Markers of Bile Acid Metabolism in Pediatric Diarrhea Predominant Irritable Bowel Syndrome and Healthy Controls

Beate C Beinvogl1, Mhd Louai Manini2, Michael Camilleri3

  • 1Center for Motility and Functional Gastrointestinal Disorders, Boston Children's Hospital, Boston, MA.

Insights

This study investigated bile acid diarrhea (BAD) in children with irritable bowel syndrome with diarrhea (IBS-D). Abnormal serum markers were found in 20% of pediatric IBS-D patients, suggesting a potential diagnostic role for C4 testing.

Area of Science:

  • Pediatric Gastroenterology
  • Hepatology
  • Digestive Diseases

Background:

  • Excessive fecal bile acids are linked to diarrhea-predominant irritable bowel syndrome (IBS-D) in adults.
  • The role of bile acid diarrhea (BAD) in pediatric IBS-D remains unclear.
  • Serum markers 7α-hydroxy-4-cholesten-3-one (C4) and fibroblast growth factor-19 (FGF-19) can detect BAD in adults.

Purpose of the Study:

  • To assess serum C4, FGF-19, and 48-hour fecal bile acid (48FBA) in pediatric IBS-D patients and healthy controls (HC).
  • To compare these markers between pediatric IBS-D patients and HC.
  • To determine the prevalence of BAD in children with IBS-D.

Main Methods:

  • Cross-sectional study involving 26 pediatric IBS-D patients and 56 HC.
  • Collected fasting serum C4 and FGF-19, and 48FBA.
  • Analyzed correlations between markers and stool frequency using Spearman correlations.

Main Results:

  • Serum C4 correlated significantly with 48FBA (r=0.48) and inversely with FGF-19 (r=-0.43).
  • No significant differences in C4, FGF-19, or 48FBA were found between IBS-D and HC groups.
  • Twenty percent of pediatric IBS-D patients exhibited elevated serum C4, and 28% had low FGF-19.

Conclusions:

  • The correlations between C4, 48FBA, and FGF-19 are confirmed in a pediatric cohort.
  • Abnormal fasting serum C4 was observed in 20% of pediatric IBS-D patients.
  • Serum C4 testing shows potential for identifying BAD in pediatric IBS-D.
Abstract

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