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Evaluation of gut dysbiosis using serum and fecal bile acid profiles
Dysbiosis in the intestinal microflora can affect the gut production of microbial metabolites, and toxic substances can disrupt the barrier function of the intestinal wall, leading to the development of various diseases. Decreased levels of Clostridium subcluster XIVa (XIVa) are associated with the...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Baishideng Publishing Group Inc
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791502/ https://www.ncbi.nlm.nih.gov/pubmed/36579096 http://dx.doi.org/10.12998/wjcc.v10.i34.12484 |
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author | Monma, Tadakuni Iwamoto, Junichi Ueda, Hajime Tamamushi, Makoto Kakizaki, Fumio Konishi, Naoki Yara, Shoichiro Miyazaki, Teruo Hirayama, Takeshi Ikegami, Tadashi Honda, Akira |
author_facet | Monma, Tadakuni Iwamoto, Junichi Ueda, Hajime Tamamushi, Makoto Kakizaki, Fumio Konishi, Naoki Yara, Shoichiro Miyazaki, Teruo Hirayama, Takeshi Ikegami, Tadashi Honda, Akira |
author_sort | Monma, Tadakuni |
collection | PubMed |
description | Dysbiosis in the intestinal microflora can affect the gut production of microbial metabolites, and toxic substances can disrupt the barrier function of the intestinal wall, leading to the development of various diseases. Decreased levels of Clostridium subcluster XIVa (XIVa) are associated with the intestinal dysbiosis found in inflammatory bowel disease (IBD) and Clostridium difficile infection (CDI). Since XIVa is a bacterial group responsible for the conversion of primary bile acids (BAs) to secondary BAs, the proportion of intestinal XIVa can be predicted by determining the ratio of deoxycholic acid (DCA)/[DCA + cholic acid (CA)] in feces orserum. For example, serum DCA/(DCA+CA) was significantly lower in IBD patients than in healthy controls, even in the remission period. These results suggest that a low proportion of intestinal XIVa in IBD patients might be a precondition for IBD onset but not a consequence of intestinal inflammation. Another report showed that a reduced serum DCA/(DCA + CA) ratio could predict susceptibility to CDI. Thus, the BA profile, particularly the ratio of secondary to primary BAs, can serve as a surrogate marker of the intestinal dysbiosis caused by decreased XIVa. |
format | Online Article Text |
id | pubmed-9791502 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-97915022022-12-27 Evaluation of gut dysbiosis using serum and fecal bile acid profiles Monma, Tadakuni Iwamoto, Junichi Ueda, Hajime Tamamushi, Makoto Kakizaki, Fumio Konishi, Naoki Yara, Shoichiro Miyazaki, Teruo Hirayama, Takeshi Ikegami, Tadashi Honda, Akira World J Clin Cases Minireviews Dysbiosis in the intestinal microflora can affect the gut production of microbial metabolites, and toxic substances can disrupt the barrier function of the intestinal wall, leading to the development of various diseases. Decreased levels of Clostridium subcluster XIVa (XIVa) are associated with the intestinal dysbiosis found in inflammatory bowel disease (IBD) and Clostridium difficile infection (CDI). Since XIVa is a bacterial group responsible for the conversion of primary bile acids (BAs) to secondary BAs, the proportion of intestinal XIVa can be predicted by determining the ratio of deoxycholic acid (DCA)/[DCA + cholic acid (CA)] in feces orserum. For example, serum DCA/(DCA+CA) was significantly lower in IBD patients than in healthy controls, even in the remission period. These results suggest that a low proportion of intestinal XIVa in IBD patients might be a precondition for IBD onset but not a consequence of intestinal inflammation. Another report showed that a reduced serum DCA/(DCA + CA) ratio could predict susceptibility to CDI. Thus, the BA profile, particularly the ratio of secondary to primary BAs, can serve as a surrogate marker of the intestinal dysbiosis caused by decreased XIVa. Baishideng Publishing Group Inc 2022-12-06 2022-12-06 /pmc/articles/PMC9791502/ /pubmed/36579096 http://dx.doi.org/10.12998/wjcc.v10.i34.12484 Text en ©The Author(s) 2022. Published by Baishideng Publishing Group Inc. All rights reserved. https://creativecommons.org/licenses/by-nc/4.0/This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. |
spellingShingle | Minireviews Monma, Tadakuni Iwamoto, Junichi Ueda, Hajime Tamamushi, Makoto Kakizaki, Fumio Konishi, Naoki Yara, Shoichiro Miyazaki, Teruo Hirayama, Takeshi Ikegami, Tadashi Honda, Akira Evaluation of gut dysbiosis using serum and fecal bile acid profiles |
title | Evaluation of gut dysbiosis using serum and fecal bile acid profiles |
title_full | Evaluation of gut dysbiosis using serum and fecal bile acid profiles |
title_fullStr | Evaluation of gut dysbiosis using serum and fecal bile acid profiles |
title_full_unstemmed | Evaluation of gut dysbiosis using serum and fecal bile acid profiles |
title_short | Evaluation of gut dysbiosis using serum and fecal bile acid profiles |
title_sort | evaluation of gut dysbiosis using serum and fecal bile acid profiles |
topic | Minireviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9791502/ https://www.ncbi.nlm.nih.gov/pubmed/36579096 http://dx.doi.org/10.12998/wjcc.v10.i34.12484 |
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