Inflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.
School of Biotechnology & Biomolecular Sciences, University of New South Wales, Sydney, NSW, Australia.
J Crohns Colitis. 2017 Oct 1;11(10):1180-1199. doi: 10.1093/ecco-jcc/jjx063.
Faecal microbiota transplantation [FMT] has been investigated as a potential treatment for inflammatory bowel disease [IBD]. We thus performed a systematic review and meta-analysis assessing the effectiveness and safety of FMT in IBD.
A systematic review was conducted until January 2017. Studies were excluded if patients had co-infection or data were pooled across disease subtypes (ulcerative colitis [UC], Crohn's disease [CD], pouchitis). Clinical remission was established as the primary outcome. Pooled effect sizes and 95% confidence intervals were obtained using the random effects model.
In all, 53 studies were included [41 in UC, 11 in CD, 4 in pouchitis]. Overall, 36% [201/555] of UC, 50.5% [42/83] of CD, and 21.5% [5/23] of pouchitis patients achieved clinical remission. Among cohort studies, the pooled proportion achieving clinical remission was 33% (95% confidence interval [CI] = 23%-43%] for UC and 52% [95% CI = 31%-72%] for CD, both with moderate risk of heterogeneity. For four RCTs in UC, significant benefit in clinical remission (pooled odds ratios [[P-OR] = 2.89, 95% CI = 1.36-6.13, p = 0.006) with moderate heterogeneity [Cochran's Q, p = 0.188; I2 = 37%] was noted. Sub-analyses suggest remission in UC improved with increased number of FMT infusions and lower gastrointestinal tract administration. Most adverse events were transient gastrointestinal complaints. Microbiota analysis was performed in 24 studies, with many identifying increased diversity and a shift in recipient microbiota profile towards the donor post-FMT.
FMT appears effective in UC remission induction, but long-term durability and safety remain unclear. Additional well-designed controlled studies of FMT in IBD are needed, especially in CD and pouchitis.
粪便微生物群移植(FMT)已被研究作为治疗炎症性肠病(IBD)的一种潜在方法。因此,我们进行了一项系统评价和荟萃分析,评估 FMT 在 IBD 中的有效性和安全性。
系统评价截至 2017 年 1 月进行。如果患者存在合并感染或数据在疾病亚型(溃疡性结肠炎[UC]、克罗恩病[CD]、 pouchitis)之间汇总,则排除研究。临床缓解被确定为主要结局。使用随机效应模型获得汇总效果大小和 95%置信区间。
共纳入 53 项研究[UC 41 项,CD 11 项, pouchitis 4 项]。总体而言,UC 患者中有 36%[201/555],CD 患者中有 50.5%[42/83], pouchitis 患者中有 21.5%[5/23]达到临床缓解。在队列研究中,UC 患者达到临床缓解的汇总比例为 33%(95%置信区间[CI] = 23%-43%),CD 患者为 52%(95% CI = 31%-72%),均存在中度异质性。在 UC 的四项 RCT 中,临床缓解的显著获益(汇总优势比[P-OR] = 2.89,95% CI = 1.36-6.13,p = 0.006),存在中度异质性[Cochran's Q,p = 0.188;I2 = 37%]。亚分析表明,UC 缓解率随 FMT 输注次数增加和下消化道给药而提高。大多数不良事件是短暂的胃肠道投诉。24 项研究进行了微生物组分析,许多研究发现,FMT 后,受体微生物组的多样性增加,并且向供体的微生物组特征发生转移。
FMT 似乎对 UC 缓解诱导有效,但长期持久性和安全性仍不清楚。需要进一步设计良好的 FMT 在 IBD 中的对照研究,特别是在 CD 和 pouchitis 中。