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Minimising the impact of high fructose foods for patients with Irritable Bowel Syndrome: investigating the use of added glucose to assist with fructose absorption from food by the small intestine in healthy volunteers and in patients with IBS

Minimising the impact of high fructose foods for patients with Irritable Bowel Syndrome: investigating the use of added glucose to assist with fructose absorption from food by the small intestine in healthy volunteers and in patients with IBS

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12616000766415
Enrollment
18
Registered
2016-06-10
Start date
2008-04-01
Completion date
2009-03-01
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Malabsorption of fructose occurs in 40% of healthy Australians but may be a major problem for individuals with Irritable Bowel Syndrome. The addition of glucose has been shown to assist in free fructose absorption in test solutions and juices however this effect has never been investigated using whole foods. The aim was to investigate the effect on fructose absorption when glucose was added to foods with naturally high levels of free fructose in a randomised, single-blinded, crossover intervention trial.

Interventions

This was a randomised, single-blind crossover trial using whole foods as the source of fructose with and without added glucose. During a 36-h low FODMAP (Fermentable, Oligosaccharides, Disacchardies, Monosaccharides and Polyols) run-in period, followed by a 24-h test day, all food was provided. Breath hydrogen samples were collected hourly for 14 h on two consecutive days, commencing before breakfast each day. For the test day, participants were randomised to either a diet high in fructose with

This was a randomised, single-blind crossover trial using whole foods as the source of fructose with and without added glucose. During a 36-h low FODMAP (Fermentable, Oligosaccharides, Disacchardies, Monosaccharides and Polyols) run-in period, followed by a 24-h test day, all food was provided. Breath hydrogen samples were collected hourly for 14 h on two consecutive days, commencing before breakfast each day. For the test day, participants were randomised to either a diet high in fructose with no added glucose (high fructose diet), or high in fructose with glucose added to give a 1:1 ratio of free fructose to free glucose (fructose/glucose co-administration diet). Following a one-week washout period, participants crossed over to the alternative diet. For both test diets, foods included were naturally high in fructose in excess of glucose (including watermelon, apple/guava juice, pear and apple muffins). The remainder of the diet was low in total FODMAP content. For the fructose/glucose co-administration diet, glucose was co-ingested by participants in tablet form (Glucodin tablets; Reckitt Benckiser, NSW Australia) when whole pieces of fruit were eaten. Participants were asked to consume the glucose tablets at the time of meal consumption. Glucose powder (Glucodin Powder; Reckitt Benckiser, NSW Australia) was added during the baking process for apple muffins and pre-mixed with apple/guava juice. For the high fructose diet, sucrose cubes and powder replaced the glucose to aid in blinding the participants. The high fructose foods provided 11 g of fructose in excess of glucose. The diets provided during the two run-in periods were identical. The two high excess-fructose diets were also identical apart from the addition of sucrose and/or glucose. There were no differences in macronutrient content between the two test diets including total carbohydrate, starch, dietary fibre and total sugar levels. The provided diet on the test day is listed below: † denotes high fructose foods Energy intake was not individualised, it was a standard amount, the same given to each participant. Total energy provided was 9.5MJ/day. Breakfast: Corn flakes (30 g), Milk (LF), Bread 2 slices (GF), Butter/margarine, Vegemite, † 1 slice fresh Watermelon (plus 1 *glucose tablet), †Apple-guava Juice (200ml + 1.5 g *glucose powder) Morning tea: † 1 fresh Pear (plus 6 *glucose tablets), Sweet biscuit (GF) Lunch: Chicken pasta bake, † Apple-guava Juice (200ml + 1.5 g glucose) Afternoon tea: † Apple muffin (GF + 0.1 g glucose) Dinner: Lasagne (GF) Supper: Drinking chocolate Note: Each glucose tablet contains 1.5g glucose. Participants completed food diaries to monitor compliance. Participants consume all meals at home at their own convenience. It was up to the participant as to what time of day each meal and snack was consumed.

Sponsors

Monash University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject)

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

Inclusion criteria required participants to be aged 18-70 years, and, within the past 3 months, to have fructose malabsorption identified by breath hydrogen rise of >15 ppm after 35 g fructose. Two groups of fructose malabsorbers were recruited: healthy subjects (without gastrointestinal symptoms) and patients with FBD, as determined by a gastroenterologist using the Rome III criteria. Those who expressed interest but had a positive fructose breath test more than 3 months prior were asked to repeat the fructose breath test prior to enrolment and only if fructose malabsorption was retained were they then invited to enrol.

Exclusion criteria

Exclusion criteria included inadequate breath hydrogen production (<15 ppm) after 35 g fructose, pregnancy or breastfeeding, diabetes, other gastrointestinal disorders such as coeliac disease, antibiotic or probiotic use in the past 2 weeks, and the taking of colonoscopy preparations in the past 4 weeks.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026