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The impact of rifaximin on inflammation and metabolism in alcoholic hepatitis: A randomized clinical trial
BACKGROUND AND AIMS: Alcoholic hepatitis (AH) is characterized by acute liver failure, neurocognitive impairment and renal failure. Severe inflammatory reactions are also known to occur in AH. Inflammation and bacterial translocation in the gut are thought to have major impact on disease development...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8920190/ https://www.ncbi.nlm.nih.gov/pubmed/35286322 http://dx.doi.org/10.1371/journal.pone.0264278 |
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author | Kimer, Nina Meldgaard, Mads Hamberg, Ole Kronborg, Thit Mynster Lund, Allan M. Møller, Holger Jon Bendtsen, Flemming Ytting, Henriette |
author_facet | Kimer, Nina Meldgaard, Mads Hamberg, Ole Kronborg, Thit Mynster Lund, Allan M. Møller, Holger Jon Bendtsen, Flemming Ytting, Henriette |
author_sort | Kimer, Nina |
collection | PubMed |
description | BACKGROUND AND AIMS: Alcoholic hepatitis (AH) is characterized by acute liver failure, neurocognitive impairment and renal failure. Severe inflammatory reactions are also known to occur in AH. Inflammation and bacterial translocation in the gut are thought to have major impact on disease development and progression. The mortality rate for AH is close to 50%. We aimed to assess the efficacy of rifaximin in treating AH and its impact on inflammation and metabolism. METHODS: The trial was approved by relevant authorities (EudraCT no: 2014-02264-33, Scientific Ethics Committee, jr. no: H-1-2014-056). Primary outcomes were changes in metabolic and inflammatory markers. Secondary outcomes were portal hypertension, kidney and neurocognitive function. RESULTS: Thirty-two patients were randomized to standard medical therapy (SMT) or SMT plus rifaximin, allocation was concealed. Four patients in the SMT group and five patients in the SMT + rifaximin group died due to AH and liver failure. No adverse events related to the study medication were observed. We found no significant differences in amino acids or inflammation markers (IL-2, IL-6, IL-8, IL-10, TNF-α, interferon-γ) between the groups after 28 and 90 days. CONCLUSION: Rifaximin does not alter inflammation or metabolism in patients with AH. |
format | Online Article Text |
id | pubmed-8920190 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-89201902022-03-15 The impact of rifaximin on inflammation and metabolism in alcoholic hepatitis: A randomized clinical trial Kimer, Nina Meldgaard, Mads Hamberg, Ole Kronborg, Thit Mynster Lund, Allan M. Møller, Holger Jon Bendtsen, Flemming Ytting, Henriette PLoS One Research Article BACKGROUND AND AIMS: Alcoholic hepatitis (AH) is characterized by acute liver failure, neurocognitive impairment and renal failure. Severe inflammatory reactions are also known to occur in AH. Inflammation and bacterial translocation in the gut are thought to have major impact on disease development and progression. The mortality rate for AH is close to 50%. We aimed to assess the efficacy of rifaximin in treating AH and its impact on inflammation and metabolism. METHODS: The trial was approved by relevant authorities (EudraCT no: 2014-02264-33, Scientific Ethics Committee, jr. no: H-1-2014-056). Primary outcomes were changes in metabolic and inflammatory markers. Secondary outcomes were portal hypertension, kidney and neurocognitive function. RESULTS: Thirty-two patients were randomized to standard medical therapy (SMT) or SMT plus rifaximin, allocation was concealed. Four patients in the SMT group and five patients in the SMT + rifaximin group died due to AH and liver failure. No adverse events related to the study medication were observed. We found no significant differences in amino acids or inflammation markers (IL-2, IL-6, IL-8, IL-10, TNF-α, interferon-γ) between the groups after 28 and 90 days. CONCLUSION: Rifaximin does not alter inflammation or metabolism in patients with AH. Public Library of Science 2022-03-14 /pmc/articles/PMC8920190/ /pubmed/35286322 http://dx.doi.org/10.1371/journal.pone.0264278 Text en © 2022 Kimer et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kimer, Nina Meldgaard, Mads Hamberg, Ole Kronborg, Thit Mynster Lund, Allan M. Møller, Holger Jon Bendtsen, Flemming Ytting, Henriette The impact of rifaximin on inflammation and metabolism in alcoholic hepatitis: A randomized clinical trial |
title | The impact of rifaximin on inflammation and metabolism in alcoholic hepatitis: A randomized clinical trial |
title_full | The impact of rifaximin on inflammation and metabolism in alcoholic hepatitis: A randomized clinical trial |
title_fullStr | The impact of rifaximin on inflammation and metabolism in alcoholic hepatitis: A randomized clinical trial |
title_full_unstemmed | The impact of rifaximin on inflammation and metabolism in alcoholic hepatitis: A randomized clinical trial |
title_short | The impact of rifaximin on inflammation and metabolism in alcoholic hepatitis: A randomized clinical trial |
title_sort | impact of rifaximin on inflammation and metabolism in alcoholic hepatitis: a randomized clinical trial |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8920190/ https://www.ncbi.nlm.nih.gov/pubmed/35286322 http://dx.doi.org/10.1371/journal.pone.0264278 |
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