Prebiotic effect of inulin-type fructans on faecal microbiota and short-chain fatty acids in type 2 diabetes: a randomised controlled trial.


Journal

European journal of nutrition
ISSN: 1436-6215
Titre abrégé: Eur J Nutr
Pays: Germany
ID NLM: 100888704

Informations de publication

Date de publication:
Oct 2020
Historique:
received: 29 01 2020
accepted: 11 05 2020
pubmed: 23 5 2020
medline: 11 6 2021
entrez: 23 5 2020
Statut: ppublish

Résumé

Compared to a healthy population, the gut microbiota in type 2 diabetes presents with several unfavourable features that may impair glucose regulation. The aim of this study was to evaluate the prebiotic effect of inulin-type fructans on the faecal microbiota and short-chain fatty acids (SCFA) in patients with type 2 diabetes. The study was a placebo controlled crossover study, where 25 patients (15 men) aged 41-71 years consumed 16 g of inulin-type fructans (a mixture of oligofructose and inulin) and 16-g placebo (maltodextrin) for 6 weeks in randomised order. A 4-week washout separated the 6 weeks treatments. The faecal microbiota was analysed by high-throughput 16S rRNA amplicon sequencing and SCFA in faeces were analysed using vacuum distillation followed by gas chromatography. Treatment with inulin-type fructans induced moderate changes in the faecal microbiota composition (1.5%, p = 0.045). A bifidogenic effect was most prominent, with highest positive effect on operational taxonomic units (OTUs) of Bifidobacterium adolescentis, followed by OTUs of Bacteroides. Significantly higher faecal concentrations of total SCFA, acetic acid and propionic acid were detected after prebiotic consumption compared to placebo. The prebiotic fibre had no effects on the concentration of butyric acid or on the overall microbial diversity. Six weeks supplementation with inulin-type fructans had a significant bifidogenic effect and induced increased concentrations of faecal SCFA, without changing faecal microbial diversity. Our findings suggest a moderate potential of inulin-type fructans to improve gut microbiota composition and to increase microbial fermentation in type 2 diabetes. The trial is registered at clinicaltrials.gov (NCT02569684).

Identifiants

pubmed: 32440730
doi: 10.1007/s00394-020-02282-5
pii: 10.1007/s00394-020-02282-5
pmc: PMC7501097
doi:

Substances chimiques

Fatty Acids, Volatile 0
Prebiotics 0
RNA, Ribosomal, 16S 0
Inulin 9005-80-5

Banques de données

ClinicalTrials.gov
['NCT02569684']

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

3325-3338

Subventions

Organisme : The DAM Foundation, Norway
ID : 2013-2-267
Organisme : Diabetesforbundet
ID : 36660
Organisme : Mills DA
ID : 36660

Commentaires et corrections

Type : ErratumIn

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Auteurs

Eline Birkeland (E)

Section of Nutrition and Dietetics, Division of Medicine, Department of Clinical Service, Oslo University Hospital, Oslo, Norway. eline.birkeland@ous-hf.no.
Institute of Clinical Medicine, University of Oslo, Oslo, Norway. eline.birkeland@ous-hf.no.

Sedegheh Gharagozlian (S)

Section of Nutrition and Dietetics, Division of Medicine, Department of Clinical Service, Oslo University Hospital, Oslo, Norway.

Kåre I Birkeland (KI)

Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
Department of Transplantation Medicine, Oslo University Hospital, Oslo, Norway.

Jørgen Valeur (J)

Department of Gastroenterology, Oslo University Hospital, Oslo, Norway.
Unger-Vetlesen Institute, Lovisenberg Diaconal Hospital, Oslo, Norway.

Ingrid Måge (I)

Nofima-Norwegian Institute of Food, Fisheries and Aquaculture Research, Ås, Norway.

Ida Rud (I)

Nofima-Norwegian Institute of Food, Fisheries and Aquaculture Research, Ås, Norway.

Anne-Marie Aas (AM)

Section of Nutrition and Dietetics, Division of Medicine, Department of Clinical Service, Oslo University Hospital, Oslo, Norway.
Institute of Clinical Medicine, University of Oslo, Oslo, Norway.

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