The impact of exclusive enteral nutrition on the gut microbiome and bile acid metabolism in pediatric Crohn's disease

Clin Nutr. 2023 Feb;42(2):116-128. doi: 10.1016/j.clnu.2022.11.018. Epub 2022 Nov 30.

Abstract

Background: Gut dysbiosis and associated bile acid (BA) metabolism play an important role in the pathogenesis of Crohn's disease (CD). We investigated the impacts of the exclusive enteral nutrition treatment (EEN) on the gut microbiome (GM) and BAs metabolism for patients with CD.

Methods: Targeted metabolomics analysis and metagenomics analysis were performed in feces to investigate the BA and GM changes of patients before and after 2-months EEN therapy. The Pediatric Crohn's Disease Activity Index (PCDAI) and fecal calprotectin were used to evaluate the severity and mucosal inflammation of CD.

Results: A total of 27 newly diagnosed pediatric patients with CD and 27 healthy controls were recruited in this study. Both GM structure and the secondary BA metabolism were significantly impaired in patients, which could return towards normal levels after EEN treatment. The most abundant taxa Firmicutes and 11 BAs were found closely associated with the PCDAI score and fecal calprotectin. Meanwhile, the close interactions between Firmicute bacteria and BAs might contribute to the remission of CD after EEN treatment. The qPCR data further confirmed that the relative expressions of Firmicutes phylum, and genus Flavonifractor and Clostridium V were improved after EEN treatment.

Conclusions: Firmicutes bacteria and the balance of primary and secondary BA compositions in the gut were closely associated with the health status of CD disease indicated by the PCDAI score and fecal calprotectin. Understanding the recovery process of gut microbiome and BA metabolism will help us to explore the potential mechanisms of EEN therapy.

Keywords: Crohn's disease; Exclusive enteral nutrition; Gut microbiota and bile acid metabolism.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bile Acids and Salts* / metabolism
  • Child
  • Crohn Disease* / diet therapy
  • Crohn Disease* / etiology
  • Crohn Disease* / metabolism
  • Crohn Disease* / microbiology
  • Dysbiosis / complications
  • Dysbiosis / metabolism
  • Dysbiosis / microbiology
  • Enteral Nutrition*
  • Feces / chemistry
  • Feces / microbiology
  • Firmicutes / isolation & purification
  • Gastrointestinal Microbiome*
  • Humans
  • Leukocyte L1 Antigen Complex / analysis
  • Remission Induction

Substances

  • Bile Acids and Salts
  • Leukocyte L1 Antigen Complex

Supplementary concepts

  • Pediatric Crohn's disease