Gastro Unit, Medical Division, Amager-Hvidovre University Hospital, Hvidovre, Denmark.
Department of Internal Medicine, Zealand University Hospital, Koege, Denmark.
PLoS One. 2022 Mar 14;17(3):e0264278. doi: 10.1371/journal.pone.0264278. eCollection 2022.
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.
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.
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.
Rifaximin does not alter inflammation or metabolism in patients with AH.
酒精性肝炎(AH)的特征为急性肝功能衰竭、神经认知障碍和肾衰竭。已知严重的炎症反应也会发生在 AH 中。肠道中的炎症和细菌易位被认为对疾病的发展和进展有重大影响。AH 的死亡率接近 50%。我们旨在评估利福昔明治疗 AH 的疗效及其对炎症和代谢的影响。
该试验得到了相关部门的批准(EudraCT 编号:2014-02264-33,科学伦理委员会,jr. 编号:H-1-2014-056)。主要结局指标是代谢和炎症标志物的变化。次要结局指标是门脉高压、肾脏和神经认知功能。
32 名患者被随机分配到标准药物治疗(SMT)或 SMT 加利福昔明组,分配是隐蔽的。SMT 组有 4 名患者和 SMT +利福昔明组有 5 名患者因 AH 和肝功能衰竭而死亡。未观察到与研究药物相关的不良事件。我们发现,在 28 天和 90 天后,两组之间的氨基酸或炎症标志物(IL-2、IL-6、IL-8、IL-10、TNF-α、干扰素-γ)没有显著差异。
利福昔明不能改变 AH 患者的炎症或代谢。