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The analysis of gut microbiota in patients with bile acid diarrhoea treated with colesevelam

  • Aditi Kumar
  • , Mohammed Nabil Quraishi
  • , Hafid O. Al-Hassi
  • , Mohammed E. El-Asrag
  • , Jonathan P. Segal
  • , Manushri Jain
  • , Helen Steed
  • , Jeffrey Butterworth
  • , Adam Farmer
  • , John Mclaughlin
  • , Andrew Beggs
  • , Matthew J. Brookes
  • Department of Pediatrics NYU Grossman School of Medicine New York City New York USA; Department of Pediatrics, Gastroenterology and Nutrition, Collegium Medicum University of Warmia and Mazury Olsztyn Poland
  • Microbiome Treatment Centre
  • University of Wolverhampton
  • Northern General Hospital Trust
  • Shrewsbury and Telford Hospital NHS Trust
  • University Hospitals of North Midlands NHS Trust
  • University of Manchester

Research output: Contribution to journalArticlepeer-review

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Abstract

INTRODUCTION: Bile acid diarrhoea (BAD) is a common disorder that results from an increased loss of primary bile acids and can result in a change in microbiome. The aims of this study were to characterise the microbiome in different cohorts of patients with BAD and to determine if treatment with a bile acid sequestrant, colesevelam, can alter the microbiome and improve microbial diversity.

MATERIALS AND METHODS: Patients with symptoms of diarrhoea underwent 75-selenium homocholic acid (75SeHCAT) testing and were categorised into four cohorts: idiopathic BAD, post-cholecystectomy BAD, post-operative Crohn's disease BAD and 75SeHCAT negative control group. Patients with a positive 75SeHCAT (<15%) were given a trial of treatment with colesevelam. Stool samples were collected pre-treatment, 4-weeks, 8-weeks and 6-12 months post-treatment. Faecal 16S ribosomal RNA gene analysis was undertaken.

RESULTS: A total of 257 samples were analysed from 134 patients. α-diversity was significantly reduced in patients with BAD and more specifically, in the idiopathic BAD cohort and in patients with severe disease (SeHCAT <5%); p < 0.05. Colesevelam did not alter bacterial α/β-diversity but patients who clinically responded to treatment had a significantly greater abundance of Fusobacteria and Ruminococcus, both of which aid in the conversion of primary to secondary bile acids.

CONCLUSION: This is the first study to examine treatment effects on the microbiome in BAD, which demonstrated a possible association with colesevelam on the microbiome through bile acid modulation in clinical responders. Larger studies are now needed to establish a causal relationship with colesevelam and the inter-crosstalk between bile acids and the microbiome.

Original languageEnglish
Article number1134105
Number of pages11
JournalFrontiers in Microbiology
Volume14
Early online date17 Mar 2023
DOIs
Publication statusPublished - 17 Mar 2023

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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