Differential expression of microRNAs following cardiopulmonary bypass in children with congenital heart diseases

J Transl Med. 2017 May 30;15(1):117. doi: 10.1186/s12967-017-1213-9.


Background: Children with congenital heart defects (CHDs) are at high risk for myocardial failure after operative procedures with cardiopulmonary bypass (CPB). Recent studies suggest that microRNAs (miRNA) are involved in the development of CHDs and myocardial failure. Therefore, the aim of this study was to determine alterations in the miRNA profile in heart tissue after cardiac surgery using CPB.

Methods: In total, 14 tissue samples from right atrium were collected from patients before and after connection of the CPB. SurePrint™ 8 × 60K Human v21 miRNA array and quantitative reverse transcription-polymerase chain reaction (RT-qPCR) were employed to determine the miRNA expression profile from three patients before and after connection of the CPB. Enrichment analyses of altered miRNA expression were predicted using bioinformatic tools.

Results: According to miRNA array, a total of 90 miRNAs were significantly altered including 29 miRNAs with increased and 61 miRNAs with decreased expression after de-connection of CPB (n = 3) compared to before CPB (n = 3). Seven miRNAs had been validated using RT-qPCR in an independent cohort of 11 patients. Enrichment analyses applying the KEGG database displayed the highest correlation for signaling pathways, cellular community, cardiovascular disease and circulatory system.

Conclusion: Our result identified the overall changes of the miRNome in right atrium tissue of patients with CHDs after CPB. The differentially altered miRNAs lay a good foundation for further understanding of the molecular function of changed miRNAs in regulating CHDs and after CPB in particular.

Keywords: Atrial myocardium; Cardiopulmonary bypass; Congenital heart disease; MicroRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cardiopulmonary Bypass*
  • Child
  • Child, Preschool
  • Cluster Analysis
  • Cohort Studies
  • Computational Biology
  • Female
  • Gene Expression Profiling*
  • Gene Expression Regulation*
  • Heart Atria / metabolism
  • Heart Defects, Congenital / metabolism*
  • Humans
  • Infant
  • Male
  • MicroRNAs / metabolism*
  • Myocardium / pathology
  • Oligonucleotide Array Sequence Analysis
  • Time Factors
  • Tissue Distribution


  • MicroRNAs