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Pathophysiology and Clinical Management of Bile Acid Diarrhea
Bile acid malabsorption (BAM) represents a common cause of chronic diarrhea whose prevalence is under-investigated. We reviewed the evidence available regarding the pathophysiology and clinical management of bile acid diarrhea (BAD). BAD results from dysregulation of the enterohepatic recirculation...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9180966/ https://www.ncbi.nlm.nih.gov/pubmed/35683489 http://dx.doi.org/10.3390/jcm11113102 |
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author | Marasco, Giovanni Cremon, Cesare Barbaro, Maria Raffaella Falangone, Francesca Montanari, Davide Capuani, Federica Mastel, Giada Stanghellini, Vincenzo Barbara, Giovanni |
author_facet | Marasco, Giovanni Cremon, Cesare Barbaro, Maria Raffaella Falangone, Francesca Montanari, Davide Capuani, Federica Mastel, Giada Stanghellini, Vincenzo Barbara, Giovanni |
author_sort | Marasco, Giovanni |
collection | PubMed |
description | Bile acid malabsorption (BAM) represents a common cause of chronic diarrhea whose prevalence is under-investigated. We reviewed the evidence available regarding the pathophysiology and clinical management of bile acid diarrhea (BAD). BAD results from dysregulation of the enterohepatic recirculation of bile acids. It has been estimated that 25–33% of patients with functional diarrhea and irritable bowel syndrome with diarrhea have BAM. Currently, the selenium homotaurocholic acid test is the gold standard for BAD diagnosis and severity assessment. However, it is an expensive method and not widely available. The validation of the utility in the clinical practice of several other serum markers, such as 7α-hydroxy-4-cholesten-3-one (C4) and the fibroblast growth factor 19 (FGF19) is ongoing. The first-line treatment of patients with BAD is bile acid sequestrants. Patients that are refractory to first-line therapy should undergo further diagnostics to confirm the diagnosis and to treat the underlying cause of BAD. An early and correct diagnosis of BAD would improve patient’s quality of life, avoiding additional diagnostic tests that burden health care systems. Considering the limited availability and tolerability of specific medications for BAD treatment, future research is awaited to identify other therapeutic approaches, such as gut microbiota modulating therapies. |
format | Online Article Text |
id | pubmed-9180966 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91809662022-06-10 Pathophysiology and Clinical Management of Bile Acid Diarrhea Marasco, Giovanni Cremon, Cesare Barbaro, Maria Raffaella Falangone, Francesca Montanari, Davide Capuani, Federica Mastel, Giada Stanghellini, Vincenzo Barbara, Giovanni J Clin Med Review Bile acid malabsorption (BAM) represents a common cause of chronic diarrhea whose prevalence is under-investigated. We reviewed the evidence available regarding the pathophysiology and clinical management of bile acid diarrhea (BAD). BAD results from dysregulation of the enterohepatic recirculation of bile acids. It has been estimated that 25–33% of patients with functional diarrhea and irritable bowel syndrome with diarrhea have BAM. Currently, the selenium homotaurocholic acid test is the gold standard for BAD diagnosis and severity assessment. However, it is an expensive method and not widely available. The validation of the utility in the clinical practice of several other serum markers, such as 7α-hydroxy-4-cholesten-3-one (C4) and the fibroblast growth factor 19 (FGF19) is ongoing. The first-line treatment of patients with BAD is bile acid sequestrants. Patients that are refractory to first-line therapy should undergo further diagnostics to confirm the diagnosis and to treat the underlying cause of BAD. An early and correct diagnosis of BAD would improve patient’s quality of life, avoiding additional diagnostic tests that burden health care systems. Considering the limited availability and tolerability of specific medications for BAD treatment, future research is awaited to identify other therapeutic approaches, such as gut microbiota modulating therapies. MDPI 2022-05-30 /pmc/articles/PMC9180966/ /pubmed/35683489 http://dx.doi.org/10.3390/jcm11113102 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Marasco, Giovanni Cremon, Cesare Barbaro, Maria Raffaella Falangone, Francesca Montanari, Davide Capuani, Federica Mastel, Giada Stanghellini, Vincenzo Barbara, Giovanni Pathophysiology and Clinical Management of Bile Acid Diarrhea |
title | Pathophysiology and Clinical Management of Bile Acid Diarrhea |
title_full | Pathophysiology and Clinical Management of Bile Acid Diarrhea |
title_fullStr | Pathophysiology and Clinical Management of Bile Acid Diarrhea |
title_full_unstemmed | Pathophysiology and Clinical Management of Bile Acid Diarrhea |
title_short | Pathophysiology and Clinical Management of Bile Acid Diarrhea |
title_sort | pathophysiology and clinical management of bile acid diarrhea |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9180966/ https://www.ncbi.nlm.nih.gov/pubmed/35683489 http://dx.doi.org/10.3390/jcm11113102 |
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