Wilson, Bridgette, Kanno, Tokuwa, Slater, Rachael, Rossi, Megan, Irving, Peter M, Lomer, Miranda C, Probert, Chris ORCID: 0000-0003-0477-6714, Mason, A James and Whelan, Kevin
(2023)
Faecal and urine metabolites, but not gut microbiota, may predict response to low FODMAP diet in irritable bowel syndrome.
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 58 (4).
pp. 404-416.
ISSN 0269-2813, 1365-2036
Text
Aliment Pharmacol Ther - 2023 - Wilson - Faecal and urine metabolites but not gut microbiota may predict response to low (1).pdf - Open Access published version Download (2MB) | Preview |
Abstract
<h4>Background</h4>The low FODMAP diet (LFD) leads to clinical response in 50%-80% of patients with irritable bowel syndrome (IBS). It is unclear why only some patients respond.<h4>Aims</h4>To determine if differences in baseline faecal microbiota or faecal and urine metabolite profiles may separate clinical responders to the diet from non-responders allowing predictive algorithms to be proposed.<h4>Methods</h4>We recruited adults fulfilling Rome III criteria for IBS to a blinded randomised controlled trial. Patients were randomised to sham diet with a placebo supplement (control) or LFD supplemented with either placebo (LFD) or 1.8 g/d B-galactooligosaccharide (LFD/B-GOS), for 4 weeks. Clinical response was defined as adequate symptom relief at 4 weeks after the intervention (global symptom question). Differences between responders and non-responders in faecal microbiota (FISH, 16S rRNA sequencing) and faecal (gas-liquid chromatography, gas-chromatography mass-spectrometry) and urine (<sup>1</sup> H NMR) metabolites were analysed.<h4>Results</h4>At 4 weeks, clinical response differed across the 3groups with adequate symptom relief of 30% (7/23) in controls, 50% (11/22) in the LFD group and 67% (16/24) in the LFD/B-GOS group (p = 0.048). In the control and the LFD/B-GOS groups, microbiota and metabolites did not separate responders from non-responders. In the LFD group, higher baseline faecal propionate (sensitivity 91%, specificity 89%) and cyclohexanecarboxylic acid esters (sensitivity 80%, specificity 78%), and urine metabolite profile (Q<sup>2</sup> 0.296 vs. randomised -0.175) predicted clinical response.<h4>Conclusions</h4>Baseline faecal and urine metabolites may predict response to the LFD.
Item Type: | Article |
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Uncontrolled Keywords: | FODMAP, IBS, microbiota, prebiotics |
Divisions: | Faculty of Health and Life Sciences Faculty of Health and Life Sciences > Institute of Systems, Molecular and Integrative Biology |
Depositing User: | Symplectic Admin |
Date Deposited: | 25 Sep 2023 08:39 |
Last Modified: | 07 Dec 2024 22:40 |
DOI: | 10.1111/apt.17609 |
Related URLs: | |
URI: | https://livrepository.liverpool.ac.uk/id/eprint/3172984 |