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A Porcine Model of Acute Autologous Pulmonary Embolism
Published on: September 6, 2024
Plasma Levels of microRNA-221 (miR-221) are Increased in Patients with Acute Pulmonary Embolism
Tingwei Liu1, Jian Kang1, Fan Liu1
1Department of Respiratory Medicine, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning, China (mainland).
Abstract:
BACKGROUND The aim of this study was to measure and compare the plasma levels of the microRNA (miRNA), miR-221, in patients with acute pulmonary embolism (PE) with healthy individuals and to evaluate the potential role of miR-221 as a diagnostic biomarker for acute PE. MATERIAL AND METHODS In blood samples collected from 60 patients with acute PE and 50 healthy volunteers, plasma levels of microRNA were identified using a microRNA microarray, and miR-221 expression was detected using real-time quantitative reverse transcription polymerase chain reaction (qRT-PCR). Brain natriuretic peptide (BNP) and troponin I were measured using an automated immunoassay analyzer. D-dimer levels were measured with an enzyme-linked immunosorbent assay (ELISA). RESULTS From the evaluation of 32 differentially expressed plasma miRNAs, miR-221 was significantly upregulated in the plasma of patients with acute PE compared with normal individuals (P<0.05). Correlation analysis showed that plasma miR-221 levels in patients with acute PE were positively correlated with levels of BNP (r=0.842, P<0.05), troponin I (r=0.853; P<0.05), and D-dimer (r=0.838; P<0.05). The receiver operating characteristic (ROC) area under the curve (AUC) for plasma miR-221 was 0.823 (95% CI, 0.757-0.906) (P<0.05), compared with the AUC for D-dimer of 0.768 (95% CI, 0.727-0.853), the AUC for troponin I of 0.713 (95% CI, 0.646-0.868), and the AUC for BNP of 0.648 (95% CI, 0.601-0.723). CONCLUSIONS Plasma levels of miR-221 were significantly increased in patients with acute PE when compared with healthy individuals.
Insights
Plasma levels of microRNA-221 (miR-221) are significantly elevated in patients with acute pulmonary embolism (PE). This finding suggests miR-221 may serve as a novel diagnostic biomarker for PE.
Area of Science:
- Biochemistry
- Molecular Biology
- Medical Diagnostics
Background:
- Acute pulmonary embolism (PE) is a critical condition requiring accurate and timely diagnosis.
- MicroRNAs (miRNAs) are emerging as potential biomarkers for various diseases.
- miR-221 has been investigated for its role in cardiovascular conditions.
Purpose of the Study:
- To quantify and compare plasma miR-221 levels in acute PE patients versus healthy individuals.
- To assess the diagnostic potential of miR-221 as a biomarker for acute PE.
Main Methods:
- Plasma samples from 60 acute PE patients and 50 healthy volunteers were analyzed.
- MicroRNA microarray and quantitative reverse transcription polymerase chain reaction (qRT-PCR) were used to detect miR-221 expression.
- Levels of Brain Natriuretic Peptide (BNP), troponin I, and D-dimer were also measured.
Main Results:
- Plasma miR-221 levels were significantly higher in acute PE patients compared to healthy individuals (P<0.05).
- miR-221 showed positive correlations with BNP, troponin I, and D-dimer levels in PE patients.
- The receiver operating characteristic (ROC) analysis indicated a strong diagnostic performance for miR-221 (AUC=0.823), outperforming D-dimer, troponin I, and BNP.
Conclusions:
- Plasma miR-221 is significantly upregulated in patients with acute PE.
- miR-221 demonstrates potential as a valuable diagnostic biomarker for acute pulmonary embolism.
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