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Gut microbiota differs between treatment outcomes early after fecal microbiota transplantation against recurrent Clostridioides difficile infection

In fecal microbiota transplantation (FMT) against recurrent Clostridioides difficile infection (CDI), clinical outcomes are usually determined after 8 weeks. We hypothesized that the intestinal microbiota changes earlier than this timepoint, and analyzed fecal samples obtained 1 week after treatment...

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Autores principales: Wei, Shaodong, Bahl, Martin Iain, Baunwall, Simon Mark Dahl, Dahlerup, Jens Frederik, Hvas, Christian Lodberg, Licht, Tine Rask
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176232/
https://www.ncbi.nlm.nih.gov/pubmed/36519447
http://dx.doi.org/10.1080/19490976.2022.2084306
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author Wei, Shaodong
Bahl, Martin Iain
Baunwall, Simon Mark Dahl
Dahlerup, Jens Frederik
Hvas, Christian Lodberg
Licht, Tine Rask
author_facet Wei, Shaodong
Bahl, Martin Iain
Baunwall, Simon Mark Dahl
Dahlerup, Jens Frederik
Hvas, Christian Lodberg
Licht, Tine Rask
author_sort Wei, Shaodong
collection PubMed
description In fecal microbiota transplantation (FMT) against recurrent Clostridioides difficile infection (CDI), clinical outcomes are usually determined after 8 weeks. We hypothesized that the intestinal microbiota changes earlier than this timepoint, and analyzed fecal samples obtained 1 week after treatment from 64 patients diagnosed with recurrent CDI and included in a randomized clinical trial, where the infection was treated with either vancomycin-preceded FMT (N = 24), vancomycin (N = 16) or fidaxomicin (N = 24). In comparison with non-responders, patients with sustained resolution after FMT had increased microbial alpha diversity, enrichment of Ruminococcaceae and Lachnospiraceae, depletion of Enterobacteriaceae, more pronounced donor microbiota engraftment, and resolution of gut microbiota dysbiosis. We found that a constructed index, based on markers for the identified genera Escherichia and Blautia, successfully predicted clinical outcomes at Week 8, which exemplifies a way to utilize clinically feasible methods to predict treatment failure. Microbiota changes were restricted to patients who received FMT rather than antibiotic monotherapy, indicating that FMT confers treatment response in a different way than antibiotics. We suggest that early identification of microbial community structures after FMT is of clinical value to predict response to the treatment.
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spelling pubmed-91762322022-06-09 Gut microbiota differs between treatment outcomes early after fecal microbiota transplantation against recurrent Clostridioides difficile infection Wei, Shaodong Bahl, Martin Iain Baunwall, Simon Mark Dahl Dahlerup, Jens Frederik Hvas, Christian Lodberg Licht, Tine Rask Gut Microbes Research Paper In fecal microbiota transplantation (FMT) against recurrent Clostridioides difficile infection (CDI), clinical outcomes are usually determined after 8 weeks. We hypothesized that the intestinal microbiota changes earlier than this timepoint, and analyzed fecal samples obtained 1 week after treatment from 64 patients diagnosed with recurrent CDI and included in a randomized clinical trial, where the infection was treated with either vancomycin-preceded FMT (N = 24), vancomycin (N = 16) or fidaxomicin (N = 24). In comparison with non-responders, patients with sustained resolution after FMT had increased microbial alpha diversity, enrichment of Ruminococcaceae and Lachnospiraceae, depletion of Enterobacteriaceae, more pronounced donor microbiota engraftment, and resolution of gut microbiota dysbiosis. We found that a constructed index, based on markers for the identified genera Escherichia and Blautia, successfully predicted clinical outcomes at Week 8, which exemplifies a way to utilize clinically feasible methods to predict treatment failure. Microbiota changes were restricted to patients who received FMT rather than antibiotic monotherapy, indicating that FMT confers treatment response in a different way than antibiotics. We suggest that early identification of microbial community structures after FMT is of clinical value to predict response to the treatment. Taylor & Francis 2022-06-05 /pmc/articles/PMC9176232/ /pubmed/36519447 http://dx.doi.org/10.1080/19490976.2022.2084306 Text en © 2022 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Wei, Shaodong
Bahl, Martin Iain
Baunwall, Simon Mark Dahl
Dahlerup, Jens Frederik
Hvas, Christian Lodberg
Licht, Tine Rask
Gut microbiota differs between treatment outcomes early after fecal microbiota transplantation against recurrent Clostridioides difficile infection
title Gut microbiota differs between treatment outcomes early after fecal microbiota transplantation against recurrent Clostridioides difficile infection
title_full Gut microbiota differs between treatment outcomes early after fecal microbiota transplantation against recurrent Clostridioides difficile infection
title_fullStr Gut microbiota differs between treatment outcomes early after fecal microbiota transplantation against recurrent Clostridioides difficile infection
title_full_unstemmed Gut microbiota differs between treatment outcomes early after fecal microbiota transplantation against recurrent Clostridioides difficile infection
title_short Gut microbiota differs between treatment outcomes early after fecal microbiota transplantation against recurrent Clostridioides difficile infection
title_sort gut microbiota differs between treatment outcomes early after fecal microbiota transplantation against recurrent clostridioides difficile infection
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9176232/
https://www.ncbi.nlm.nih.gov/pubmed/36519447
http://dx.doi.org/10.1080/19490976.2022.2084306
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