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Updated: Jan 18, 2026

Digital PCR for Quantifying Circulating MicroRNAs in Acute Myocardial Infarction and Cardiovascular Disease
Published on: July 3, 2018
Serum hsa-miR-21 expression and its clinical value in pediatric patients with fulminant myocarditis
Wenwen Wang1, Jingmin Sun1, Jing Li1
1The First Affiliated Hospital of Anhui Medical University, Department of Pediatrics, Hefei, Anhui Province, China.
Insights
Serum hsa-miR-21 is elevated in pediatric fulminant myocarditis (FM) patients and correlates with poor prognoses. This microRNA is an independent risk factor and aids in predicting poor outcomes in FM children.
Area of Science:
- Cardiology
- Molecular Biology
- Pediatrics
Background:
- Fulminant myocarditis (FM) is a rare and severe form of myocarditis in children.
- Understanding biomarkers for predicting FM prognosis is crucial for timely intervention.
Purpose of the Study:
- To investigate the expression levels of hsa-miR-21 in pediatric FM patients.
- To evaluate the clinical significance and predictive value of hsa-miR-21 for prognosis in pediatric FM.
Main Methods:
- Serum hsa-miR-21 levels were quantified using RT-qPCR in 88 pediatric FM patients and 90 healthy controls.
- Correlations with myocardial injury markers (cTnI, CK-MB) and risk factors for poor prognosis were analyzed.
- Receiver operating characteristic (ROC) curve analysis was employed to assess the predictive value of hsa-miR-21.
Main Results:
- Serum hsa-miR-21 levels were significantly higher in FM patients compared to healthy controls.
- Elevated hsa-miR-21 correlated positively with myocardial injury markers (MYO, BNP, cTnI, CK-MB).
- hsa-miR-21, along with CK-MB and other markers, was identified as an independent risk factor for poor prognosis in pediatric FM, with an AUC of 0.790 for prediction.
Conclusions:
- Serum hsa-miR-21 is upregulated in pediatric FM and associated with myocardial injury.
- hsa-miR-21 serves as an independent risk factor and offers some predictive value for poor prognosis in pediatric FM.
- While promising, the diagnostic accuracy of hsa-miR-21 for predicting FM prognosis requires further investigation.
Objective:
Fulminant myocarditis (FM) is a distinct and rare form of myocarditis. This study probed hsa-miR-21 expression in FM pediatric patients and its clinical value.
Methods:
This study enrolled 88 FM pediatric patients and 90 healthy children (normal controls), with serum sample hsa-miR-21 levels measured by RT-qPCR. FM children were categorized into the good and poor prognosis groups. Correlations of hsa-miR-21 expression with myocardial injury markers [cardiac troponin I (cTnI), creatine kinase isoenzyme (CK-MB)], and independent risk factors and predictive value of hsa-miR-21 expression for FM patients' poor prognoses were analyzed by Pearson's, logistic regression, and receiver operating characteristic (ROC) curve analyses.
Results:
Serum hsa-miR-21 levels were elevated in FM children relative to the healthy controls and linked with poor prognoses. hsa-miR-21 levels positively correlated with myoglobin (MYO), B-type natriuretic peptide (BNP), cTnI, and CK-MB levels. Elevated hsa-miR-21, CK-MB, left ventricular ejection fraction, C-reactive protein, lactate dehydrogenase, and lactate were independent risk factors for FM children's poor prognoses. Serum hsa-miR-21 levels yielded an area under the ROC curve of 0.790 in predicting FM pediatric patients' poor prognoses (58.1 % sensitivity, 87.7 % specificity), with positive and negative predictive values of 74.07 % and 81.97 %, respectively, demonstrating that hsa-miR-21 aided in predicting FM pediatric patients' poor prognoses to some extent.
Conclusion:
Serum hsa-miR-21 was up-regulated in FM pediatric patients, and positively correlated with MYO, BNP, cTnI, and CK-MB. hsa-miR-21 expression was an independent risk factor for FM pediatric patients' poor prognosis, and predicted prognoses to some extent; however, the diagnostic accuracy was limited.
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