Cui Bota, Feng Qiang, Wang Honggang, Wang Min, Peng Zhaoyuan, Li Pan, Huang Guangming, Liu Zheng, Wu Ping, Fan Zhining, Ji Guozhong, Wang Xin, Wu Kaichun, Fan Daiming, Zhang Faming
Medical Center for Digestive Diseases, the Second Affiliated Hospital of Nanjing Medical University, Nanjing, China.
J Gastroenterol Hepatol. 2015 Jan;30(1):51-8. doi: 10.1111/jgh.12727.
The gut microbiota plays a pivotal role in the intestinal diseases. Fecal microbiota transplantation (FMT) might be a rescue therapy for refractory inflammatory bowel disease. This study aimed to evaluate the safety, feasibility, and efficacy of FMT through mid-gut for refractory Crohn's disease (CD).
We established standardized laboratory protocol and clinical work flow for FMT. Only refractory CD patients with Harvey-Bradshaw Index (HBI) score ≥ 7 were enrolled for this study. All included patients were treated with single FMT through mid-gut and assessed during follow-up.
Metagenomics analysis showed a high concordance between feces sample and purified fecal microbiota from same donors. Standardized fecal microbiota preparation and clinical flow significantly simplified the practical aspects of FMT. Totally, 30 patients were qualified for the present analysis. The rate of clinical improvement and remission based on clinical activity at the first month was 86.7% (26/30) and 76.7% (23/30), respectively, which was higher than other assessment points within 15-month follow-up. Patients' body weight increased after FMT, and the lipid profile improved as well. FMT also showed a fast and continuous significant effect in relieving the sustaining abdominal pain associated with sustaining CD.
This is a pilot study with the largest sample of patients with refractory CD who underwent single FMT. The results demonstrated that FMT through mid-gut might be a safe, feasible, and efficient rescue therapy for refractory CD.
肠道微生物群在肠道疾病中起关键作用。粪便微生物群移植(FMT)可能是难治性炎症性肠病的一种挽救疗法。本研究旨在评估经中肠进行FMT治疗难治性克罗恩病(CD)的安全性、可行性和疗效。
我们建立了FMT的标准化实验室方案和临床工作流程。本研究仅纳入哈维-布拉德肖指数(HBI)评分≥7的难治性CD患者。所有纳入患者均接受单次经中肠FMT治疗,并在随访期间进行评估。
宏基因组学分析显示粪便样本与来自同一供体的纯化粪便微生物群之间具有高度一致性。标准化的粪便微生物群制备和临床流程显著简化了FMT的实际操作。共有30例患者符合本分析标准。基于第一个月临床活动的临床改善率和缓解率分别为86.7%(26/30)和76.7%(23/30),高于15个月随访期内的其他评估点。FMT后患者体重增加,血脂情况也有所改善。FMT在缓解与持续性CD相关的持续性腹痛方面也显示出快速且持续的显著效果。
这是一项针对接受单次FMT的难治性CD患者样本量最大的试点研究。结果表明,经中肠FMT可能是难治性CD一种安全、可行且有效的挽救疗法。