Trials / Active Not Recruiting
Active Not RecruitingNCT05795049
Genetic Carbohydrate Maldigestion as a Model to Study Food Hypersensitivity
Genetic Carbohydrate Maldigestion as a Model to Study Food Hypersensitivity Mechanism and Guide Personalised Treatment Using a Non-invasive Multiparametric Test (Work Package 1)
- Status
- Active Not Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 2,000 (estimated)
- Sponsor
- Nottingham University Hospitals NHS Trust · Academic / Other
- Sex
- All
- Age
- 5 Years – 70 Years
- Healthy volunteers
- Accepted
Summary
Irritable bowel syndrome (IBS) affects one in seven people with gastrointestinal (GI) symptoms. IBS strongly impacts quality of life, is a leading cause of work absenteeism, and consumes 0.5% of the healthcare annual budget. It manifests in women more than men with symptoms including abdominal pain, bloating, constipation (IBS-C), diarrhoea (IBS-D), and mixed presentations (IBS-M) (1). The development of therapeutic options is hampered by the poor understanding of the underlying cause of symptoms. Many patients find that certain foods (particularly carbohydrates) trigger their symptoms, and avoiding such foods has been shown effective in IBS, like in the low-FODMAP (fermentable oligo-, di-, mono-saccharides and polyols) exclusion diet. This has suggested that the food-symptom relation may involve malabsorption of carbohydrates due to inefficient digestion. However only a percentage of patients respond to this diet. Recently it has been reported that a subset of IBS carries hypomorphic (defective) gene variant of the sucrase isomaltase (SI), the enzyme that normally digests carbohydrates, sucrose and starch. This carbohydrate maldigestion (the breakdown of complex carbohydrates by a person's small bowel enzymes) is characterized by diarrhoea, abdominal pain and bloating, which are also features of IBS. This possibly occurs via accumulation of undigested carbohydrates in the large bowel, where they cause symptoms due to gas production following bacterial fermentation. Similar mechanisms may be acting at the level of other enzymes involved in the digestion, breakdown and absorption of carbohydrates (carb digestion genes -CDGs). Aim of the study is to study the prevalence of this genetic alteration in a large number of IBS patients as compared to asymptomatic controls.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Stool and saliva sample collection | Stool and saliva samples collection |
| OTHER | Questionnaire completion | Questionnaire on; * demographic, ethnicity, IBS subtype, post-infection onset, previous surgeries * IBS severity score for adults * Hospital Anxiety and Depression scores for adults * Somatization score for adults * Total glucose and fructose and excess fructose, lactose, sorbitol, mannitol, oligosaccharides (Fructans and GOS) as measured by CNAQ questionnaire for adults and children * Quality of Life as measured by the PedsQL™ GI Symptoms Module * GI symptoms as measured by the PedsQL™ GI Symptoms Module * Anxiety, Depression as measured by the Pediatric PROMIS® |
Timeline
- Start date
- 2024-07-23
- Primary completion
- 2025-09-30
- Completion
- 2026-03-31
- First posted
- 2023-04-03
- Last updated
- 2025-12-19
Locations
1 site across 1 country: United Kingdom
Source: ClinicalTrials.gov record NCT05795049. Inclusion in this directory is not an endorsement.