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原发性硬化性胆管炎粪便微生物群移植(FARGO):一项随机、多中心、IIa期、安慰剂对照试验的研究方案

FAecal micRobiota transplantation in primary sclerosinG chOlangitis (FARGO): study protocol for a randomised, multicentre, phase IIa, placebo-controlled trial.

作者信息

Al-Shakhshir Sarah, Quraishi Mohammed Nabil, Mullish Benjamin, Patel Arzoo, Vince Alexandra, Rowe Anna, Homer Victoria, Jackson Nicola, Gyimah Derick, Shabir Sahida, Manzoor Susan, Cooney Rachel, Alrubaiy Laith, Quince Christopher, van Schaik Willem, Hares Miriam, Beggs Andrew D, Efstathiou Elena, Rimmer Peter, Weston Chris, Iqbal Tariq, Trivedi Palak J

机构信息

National Institute of Health and Care Research (NIHR) Birmingham Biomedical Research Centre (BRC) Center for Liver and Gastrointestinal Research, University of Birmingham, Birmingham, England, UK.

University Hospitals Birmingham NHS Foundation Trust, Birmingham, UK.

出版信息

BMJ Open. 2025 Jan 6;15(1):e095392. doi: 10.1136/bmjopen-2024-095392.

Abstract

INTRODUCTION

Primary sclerosing cholangitis (PSC) is the classical hepatobiliary manifestation of inflammatory bowel disease (IBD). The strong association between gut and liver inflammation has driven several pathogenic hypotheses to which the intestinal microbiome is proposed to contribute. Pilot studies of faecal microbiota transplantation (FMT) in PSC and IBD are demonstrated to be safe and associated with increased gut bacterial diversity. However, the longevity of such changes and the impact on markers of disease activity and disease progression have not been studied. The aim of this clinical trial is to determine the effects of repeated FMT as a treatment for PSC-IBD.

METHODS AND ANALYSIS

FAecal micRobiota transplantation in primary sclerosinG chOlangitis (FARGO) is a phase IIa randomised placebo-controlled trial to assess the efficacy and safety of repeated colonic administration of FMT in patients with non-cirrhotic PSC-IBD. Fifty-eight patients will be recruited from six sites across England and randomised in a 1:1 ratio between active FMT or FMT placebo arms. FMT will be manufactured by the University of Birmingham Microbiome Treatment Centre, using stool collected from rigorously screened healthy donors. A total of 8 weekly treatments will be delivered; the first through colonoscopic administration (week 1) and the remaining seven via once-weekly enema (up to week 8). Participants will then be followed on a 12-weekly basis until week 48 from the first treatment visit. The primary efficacy outcome will be to determine the effect of FMT on serum alkaline phosphatase values over time (end of study at 48 weeks). Key secondary outcomes will be to evaluate the impact of FMT on other liver biochemical parameters, PSC risk scores, circulating and imaging markers of liver fibrosis, health-related quality of life measures, IBD activity and the incidence of PSC-related clinical events. Key translational objectives will be to identify mucosal metagenomic, metatranscriptomic, metabolomic and immunological pathways associated with the administration of FMT.

ETHICS AND DISSEMINATION

The protocol was approved by the South Central-Hampshire B Research Ethics Committee (REC 23/SC/0147). Participants will be required to provide written informed consent. The results of this trial will be disseminated through national and international presentations and peer-reviewed publications.

TRIAL REGISTRATION NUMBER

The trial was registered at ClinicalTrials.gov on 23 February 2024 (NCT06286709). Weblink: Study Details | FAecal Microbiota Transplantation in primaRy sclerosinG chOlangitis | ClinicalTrials.gov.

摘要

引言

原发性硬化性胆管炎(PSC)是炎症性肠病(IBD)的典型肝胆表现。肠道与肝脏炎症之间的密切关联催生了多种致病假说,其中提出肠道微生物群也参与其中。粪便微生物群移植(FMT)在PSC和IBD中的初步研究表明是安全的,并且与肠道细菌多样性增加有关。然而,这种变化的持久性以及对疾病活动标志物和疾病进展的影响尚未得到研究。本临床试验的目的是确定重复进行FMT作为PSC-IBD治疗方法的效果。

方法与分析

原发性硬化性胆管炎粪便微生物群移植(FARGO)是一项IIa期随机安慰剂对照试验,旨在评估对非肝硬化PSC-IBD患者重复进行结肠内FMT给药的疗效和安全性。将从英格兰的六个地点招募58名患者,并以1:1的比例随机分配至活性FMT组或FMT安慰剂组。FMT将由伯明翰大学微生物组治疗中心生产,使用从经过严格筛选的健康供体收集的粪便。总共将进行8次每周一次的治疗;第一次通过结肠镜给药(第1周),其余7次通过每周一次灌肠(直至第8周)。然后,参与者将每12周接受一次随访,直至首次治疗访视后的第48周。主要疗效指标将是确定FMT随时间推移对血清碱性磷酸酶值的影响(研究结束时为48周)。关键次要指标将是评估FMT对其他肝脏生化参数、PSC风险评分、肝纤维化的循环和影像学标志物、健康相关生活质量指标、IBD活动以及PSC相关临床事件发生率的影响。关键转化目标将是确定与FMT给药相关的黏膜宏基因组、宏转录组、代谢组和免疫途径。

伦理与传播

该方案已获得中南汉普郡B研究伦理委员会(REC 23/SC/0147)的批准。参与者将被要求提供书面知情同意书。本试验的结果将通过国内和国际会议报告以及同行评审出版物进行传播。

试验注册号

该试验于2024年2月23日在ClinicalTrials.gov注册(NCT06286709)。网址:研究详情 | 原发性硬化性胆管炎粪便微生物群移植 | ClinicalTrials.gov 。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc2f/11749870/6508bc2a8329/bmjopen-15-1-g001.jpg

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