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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...

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Autores principales: Marasco, Giovanni, Cremon, Cesare, Barbaro, Maria Raffaella, Falangone, Francesca, Montanari, Davide, Capuani, Federica, Mastel, Giada, Stanghellini, Vincenzo, Barbara, Giovanni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
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.
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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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