Allogenic Fecal Microbiota Transplantation in Patients With Nonalcoholic Fatty Liver Disease Improves Abnormal Small Intestinal Permeability: A Randomized Control Trial.


Journal

The American journal of gastroenterology
ISSN: 1572-0241
Titre abrégé: Am J Gastroenterol
Pays: United States
ID NLM: 0421030

Informations de publication

Date de publication:
07 2020
Historique:
entrez: 4 7 2020
pubmed: 4 7 2020
medline: 29 9 2020
Statut: ppublish

Résumé

Nonalcoholic fatty liver disease (NAFLD) is an obesity-related disorder that is rapidly increasing in incidence and is considered the hepatic manifestation of the metabolic syndrome. The gut microbiome plays a role in metabolism and maintaining gut barrier integrity. Studies have found differences in the microbiota between NAFLD and healthy patients and increased intestinal permeability in patients with NAFLD. Fecal microbiota transplantation (FMT) can be used to alter the gut microbiome. It was hypothesized that an FMT from a thin and healthy donor given to patients with NAFLD would improve insulin resistance (IR), hepatic proton density fat fraction (PDFF), and intestinal permeability. Twenty-one patients with NAFLD were recruited and randomized in a ratio of 3:1 to either an allogenic (n = 15) or an autologous (n = 6) FMT delivered by using an endoscope to the distal duodenum. IR was calculated by HOMA-IR, hepatic PDFF was measured by MRI, and intestinal permeability was tested using the lactulose:mannitol urine test. Additional markers of metabolic syndrome and the gut microbiota were examined. Patient visits occurred at baseline, 2, 6 weeks, and 6 months post-FMT. There were no significant changes in HOMA-IR or hepatic PDFF in patients who received the allogenic or autologous FMT. Allogenic FMT patients with elevated small intestinal permeability (>0.025 lactulose:mannitol, n = 7) at baseline had a significant reduction 6 weeks after allogenic FMT. FMT did not improve IR as measured by HOMA-IR or hepatic PDFF but did have the potential to reduce small intestinal permeability in patients with NAFLD.

Identifiants

pubmed: 32618656
doi: 10.14309/ajg.0000000000000661
pii: 00000434-202007000-00019
doi:

Banques de données

ClinicalTrials.gov
['NCT02496390']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1055-1065

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Auteurs

Laura Craven (L)

Department of Microbiology and Immunology, Western University, London, Ontario, Canada.

Adam Rahman (A)

Lawson Health Research Institute, London, Ontario, Canada.
Division of Gastroenterology, London Health Sciences, London, Ontario, Canada.

Seema Nair Parvathy (S)

Division of Infectious Disease, St. Joseph's Health Care, London, Ontario, Canada.

Melanie Beaton (M)

Lawson Health Research Institute, London, Ontario, Canada.
Division of Gastroenterology, London Health Sciences, London, Ontario, Canada.

Justin Silverman (J)

Program in Computational Biology and Bioinformatics, Duke University, Durham, North Carolina, USA.

Karim Qumosani (K)

Lawson Health Research Institute, London, Ontario, Canada.
Division of Gastroenterology, London Health Sciences, London, Ontario, Canada.

Irene Hramiak (I)

Lawson Health Research Institute, London, Ontario, Canada.
Division of Endocrinology, St Joseph's Health Care, London, Ontario, Canada.

Rob Hegele (R)

Lawson Health Research Institute, London, Ontario, Canada.
Division of Endocrinology, St Joseph's Health Care, London, Ontario, Canada.
Department of Medical Biophysics, Western University, London, Ontario, Canada.

Tisha Joy (T)

Lawson Health Research Institute, London, Ontario, Canada.
Division of Endocrinology, St Joseph's Health Care, London, Ontario, Canada.

Jon Meddings (J)

Department of Medicine, University of Calgary, Alberta, Canada.

Brad Urquhart (B)

Lawson Health Research Institute, London, Ontario, Canada.

Ruth Harvie (R)

The Canadian Centre for Microbiome and Probiotic Research, London, Ontario, Canada.

Charles McKenzie (C)

Lawson Health Research Institute, London, Ontario, Canada.
Department of Medical Biophysics, Western University, London, Ontario, Canada.

Kelly Summers (K)

Department of Microbiology and Immunology, Western University, London, Ontario, Canada.
Lawson Health Research Institute, London, Ontario, Canada.

Gregor Reid (G)

Department of Microbiology and Immunology, Western University, London, Ontario, Canada.
Lawson Health Research Institute, London, Ontario, Canada.
The Canadian Centre for Microbiome and Probiotic Research, London, Ontario, Canada.

Jeremy P Burton (JP)

Department of Microbiology and Immunology, Western University, London, Ontario, Canada.
Lawson Health Research Institute, London, Ontario, Canada.
The Canadian Centre for Microbiome and Probiotic Research, London, Ontario, Canada.

Michael Silverman (M)

Department of Microbiology and Immunology, Western University, London, Ontario, Canada.
Lawson Health Research Institute, London, Ontario, Canada.
Division of Infectious Disease, St. Joseph's Health Care, London, Ontario, Canada.

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