The association between the adenoid microbiome and chronic otitis media with effusion in children differs according

Jae-Won Jo1,2, Sung Kyun Kim3, Jae Yong Byun4

  • 1Department of Life Science, Multidisciplinary Genome Institute, Hallym University, Chuncheon, Gangwon-do, Republic of Korea.

Insights

The adenoid microbiome, not the gut microbiome, is linked to chronic otitis media with effusion (COME) in children. Age-specific adenoid microbiome changes, especially in 6-12 year olds, are associated with COME development.

Area of Science:

  • Microbiology
  • Pediatrics
  • Otolaryngology

Background:

  • Chronic otitis media with effusion (COME) impacts child development.
  • The adenoid's role as a bacterial reservoir in COME pathogenesis is suspected but not fully understood.
  • The adenoid microbiome's specific contribution to COME requires further investigation.

Purpose of the Study:

  • To analyze and compare adenoid and gut microbiomes in children with and without COME.
  • To identify the potential roles of these microbiomes in COME pathogenesis.
  • To investigate age-dependent variations in the adenoid microbiome related to COME.

Main Methods:

  • Whole metagenome sequencing of adenoid and fecal samples from children with and without COME.
  • Bioinformatic analysis to characterize microbiome composition and function.
  • Correlation analysis between microbiome profiles, age, and COME status.

Main Results:

  • A significant association was found between the adenoid microbiome and COME, but not the gut microbiome.
  • Adenoid microbiome composition varied with age in controls, with this pattern disrupted in COME patients.
  • In children aged 6-12 years, specific bacteria like *Streptococcus pneumoniae* and *Haemophilus influenzae* in the adenoid microbiome were linked to mucoid COME, with implications for serous COME.

Conclusions:

  • The adenoid microbiome plays a significant, age-dependent role in the pathogenesis of COME, particularly in children aged 6-12 years.
  • Altered adenoid microbiome may influence immune responses via metabolites like spermidine and acetate, contributing to COME.
  • Findings highlight the adenoid microbiome as a key factor in COME development and suggest potential therapeutic targets.
Abstract

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