF, or between primary and secondary dengue infections (p > 0.05).
- CmiR-126-3p levels increased significantly from the febrile to convalescent phase in DF patients (p = 0.025), but showed no correlation with hematocrit, WBC, platelets, or viral load.
Conclusions:
- Hsa-miR-126-3p is involved in the pathogenesis of dengue infection.
- Hsa-miR-126-3p may serve as a promising early and late biomarker for dengue virus infection (DENV).
- Hsa-miR-126-3p alone cannot predict dengue severity.

