The completion of the Trial to Reduce Insulin Dependent Diabetes in the Genetically at Risk ('TRIGR') will determine whether weaning to a formula in which (foreign) proteins have been extensively hydrolyzed, reduces disease risk for type 1 diabetes (T1D) in genetically susceptible children, as it does in rodent models.
The Specific Aims are: I-a: To determine whether weaning to casein hydrolysate reduces the frequency of clinical diabetes; and I-b: To assess a potential shift in the age-adjusted incidence (not the cumulative incidence) of autoantibodies and T1D to a later time period in the group treated with the hydrolyzed study formula. This longest and largest, double-blind, randomized controlled trial in subjects with an affected first-degree relative and risk-associated HLA genotypes is currently in its 14th year. An international, multicenter consortium has been developed comprising 77 centers in 15 countries. Enrollment of 2159 eligible infants was completed successfully, providing a cushion above the required 2032 infants. The 6-8 month intervention designed to compare the effects of either hydrolyzed casein or standard cow milk based weaning formula was completed in 2007. Duration of breast-feeding was at the mothers' discretion and similar to or above background populations. All subjects are followed during and after the intervention period for at least 10 years with measurements of immune markers of intact cow milk exposure, diabetes predictive autoantibodies and the clinical and/or metabolic indices of diabetes (the end point at age 10-14 years). Currently all planning parameters have been met and drop- out rate is 2% with compliance at expected level. A large, cross-linked repository of stored sera, DNA, T-cell data, and cryopreserved peripheral blood mononuclear cells allows independently funded ancillary and mechanistic studies related to the natural history of prediabetes and the hypothesis to be tested. This application covers years 16- 18 for the International Coordinating Center and the Core Autoantibody Laboratory at the University of Helsinki and for the study centers in Europe and Australia which is submitted in tandem with those of the US coordinating center and clinical centers and that of the Data Management Unit. Funding is requested for completing the trial and reporting the outcome.

Public Health Relevance

TRIGR is the largest primary prevention trial ever for T1D which is close to its completion. It tests the longstanding controversy whether weaning to hydrolyzed (non-intact) cow's milk protein protects against the development of T1D. It has been conducted extremely successfully and generated a highly valuable set of data and biological samples. Funding for completing the trial and reporting the outcome is requested.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
2R01HD051997-11
Application #
9027657
Study Section
Biobehavioral and Behavioral Sciences Subcommittee (CHHD)
Program Officer
Grave, Gilman D
Project Start
2006-07-10
Project End
2019-06-30
Budget Start
2016-07-01
Budget End
2017-06-30
Support Year
11
Fiscal Year
2016
Total Cost
Indirect Cost
Name
University of South Florida
Department
Pediatrics
Type
Schools of Medicine
DUNS #
069687242
City
Tampa
State
FL
Country
United States
Zip Code
33612
Writing Group for the TRIGR Study Group; Knip, Mikael; Ã…kerblom, Hans K et al. (2018) Effect of Hydrolyzed Infant Formula vs Conventional Formula on Risk of Type 1 Diabetes: The TRIGR Randomized Clinical Trial. JAMA 319:38-48
Nucci, Anita M; Virtanen, Suvi M; Sorkio, Susa et al. (2017) Regional differences in milk and complementary feeding patterns in infants participating in an international nutritional type 1 diabetes prevention trial. Matern Child Nutr 13:
Lehtonen, Eveliina; Ormisson, Anne; Nucci, Anita et al. (2014) Use of vitamin D supplements during infancy in an international feeding trial. Public Health Nutr 17:810-22
Knip, Mikael; Ã…kerblom, Hans K; Becker, Dorothy et al. (2014) Hydrolyzed infant formula and early ?-cell autoimmunity: a randomized clinical trial. JAMA 311:2279-87
Hadley, David; Cheung, Roy K; Becker, Dorothy J et al. (2014) Large-scale prospective T cell function assays in shipped, unfrozen blood samples: experiences from the multicenter TRIGR trial. Clin Vaccine Immunol 21:203-11
Franciscus, Margaret; Nucci, Anita; Bradley, Brenda et al. (2014) Recruitment and retention of participants for an international type 1 diabetes prevention trial: a coordinators' perspective. Clin Trials 11:150-8
Kingery, Suzanne E; Wu, Yee Ling; Zhou, Bi et al. (2012) Gene CNVs and protein levels of complement C4A and C4B as novel biomarkers for partial disease remissions in new-onset type 1 diabetes patients. Pediatr Diabetes 13:408-18
Nucci, Anita M; Becker, Dorothy J; Virtanen, Suvi M et al. (2012) Growth differences between North American and European children at risk for type 1 diabetes. Pediatr Diabetes 13:425-31
Vehik, Kendra; Cuthbertson, David; Boulware, David et al. (2012) Performance of HbA1c as an early diagnostic indicator of type 1 diabetes in children and youth. Diabetes Care 35:1821-5
Knip, Mikael; Virtanen, Suvi M; Becker, Dorothy et al. (2011) Early feeding and risk of type 1 diabetes: experiences from the Trial to Reduce Insulin-dependent diabetes mellitus in the Genetically at Risk (TRIGR). Am J Clin Nutr 94:1814S-1820S

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