Exploring Longitudinal Gut Microbiome towards Metabolic Functional Changes Associated in Atopic Dermatitis in Early

Preecha Patumcharoenpol1, Amornthep Kingkaw1, Massalin Nakphaichit2

  • 1Interdisciplinary Graduate Program in Bioscience, Faculty of Science, Kasetsart University, Bangkok 10900, Thailand.

Biology
|September 28, 2023
PubMed

Insights

Early childhood atopic dermatitis (AD) is linked to specific gut bacteria, even without changes in overall gut microbiome diversity. This study highlights key bacterial differences and metabolic functions in Thai children with AD.

Area of Science:

  • Microbiology
  • Immunology
  • Pediatric Health

Background:

  • Atopic dermatitis (AD) is a common inflammatory skin condition.
  • Gut microbiome alterations in early life are linked to AD.
  • Limited longitudinal studies exist on the gut microbiome in AD.

Purpose of the Study:

  • To investigate taxonomic and metabolic functions of longitudinal gut microbiomes in Thai children with AD.
  • To analyze gut microbial changes from 9 to 30 months of age.
  • To establish a framework for monitoring microbial imbalances in allergic diseases.

Main Methods:

  • Longitudinal analysis of gut microbiomes in Thai children (9-30 months).
  • Integrative data analysis to compare healthy and AD groups.
  • Taxonomic and functional profiling of microbial communities.

Main Results:

  • No significant difference in gut microbiome diversity between healthy and AD groups.
  • Increased abundance of SCFA-producing bacteria (e.g., *Anaerostipes*, *Butyricicoccus*, *Ruminococcus*, *Lactobacillus*) in the AD group.
  • Observed metabolic alterations related to vitamin production and immune response (e.g., menaquinol, succinate, (Kdo)2-lipid A biosynthesis).

Conclusions:

  • Specific gut bacteria and metabolic functions are associated with AD in Thai children.
  • Longitudinal microbiome analysis provides insights into AD development.
  • This study offers a framework for understanding microbial roles in pediatric allergic diseases.