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Prevalence of biliary acid malabsorption in patients with chronic diarrhoea of functional characteristics: a prospective study

BACKGROUND: Bile acid malabsorption occurs in up to one third of patients with chronic diarrhoea of functional characteristics. The gold standard test for its diagnosis is the (75)Selenium homocholic acid taurine ((75)SeHCAT) test. The aim of this work is to confirm previous data suggesting that bil...

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Autores principales: Flores, Virginia, Martínez-Lozano, Helena, Bighelli, Federico, Orcajo, Javier, García-Lledó, Javier, Alonso-Farto, Juan Carlos, Menchén, Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7871394/
https://www.ncbi.nlm.nih.gov/pubmed/33563227
http://dx.doi.org/10.1186/s12876-021-01637-4
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author Flores, Virginia
Martínez-Lozano, Helena
Bighelli, Federico
Orcajo, Javier
García-Lledó, Javier
Alonso-Farto, Juan Carlos
Menchén, Luis
author_facet Flores, Virginia
Martínez-Lozano, Helena
Bighelli, Federico
Orcajo, Javier
García-Lledó, Javier
Alonso-Farto, Juan Carlos
Menchén, Luis
author_sort Flores, Virginia
collection PubMed
description BACKGROUND: Bile acid malabsorption occurs in up to one third of patients with chronic diarrhoea of functional characteristics. The gold standard test for its diagnosis is the (75)Selenium homocholic acid taurine ((75)SeHCAT) test. The aim of this work is to confirm previous data suggesting that bile acid malabsorption, diagnosed by (75)Se-HCAT test, is the underlying cause of diarrhoea in a significant proportion of patients previously diagnosed with a functional disorder. In addition, we have analysed the clinical response of bile acid sequestrants in those patients with a bile acid diarrhoea diagnosis. METHODS: This is a prospective, single-centre study including consecutive adult patients diagnosed with chronic diarrhoea of unknown origin and with functional characteristics; systematic rule out of common causes of chronic diarrhoea was performed before bile acid malabsorption evaluation by (75)SeHCAT scanning. A retention percentage less than 10% was considered positive. Clinical response to cholestyramine was further evaluated in those patients with a positive diagnosis of bile acid diarrhoea RESULTS: 38 patients (20 male, mean age 37.5 years) were finally included. Twenty (52.6%) patients included had a positive (75)SeHCAT test. Median body mass index was significantly higher in those patients. We did not find significant differences in other clinical or biochemical variables (75)SeHCAT-positive and (75)SeHCAT-negative groups. Only 6 of 17 (35.3%) patients responded to cholestyramine treatment; 10 patients did not have response or withdraw the drug due to adverse events. Logistic regression analysis showed that none of the included variables was a predictor of clinical response to cholestyramine. CONCLUSIONS: Bile acid malabsorption occurs in a high proportion of patients suffering from chronic diarrhoea with functional characteristics. Systematic investigation of bile acid malabsorption should be included in the diagnostic algorithms of patients with chronic watery diarrhoea in the routine clinical practice. Absence of response to cholestyramine does not rule out bile acid diarrhoea.
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spelling pubmed-78713942021-02-09 Prevalence of biliary acid malabsorption in patients with chronic diarrhoea of functional characteristics: a prospective study Flores, Virginia Martínez-Lozano, Helena Bighelli, Federico Orcajo, Javier García-Lledó, Javier Alonso-Farto, Juan Carlos Menchén, Luis BMC Gastroenterol Research Article BACKGROUND: Bile acid malabsorption occurs in up to one third of patients with chronic diarrhoea of functional characteristics. The gold standard test for its diagnosis is the (75)Selenium homocholic acid taurine ((75)SeHCAT) test. The aim of this work is to confirm previous data suggesting that bile acid malabsorption, diagnosed by (75)Se-HCAT test, is the underlying cause of diarrhoea in a significant proportion of patients previously diagnosed with a functional disorder. In addition, we have analysed the clinical response of bile acid sequestrants in those patients with a bile acid diarrhoea diagnosis. METHODS: This is a prospective, single-centre study including consecutive adult patients diagnosed with chronic diarrhoea of unknown origin and with functional characteristics; systematic rule out of common causes of chronic diarrhoea was performed before bile acid malabsorption evaluation by (75)SeHCAT scanning. A retention percentage less than 10% was considered positive. Clinical response to cholestyramine was further evaluated in those patients with a positive diagnosis of bile acid diarrhoea RESULTS: 38 patients (20 male, mean age 37.5 years) were finally included. Twenty (52.6%) patients included had a positive (75)SeHCAT test. Median body mass index was significantly higher in those patients. We did not find significant differences in other clinical or biochemical variables (75)SeHCAT-positive and (75)SeHCAT-negative groups. Only 6 of 17 (35.3%) patients responded to cholestyramine treatment; 10 patients did not have response or withdraw the drug due to adverse events. Logistic regression analysis showed that none of the included variables was a predictor of clinical response to cholestyramine. CONCLUSIONS: Bile acid malabsorption occurs in a high proportion of patients suffering from chronic diarrhoea with functional characteristics. Systematic investigation of bile acid malabsorption should be included in the diagnostic algorithms of patients with chronic watery diarrhoea in the routine clinical practice. Absence of response to cholestyramine does not rule out bile acid diarrhoea. BioMed Central 2021-02-09 /pmc/articles/PMC7871394/ /pubmed/33563227 http://dx.doi.org/10.1186/s12876-021-01637-4 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Flores, Virginia
Martínez-Lozano, Helena
Bighelli, Federico
Orcajo, Javier
García-Lledó, Javier
Alonso-Farto, Juan Carlos
Menchén, Luis
Prevalence of biliary acid malabsorption in patients with chronic diarrhoea of functional characteristics: a prospective study
title Prevalence of biliary acid malabsorption in patients with chronic diarrhoea of functional characteristics: a prospective study
title_full Prevalence of biliary acid malabsorption in patients with chronic diarrhoea of functional characteristics: a prospective study
title_fullStr Prevalence of biliary acid malabsorption in patients with chronic diarrhoea of functional characteristics: a prospective study
title_full_unstemmed Prevalence of biliary acid malabsorption in patients with chronic diarrhoea of functional characteristics: a prospective study
title_short Prevalence of biliary acid malabsorption in patients with chronic diarrhoea of functional characteristics: a prospective study
title_sort prevalence of biliary acid malabsorption in patients with chronic diarrhoea of functional characteristics: a prospective study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7871394/
https://www.ncbi.nlm.nih.gov/pubmed/33563227
http://dx.doi.org/10.1186/s12876-021-01637-4
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