Cited by 681Gut microbiota and healthGastrointestinal motility and disordersMicrobial Metabolites in Food Biotechnology

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Diets that differ in their FODMAP content alter the colonic luminal microenvironment

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Halmos, Emma P, Christophersen, Claus T, Bird, Anthony R, Shepherd, Susan J, Gibson, Peter R, Muir, Jane G·2015·Gut

DOI 10.1136/gutjnl-2014-307264

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Abstract

Objective: A low FODMAP (Fermentable Oligosaccharides, Disaccharides, Monosaccharides And Polyols) diet reduces symptoms of IBS, but reduction of potential prebiotic and fermentative effects might adversely affect the colonic microenvironment. The effects of a low FODMAP diet with a typical Australian diet on biomarkers of colonic health were compared in a single-blinded, randomised, cross-over trial. Design: Twenty-seven IBS and six healthy subjects were randomly allocated one of two 21-day provided diets, differing only in FODMAP content (mean (95% CI) low 3.05 (1.86 to 4.25) g/day vs Australian 23.7 (16.9 to 30.6) g/day), and then crossed over to the other diet with ≥21-day washout period. Faeces passed over a 5-day run-in on their habitual diet and from day 17 to day 21 of the interventional diets were pooled, and pH, short-chain fatty acid concentrations and bacterial abundance and diversity were assessed. Results: Faecal indices were similar in IBS and healthy subjects during habitual diets. The low FODMAP diet was associated with higher faecal pH (7.37 (7.23 to 7.51) vs 7.16 (7.02 to 7.30); p=0.001), similar short-chain fatty acid concentrations, greater microbial diversity and reduced total bacterial abundance (9.63 (9.53 to 9.73) vs 9.83 (9.72 to 9.93) log 10 copies/g; p<0.001) compared with the Australian diet. To indicate direction of change, in comparison with the habitual diet the low FODMAP diet reduced total bacterial abundance and the typical Australian diet increased relative abundance for butyrate-producing Clostridium cluster XIVa (median ratio 6.62; p<0.001) and mucus-associated Akkermansia muciniphila (19.3; p<0.001), and reduced Ruminococcus torques . Conclusions: Diets differing in FODMAP content have marked effects on gut microbiota composition. The implications of long-term reduction of intake of FODMAPs require elucidation. Trial registration number: ACTRN12612001185853.

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Improved extraction of PCR-quality community DNA from digesta and fecal samples
Yu, Z., & Morrison, M. (2004) · BioTechniques · doi:10.2144/04365st04 · Cited by 1,663
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Png, C. W., Lindén, S. K., Gilshenan, K. S., Zoetendal, E. G., McSweeney, C. S., Sly, L. I., McGuckin, M. A., & Florin, T. H. J. (2010) · American Journal of Gastroenterology · doi:10.1038/ajg.2010.281 · Cited by 1,364
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Murillo, A. Z., Estremera, F., & Jáuregui, E. P. (2016) · Endocrinología y Nutrición (English Edition) · doi:10.1016/j.endoen.2015.10.014 · Cited by 13

Authors: Halmos, E. P., Christophersen, C. T., Bird, A. R., Shepherd, S. J., Gibson, P. R., & Muir, J. G.
Affiliations: The Alfred Hospital (AU)
Commonwealth Scientific and Industrial Research Organisation (AU)
Eastern Health (AU)
Corresponding author: Halmos, Emma P
ORCID: Halmos, Emma P
Christophersen, Claus T
Bird, Anthony R
Shepherd, Susan J
Muir, Jane G
Venue: Gut
Publisher: BMJ
Published: 2014-07-12
Volume: 64
Issue: 1
Pages: 93-100
ISSN: 0017-5749 (ISSN-L)
1468-3288
DOI: 10.1136/gutjnl-2014-307264
OpenAlex: W2167428741
Cited by: 681
References: 37
Citations by year: 2026: 21 · 2025: 31 · 2024: 37 · 2023: 45 · 2022: 56 · 2021: 64 · 2020: 63 · 2019: 76 · 2018: 66 · 2017: 87 · 2016: 79 · 2015: 47 · 2014: 8
FWCI: 30.18
Type: journal article
Language: en
Open access: bronze
doi.org
Locations: Gut (publishedVersion)
PubMed (publishedVersion)
Research Online (Edith Cowan University) (submittedVersion)
eSpace (Curtin University) (submittedVersion)
HighWire Press Open Archive (submittedVersion)
Funders: Commonwealth Scientific and Industrial Research Organisation
Monash University
Medical Research Council
National Health and Medical Research Council
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
Health Sciences › Nursing › Nutrition and Dietetics › Microbial Metabolites in Food Biotechnology
Keywords: low FODMAP diet, FODMAPs, irritable bowel syndrome, gut microbiota, fecal pH, short-chain fatty acids, butyrate-producing bacteria, Clostridium cluster XIVa, Akkermansia muciniphila, Ruminococcus torques, dietary intervention, prebiotics
MeSH terms: Adult, Colon, Diet, Disaccharides, Feces, Female, Fermentation, Humans, Male, Middle Aged, Monosaccharides, Oligosaccharides, Single-Blind Method, Cross-Over Studies, Irritable Bowel Syndrome, Young Adult

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Diets that differ in their FODMAP content alter the colonic luminal microenvironment

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