Literature DB >> 23639599

Bowel functions, fecal unconjugated primary and secondary bile acids, and colonic transit in patients with irritable bowel syndrome.

Andrea Shin1, Michael Camilleri, Priya Vijayvargiya, Irene Busciglio, Duane Burton, Michael Ryks, Deborah Rhoten, Alan Lueke, Amy Saenger, Adam Girtman, Alan R Zinsmeister.   

Abstract

BACKGROUND & AIMS: There is an unclear relationship among bowel symptoms, excretion of unconjugated fecal bile acid (UBA), and colonic transit in irritable bowel syndrome (IBS). We measured total and main individual UBA in fecal samples of patients with IBS and assessed relationships among stool frequency or consistency, fecal UBA (total and individual), and colonic transit.
METHODS: In this study 30 healthy volunteers (controls), 31 subjects with IBS with diarrhea (IBS-D), and 30 with IBS with constipation (IBS-C) were placed on 4-day diets containing 100 g fat; we measured stool characteristics, total fecal UBA and fat levels, and overall colonic transit. We assessed univariate associations of total and individual levels of fecal UBA with phenotype (controls, IBS-D, IBS-C) by using the Kruskal-Wallis test; associations between end points were assessed by using Spearman correlations. With response surface regression models, we assessed relationships between stool, colonic transit, and fecal total and secretory UBA.
RESULTS: There was a significant association between total fecal UBA and phenotype (P = .029); the association was greater for IBS-D than IBS-C, compared with controls. Fecal levels of primary UBAs (cholic and chenodeoxycholic acids) were higher in subjects with IBS-D, compared with controls (both P < .01). Levels of fecal secretory UBAs (chenodeoxycholic acid, P = .019; deoxycholic acid, P = .025) were lower in subjects with IBS-C compared with controls, whereas levels of the nonsecretory UBA, lithocholic acid, were higher (P = .020). There were significant univariate associations between stool number and form and total fecal UBA (including percentages of lithocholic acid, chenodeoxycholic acid and cholic acid), fecal fat, and colonic transit at 24 and 48 hours after eating. In the regression models, the relative contribution of colonic transit was consistently greater and largely independent of the contribution of bile acids.
CONCLUSIONS: Measurements of individual UBAs identify changes associated with stool characteristics in patients with IBS; these effects are independent of the effects of colonic transit.
Copyright © 2013 AGA Institute. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Abdominal Pain; BA; C; CA; CDCA; CT; Constipation; D; DCA; Diarrhea; FGID; GC; HAD; HV; Hospital Anxiety and Depression Scale; IBS; LCA; Secretory; UBA; UDCA; bile acid; chenodeoxycholic acid; cholic acid; colonic transit; constipation; deoxycholic acid; diarrhea; functional gastrointestinal disorder; geometric center; healthy volunteers; irritable bowel syndrome; lithocholic acid; unconjugated bile acid; ursodeoxycholic acid

Mesh:

Substances:

Year:  2013        PMID: 23639599      PMCID: PMC3778140          DOI: 10.1016/j.cgh.2013.04.020

Source DB:  PubMed          Journal:  Clin Gastroenterol Hepatol        ISSN: 1542-3565            Impact factor:   11.382


  27 in total

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3.  Octreotide induced prolongation of colonic transit increases faecal anaerobic bacteria, bile acid metabolising enzymes, and serum deoxycholic acid in patients with acromegaly.

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4.  Recombinant human neurotrophic factors accelerate colonic transit and relieve constipation in humans.

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Journal:  Gastroenterology       Date:  2000-07       Impact factor: 22.682

5.  Prevalence of psychiatric disorders in patients with irritable bowel syndrome.

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Journal:  Psychosomatics       Date:  1993 May-Jun       Impact factor: 2.386

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Journal:  Am J Clin Nutr       Date:  1976-12       Impact factor: 7.045

7.  Bile acid malabsorption in Crohn's disease and indications for its assessment using SeHCAT.

Authors:  H Nyhlin; M V Merrick; M A Eastwood
Journal:  Gut       Date:  1994-01       Impact factor: 23.059

8.  Perfusion of the canine colon with unconjugated bile acids. Effect on water and electrolyte transport, morphology, and bile acid absorption.

