Fecal Microbiota Transplantation Commonly Failed in Children With Co-Morbidities

Richard Kellermayer1,2, Qinglong Wu3,4, Dorottya Nagy-Szakal1

  • 1Gastroenterology, Hepatology & Nutrition, Department of Pediatrics, Baylor College of Medicine and Texas Children's Hospital.

Abstract

Insights

Fecal microbiota transplantation (FMT) effectively treats recurrent Clostridioides difficile infection (rCDI) in children without comorbidities. However, underlying health issues in pediatric rCDI patients receiving FMT can impact treatment success and microbiome restoration.

Area of Science:

  • Microbiology
  • Gastroenterology
  • Pediatric Medicine

Background:

  • Recurrent Clostridioides difficile infection (rCDI) poses a significant challenge in pediatric populations.
  • Fecal microbiota transplantation (FMT) is a highly effective treatment for rCDI, but its efficacy in children with co-morbidities requires further investigation.
  • Systematic evaluation of microbiome restoration in pediatric FMT recipients with co-existing conditions is lacking.

Purpose of the Study:

  • To determine if recipient age and underlying co-morbidities influence clinical outcomes and microbiome restoration in pediatric patients undergoing FMT for rCDI.
  • To compare microbiome restoration in pediatric FMT recipients with healthy children and pediatric ulcerative colitis (UC) cases using shared fecal donors.
  • To identify factors affecting FMT success in pediatric rCDI.

Main Methods:

  • A single-center, open-label prospective cohort study involving 18 pediatric rCDI patients receiving FMT.
  • Fecal specimens were collected longitudinally for microbiome analysis using 16S rRNA gene sequencing.
  • Comparison with 12 healthy children and 4 pediatric UC cases from a separate FMT trial utilizing shared fecal donors.

Main Results:

  • FMT demonstrated significantly higher efficacy in pediatric rCDI recipients without chronic co-morbidities.
  • Microbiome composition in responders without co-morbidities was restored to levels observed in healthy children.
  • Microbiome reconstitution did not consistently correlate with symptomatic resolution in pediatric rCDI patients with co-morbidities.
  • Specific bacterial families (Bacteroidaceae, Bifidobacteriaceae, Lachnospiraceae, Ruminococcaceae, Erysipelotrichaceae) increased, while Enterobacteriaceae decreased in pediatric rCDI responders.

Conclusions:

  • Underlying co-morbidities in pediatric rCDI patients are a significant risk factor influencing FMT outcomes.
  • Careful consideration is warranted when implementing FMT for pediatric rCDI patients with co-existing health conditions.
  • Further research is needed to optimize FMT strategies for pediatric rCDI patients with co-morbidities.