Mizuno Shinta, Nanki Kosaku, Matsuoka Katsuyoshi, Saigusa Keiichiro, Ono Keiko, Arai Mari, Sugimoto Shinya, Kiyohara Hiroki, Nakashima Moeko, Takeshita Kozue, Naganuma Makoto, Suda Wataru, Hattori Masahira, Kanai Takanori
Division of Gastroenterology and Hepatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.
Division of Gastroenterology and Hepatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan.; Department of Immunology, Keio University School of Medicine, Tokyo, Japan.
Intest Res. 2017 Jan;15(1):68-74. doi: 10.5217/ir.2017.15.1.68. Epub 2017 Jan 31.
BACKGROUND/AIMS: Recent developments in analytical techniques including next-generation sequencing have clarified the correlation between intestinal microbiota and inflammatory bowel disease. Fecal microbiota transplantation (FMT) for patients with ulcerative colitis (UC) is proposed as a potential approach to resolving their dysbiosis; however, its safety and efficacy have not been confirmed. This single-arm, open-label, non-randomized study aimed to evaluate the safety and efficacy of FMT for Japanese patients with UC as the first registered clinical trial in Japan. METHODS: We enrolled 10 patients with active UC despite medical therapy. The donors were the patients' relatives and were carefully screened for infectious diseases. Fecal material was administered via colonoscopy, and the primary endpoint was the presence or absence of serious adverse events related to FMT. The secondary endpoint was a change in partial Mayo score at 12 weeks post-FMT. Scores ≤2 were considered a clinical response. Fecal samples were collected to follow changes in gut microbiota, while extracted complementary DNA were analyzed by a next-generation sequencer. We obtained written informed consent from all patients and donors. This study was approved by our Institutional Review Board and is registered in the University hospital Medical Information Network (UMIN) Clinical Trials Registry (UMIN 000012814). RESULTS: Five patients with moderate disease and five with severe disease were enrolled. No severe adverse effects were observed. One patient achieved clinical response; however, none of the patients' microbiota diversity recovered to the donor levels. CONCLUSIONS: The use of single FMT for UC was safe; however, we failed to show its clinical efficacy and potential to change the intestinal microbiota.
背景/目的:包括新一代测序在内的分析技术的最新进展已阐明肠道微生物群与炎症性肠病之间的相关性。对于溃疡性结肠炎(UC)患者,粪便微生物群移植(FMT)被提议作为解决其生态失调的一种潜在方法;然而,其安全性和有效性尚未得到证实。这项单臂、开放标签、非随机研究旨在评估FMT对日本UC患者的安全性和有效性,这是日本首个注册的临床试验。 方法:我们纳入了10例尽管接受了药物治疗仍患有活动性UC的患者。供体为患者亲属,并对其进行了仔细的传染病筛查。通过结肠镜检查给予粪便样本,主要终点是与FMT相关的严重不良事件的有无。次要终点是FMT后12周时部分梅奥评分的变化。评分≤2被认为是临床反应。收集粪便样本以追踪肠道微生物群的变化,同时通过新一代测序仪分析提取的互补DNA。我们获得了所有患者和供体的书面知情同意。本研究经我们的机构审查委员会批准,并在大学医院医学信息网络(UMIN)临床试验注册中心(UMIN 000012814)注册。 结果:纳入了5例中度疾病患者和5例重度疾病患者。未观察到严重不良反应。1例患者达到临床反应;然而,没有患者的微生物群多样性恢复到供体水平。 结论:对UC使用单次FMT是安全的;然而,我们未能证明其临床疗效以及改变肠道微生物群的潜力。
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