Effects of Low FODMAP Diet on Symptoms, Fecal Microbiome, and Markers of Inflammation in Patients With Quiescent Inflammatory Bowel Disease in a Randomized Trial.


Journal

Gastroenterology
ISSN: 1528-0012
Titre abrégé: Gastroenterology
Pays: United States
ID NLM: 0374630

Informations de publication

Date de publication:
01 2020
Historique:
received: 02 04 2019
revised: 17 09 2019
accepted: 19 09 2019
pubmed: 6 10 2019
medline: 15 2 2020
entrez: 6 10 2019
Statut: ppublish

Résumé

There is limited evidence that a diet low in fermentable oligosaccharides, disaccharides, monosaccharides, and polyols (FODMAPs) reduces gut symptoms in quiescent inflammatory bowel disease (IBD). We performed a randomized, controlled trial to investigate the effects of a low FODMAP diet on persistent gut symptoms, the intestinal microbiome, and circulating markers of inflammation in patients with quiescent IBD. We performed a single-blind trial of 52 patients with quiescent Crohn's disease or ulcerative colitis and persistent gut symptoms at 2 large gastroenterology clinics in the United Kingdom. Patients were randomly assigned to groups that followed a diet low in FODMAPs (n = 27) or a control diet (n = 25), with dietary advice, for 4 weeks. Gut symptoms and health-related quality of life were measured using validated questionnaires. Stool and blood samples were collected at baseline and end of trial. We assessed fecal microbiome composition and function using shotgun metagenomic sequencing and phenotypes of T cells in blood using flow cytometry. A higher proportion of patients reported adequate relief of gut symptoms following the low FODMAP diet (14/27, 52%) than the control diet (4/25, 16%, P=.007). Patients had a greater reduction in irritable bowel syndrome severity scores following the low FODMAP diet (mean reduction of 67; standard error, 78) than the control diet (mean reduction of 34; standard error, 50), although this difference was not statistically significant (P = .075). Following the low FODMAP diet, patients had higher health-related quality of life scores (81.9 ± 1.2) than patients on the control diet (78.3 ± 1.2, P = .042). A targeted analysis revealed that in stool samples collected at the end of the study period, patients on the low FODMAP diet had significantly lower abundance of Bifidobacterium adolescentis, Bifidobacterium longum, and Faecalibacterium prausnitzii than patients on control diet. However, microbiome diversity and markers of inflammation did not differ significantly between groups. In a trial of the low FODMAP diet vs a control diet in patients with quiescent IBD, we found no significant difference after 4 weeks in change in irritable bowel syndrome severity scores, but significant improvements in specific symptom scores and numbers reporting adequate symptom relief. The low FODMAP diet reduced fecal abundance of microbes believed to regulate the immune response, compared with the control diet, but had no significant effect on markers of inflammation. We conclude that a 4-week diet low in FODMAPs is safe and effective for managing persistent gut symptoms in patients with quiescent IBD. www.isrctn.com no.: ISRCTN17061468.

