Dietary Triggers of Abdominal Symptoms in Patients With Irritable Bowel Syndrome: Randomized Placebo-Controlled Evidence
Abstract
Background & aims Observational studies suggest dietary fructose restriction might lead to sustained symptomatic response in patients with irritable bowel syndrome (IBS) and fructose malabsorption. The aims of this study were first to determine whether the efficacy of this dietary change is due to dietary fructose restriction and second to define whether symptom relief was specific to free fructose or to poorly absorbed short-chain carbohydrates in general. Methods The double-blinded, randomized, quadruple arm, placebo-controlled rechallenge trial took place in the general community. The 25 patients who had responded to dietary change were provided all food, low in free fructose and fructans, for the duration of the study. Patients were randomly challenged by graded dose introduction of fructose, fructans, alone or in combination, or glucose taken as drinks with meals for maximum test period of 2 weeks, with at least 10-day washout period between. For the main outcome measures, symptoms were monitored by daily diary entries and responses to a global symptom question. Results Seventy percent of patients receiving fructose, 77% receiving fructans, and 79% receiving a mixture reported symptoms were not adequately controlled, compared with 14% receiving glucose (P Conclusions In patients with IBS and fructose malabsorption, dietary restriction of fructose and/or fructans is likely to be responsible for symptomatic improvement, suggesting efficacy is due to restriction of poorly a…
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Genome-wide association studies have provided associations with variants on chromosome 9 (9q31.2 locus) that are linked to the functions of diverse ion channels and autonomic dysfunction, and mutations in the sucrase-isomaltase gene.
“genome-wide association studies have provided associations with variants on chromosome 9 (9q31.2 locus) that are linked to the functions of diverse ion channels and autonomic dysfunction, 56 and mutations in the sucrase-isomaltase gene, 38,39 as previously discussed.”
From Irritable bowel syndrome (2020) · cites this paper as [39]
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- Authors
- Shepherd, S. J., Parker, F. C., Muir, J. G., & Gibson, P. R.
- Affiliations
- Box Hill Hospital (AU)
- Corresponding author
- Shepherd, Susan J.
- Venue
- Clinical Gastroenterology and Hepatology
- Publisher
- Elsevier BV
- Published
- 2008-07
- Volume
- 6
- Issue
- 7
- Pages
- 765-771
- ISSN
- 1542-3565 (ISSN-L)
- OpenAlex
- W2155620449
- Cited by
- 549
- References
- 5
- Citations by year
- 2026: 8 · 2025: 19 · 2024: 13 · 2023: 23 · 2022: 27 · 2021: 32 · 2020: 27 · 2019: 34 · 2018: 35 · 2017: 56 · 2016: 53 · 2015: 33 · 2014: 40 · 2013: 42 · 2012: 31
- FWCI
- 24.30
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Clinical Gastroenterology and Hepatology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Gastroenterology › Gastrointestinal motility and disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Nursing › Nutrition and Dietetics › Microbial Metabolites in Food Biotechnology
- Keywords
- irritable bowel syndrome, fructose malabsorption, fructose restriction, fructans, short-chain carbohydrates, abdominal symptoms, fructose intolerance
- MeSH terms
- Adult, Diarrhea, Diet, Female, Fructans, Fructose, Glucose, Humans, Male, Middle Aged, Placebos, Abdominal Pain, Irritable Bowel Syndrome
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