scholarly journals Effect of colesevelam on faecal bile acids and bowel functions in diarrhoea-predominant irritable bowel syndrome

2015 ◽  
Vol 41 (5) ◽  
pp. 438-448 ◽  
Author(s):  
M. Camilleri ◽  
A. Acosta ◽  
I. Busciglio ◽  
A. Boldingh ◽  
R. B. Dyer ◽  
...  
2018 ◽  
Vol 1 (1) ◽  
Author(s):  
Chirag Patel ◽  
Carolyn Lockett ◽  
Huiping Xu ◽  
Andrea Shin

Background and Aims: Fecal bile acids (BAs), short chain fatty acids (SCFAs), and gut microbiome may be implicated in irritable bowel syndrome (IBS) pathophysiology. Our aim was to compare fecal organic acids between IBS with constipation (IBS-C), IBS with diarrhea (IBS-D), and controls.   Methods: Stool samples were collected from 17 controls, 5 IBS-C, and 5 IBS-D volunteers during a 4-day high fat diet. Aliquots were stored for future analysis of the fecal microbiota. Fecal SCFA and BA analyses were conducted at the Metabolite Profiling Facility at Purdue University and Laboratory Medicine and Pathology at Mayo Clinic. We compared SCFA and BA levels among groups using the Wilcoxon rank sum test. Gamma and linear regression were used to compare SCFAs and BAs adjusting for age and body mass index (BMI).  Results: Fecal acetate levels (mean+SD, µg/mg) were higher in IBS-C (11.3±7) than in controls (6.1±3.3) or IBS-D (7.7±2), although not statistically significant (p=0.19). Total fecal BAs (median [IQR], %) were higher in IBS-D (675 [484-778]) than in controls (342 [130-640]) or IBS-C (321.5 (34.5-718); however, differences were not significant. No significant differences were observed in BAs or SCFAs between groups in multivariate analyses.  Conclusion: We are unable to show significant differences in organic acid levels in IBS and controls. Lack of association may be due to small sample size. Future investigation of larger patient numbers with incorporation of transit and microbiome analyses may shed further light on the role of organic acids in IBS to identify new biomarkers and treatment targets.


2013 ◽  
Vol 11 (10) ◽  
pp. 1270-1275.e1 ◽  
Author(s):  
Andrea Shin ◽  
Michael Camilleri ◽  
Priya Vijayvargiya ◽  
Irene Busciglio ◽  
Duane Burton ◽  
...  

2013 ◽  
Vol 144 (5) ◽  
pp. S-60
Author(s):  
Dior Marie ◽  
Heloise Delagreverie ◽  
Henri Duboc ◽  
Pauline Jouet ◽  
Benoit Coffin ◽  
...  

2012 ◽  
Vol 24 (6) ◽  
pp. 513-e247 ◽  
Author(s):  
H. Duboc ◽  
D. Rainteau ◽  
S. Rajca ◽  
L. Humbert ◽  
D. Farabos ◽  
...  

2019 ◽  
Vol 156 (6) ◽  
pp. S-570
Author(s):  
Crystal S. James ◽  
Karl Fraser ◽  
Wayne Young ◽  
Warren McNabb ◽  
Richard B. Gearry ◽  
...  

2021 ◽  
Vol 12 ◽  
Author(s):  
Róisín Ní Dhonnabháín ◽  
Qiao Xiao ◽  
Dervla O’Malley

Functional bowel disorders such as irritable bowel syndrome (IBS) are common, multifactorial and have a major impact on the quality of life of individuals diagnosed with the condition. Heterogeneity in symptom manifestation, which includes changes in bowel habit and visceral pain sensitivity, are an indication of the complexity of the underlying pathophysiology. It is accepted that dysfunctional gut-brain communication, which incorporates efferent and afferent branches of the peripheral nervous system, circulating endocrine hormones and local paracrine and neurocrine factors, such as host and microbially-derived signaling molecules, underpins symptom manifestation. This review will focus on the potential role of hepatic bile acids in modulating gut-to-brain signaling in IBS patients. Bile acids are amphipathic molecules synthesized in the liver, which facilitate digestion and absorption of dietary lipids. They are also important bioactive signaling molecules however, binding to bile acid receptors which are expressed on many different cell types. Bile acids have potent anti-microbial actions and thereby shape intestinal bacterial profiles. In turn, bacteria with bile salt hydrolase activity initiate the critical first step in transforming primary bile acids into secondary bile acids. Individuals with IBS are reported to have altered microbial profiles and modified bile acid pools. We have assessed the evidence to support a role for bile acids in the pathophysiology underlying the manifestation of IBS symptoms.


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