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Gut fermentation syndrome: A systematic review of case reports
BACKGROUND: The gut fermentation syndrome (GFS), also known as the endogenous alcohol fermentation syndrome or auto brewery syndrome, is a rare and underdiagnosed medical condition where consumed carbohydrates are converted to alcohol by the microbiota in the gastrointestinal or urinary tract. The s...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8259373/ https://www.ncbi.nlm.nih.gov/pubmed/33887125 http://dx.doi.org/10.1002/ueg2.12062 |
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author | Bayoumy, Ahmed B. Mulder, Chris J. J. Mol, Jaap J. Tushuizen, Maarten E. |
author_facet | Bayoumy, Ahmed B. Mulder, Chris J. J. Mol, Jaap J. Tushuizen, Maarten E. |
author_sort | Bayoumy, Ahmed B. |
collection | PubMed |
description | BACKGROUND: The gut fermentation syndrome (GFS), also known as the endogenous alcohol fermentation syndrome or auto brewery syndrome, is a rare and underdiagnosed medical condition where consumed carbohydrates are converted to alcohol by the microbiota in the gastrointestinal or urinary tract. The symptoms of GFS can have severe impact on patients' wellbeing and can have social and legal consequences. Unfortunately, not much is reported about GFS. The aim of this systematic review was to assess the evidence for GFS, causal micro‐organisms, diagnostics, and possible treatments. METHODS: A protocol was developed prior to initiation of the systematic review (PROSPERO 207182). We performed a literature search for clinical studies on 1 September 2020 using PubMed and Embase. We included all clinical studies, including case reports that described the GFS. RESULTS: In total, 17 case reports were included, consisting of 20 patients diagnosed with GFS. The species that caused the GFS included Klebsiella pneumoniae, Candida albicans, C. glabrata, Saccharomyces cerevisiae, C. intermedia, C. parapsilosis, and C. kefyr. CONCLUSIONS: GFS is a rare but underdiagnosed disease in daily practice. The disease is mostly reported by Saccharomyces and Candida genera, and some cases were previously treated with antibiotics. Studies in Nonalcoholic Fatty Liver disease suggest a bacterial origin of endogenous alcohol‐production, which might also be causal micro‐organisms in GFS. Current treatments for GFS include antibiotics, antifungal medication, low carbohydrate diet, and probiotics. There might be a potential role of fecal microbiota transplant in the treatment of GFS. |
format | Online Article Text |
id | pubmed-8259373 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82593732021-07-12 Gut fermentation syndrome: A systematic review of case reports Bayoumy, Ahmed B. Mulder, Chris J. J. Mol, Jaap J. Tushuizen, Maarten E. United European Gastroenterol J Neurogastroenterology BACKGROUND: The gut fermentation syndrome (GFS), also known as the endogenous alcohol fermentation syndrome or auto brewery syndrome, is a rare and underdiagnosed medical condition where consumed carbohydrates are converted to alcohol by the microbiota in the gastrointestinal or urinary tract. The symptoms of GFS can have severe impact on patients' wellbeing and can have social and legal consequences. Unfortunately, not much is reported about GFS. The aim of this systematic review was to assess the evidence for GFS, causal micro‐organisms, diagnostics, and possible treatments. METHODS: A protocol was developed prior to initiation of the systematic review (PROSPERO 207182). We performed a literature search for clinical studies on 1 September 2020 using PubMed and Embase. We included all clinical studies, including case reports that described the GFS. RESULTS: In total, 17 case reports were included, consisting of 20 patients diagnosed with GFS. The species that caused the GFS included Klebsiella pneumoniae, Candida albicans, C. glabrata, Saccharomyces cerevisiae, C. intermedia, C. parapsilosis, and C. kefyr. CONCLUSIONS: GFS is a rare but underdiagnosed disease in daily practice. The disease is mostly reported by Saccharomyces and Candida genera, and some cases were previously treated with antibiotics. Studies in Nonalcoholic Fatty Liver disease suggest a bacterial origin of endogenous alcohol‐production, which might also be causal micro‐organisms in GFS. Current treatments for GFS include antibiotics, antifungal medication, low carbohydrate diet, and probiotics. There might be a potential role of fecal microbiota transplant in the treatment of GFS. John Wiley and Sons Inc. 2021-04-22 /pmc/articles/PMC8259373/ /pubmed/33887125 http://dx.doi.org/10.1002/ueg2.12062 Text en © 2021 The Authors. United European Gastroenterology Journal published by Wiley Periodicals LLC. on behalf of United European Gastroenterology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Neurogastroenterology Bayoumy, Ahmed B. Mulder, Chris J. J. Mol, Jaap J. Tushuizen, Maarten E. Gut fermentation syndrome: A systematic review of case reports |
title | Gut fermentation syndrome: A systematic review of case reports |
title_full | Gut fermentation syndrome: A systematic review of case reports |
title_fullStr | Gut fermentation syndrome: A systematic review of case reports |
title_full_unstemmed | Gut fermentation syndrome: A systematic review of case reports |
title_short | Gut fermentation syndrome: A systematic review of case reports |
title_sort | gut fermentation syndrome: a systematic review of case reports |
topic | Neurogastroenterology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8259373/ https://www.ncbi.nlm.nih.gov/pubmed/33887125 http://dx.doi.org/10.1002/ueg2.12062 |
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