TY - JOUR
T1 - Microbial Engraftment and Efficacy of Fecal Microbiota Transplant for Clostridium Difficile in Patients with and without Inflammatory Bowel Disease
AU - Hirten, Robert P.
AU - Grinspan, Ari
AU - Fu, Shih Chen
AU - Luo, Yuying
AU - Suarez-Farinas, Mayte
AU - Rowland, John
AU - Contijoch, Eduardo J.
AU - Mogno, Ilaria
AU - Yang, Nancy
AU - Luong, Tramy
AU - Labrias, Philippe R.
AU - Peter, Inga
AU - Cho, Judy H.
AU - Sands, Bruce E.
AU - Colombel, Jean Frederic
AU - Faith, Jeremiah J.
AU - Clemente, Jose C.
N1 - Funding Information:
Supported in part by the SUCCESS (Sinai Ulcerative Colitis Clinical, Experimental and System Studies) grant from the Bacchetta Foundation (SCF, IP, JHC, JFC, JJF, JCC), the Crohn's and Colitis Foundation of America grant #362048 (JJF, JCC), the George Waechter Memorial Foundation grant (AG), and NIH/ NIDDK R01 DK114038 (JCC).
Funding Information:
Abbreviations: Anti-TNF, anti-tumor necrosis factor; AZA, azathioprine; BMI, body mass index; CD, Crohn’s disease; CDI, clostridium difficile infection; CDIR, clostridium difficile infection relapse; CRP, c-reactive protein; ESR, erythrocyte sedimentation rate; FMT, fecal microbiota transplant; GERD, gastroesophageal reflux disease; HBI, Harvey Bradshaw Index; IBD, inflammatory bowel disease; Non-IBD, non-inflammatory bowel disease group; IBDe, inflammatory bowel disease medication escalation; IBDs, inflammatory bowel disease no medication escalation; J tube, jejunal tube; LSM, least-squares means; MP, mercaptopurine; MTX, methotrexate; OTU, operational taxonomic unit; PCoA, principal coordinate analysis; PEG, percutaneous endoscopic gastrostomy; PPI, proton pump inhibitor; PUD, peptic ulcer disease; SD, standard deviation; SES-CD, simple endoscopic score for Crohn’s disease; UC, ulcerative colitis; WBC, white blood cell count Supported in part by the SUCCESS (Sinai Ulcerative Colitis Clinical, Experimental and System Studies) grant from the Bacchetta Foundation (SCF, IP, JHC, JFC, JJF, JCC), the Crohn’s and Colitis Foundation of America grant #362048 (JJF, JCC), the George Waechter Memorial Foundation grant (AG), and NIH/ NIDDK R01 DK114038 (JCC).
Publisher Copyright:
© 2019 Crohn's & Colitis Foundation.
PY - 2019/5/4
Y1 - 2019/5/4
N2 - Background: Recurrent and severe Clostridium difficile infections (CDI) are treated with fecal microbiota transplant (FMT). Uncertainty exists regarding FMT effectiveness for CDI with underlying inflammatory bowel disease (IBD) and regarding its effects on disease activity and effectiveness in transferring the donor microbiota to patients with and without IBD. Methods: Subjects with and without IBD who underwent FMT for recurrent or severe CDI between 2013 and 2016 at The Mount Sinai Hospital were followed for up to 6 months. The primary outcome was CDI recurrence 6 months after FMT. Secondary outcomes were (1) CDI recurrence 2 months after FMT; (2) frequency of IBD flare after FMT; (3) microbiota engraftment after FMT; (and 4) predictors of CDI recurrence. Results: One hundred thirty-four patients, 46 with IBD, were treated with FMT. Follow-up was available in 83 and 118 patients at 6 and 2 months, respectively. There was no difference in recurrence in patients with and without IBD at 6 months (38.7% vs 36.5%; P > 0.99) and 2 months (22.5% vs 17.9%; P = 0.63). Proton pump inhibitor use, severe CDI, and comorbid conditions were predictors of recurrence. Pre-FMT microbiota was not predictive of CDI recurrence. Subjects with active disease requiring medication escalation had reduced engraftment, with no difference in engraftment based on CDI recurrence or IBD endoscopic severity at FMT. Conclusions: Inflammatory bowel disease did not affect CDI recurrence rates 6 months after FMT. Pre-FMT microbiota was not predictive of recurrence, and microbial engraftment was impacted in those requiring IBD treatment escalation, though not by CDI recurrence or IBD disease severity.
AB - Background: Recurrent and severe Clostridium difficile infections (CDI) are treated with fecal microbiota transplant (FMT). Uncertainty exists regarding FMT effectiveness for CDI with underlying inflammatory bowel disease (IBD) and regarding its effects on disease activity and effectiveness in transferring the donor microbiota to patients with and without IBD. Methods: Subjects with and without IBD who underwent FMT for recurrent or severe CDI between 2013 and 2016 at The Mount Sinai Hospital were followed for up to 6 months. The primary outcome was CDI recurrence 6 months after FMT. Secondary outcomes were (1) CDI recurrence 2 months after FMT; (2) frequency of IBD flare after FMT; (3) microbiota engraftment after FMT; (and 4) predictors of CDI recurrence. Results: One hundred thirty-four patients, 46 with IBD, were treated with FMT. Follow-up was available in 83 and 118 patients at 6 and 2 months, respectively. There was no difference in recurrence in patients with and without IBD at 6 months (38.7% vs 36.5%; P > 0.99) and 2 months (22.5% vs 17.9%; P = 0.63). Proton pump inhibitor use, severe CDI, and comorbid conditions were predictors of recurrence. Pre-FMT microbiota was not predictive of CDI recurrence. Subjects with active disease requiring medication escalation had reduced engraftment, with no difference in engraftment based on CDI recurrence or IBD endoscopic severity at FMT. Conclusions: Inflammatory bowel disease did not affect CDI recurrence rates 6 months after FMT. Pre-FMT microbiota was not predictive of recurrence, and microbial engraftment was impacted in those requiring IBD treatment escalation, though not by CDI recurrence or IBD disease severity.
KW - Clostridium difficile
KW - fecal microbiota transplant
KW - inflammatory bowel disease
KW - microbiome
UR - http://www.scopus.com/inward/record.url?scp=85065557049&partnerID=8YFLogxK
U2 - 10.1093/ibd/izy398
DO - 10.1093/ibd/izy398
M3 - Article
C2 - 30852592
AN - SCOPUS:85065557049
SN - 1078-0998
VL - 25
SP - 969
EP - 979
JO - Inflammatory Bowel Diseases
JF - Inflammatory Bowel Diseases
IS - 6
ER -