Exosomal miRNAs as potential biomarkers for acute myocardial infarction

Jia Su1, Jiyi Li1,2, Qinglin Yu3

  • 1Department of Cardiology, Ningbo No. 1 Hospital, Ningbo, Zhejiang, People's Republic of China.

IUBMB Life
|November 2, 2019
PubMed

Insights

Serum exosomal microRNAs (miRNAs) show potential as early diagnostic biomarkers for acute myocardial infarction (AMI). Lower levels of specific miRNAs like miR-1915-3p were observed in AMI patients compared to stable coronary artery disease (SCAD) patients.

Area of Science:

  • Biochemistry
  • Molecular Biology
  • Cardiovascular Medicine

Background:

  • MicroRNAs (miRNAs) are recognized biomarkers for acute myocardial infarction (AMI).
  • The role of exosomal miRNAs in the transition from stable coronary artery disease (SCAD) to AMI remains under-explored.
  • Understanding these mechanisms is crucial for early diagnosis and intervention.

Purpose of the Study:

  • To investigate the diagnostic value of exosomal miRNAs in differentiating SCAD from AMI.
  • To explore the potential role of exosomal miRNAs in the pathophysiology of AMI progression.
  • To identify specific exosomal miRNAs as predictive biomarkers for early-stage AMI.

Main Methods:

  • Serum exosomes were isolated using ultracentrifugation and characterized by electron microscopy, western blotting, and nanoparticle tracking analysis.
  • Differential expression of miRNAs between SCAD and AMI patients was screened using microarray analysis.
  • Target gene prediction and pathway analysis were performed using bioinformatics tools.
  • Quantitative real-time PCR validated the expression of candidate miRNAs in a larger cohort.

Main Results:

  • Thirteen miRNAs were significantly downregulated in AMI exosome samples compared to SCAD samples.
  • Target genes of these miRNAs are primarily involved in cardiac rehabilitation and remodeling pathways.
  • Exosomal miR-1915-3p, miR-4,507, and miR-3,656 showed significantly lower expression in AMI patients.
  • Receiver-operating-characteristic curve analysis indicated good predictive accuracy for these miRNAs (AUCs ranging from 0.684 to 0.772).

Conclusions:

  • Serum exosomal miRNAs, particularly miR-1915-3p, miR-4,507, and miR-3,656, may serve as valuable early diagnostic biomarkers for AMI.
  • These miRNAs potentially play a significant role in the pathophysiology of AMI.
  • Further research into exosomal miRNAs could lead to improved diagnostic strategies for cardiovascular diseases.

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