Decreased miRNA-320e correlates with allergy in children with otitis media with effusion

Paulina Adamczyk1, Beata Narożna2, Aleksandra Szczepankiewicz2

  • 1Department of Pediatric Otolaryngology, Poznan University of Medical Sciences, Szpitalna 27/33 60-572 Poznań, Poland.

Auris, Nasus, Larynx
|April 4, 2021
PubMed
Abstract

Insights

MicroRNA (miRNA) expression in middle ear fluid differs between allergic and non-allergic children with otitis media with effusion (OME). Specifically, miR-320e levels were significantly lower in allergic children, suggesting a role in OME.

Area of Science:

  • Biochemistry
  • Molecular Biology
  • Pediatrics

Background:

  • Otitis media with effusion (OME) is a leading cause of conductive hearing loss in children.
  • The role of allergy in OME pathogenesis is debated.
  • MicroRNAs (miRNAs) are implicated in allergic responses and may influence middle ear effusion.

Purpose of the Study:

  • To investigate differential miRNA expression in middle ear effusions from allergic and non-allergic children with OME.
  • To explore the potential role of miRNAs in the distinct molecular mechanisms of OME in allergic versus non-allergic individuals.

Main Methods:

  • Quantification of 5 specific miRNAs (miR-223-3p, miR-451a, miR-16-5p, miR-320e, miR-25-3p) in middle ear fluid from 54 children with OME.
  • miRNA isolation, cDNA transcription, and expression analysis using TaqMan™ MicroRNA Assays.
  • Relative gene expression calculated via the comparative CT method using U6 snRNA as a control.

Main Results:

  • Significantly decreased expression of miR-320e was observed in the middle ear effusions of allergic children with OME.
  • Other tested miRNAs showed a trend towards reduced expression in allergic children, but did not reach statistical significance.

Conclusions:

  • MiRNA expression profiles in middle ear effusions differ between allergic and non-allergic children with OME.
  • Further research is warranted to elucidate the specific function of miR-320e and its targets in allergic OME.
  • These findings may offer insights into the molecular basis of OME in allergic pediatric populations.