Sections du résumé

BACKGROUND & AIMS
There is limited evidence that a diet low in fermentable oligosaccharides, disaccharides, monosaccharides, and polyols (FODMAPs) reduces gut symptoms in quiescent inflammatory bowel disease (IBD). We performed a randomized, controlled trial to investigate the effects of a low FODMAP diet on persistent gut symptoms, the intestinal microbiome, and circulating markers of inflammation in patients with quiescent IBD.
METHODS
We performed a single-blind trial of 52 patients with quiescent Crohn's disease or ulcerative colitis and persistent gut symptoms at 2 large gastroenterology clinics in the United Kingdom. Patients were randomly assigned to groups that followed a diet low in FODMAPs (n = 27) or a control diet (n = 25), with dietary advice, for 4 weeks. Gut symptoms and health-related quality of life were measured using validated questionnaires. Stool and blood samples were collected at baseline and end of trial. We assessed fecal microbiome composition and function using shotgun metagenomic sequencing and phenotypes of T cells in blood using flow cytometry.
RESULTS
A higher proportion of patients reported adequate relief of gut symptoms following the low FODMAP diet (14/27, 52%) than the control diet (4/25, 16%, P=.007). Patients had a greater reduction in irritable bowel syndrome severity scores following the low FODMAP diet (mean reduction of 67; standard error, 78) than the control diet (mean reduction of 34; standard error, 50), although this difference was not statistically significant (P = .075). Following the low FODMAP diet, patients had higher health-related quality of life scores (81.9 ± 1.2) than patients on the control diet (78.3 ± 1.2, P = .042). A targeted analysis revealed that in stool samples collected at the end of the study period, patients on the low FODMAP diet had significantly lower abundance of Bifidobacterium adolescentis, Bifidobacterium longum, and Faecalibacterium prausnitzii than patients on control diet. However, microbiome diversity and markers of inflammation did not differ significantly between groups.
CONCLUSIONS
In a trial of the low FODMAP diet vs a control diet in patients with quiescent IBD, we found no significant difference after 4 weeks in change in irritable bowel syndrome severity scores, but significant improvements in specific symptom scores and numbers reporting adequate symptom relief. The low FODMAP diet reduced fecal abundance of microbes believed to regulate the immune response, compared with the control diet, but had no significant effect on markers of inflammation. We conclude that a 4-week diet low in FODMAPs is safe and effective for managing persistent gut symptoms in patients with quiescent IBD. www.isrctn.com no.: ISRCTN17061468.

Identifiants

pubmed: 31586453
pii: S0016-5085(19)41366-8
doi: 10.1053/j.gastro.2019.09.024
pii:
doi:

Substances chimiques

Biomarkers 0
Disaccharides 0
Monosaccharides 0

Banques de données

ISRCTN
['ISRCTN17061468']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

176-188.e7

Commentaires et corrections

Type : CommentIn

Informations de copyright

Copyright © 2020 AGA Institute. Published by Elsevier Inc. All rights reserved.

Auteurs

Selina R Cox (SR)

Department of Nutritional Sciences, King's College London, London, United Kingdom.

James O Lindsay (JO)

Barts Health NHS Trust, Department of Gastroenterology, Royal London Hospital, London, United Kingdom; Blizard Institute, Queen Mary University of London, Centre for Immunobiology, London, United Kingdom.

Sébastien Fromentin (S)

Metagénopolis, Institut National de la Recherche Agronomique, Université Paris-Saclay, Paris, France.

Andrew J Stagg (AJ)

Blizard Institute, Queen Mary University of London, Centre for Immunobiology, London, United Kingdom.

Neil E McCarthy (NE)

Blizard Institute, Queen Mary University of London, Centre for Immunobiology, London, United Kingdom.

Nathalie Galleron (N)

Metagénopolis, Institut National de la Recherche Agronomique, Université Paris-Saclay, Paris, France.

Samar B Ibraim (SB)

Metagénopolis, Institut National de la Recherche Agronomique, Université Paris-Saclay, Paris, France.

Hugo Roume (H)

Metagénopolis, Institut National de la Recherche Agronomique, Université Paris-Saclay, Paris, France.

Florence Levenez (F)

Metagénopolis, Institut National de la Recherche Agronomique, Université Paris-Saclay, Paris, France.

Nicolas Pons (N)

Metagénopolis, Institut National de la Recherche Agronomique, Université Paris-Saclay, Paris, France.

Nicolas Maziers (N)

Metagénopolis, Institut National de la Recherche Agronomique, Université Paris-Saclay, Paris, France.

Miranda C Lomer (MC)

Department of Nutritional Sciences, King's College London, London, United Kingdom; Department of Nutrition and Dietetics, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.

S Dusko Ehrlich (SD)

Metagénopolis, Institut National de la Recherche Agronomique, Université Paris-Saclay, Paris, France.

Peter M Irving (PM)

Department of Gastroenterology, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.

Kevin Whelan (K)

Department of Nutritional Sciences, King's College London, London, United Kingdom. Electronic address: kevin.whelan@kcl.ac.uk.

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Classifications MeSH