Long-term efficacy and safety of monotherapy with a single fresh fecal microbiota transplant for recurrent active ulcerative colitis: a prospective randomized pilot study

被引:64
作者
Fang, Haiming [1 ,2 ]
Fu, Lian [1 ,2 ]
Li, Xuejun [3 ]
Lu, Chunxia [1 ,2 ]
Su, Yuan [1 ,2 ]
Xiong, Kangwei [1 ,2 ]
Zhang, Lijiu [1 ,2 ]
机构
[1] Anhui Med Univ, Hosp 2, Dept Gastroenterol & Hepatol, Hefei, Peoples R China
[2] Anhui Med Univ, Hosp 2, Ctr Gut Microbiota Res, Hefei, Peoples R China
[3] Anhui Univ Chinese Med, Hosp 2, Dept Gastroenterol, Hefei, Peoples R China
基金
安徽省自然科学基金;
关键词
Fecal microbiota transplantation; Inflammatory bowel disease; Ulcerative colitis; Gut microbiota; Intestinal flora;
D O I
10.1186/s12934-021-01513-6
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
BackgroundTo assess the long-term safety and efficacy of monotherapy with a single fresh fecal microbiota transplant (FMT) for recurrent ulcerative colitis (UC).ResultsTwenty-six eligible patients were enrolled, and 6 patients were excluded. Ultimately, 20 patients were randomized to the FMT group (n=10) and the control group (n=10); 80% were females (F/M=16/4), the mean age was 4814 years, and the mean duration was 6.4 +/- 8.2 years. The mean length of post-FMT follow-up was 19.1 +/- 10.1 months (6-38). No statistically significant differences in baseline demographic or clinical characteristics were found between the groups. Ninety percent of patients in the FMT group and 50% of patients in the control group met the primary endpoint at week 8. The Mayo score was significantly decreased compared with that of the control group (n=10) when reassessed at week 4 (P=0.001) and week 8 (P=0.019) after FMT; there was no significant difference 6 months after treatment. The median remission time was 24 months (95% CI 68.26-131.7%) in both the FMT (range 6-38 months) and control groups (range 7-35 months), with no significant difference (P=0.895). Participants tolerated FMT treatment, and no adverse events occurred during long-term follow-up, with one treatment-related significant adverse event (EBV infection) occurring within 2 weeks after FMT. Stool microbiota composition analysis indicated improved gut microbiota diversity after FMT, with expansion of stool-donor taxa. Bacteroidetes, Firmicutes and Proteobacteria were the dominant bacterial phyla of the gut microbiota in active UC patients. The relative abundance of Bacteroidetes decreased and that of Proteobacteria increased significantly in active UC patients compared with donors, while Firmicutes showed no significant changes. A single fresh FMT could effectively reconstruct the gut microbiota composition in patients with active UC and maintain stability, with increased Bacteroidetes and decreased Proteobacteria abundance. FMT significantly reduced the relative abundance of Escherichia and increased the relative abundance of Prevotella at the genus level. Pyruvate metabolism, glyoxylate and dicarboxylate metabolism, and pantothenate and CoA biosynthesis showed significant differences after transplantation.Conclusions Monotherapy with a single fresh FMT is an effective and safe strategy to induce long-term remission without drugs in patients with active UC and may be an alternative induction therapy for recurrent UC or even primary UC.
引用
收藏
页数:14
相关论文
共 44 条
[1]  
Agrawal M, 2016, J CLIN GASTROENTEROL, V50, P403, DOI 10.1097/MCG.0000000000000410
[2]   The evolution of the use of faecal microbiota transplantation and emerging therapeutic indications [J].
Allegretti, Jessica R. ;
Mullish, Benjamin H. ;
Kelly, Colleen ;
Fischer, Monika .
LANCET, 2019, 394 (10196) :420-431
[3]   Systematic review: faecal microbiota transplantation in the management of inflammatory bowel disease [J].
Anderson, J. L. ;
Edney, R. J. ;
Whelan, K. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2012, 36 (06) :503-516
[4]  
[Anonymous], 2018, COCHRANE DATABASE SY
[5]   Evolving Role of IBD Surgery [J].
Bemelman, W. A. .
JOURNAL OF CROHNS & COLITIS, 2018, 12 (08) :1005-1007
[6]  
BENNET JD, 1989, LANCET, V1, P164
[7]   Treatment of ulcerative colitis using fecal bacteriotherapy [J].
Borody, TJ ;
Warren, EF ;
Leis, S ;
Surace, R ;
Ashman, O .
JOURNAL OF CLINICAL GASTROENTEROLOGY, 2003, 37 (01) :42-47
[8]   Genetic Factors and the Intestinal Microbiome Guide Development of Microbe-Based Therapies for Inflammatory Bowel Diseases [J].
Cohen, Louis J. ;
Cho, Judy H. ;
Gevers, Dirk ;
Chu, Hiutung .
GASTROENTEROLOGY, 2019, 156 (08) :2174-2189
[9]   Multidonor FMT capsules improve symptoms and decrease fecal calprotectin in ulcerative colitis patients while treated - an open-label pilot study [J].
Cold, F. ;
Browne, P. D. ;
Guenther, S. ;
Halkjaer, S. I. ;
Petersen, A. M. ;
Al-Gibouri, Z. ;
Hansen, L. H. ;
Christensen, A. H. .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2019, 54 (03) :289-296
[10]   Fecal microbiota transplantation as therapy for inflammatory bowel disease: A systematic review and meta-analysis (Publication with Expression of Concern) [J].
Colman, Ruben J. ;
Rubin, David T. .
JOURNAL OF CROHNS & COLITIS, 2014, 8 (12) :1569-1581