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Dysbiosis-Associated Polyposis of the Colon—Cap Polyposis

Cap polyposis is a rare gastrointestinal disease characterized by multiple inflammatory polyps located between the distal colon and the rectum. Despite the lack of clarity regarding its pathogenesis, mucosal prolapse, chronic inflammatory responses, and Helicobacter pylori infection are considered k...

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Autores principales: Okamoto, Kazuki, Watanabe, Tomohiro, Komeda, Yoriaki, Okamoto, Ayana, Minaga, Kosuke, Kamata, Ken, Yamao, Kentaro, Takenaka, Mamoru, Hagiwara, Satoru, Sakurai, Toshiharu, Tanaka, Tomonori, Sakamoto, Hiroki, Fujimoto, Kiyoshige, Nishida, Naoshi, Kudo, Masatoshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5949673/
https://www.ncbi.nlm.nih.gov/pubmed/29867933
http://dx.doi.org/10.3389/fimmu.2018.00918
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author Okamoto, Kazuki
Watanabe, Tomohiro
Komeda, Yoriaki
Okamoto, Ayana
Minaga, Kosuke
Kamata, Ken
Yamao, Kentaro
Takenaka, Mamoru
Hagiwara, Satoru
Sakurai, Toshiharu
Tanaka, Tomonori
Sakamoto, Hiroki
Fujimoto, Kiyoshige
Nishida, Naoshi
Kudo, Masatoshi
author_facet Okamoto, Kazuki
Watanabe, Tomohiro
Komeda, Yoriaki
Okamoto, Ayana
Minaga, Kosuke
Kamata, Ken
Yamao, Kentaro
Takenaka, Mamoru
Hagiwara, Satoru
Sakurai, Toshiharu
Tanaka, Tomonori
Sakamoto, Hiroki
Fujimoto, Kiyoshige
Nishida, Naoshi
Kudo, Masatoshi
author_sort Okamoto, Kazuki
collection PubMed
description Cap polyposis is a rare gastrointestinal disease characterized by multiple inflammatory polyps located between the distal colon and the rectum. Despite the lack of clarity regarding its pathogenesis, mucosal prolapse, chronic inflammatory responses, and Helicobacter pylori infection are considered key contributors to the development of this disease entity. Although it is now generally accepted that dysbiosis of gut microbiota is associated with intestinal and extra-intestinal diseases, alterations of intestinal microbiota have been poorly defined in cap polyposis. Here, we report a patient with H. pylori-negative cap polyposis who was successfully treated with antibiotics and exhibited dramatic alterations in intestinal microbiota composition after antibiotic treatment. The patient was treated with oral administration of ampicillin and metronidazole and showed regression of cap polyposis 6 months after antibiotic treatment. Fecal microbiota analysis using the next-generation sequencing technology revealed a significant alteration in the intestinal microbiota composition following antibiotic treatment—a marked reduction of Blautia, Dorea, and Sutterella was observed concomitant with a marked increase in Fusobacterium. These data suggest that cap polyposis may originate from dysbiosis and that microbiome-targeted therapy may be useful in this disorder.
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spelling pubmed-59496732018-06-04 Dysbiosis-Associated Polyposis of the Colon—Cap Polyposis Okamoto, Kazuki Watanabe, Tomohiro Komeda, Yoriaki Okamoto, Ayana Minaga, Kosuke Kamata, Ken Yamao, Kentaro Takenaka, Mamoru Hagiwara, Satoru Sakurai, Toshiharu Tanaka, Tomonori Sakamoto, Hiroki Fujimoto, Kiyoshige Nishida, Naoshi Kudo, Masatoshi Front Immunol Immunology Cap polyposis is a rare gastrointestinal disease characterized by multiple inflammatory polyps located between the distal colon and the rectum. Despite the lack of clarity regarding its pathogenesis, mucosal prolapse, chronic inflammatory responses, and Helicobacter pylori infection are considered key contributors to the development of this disease entity. Although it is now generally accepted that dysbiosis of gut microbiota is associated with intestinal and extra-intestinal diseases, alterations of intestinal microbiota have been poorly defined in cap polyposis. Here, we report a patient with H. pylori-negative cap polyposis who was successfully treated with antibiotics and exhibited dramatic alterations in intestinal microbiota composition after antibiotic treatment. The patient was treated with oral administration of ampicillin and metronidazole and showed regression of cap polyposis 6 months after antibiotic treatment. Fecal microbiota analysis using the next-generation sequencing technology revealed a significant alteration in the intestinal microbiota composition following antibiotic treatment—a marked reduction of Blautia, Dorea, and Sutterella was observed concomitant with a marked increase in Fusobacterium. These data suggest that cap polyposis may originate from dysbiosis and that microbiome-targeted therapy may be useful in this disorder. Frontiers Media S.A. 2018-05-07 /pmc/articles/PMC5949673/ /pubmed/29867933 http://dx.doi.org/10.3389/fimmu.2018.00918 Text en Copyright © 2018 Okamoto, Watanabe, Komeda, Okamoto, Minaga, Kamata, Yamao, Takenaka, Hagiwara, Sakurai, Tanaka, Sakamoto, Fujimoto, Nishida and Kudo. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Okamoto, Kazuki
Watanabe, Tomohiro
Komeda, Yoriaki
Okamoto, Ayana
Minaga, Kosuke
Kamata, Ken
Yamao, Kentaro
Takenaka, Mamoru
Hagiwara, Satoru
Sakurai, Toshiharu
Tanaka, Tomonori
Sakamoto, Hiroki
Fujimoto, Kiyoshige
Nishida, Naoshi
Kudo, Masatoshi
Dysbiosis-Associated Polyposis of the Colon—Cap Polyposis
title Dysbiosis-Associated Polyposis of the Colon—Cap Polyposis
title_full Dysbiosis-Associated Polyposis of the Colon—Cap Polyposis
title_fullStr Dysbiosis-Associated Polyposis of the Colon—Cap Polyposis
title_full_unstemmed Dysbiosis-Associated Polyposis of the Colon—Cap Polyposis
title_short Dysbiosis-Associated Polyposis of the Colon—Cap Polyposis
title_sort dysbiosis-associated polyposis of the colon—cap polyposis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5949673/
https://www.ncbi.nlm.nih.gov/pubmed/29867933
http://dx.doi.org/10.3389/fimmu.2018.00918
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