Article (Scientific journals)
The Trial to Reduce IDDM in the Genetically at Risk (TRIGR) study: recruitment, intervention and follow-up.
Akerblom, H.K.; Krischer, J; Virtanen, SM et al.
2011In Diabetologia, 54 (3), p. 627-633
Peer Reviewed verified by ORBi
 

Files


Full Text
akerblom et al. 2011 the trial to reduce IDDM.pdf
Publisher postprint (152.66 kB)
Download

All documents in ORBilu are protected by a user license.

Send to



Details



Keywords :
IDDM reduction; TRIGR study; genetic risk; hydrolysed formula; infancy; children; risk of diabetes; diabetes type 1
Abstract :
[en] AIMS/HYPOTHESIS: The Trial to Reduce IDDM in the Genetically at Risk (TRIGR) study was designed to establish whether weaning to a highly hydrolysed formula in infancy subsequently reduces the risk of type 1 diabetes. METHODS: The study population comprises newborn infants who have first-degree relatives with type 1 diabetes and meet the increased risk HLA inclusion, but not exclusion criteria. The study is being performed in 15 countries in three continents. First-degree relatives of patients with type 1 diabetes were identified from diabetes clinics, diabetes registries, and from other endocrinology or obstetrics offices and websites. HLA typing was performed at birth from cord or heel stick blood, and the results sent to the study's Data Management Unit within 2 weeks for communication of eligibility to the clinical study centre. All mothers recruited were encouraged to breastfeed. The intervention lasted for 6 to 8 months, and weaning formulas based on hydrolysed casein and standard cow's milk were compared. RESULTS: TRIGR recruited 5,606 infants, of whom 2,160 were enrolled as eligible participants, 6% more than the target of 2,032. Of those enrolled, 80% were exposed to the study formula. The overall retention rate over the first 5 years is 87%, with protocol compliance at 94%. The randomisation code will be opened when the last recruited child turns 10 years of age, i.e. in 2017. CONCLUSIONS/INTERPRETATION: The TRIGR experience demonstrates the feasibility and successful implementation of an international dietary intervention study. TRIGR is the first ever primary prevention trial for type 1 diabetes and, if completed successfully, will provide a definite answer to the research question. TRIAL REGISTRATION: ClinicalTrials.gov NCT00179777 FUNDING: The study was funded by the National Institute of Child Health and Development (NICHD) and National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), National Institutes of Health (NIH) (grant numbers HD040364, HD042444 and HD051997), Canadian Institutes of Health Research, the Juvenile Diabetes Research Foundation International and the Commission of the European Communities (specific RTD programme 'Quality of Life and Management of Living Resources', contract number QLK1-2002-00372 'Diabetes Prevention'. Other funding came from the EFSD/JDRF/Novo Nordisk Focused Research Grant, Academy of Finland, Dutch Diabetes Research Foundation and Finnish Diabetes Research Foundation).
Disciplines :
Human health sciences: Multidisciplinary, general & others
Author, co-author :
Akerblom, H.K.
Krischer, J
Virtanen, SM
Berseth, C
Becker, D
Dupré, J
Ilonen, J
Trucco, M
Savilahti, E
Koski, K
Pajakkala, E
Fransiscus, M
Lough, G
Bradley, B
Koski, M
Knip, M
De Beaufort, Carine ;  University of Luxembourg > Luxembourg Centre for Systems Biomedicine (LCSB)
More authors (7 more) Less
External co-authors :
yes
Language :
English
Title :
The Trial to Reduce IDDM in the Genetically at Risk (TRIGR) study: recruitment, intervention and follow-up.
Publication date :
March 2011
Journal title :
Diabetologia
ISSN :
1432-0428
Publisher :
Springer Verlag, Berlin, Germany
Volume :
54
Issue :
3
Pages :
627-633
Peer reviewed :
Peer Reviewed verified by ORBi
Name of the research project :
TRIGR STUDY GROUP
Available on ORBilu :
since 20 May 2016

Statistics


Number of views
62 (0 by Unilu)
Number of downloads
106 (0 by Unilu)

Scopus citations®
 
77
Scopus citations®
without self-citations
47
OpenCitations
 
53
WoS citations
 
53

Bibliography


Similar publications



Contact ORBilu