GlutDigest: Digestion of Gluten in the Presence of Enzymes

Sponsor
Deerland Enzymes (Industry)
Overall Status
Recruiting
CT.gov ID
NCT04489810
Collaborator
Teagasc (Industry), Atlantia Food Clinical Trials (Industry)
15
1
4
6.4
2.4

Study Details

Study Description

Brief Summary

This study evaluates the impact of two dietary supplements (Glutalytic® and DE111®) and of oatmeal properties on the digestion of gluten and starch and on the glycemic response.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Placebo
  • Dietary Supplement: Glutalytic®
  • Dietary Supplement: DE111®
  • Other: Meal A
  • Other: Meal B
N/A

Detailed Description

RATIONALE Two important factors can influence the proportions of gluten and starch that resist digestion: (1) enzyme availability and specificity and (2) the structural properties of the food.

Glutalytic®, is a dietary supplement based on an enzyme preparation which effectively degrades gluten in vitro (Healey, Hall et al. unpublished). As it has also been found that the rate of wheat protein digestion can be increased in the presence of amylases (Smith, Pan et al. 2015), Glutalytic ® is also enriched with amylase to aid in starch digestion.

The structural properties of food are influenced by numerous factors including meal preparation practices. Two common practices that can influence nutrient availability differently are heating vs. refrigerating (e.g. oat porridge vs. soaked and refrigerated oats).

Bacillus subtilis DE111® can produce and secrete many enzymes, including proteases, which, if secreted into the environment of the digestive tract, could support digestion and, in particular, the digestion of gluten. However, it is not clear whether diet supplementation with DE111 is a physiologically viable approach in terms of probiotic survival in the gastrointestinal tract.

PURPOSE The aims of this study are to better understand the impact of each of these factors and whether supplementation with probiotic spores is a viable option.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
15 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Primary Purpose:
Other
Official Title:
GlutDigest - Enzymes-assisted Gluten Digestion
Actual Study Start Date :
Sep 19, 2020
Anticipated Primary Completion Date :
Mar 1, 2021
Anticipated Study Completion Date :
Apr 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Meal A + Placebo

350 mg Placebo capsule, taken by mouth, once, with Meal A

Dietary Supplement: Placebo
Maltodextrin capsule manufactured to mimic the Glutalytic® and DE111® capsules

Other: Meal A
Oatmeal porridge - serving of cooked oats containing 50g of carbohydrates (excluding sugars); Wheat cereal - serving of wheat cereal providing 1g of gluten; Water - 125 mL

Experimental: Meal A + Glutalytic®

350 mg Glutalytic® capsule, taken by mouth, once, with Meal A

Dietary Supplement: Glutalytic®
1 capsule containing 350 mg of Glutalyltic®

Other: Meal A
Oatmeal porridge - serving of cooked oats containing 50g of carbohydrates (excluding sugars); Wheat cereal - serving of wheat cereal providing 1g of gluten; Water - 125 mL

Experimental: Meal A + DE111®

350 mg DE111® capsule, taken by mouth, once, with Meal A

Dietary Supplement: DE111®
1 capsule containing Bacillus subtilis DE111

Other: Meal A
Oatmeal porridge - serving of cooked oats containing 50g of carbohydrates (excluding sugars); Wheat cereal - serving of wheat cereal providing 1g of gluten; Water - 125 mL

Experimental: Meal B + Placebo

350 mg Placebo capsule, taken by mouth, once, with Meal B

Dietary Supplement: Placebo
Maltodextrin capsule manufactured to mimic the Glutalytic® and DE111® capsules

Other: Meal B
Refrigerated oatmeal - serving of refrigerated oats containing 50g of carbohydrates (excluding sugars); Wheat cereal - serving of wheat cereal providing 1g of gluten; Water - 125 mL

Outcome Measures

Primary Outcome Measures

  1. Undigested wheat protein [9-hour period after the test meal]

    Difference between the mean concentration of undigested wheat protein in ileal effluent samples.

Secondary Outcome Measures

  1. Vegetative DE111 cells [9-hour period after the test meal]

    Mean concentration of DE111® cells recovered in the ileal effluent in the vegetative state.

  2. Glycemic response [At baseline, and at different time-points during 9 hours after after consuming the test meal.]

    Difference between the mean area under the glucose concentration (measured in the interstitial fluid) curves following each treatment

  3. Undigested starch [At baseline and once every hour in the 9-hour period after consumption of the test meal.]

    Difference between the mean concentration of undigested starch in ileal effluent samples.

  4. Undigested food particles [9-hour period after the test meal]

    Pictures of undigested foods particles and microscopy will be combined for a combined assessment of macro- and micro- structural characteristics of the food particles recovered in ileal effluent samples.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Subject has given written informed consent

  • Subject has an ileostomy stable for at least 3 months post-operative and shows normal stoma functions

  • Subject is otherwise healthy

  • Subject is available to participate in the study sessions on the proposed dates

Exclusion Criteria:
  • Subject has coeliac disease or allergy to wheat products and/or any other ingredients in the test meal and standard meals

  • Case of obstruction of the stoma in the past 3 months

  • Body mass index < 18 kg/m2 or > 30 kg/m2.

  • Diagnosed mouth, throat or active gastrointestinal pathology (other than ileostomy) that may affect normal ingestion and digestion of food.

  • History of pancreatic disease

  • Subject is immunocompromised (HIV positive, transplant patient, on antirejection medications, on a steroid for >30 days, or chemotherapy or radiotherapy within the last year)

  • Subject has Type 1 or Type 2 diabetes mellitus.

  • Subject has a history of bariatric surgery.

  • Subject has a history of drug and/or alcohol abuse at the time of enrolment

  • Subject is currently participating in another study, or plans to participate in another study during the study period

  • Women of child-bearing potential who do not use an acceptable method of contraception

  • Pregnant or nursing (lactating) women

Contacts and Locations

Locations

Site City State Country Postal Code
1 Atlantia Food Clinical Trials Cork Ireland

Sponsors and Collaborators

  • Deerland Enzymes
  • Teagasc
  • Atlantia Food Clinical Trials

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Deerland Enzymes
ClinicalTrials.gov Identifier:
NCT04489810
Other Study ID Numbers:
  • Project 0470
First Posted:
Jul 28, 2020
Last Update Posted:
Feb 15, 2021
Last Verified:
Oct 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Deerland Enzymes

Study Results

No Results Posted as of Feb 15, 2021