期刊
FRONTIERS IN MICROBIOLOGY
卷 14, 期 -, 页码 -出版社
FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2023.1134105
关键词
microbiome; Crohn's disease; bile acid diarrhoea; colesevelam; post-cholecystectomy
类别
This study aimed to characterize the microbiome in different cohorts of patients with bile acid diarrhea (BAD) and determine if treatment with the bile acid sequestrant colesevelam could alter the microbiome. The study found that BAD patients had reduced microbiome diversity, but patients who responded to colesevelam treatment had increased abundance of certain bacteria. This is the first study to examine the treatment effects on the microbiome in BAD, suggesting a possible association between colesevelam and the microbiome through bile acid modulation in clinical responders.
IntroductionBile 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 methodsPatients with symptoms of diarrhoea underwent 75-selenium homocholic acid ((75)SeHCAT) testing and were categorised into four cohorts: idiopathic BAD, post-cholecystectomy BAD, post-operative Crohn's disease BAD and (75)SeHCAT negative control group. Patients with a positive (75)SeHCAT (<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. ResultsA total of 257 samples were analysed from 134 patients. alpha-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 alpha/beta-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. ConclusionThis 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.
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