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).

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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