Alterations in intestinal microbiota composition in children with Hhirschsprung disease: A comparative study with

M Makkadafi1, W Warsinggih2, S As'ad3

  • 1Department of Surgery, Faculty of Medicine, Hasanuddin University, Makassar, Indonesia. munamakkadafi@gmail.com.

PubMed

Insights

Children with Hirschsprung disease (HSCR) have altered gut bacteria, showing fewer beneficial microbes and more harmful ones like Enterobacteriaceae. This dysbiosis may offer new treatment targets for HSCR.

Area of Science:

  • Microbiology
  • Pediatric Gastroenterology
  • Genetics

Background:

  • Hirschsprung disease (HSCR) is a congenital disorder affecting the colon's nerves, leading to bowel obstruction.
  • The role of the gut microbiome in HSCR pathogenesis is not well understood.
  • Investigating microbial alterations in HSCR is crucial for understanding disease mechanisms.

Purpose of the Study:

  • To characterize the fecal microbiota composition in children with Hirschsprung disease.
  • To compare the microbiota of HSCR patients with that of healthy controls.
  • To identify potential microbial biomarkers associated with HSCR.

Main Methods:

  • A comparative cross-sectional study involving 7 preoperative HSCR patients and 3 healthy controls.
  • 16S rRNA gene sequencing was used to analyze fecal microbiota composition.
  • Clinical data, including nutritional status and medication history, were collected.

Main Results:

  • HSCR patients exhibited an eleven-fold increase in Enterobacteriaceae compared to controls.
  • A decrease in beneficial bacteria (e.g., Lactobacillus, Bifidobacterium) was observed in HSCR patients.
  • An increase in potentially pathogenic bacteria (e.g., Escherichia-Shigella) and a decrease in Firmicutes and Actinobacteria were noted.

Conclusions:

  • Children with HSCR present a distinct gut dysbiosis characterized by reduced beneficial bacteria and elevated Enterobacteriaceae.
  • These findings suggest that the gut microbiome plays a significant role in HSCR.
  • Microbiota-targeted therapies could be a potential strategy for managing HSCR.
Abstract

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