The impact of rifaximin on inflammation and metabolism in alcoholic hepatitis: A randomized clinical trial

被引:21
作者
Kimer, Nina [1 ]
Meldgaard, Mads [2 ]
Hamberg, Ole [2 ,3 ]
Kronborg, Thit Mynster [1 ]
Lund, Allan M. [4 ,5 ]
Moller, Holger Jon [6 ]
Bendtsen, Flemming [1 ]
Ytting, Henriette [1 ,3 ]
机构
[1] Amager Hvidovre Univ Hosp, Med Div, Gastro Unit, Hvidovre, Denmark
[2] Zealand Univ Hosp, Dept Internal Med, Koege, Denmark
[3] Rigshosp, Dept Hepatol & Gastroenterol, Copenhagen, Denmark
[4] Rigshosp, Ctr Inherited Metab Dis, Dept Clin Genet, Copenhagen, Denmark
[5] Rigshosp, Ctr Inherited Metab Dis, Dept Pediat, Copenhagen, Denmark
[6] Aarhus Univ Hosp, Dept Clin Biochem, Aarhus, Denmark
来源
PLOS ONE | 2022年 / 17卷 / 03期
关键词
DECOMPENSATED CIRRHOSIS; BACTERIAL TRANSLOCATION; SCORING SYSTEM; LIVER-INJURY; HEMODYNAMICS; IMPROVES; ENDOTOXEMIA; MECHANISMS; MANAGEMENT; PROGNOSIS;
D O I
10.1371/journal.pone.0264278
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background and aimsAlcoholic 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. MethodsThe 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. ResultsThirty-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-alpha, interferon-gamma) between the groups after 28 and 90 days. ConclusionRifaximin does not alter inflammation or metabolism in patients with AH.
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页数:13
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