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Interaction Between Dietary Iron Intake and Genetically Determined Iron Overload: Risk of Islet Autoimmunity and Progression to Type 1 Diabetes in the TEDDY Study




TekijätThorsen Steffen U., Liu Xiang, Kataria Yachana, Mandrup-Poulsen Thomas, Kaur Simranjeet, Uusitalo Ulla, Virtanen Suvi M., Norris Jill M., Rewers Marian, Hagopian William, Yang Jimin, She Jin-Xiong, Akolkar Beena, Andrén Aronsson Carin, Lernmark Åke, Ziegler Anette-Gabriele, Toppari Jorma, Krischer Jeffrey, Parikh Hemang M., Ellervik Christina, Svensson Jannet; TEDDY Study Group

Julkaisuvuosi2023

JournalDiabetes Care

Tietokannassa oleva lehden nimiDiabetes care

Lehden akronyymiDiabetes Care

Vuosikerta46

Numero5

Aloitussivu1014

Lopetussivu1018

ISSN0149-5992

eISSN1935-5548

DOIhttps://doi.org/10.2337/dc22-1359

Verkko-osoitehttps://diabetesjournals.org/care/article-abstract/46/5/1014/148558/Interaction-Between-Dietary-Iron-Intake-and?redirectedFrom=fulltext


Tiivistelmä
OBJECTIVE

To examine whether iron intake and genetically determined iron overload interact in predisposing to the development of childhood islet autoimmunity (IA) and type 1 diabetes (T1D).

RESEARCH DESIGN AND METHODS

In The Environmental Determinants of Diabetes in the Young (TEDDY) study, 7,770 genetically high-risk children were followed from birth until the development of IA and progression to T1D. Exposures included energy-adjusted iron intake in the first 3 years of life and a genetic risk score (GRS) for increased circulating iron.

RESULTS

We found a U-shaped association between iron intake and risk of GAD antibody as the first autoantibody. In children with GRS ≥2 iron risk alleles, high iron intake was associated with an increased risk of IA, with insulin as first autoantibody (adjusted hazard ratio 1.71 [95% CI 1.14; 2.58]) compared with moderate iron intake.

CONCLUSIONS

Iron intake may alter the risk of IA in children with high-risk HLA haplogenotypes.



Last updated on 2025-27-03 at 21:52