Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kimer, Nina, Meldgaard, Mads, Hamberg, Ole, Kronborg, Thit Mynster, Lund, Allan M., Møller, Holger Jon, Bendtsen, Flemming, Ytting, Henriette
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
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
_version_ 1784669072877682688
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
work_keys_str_mv AT kimernina theimpactofrifaximinoninflammationandmetabolisminalcoholichepatitisarandomizedclinicaltrial
AT meldgaardmads theimpactofrifaximinoninflammationandmetabolisminalcoholichepatitisarandomizedclinicaltrial
AT hambergole theimpactofrifaximinoninflammationandmetabolisminalcoholichepatitisarandomizedclinicaltrial
AT kronborgthitmynster theimpactofrifaximinoninflammationandmetabolisminalcoholichepatitisarandomizedclinicaltrial
AT lundallanm theimpactofrifaximinoninflammationandmetabolisminalcoholichepatitisarandomizedclinicaltrial
AT møllerholgerjon theimpactofrifaximinoninflammationandmetabolisminalcoholichepatitisarandomizedclinicaltrial
AT bendtsenflemming theimpactofrifaximinoninflammationandmetabolisminalcoholichepatitisarandomizedclinicaltrial
AT yttinghenriette theimpactofrifaximinoninflammationandmetabolisminalcoholichepatitisarandomizedclinicaltrial
AT kimernina impactofrifaximinoninflammationandmetabolisminalcoholichepatitisarandomizedclinicaltrial
AT meldgaardmads impactofrifaximinoninflammationandmetabolisminalcoholichepatitisarandomizedclinicaltrial
AT hambergole impactofrifaximinoninflammationandmetabolisminalcoholichepatitisarandomizedclinicaltrial
AT kronborgthitmynster impactofrifaximinoninflammationandmetabolisminalcoholichepatitisarandomizedclinicaltrial
AT lundallanm impactofrifaximinoninflammationandmetabolisminalcoholichepatitisarandomizedclinicaltrial
AT møllerholgerjon impactofrifaximinoninflammationandmetabolisminalcoholichepatitisarandomizedclinicaltrial
AT bendtsenflemming impactofrifaximinoninflammationandmetabolisminalcoholichepatitisarandomizedclinicaltrial
AT yttinghenriette impactofrifaximinoninflammationandmetabolisminalcoholichepatitisarandomizedclinicaltrial