GRAIN: Gluten Reduction and Risk of Celiac Disease

Sponsor
Lund University (Other)
Overall Status
Recruiting
CT.gov ID
NCT04593888
Collaborator
(none)
2,000
1
2
175.9
11.4

Study Details

Study Description

Brief Summary

Celiac disease shares many features of other autoimmune diseases such as type 1 diabetes. Recently, it was published that higher amounts of gluten intake increased the risk for celiac disease. Optimal amounts of gluten to be introduced during weaning have not yet been established. The aim is to investigate if a gluten-restricted diet (e.g. below 3 gram per day) will reduce the risk of develop CDA and IA in genetically predisposed children by the age of 5 years. Children who screened positive for HLA DQ2/X (X is neither DQ2 nor DQ8) in the GPPAD-02 (ASTR1D [ClinicalTrials.gov Identifier NCT03316261]) screening will be contacted by a study nurse.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Gluten reduced diet
N/A

Detailed Description

Gluten is a complex mixture of proteins, mainly gliadin and glutenin, rich in proline and glutamine amino acids which make these proteins resistant to complete degradation by enzymes in the small intestinal. Intolerance to gluten leads to inflammation of the intestinal epithelium and villous atrophy, a disorder called celiac disease. Celiac disease shares many features of other autoimmune diseases such as type 1 diabetes (T1D). First, celiac disease is associated with certain HLA genotypes of whom 95% of all patients with celiac disease carry the haplotypes DQA10501-DQB10201 (abbreviated DQ2) and the reminder 5% DQA10301-DQB10302 (abbreviated DQ8). There is a gene dose effect of HLA-DQ on the risk of develop celiac disease; 20% of the children homozygous for HLA-DQ2/DQ2 will develop celiac disease by 10 years of age. Second, celiac disease is also strongly associated with the presence of autoantibodies directed against tissue transglutaminase (tTGA) that occurs in 100% of children with celiac disease. Timing of gluten introduction and breastfeeding duration have previously been proposed to influence risk for celiac disease. However, based on the results from the multinational birth cohort study The Environmental determinants of Diabetes in the Young (TEDDY) study and other observational studies, timing of gluten introduction seems not associated with celiac disease in genetically at-risk children. In an RCT, introduction of small amounts of gluten at the age of 4-6 months did not reduce the risk for celiac disease by the age of 3 years in genetically at-risk children. Current international infant feeding recommendations recommend that gluten is introduced into the infant's diet anytime between 4-12 months of age and that consumption of large quantities of gluten should be avoided during the first month after gluten introduction and during infancy. Recently, the TEDDY study published that higher amounts of gluten intake increased the risk for celiac disease, which have been confirmed in two other observational cohort studies. In the TEDDY study, daily gluten intake was associated with higher increased risk of developing persistently positive tTGA, a definition coined celiac disease autoimmunity (CDA), as well as with celiac disease for every 1-g/day increase in gluten intake. Optimal amounts of gluten to be introduced during weaning have not yet been established. It is well known that an overlap between celiac disease and T1D exists most likely due to shared genetic risks of HLA-DQ2 and/or DQ8 in both disorders. Prospective studies in infants genetically predisposed to T1D and celiac disease showed that antibody positivity to both disorders begins in the first 1-3 years of life. The study aim is to investigate if a gluten-restricted diet will reduce the risk of develop CDA and IA in genetically predisposed children by the age of 5 years.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
2000 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Masking Description:
study participants will be randomized to either the "gluten-reduced" or "no intervention" arm on-going after enrolment.
Primary Purpose:
Prevention
Official Title:
Gluten Reduction After Infancy and Risk of Celiac Disease Study
Actual Study Start Date :
May 5, 2021
Anticipated Primary Completion Date :
Dec 31, 2025
Anticipated Study Completion Date :
Dec 31, 2035

Arms and Interventions

Arm Intervention/Treatment
No Intervention: No intervention

The group will be followed without any intervention, with regular visits at the research clinic.

Experimental: Gluten reduced diet

Subjects will follow a diet that does not exceed a daily intake of 3 gram gluten. The group will be followed with regular visits at the research clinic.

Behavioral: Gluten reduced diet
Dietary advice focusing on reducing gluten intake in children

Outcome Measures

Primary Outcome Measures

  1. Celiac disease autoimmunity (CDA) [from 6 months of age up until 10 years of age]

    Children tested positive for tissue transglutaminase autoantibodies (tTGA) in two consecutive serum samples 3-6 months apart.

Secondary Outcome Measures

  1. Celiac disease (CD) [from 6 months of age up until 10 years of age]

    celiac disease diagnosed, defined by intestinal biopsy showing a Marsh score of >2 or by high levels of tTGA with symptoms.

Other Outcome Measures

  1. Islet autoimmunity [from 6 months of age up until 10 years of age]

    Children tested positive for typ1 1 diabetes related autoantibodies (IAA, GADA, IA2A) in two consecutive serum samples 3-6 months apart.

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Months to 6 Months
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • children screened positive for HLA DQ2/X (X is neither DQ2 or DQ8)

  • children who refused enrolment to the on-going study PreSiCe (ClinicalTrials.gov Identifier NCT03562221)

Exclusion Criteria:
  • congenital chronic disorder where intervention with diet may be affected

  • written informed consent from both caregivers are missing

Contacts and Locations

Locations

Site City State Country Postal Code
1 Clinical Research Center (CRC), Bldng 60:11 Malmö Sweden 20502

Sponsors and Collaborators

  • Lund University

Investigators

  • Principal Investigator: Daniel Agardh, MD, PhD, Lund University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Lund University
ClinicalTrials.gov Identifier:
NCT04593888
Other Study ID Numbers:
  • 2020-00446
First Posted:
Oct 20, 2020
Last Update Posted:
May 12, 2021
Last Verified:
May 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Lund University
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 12, 2021