Age-dependent fecal bacterial correlation to inflammatory bowel disease for newly diagnosed untreated children

Felix Chinweije Nwosu1, Lill-Therse Thorkildsen, Ekaterina Avershina

  • 1Hedmark University College, Hamar, Norway ; Department of Chemistry, Biotechnology and Food Science, Norwegian University for Life Sciences, Ås, Oslo, Norway.

Insights

This study reveals age-dependent fecal microbiota patterns in pediatric inflammatory bowel diseases (IBD). Specific bacterial correlations with age differ between Crohn's disease (CD) and ulcerative colitis (UC), suggesting age-specific immune responses.

Area of Science:

  • Microbiome research
  • Pediatric gastroenterology
  • Immunology

Background:

  • Limited understanding of fecal microbiota in newly diagnosed, treatment-naive pediatric inflammatory bowel diseases (IBD).
  • IBD comprises Crohn's disease (CD) and ulcerative colitis (UC), with distinct pathologies.
  • Investigating age-related microbial shifts is crucial for understanding pediatric IBD development.

Purpose of the Study:

  • To investigate the correlation between fecal microbiota and age in children with newly diagnosed CD and UC.
  • To identify specific bacterial taxa associated with age in pediatric IBD subtypes.
  • To propose a model for IBD etiology based on age-dependent immune-microbiota interactions in children.

Main Methods:

  • Analysis of fecal specimens from children (<18 years) with CD (n=27), UC (n=16), and non-IBD controls (n=30).
  • Utilized bacterial small subunit (SSU) rRNA sequencing to characterize the fecal microbiota.
  • Statistical analysis to determine correlations between bacterial abundance, age, and IBD status.

Main Results:

  • Significant age-dependent correlations were observed between fecal microbiota and IBD in children.
  • For CD, E. coli showed a positive correlation with age, while Bacteroidetes showed a negative correlation.
  • UC exhibited opposite age-related correlations for Bacteroides and Escherichia, with an overrepresentation of Haemophilus.

Conclusions:

  • The etiology of pediatric IBD may involve age-dependent immunological responses to specific bacterial stimuli.
  • Findings suggest a need for age stratification in understanding and treating pediatric IBD.
  • This research provides novel insights into the interplay between the microbiome, immune system, and age in pediatric IBD.

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