Inflammatory Bowel Disease Outcomes Following Fecal Microbiota Transplantation for Recurrent C. difficile Infection

Author:

Allegretti Jessica R12,Kelly Colleen R3,Grinspan Ari4,Mullish Benjamin H5,Hurtado Jonathan1,Carrellas Madeline1,Marcus Jenna1,Marchesi Julian R56,McDonald Julie A K57,Gerardin Ylaine8,Silverstein Michael8,Pechlivanis Alexandros59,Barker Grace F5,Miguens Blanco Jesus5,Alexander James L5,Gallagher Kate I5,Pettee Will10,Phelps Emmalee11,Nemes Sara11,Sagi Sashidhar V11,Bohm Matthew11,Kassam Zain8,Fischer Monika11

Affiliation:

1. Division of Gastroenterology, Hepatology and Endoscopy, Brigham and Women’s Hospital, Boston, MA, USA

2. Harvard Medical School, Boston, MA, USA

3. Division of Gastroenterology, Alpert Medical School of Brown University, Providence, RI, USA

4. The Henry D. Janowitz Division of Gastroenterology, Icahn School of Medicine at Mount Sinai, New York, NY, USA

5. Division of Digestive Diseases, Department of Metabolism, Digestion and Reproduction, Faculty of Medicine, Imperial College London, London, UK

6. School of Biosciences, Cardiff University, Cardiff, UK

7. MRC Centre for Molecular Bacteriology and Infection, Imperial College London, London, UK

8. Finch Therapeutics, Somerville, MA, USA

9. Center for Interdisciplinary Research and Innovation, School of Chemistry, Aristotle University of Thessaloniki, Thessaloniki, Greece

10. OpenBiome, Cambridge, MA, USA

11. Division of Gastroenterology, Indiana University School of Medicine, Indianapolis, IN, USA

Abstract

Abstract Background Recurrent Clostridioides difficile infection (CDI) in patients with inflammatory bowel disease (IBD) is a clinical challenge. Fecal microbiota transplantation (FMT) has emerged as a recurrent CDI therapy. Anecdotal concerns exist regarding worsening of IBD activity; however, prospective data among IBD patients are limited. Methods Secondary analysis from an open-label, prospective, multicenter cohort study among IBD patients with 2 or more CDI episodes was performed. Participants underwent a single FMT by colonoscopy (250 mL, healthy universal donor). Secondary IBD-related outcomes included rate of de novo IBD flares, worsening IBD, and IBD improvement—all based on Mayo or Harvey-Bradshaw index (HBI) scores. Stool samples were collected for microbiome and targeted metabolomic profiling. Results Fifty patients enrolled in the study, among which 15 had Crohn’s disease (mean HBI, 5.8 ± 3.4) and 35 had ulcerative colitis (mean partial Mayo score, 4.2 ± 2.1). Overall, 49 patients received treatment. Among the Crohn’s disease cohort, 73.3% (11 of 15) had IBD improvement, and 4 (26.6%) had no disease activity change. Among the ulcerative colitis cohort, 62% (22 of 34) had IBD improvement, 29.4% (11 of 34) had no change, and 4% (1 of 34) experienced a de novo flare. Alpha diversity significantly increased post-FMT, and ulcerative colitis patients became more similar to the donor than Crohn’s disease patients (P = 0.04). Conclusion This prospective trial assessing FMT in IBD-CDI patients suggests IBD outcomes are better than reported in retrospective studies.

Funder

Crohn's and Colitis Foundation

Harvard Digestive Disease Center

National Institutes of Health

Medical Research Council

Publisher

Oxford University Press (OUP)

Subject

Gastroenterology,Immunology and Allergy

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