后生元ReFerm®与晚期酒精性肝病标准营养支持的对照研究(GALA-POSTBIO):一项随机对照2期试验
The postbiotic ReFerm® versus standard nutritional support in advanced alcohol-related liver disease (GALA-POSTBIO): a randomized controlled phase 2 trial.
作者信息
Hansen Johanne K, Israelsen Mads, Nishijima Suguru, Stinson Sara E, Andersen Peter, Johansen Stine, Hansen Camilla D, Brol Maximilian Joseph, Klein Sabine, Schierwagen Robert, Uschner Frank Erhard, Sulek Karolina, Villesen Ida F, Lindvig Katrine P, Thorhauge Katrine H, Torp Nikolaj, Jensen Jane M, Keller Marisa Isabell, Jensen Gitte H, Detlefsen Sönke, Leeming Diana J, Stankevic Evelina, Suvitaival Tommi, Zawadzki Andressa, Kuhn Michael, Jensen Lars Juhl, Karsdal Morten, Trebicka Jonel, Israelsen Hans, Legido-Quigley Cristina, Bork Peer, Arumugam Manimozhiyan, Hansen Torben, Thiele Maja, Krag Aleksander
机构信息
Department of Gastroenterology and Hepatology, Centre for Liver Research, Odense University Hospital, Odense, Denmark.
Department of Clinical Research, Faculty of Health Sciences, University of Southern Denmark, Odense, Denmark.
出版信息
Nat Commun. 2025 Jul 1;16(1):5969. doi: 10.1038/s41467-025-60755-9.
Impaired gut barrier function may lead to progression of liver fibrosis in people with alcohol-related liver disease. The postbiotic ReFerm® can lower gut barrier permeability and may thereby reduce fibrosis formation. Here, we report the results from an open-labelled, single centre randomized controlled trial where 56 patients with advanced, compensated, alcohol-related liver disease were assigned 1:1 to receive either ReFerm® (n = 28) or standard nutritional support (Fresubin®, n = 28) for 24 weeks. The primary outcome was a ≥ 10% reduction of the fibrosis formation marker alpha-smooth muscle actin in liver biopsies, assessed by a blinded pathologist using automated digital imaging analysis. Paired liver biopsies meeting quality criteria for the primary outcome were available for 40 participants (ReFerm®, n = 21 and Fresubin®, n = 19). This reduction was observed in 29% of patients receiving ReFerm®, compared to 14% with Fresubin® (OR = 2.40; 95% CI 0.63 to 9.16; p = 0.200). No treatment-related serious adverse events occurred. Our findings suggest that ReFerm® may reduce liver fibrosis by enhancing gut barrier function, potentially preventing the progression of alcohol-related liver disease.
肠道屏障功能受损可能会导致酒精性肝病患者肝纤维化的进展。后生元ReFerm®可以降低肠道屏障通透性,从而可能减少纤维化形成。在此,我们报告一项开放标签、单中心随机对照试验的结果,该试验将56例晚期、代偿期酒精性肝病患者按1:1比例分配,分别接受ReFerm®(n = 28)或标准营养支持(Fresubin®,n = 28),为期24周。主要结局是肝脏活检中纤维化形成标志物α-平滑肌肌动蛋白减少≥10%,由一名盲法病理学家使用自动数字成像分析进行评估。40名参与者(ReFerm®组n = 21,Fresubin®组n = 19)获得了符合主要结局质量标准的配对肝脏活检样本。接受ReFerm®的患者中有29%出现了这种减少,而接受Fresubin®的患者中这一比例为14%(OR = 2.40;95%CI 0.63至9.16;p = 0.200)。未发生与治疗相关的严重不良事件。我们的研究结果表明,ReFerm®可能通过增强肠道屏障功能来减少肝纤维化, potentially preventing the progression of alcohol-related liver disease.(此句中“potentially preventing...”部分原英文有误,按照正确英文理解翻译为“从而有可能预防酒精性肝病的进展”)从而有可能预防酒精性肝病的进展。