AI Article Synopsis

  • Exclusive enteral nutrition (EEN) is effective at inducing remission in pediatric Crohn's disease but leads to high relapse rates once regular diets are resumed.
  • The study involved collecting fecal samples from pediatric patients on EEN, which were processed into FMT capsules after pathogen safety screening.
  • Results showed that while FMT capsule generation was mostly successful, issues like a high pathogen burden and low microbial diversity in the samples suggest that using this method for long-term maintenance therapy in pediatric Crohn's disease may not be feasible.

Article Abstract

Background: Exclusive enteral nutrition (EEN) is a highly effective therapy for remission induction in pediatric Crohn's disease (CD), but relapse rates after return to a regular diet are high. Autologous fecal microbiota transfer (FMT) using stool collected during EEN-induced clinical remission might represent a novel approach to maintaining the benefits of EEN.

Methods: Pediatric CD patients provided fecal material at home, which was shipped at 4 °C to an FMT laboratory for FMT capsule generation and extensive pathogen safety screening. The microbial community composition of samples taken before and after shipment and after encapsulation was characterized using 16S rRNA amplicon sequencing.

Results: Seven pediatric patients provided fecal material for nine test runs after at least three weeks of nutritional therapy. FMT capsules were successfully generated in 6/8 deliveries, but stool weight and consistency varied widely. Transport and processing of fecal material into FMT capsules did not fundamentally change microbial composition, but microbial richness was <30 genera in 3/9 samples. Stool safety screening was positive for potential pathogens or drug resistance genes in 8/9 test runs.

Conclusions: A high pathogen burden, low-diversity microbiota, and practical deficiencies of EEN-conditioned fecal material might render autologous capsule-FMT an unsuitable approach as maintenance therapy for pediatric CD patients.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10096730PMC
http://dx.doi.org/10.3390/nu15071742DOI Listing

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