Authors:  H S Mekhjian; S F Phillips
Journal:  Gastroenterology       Date:  1970-07       Impact factor: 22.682

9.  The hospital anxiety and depression scale.

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Journal:  Acta Psychiatr Scand       Date:  1983-06       Impact factor: 6.392

10.  Effect of molecular structure on bile acid-induced alterations in absorptive function, permeability, and morphology in the perfused rabbit colon.

Authors:  V S Chadwick; T S Gaginella; G L Carlson; J C Debongnie; S F Phillips; A F Hofmann
Journal:  J Lab Clin Med       Date:  1979-11
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  58 in total

1.  Colonic mucosal gene expression and genotype in irritable bowel syndrome patients with normal or elevated fecal bile acid excretion.

Authors:  Michael Camilleri; Paula Carlson; Andres Acosta; Irene Busciglio
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2015-04-30       Impact factor: 4.052

2.  Irritable bowel syndrome-diarrhea: characterization of genotype by exome sequencing, and phenotypes of bile acid synthesis and colonic transit.

Authors:  Michael Camilleri; Eric W Klee; Andrea Shin; Paula Carlson; Ying Li; Madhusudan Grover; Alan R Zinsmeister
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2013-11-07       Impact factor: 4.052

3.  RNA sequencing shows transcriptomic changes in rectosigmoid mucosa in patients with irritable bowel syndrome-diarrhea: a pilot case-control study.

Authors:  Michael Camilleri; Paula Carlson; Andres Acosta; Irene Busciglio; Asha A Nair; Simon J Gibbons; Gianrico Farrugia; Eric W Klee
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2014-04-24       Impact factor: 4.052

4.  Bile Acid Deficiency in a Subgroup of Patients With Irritable Bowel Syndrome With Constipation Based on Biomarkers in Serum and Fecal Samples.

Authors:  Priya Vijayvargiya; Irene Busciglio; Duane Burton; Leslie Donato; Alan Lueke; Michael Camilleri
Journal:  Clin Gastroenterol Hepatol       Date:  2017-06-27       Impact factor: 11.382

Review 5.  Advances in understanding of bile acid diarrhea.

Authors:  Michael Camilleri
Journal:  Expert Rev Gastroenterol Hepatol       Date:  2013-11-25       Impact factor: 3.869

Review 6.  Chemical and molecular factors in irritable bowel syndrome: current knowledge, challenges, and unanswered questions.

Authors:  Michael Camilleri; Ibironke Oduyebo; Houssam Halawi
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2016-09-08       Impact factor: 4.052

7.  Colonic Transit and Bile Acid Synthesis or Excretion in Patients With Irritable Bowel Syndrome-Diarrhea Without Bile Acid Malabsorption.

Authors:  Cédric Peleman; Michael Camilleri; Irene Busciglio; Duane Burton; Leslie Donato; Alan R Zinsmeister
Journal:  Clin Gastroenterol Hepatol       Date:  2016-11-14       Impact factor: 11.382

8.  Microbiota transplantation restores normal fecal bile acid composition in recurrent Clostridium difficile infection.

Authors:  Alexa R Weingarden; Chi Chen; Aleh Bobr; Dan Yao; Yuwei Lu; Valerie M Nelson; Michael J Sadowsky; Alexander Khoruts
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2013-11-27       Impact factor: 4.052

9.  Analysis of Fecal Primary Bile Acids Detects Increased Stool Weight and Colonic Transit in Patients With Chronic Functional Diarrhea.

Authors:  Priya Vijayvargiya; Michael Camilleri; Victor Chedid; Paula Carlson; Irene Busciglio; Duane Burton; Leslie J Donato
Journal:  Clin Gastroenterol Hepatol       Date:  2018-06-12       Impact factor: 11.382

10.  New and Emerging Treatment Options for Irritable Bowel Syndrome.

Authors:  Brian E Lacy; William D Chey; Anthony J Lembo
Journal:  Gastroenterol Hepatol (N Y)       Date:  2015-04
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