1241
IRUS Total
Downloads
  Altmetric

Fecal microbiota transplantation in patients with primary sclerosing cholangitis: A pilot clinical trial

File Description SizeFormat 
_system_appendPDF_proof_hi (2).pdfAccepted version125.94 kBAdobe PDFView/Open
Title: Fecal microbiota transplantation in patients with primary sclerosing cholangitis: A pilot clinical trial
Authors: Allegretti, JA
Kassam, Z
Carrellas, M
Mullish, BH
Marchesi, JR
Pechlivanis, A
Smith, M
Gerardin, Y
Timberlake, S
Pratt, DS
Korzenik, JR
Item Type: Journal Article
Abstract: Background: Primary sclerosing cholangitis (PSC) is a cholestatic liver disease with no effective medical therapies. A perturbation of the gut microbiota has been described in association with PSC, and fecal microbiota transplantation (FMT) has been reported to restore the microbiome in other disease states. Accordingly, we aimed to evaluate the safety, change in liver enzymes, microbiota and metabolomic profiles in PSC patients after FMT. Methods: Open-label pilot study of PSC patients with concurrent inflammatory bowel disease (IBD) and ALP > 1.5X the upper limit of normal. Participants underwent a single FMT by colonoscopy. Liver enzyme profiles and stool microbiome and metabolomic analysis was conducted at baseline and week 1, 4, 8, 12 and 24 post-FMT. The primary outcome was safety and secondary outcomes include a decrease in ALP ≥50% from baseline by week 24 post-FMT, as well as stool microbiota (by 16S rRNA gene profiling) and metabonomic dynamics were assessed. Results. Ten patients underwent FMT. Nine patients had ulcerative colitis and 1 with Crohn’s colitis. The mean baseline ALP was 489 U/L. There were no related adverse events. Overall, 30% (3/10) experienced a ≥50% decrease ALP. The diversity increased in all patients post-FMT, as early as week 1 (p<0.01). Importantly, abundance of engrafter operational taxanomic units (OTUs) in patients post-FMT correlated with decreased ALP (p=0.02). Conclusion: To our knowledge, this first study to demonstrate that FMT in PSC is safe. Additionally, increases in bacterial diversity and engraftment may correlate with an improvement in ALP among PSC patients.
Issue Date: 1-Jul-2019
Date of Acceptance: 10-Dec-2018
URI: http://hdl.handle.net/10044/1/66365
DOI: https://dx.doi.org/10.14309/ajg.0000000000000115
ISSN: 1572-0241
Publisher: Wolters Kluwer
Start Page: 1071
End Page: 1079
Journal / Book Title: American Journal of Gastroenterology
Volume: 114
Issue: 7
Copyright Statement: © The American College of Gastroenterology 2019. All Rights Reserved.
Sponsor/Funder: Medical Research Council
Medical Research Council (MRC)
Funder's Grant Number: MR/R00875/1
MR/R000875/1
Keywords: Science & Technology
Life Sciences & Biomedicine
Gastroenterology & Hepatology
INFLAMMATORY-BOWEL-DISEASE
ACTIVE ULCERATIVE-COLITIS
URSODEOXYCHOLIC ACID
ORAL VANCOMYCIN
METRONIDAZOLE
PROFILES
STRATEGY
CHILDREN
1103 Clinical Sciences
Gastroenterology & Hepatology
Publication Status: Published
Appears in Collections:Department of Metabolism, Digestion and Reproduction