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Celiac Disease and Gallbladder: Pathophysiological Aspects and Clinical Issues

Background: Celiac Disease (CD) is an immune-mediated disorder which primarily affects the small intestine; however, extra-intestinal organs are often affected by the pathological process, too. As regards the digestive system, liver alterations in CD patients have been widely described, which can al...

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Autores principales: Poddighe, Dimitri, Dossybayeva, Kuanysh, Abdukhakimova, Diyora, Akhmaltdinova, Lyudmila, Ibrayeva, Aigul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612360/
https://www.ncbi.nlm.nih.gov/pubmed/36297063
http://dx.doi.org/10.3390/nu14204379
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author Poddighe, Dimitri
Dossybayeva, Kuanysh
Abdukhakimova, Diyora
Akhmaltdinova, Lyudmila
Ibrayeva, Aigul
author_facet Poddighe, Dimitri
Dossybayeva, Kuanysh
Abdukhakimova, Diyora
Akhmaltdinova, Lyudmila
Ibrayeva, Aigul
author_sort Poddighe, Dimitri
collection PubMed
description Background: Celiac Disease (CD) is an immune-mediated disorder which primarily affects the small intestine; however, extra-intestinal organs are often affected by the pathological process, too. As regards the digestive system, liver alterations in CD patients have been widely described, which can also extend to the biliary tract. Notably, gallbladder function can be altered in CD patients. In this review, we specifically analyze and summarize the main pathophysiological aspects and clinical evidence of gallbladder dysfunction in CD patients, in order to discuss the potential medical complications and clinical research gaps. In addition to some perturbations of bile composition, CD patients can develop gallbladder dysmotility, which mainly expresses with an impaired emptying during the digestive phase. The main pathophysiological determinant is a perturbation of cholecystokinin secretion by the specific duodenal enteroendocrine cells in response to the appropriate nutrient stimulation in CD patients. This situation appears to be reversible with a gluten-free diet in most cases. Despite this gallbladder impairment, CD patients do not seem to be more predisposed to gallbladder complications, such as calculous and acalculous cholecystitis. However, very few clinical studies have actively investigated these clinical aspects, which may not be completely evidenced so far; alternatively, the substantial improvements in the last two decades regarding CD diagnosis, which have reduced the diagnostic delay (and related dietary treatment), may have lessened the potential clinical consequences of CD-related gallbladder dysfunction. Specific clinical studies focused on these aspects are needed for a better understanding of the clinical implications of gallbladder alterations in CD patients.
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spelling pubmed-96123602022-10-28 Celiac Disease and Gallbladder: Pathophysiological Aspects and Clinical Issues Poddighe, Dimitri Dossybayeva, Kuanysh Abdukhakimova, Diyora Akhmaltdinova, Lyudmila Ibrayeva, Aigul Nutrients Review Background: Celiac Disease (CD) is an immune-mediated disorder which primarily affects the small intestine; however, extra-intestinal organs are often affected by the pathological process, too. As regards the digestive system, liver alterations in CD patients have been widely described, which can also extend to the biliary tract. Notably, gallbladder function can be altered in CD patients. In this review, we specifically analyze and summarize the main pathophysiological aspects and clinical evidence of gallbladder dysfunction in CD patients, in order to discuss the potential medical complications and clinical research gaps. In addition to some perturbations of bile composition, CD patients can develop gallbladder dysmotility, which mainly expresses with an impaired emptying during the digestive phase. The main pathophysiological determinant is a perturbation of cholecystokinin secretion by the specific duodenal enteroendocrine cells in response to the appropriate nutrient stimulation in CD patients. This situation appears to be reversible with a gluten-free diet in most cases. Despite this gallbladder impairment, CD patients do not seem to be more predisposed to gallbladder complications, such as calculous and acalculous cholecystitis. However, very few clinical studies have actively investigated these clinical aspects, which may not be completely evidenced so far; alternatively, the substantial improvements in the last two decades regarding CD diagnosis, which have reduced the diagnostic delay (and related dietary treatment), may have lessened the potential clinical consequences of CD-related gallbladder dysfunction. Specific clinical studies focused on these aspects are needed for a better understanding of the clinical implications of gallbladder alterations in CD patients. MDPI 2022-10-19 /pmc/articles/PMC9612360/ /pubmed/36297063 http://dx.doi.org/10.3390/nu14204379 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
Poddighe, Dimitri
Dossybayeva, Kuanysh
Abdukhakimova, Diyora
Akhmaltdinova, Lyudmila
Ibrayeva, Aigul
Celiac Disease and Gallbladder: Pathophysiological Aspects and Clinical Issues
title Celiac Disease and Gallbladder: Pathophysiological Aspects and Clinical Issues
title_full Celiac Disease and Gallbladder: Pathophysiological Aspects and Clinical Issues
title_fullStr Celiac Disease and Gallbladder: Pathophysiological Aspects and Clinical Issues
title_full_unstemmed Celiac Disease and Gallbladder: Pathophysiological Aspects and Clinical Issues
title_short Celiac Disease and Gallbladder: Pathophysiological Aspects and Clinical Issues
title_sort celiac disease and gallbladder: pathophysiological aspects and clinical issues
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9612360/
https://www.ncbi.nlm.nih.gov/pubmed/36297063
http://dx.doi.org/10.3390/nu14204379
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