Gfree - For Improved Blood Sugar and Reduced Inflammation.

Sponsor
Göteborg University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05894746
Collaborator
University of Skövde (Other), Sahlgrenska University Hospital, Sweden (Other), Ekhaga foundation (Other)
60
2
3
90.9
30
0.3

Study Details

Study Description

Brief Summary

The goal of this clinical trial is to reduce inflammation and improve glycemic control in healthy volunteers, parents, as well as children, adolescents and adults with or without diabetes. The main questions it aims to answer are: • does a reduction wheat gluten improve glycemic control and/or inflammatory biomarkers • does a reduction in certain amino acids (which is most common in wheat gluten) improve glycemic control and/or inflammatory biomarkers • can we identify individuals with an inflammatory response, which leads to poor glycemic control. Participants will eat gluten-free products as well as similar products containing gluten. They will also eat gluten together with probiotics to see if an effect of gluten can be reduced. Researchers will compare everyone with themselves (cross-over design) and if possible individuals with and without diabetes.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: gluten-free
  • Dietary Supplement: probiotic
  • Dietary Supplement: gluten
N/A

Detailed Description

BACKGROUND AND PURPOSE Many diseases, which are common in high-income countries, have an inflammatory component. In the world's rich countries, about 10% of the population will be diagnosed with a traditional inflammatory autoimmune disease during their lifetime. In an autoimmune disease, the body produces auto-antibodies against the body's own protein and the immune system destroys the body's own tissues. There are hundreds of different types of autoimmune diseases where some of the most common are; celiac disease (gluten intolerance), psoriasis, type 1 diabetes (T1D), multiple sclerosis, rheumatic diseases or thyroid diseases. Diseases such as cardiovascular disease, type 2 diabetes (T2D) and Alzheimer's disease are now also considered to have inflammatory components, and so-called auto-antibodies have been identified that indicate autoimmunity also in these diseases. Autoantibodies have also been identified in COVID-19 patients.

To try to understand the biology behind autoimmunity and inflammatory disease, the investigators have analyzed the entire genome of patients with celiac disease as a model for autoimmunity. Celiac disease is a good so-called model disease for autoimmunity because the autoimmune reaction can be switched on and off with the help of gluten in the diet. With a strict gluten-free diet, virtually all signs of illness disappear and the inflammation ceases. The results from our whole genome analysis showed that genes involved in amino acid signaling were important for disease development and pointed to associations between celiac disease, T2D and anorexia. These results were somewhat surprising and the investigators began to look at the role of nutritional signaling and amino acids in inflammatory processes further.

The purpose of this study is to test whether a reduction in certain amino acids (which is most common in wheat gluten) can improve glycemic control in healthy volunteers, parents, as well as children, adolescents and adults with diabetes and whether levels of inflammatory amino acids may be one of the factors behind the link between diabetes and severe COVID-19 infection.

The participants will, for 4 weeks, eat one week as usual, eat one week wheat gluten-free, one week wheat gluten and one week with gluten and probiotics. The participants will be provided with continuous glucose monitors and activity-tracking bracelets. The investigators will analyze the efficiency of glucose uptake using continuous glucose monitors (CGM). During these four weeks, the research subjects will be admitted for 4 clinical visits (baseline, after 1 week, 2 weeks, 3 weeks) where blood samples will be taken. Also, during these weeks the participant will take capillary blood samples, faeces, urine, buccal swabs and saliva at home and fill out a questionnaire based on diet and risk factors for diabetes and questions about COVID-19.

Total number of participants: 60 Sampling occasions per participant: 15 Follow-up period per participant: 4 weeks Number of years for inclusion: 2 years (20221201-20241201)

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Non-Randomized
Intervention Model:
Crossover Assignment
Intervention Model Description:
Four week crossover trial with three arms, gluten-free, gluten and gluten with probioticFour week crossover trial with three arms, gluten-free, gluten and gluten with probiotic
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
GFREE - A Study for Improved Blood Sugar Levels, Reduced Inflammation and for Increasing Knowledge of the Connection Between Diabetes and COVID-19.
Actual Study Start Date :
May 4, 2023
Anticipated Primary Completion Date :
Dec 1, 2024
Anticipated Study Completion Date :
Dec 1, 2030

Arms and Interventions

Arm Intervention/Treatment
Experimental: gluten-free

The study participants will start the gluten-free diet and be asked to exchange any products they normally buy with similar products. Three days in the week they will eat a meal with gluten free pasta. Two to six hours after the meal they will take samples at home and store until they return to the clinic.

Dietary Supplement: gluten-free
see info in arm description

Active Comparator: gluten

The study participants will continue the gluten-free diet and be asked to exchange any products they normally buy with similar products. Three days however, in the week they will eat a meal with regular gluten containing pasta. Two to six hours after the meal they will take samples at home and store until they return to the clinic.

Dietary Supplement: gluten-free
see info in arm description

Dietary Supplement: gluten
see info in arm description

Active Comparator: probiotic

The study participants will continue the gluten-free diet and be asked to exchange any products they normally buy with similar products. During the week they will also take probiotic (Probion, Active) every morning and every evening. Three days however, in the week they will eat a meal with regular gluten containing pasta. Two to six hours after the meal they will take samples at home and store until they return to the clinic.

Dietary Supplement: gluten-free
see info in arm description

Dietary Supplement: probiotic
see info in arm description

Outcome Measures

Primary Outcome Measures

  1. Stabilizing of blood sugar levels [0 days to 4 weeks]

    Continuous glucose monitoring (CGM) data will be analysed together with activity level data, lower glucose peaks after a meal, adjusted for activity level.

  2. Amino acid metabolism [0 days to 4 weeks]

    Lowering of the aminoacid proline

Secondary Outcome Measures

  1. Blood Lipids [0 days to 4 weeks]

    LDL, improved apolipoprotein B (APOB)

  2. Glutathione S Transferases [0 days to 4 weeks]

    Relative Glutathione S Transferases expression levels

  3. Fibrinogen [0 days to 4 weeks]

    Relative Fibrinogen expression levels

Other Outcome Measures

  1. multiomics explorative analyses [0 days to 4 weeks]

    Genomics, transcriptomics2, metabolomics and proteomics analyses are planned

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • none
Exclusion Criteria:
  • A diagnosis of celiac disease

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sahlgrenska University Hospital Gothenburg Sweden
2 University of Skövde Skövde Sweden

Sponsors and Collaborators

  • Göteborg University
  • University of Skövde
  • Sahlgrenska University Hospital, Sweden
  • Ekhaga foundation

Investigators

  • Principal Investigator: Åsa Torinsson Naluai, PhD, Göteborg University
  • Study Director: Katarina Ejeskär, PhD, University of Skövde

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Göteborg University
ClinicalTrials.gov Identifier:
NCT05894746
Other Study ID Numbers:
  • GFREE
First Posted:
Jun 8, 2023
Last Update Posted:
Jun 8, 2023
Last Verified:
Jun 1, 2023
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 Göteborg University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 8, 2023