Thyroid autoimmunity and the subsequent development of islet and celiac autoimmunity in the TEDDY study
(2026) In American Journal of Epidemiology- Abstract
We aimed to determine if thyroid autoimmunity is associated with a child's risk for subsequent development of islet or celiac autoantibodies. Children at high genetic risk of type 1 diabetes were followed for thyroid autoimmunity (thyroid peroxidase antibodies [TPOAb] and thyroglobulin antibodies [TGAb]), islet autoimmunity (IA), and celiac disease autoimmunity [CDA] in The Environmental Determinants of Diabetes in the Young (TEDDY) study. Out of 5482 children tested for thyroid autoimmunity, IA, and CDA, 39% developed at least one autoantibody. At age 14 years, thyroid autoimmunity co-occurred with IA in 59 children (15 more cases than expected by chance alone, p = 0.02), and with CDA in 125 children (26 cases above expected, p =... (More)
We aimed to determine if thyroid autoimmunity is associated with a child's risk for subsequent development of islet or celiac autoantibodies. Children at high genetic risk of type 1 diabetes were followed for thyroid autoimmunity (thyroid peroxidase antibodies [TPOAb] and thyroglobulin antibodies [TGAb]), islet autoimmunity (IA), and celiac disease autoimmunity [CDA] in The Environmental Determinants of Diabetes in the Young (TEDDY) study. Out of 5482 children tested for thyroid autoimmunity, IA, and CDA, 39% developed at least one autoantibody. At age 14 years, thyroid autoimmunity co-occurred with IA in 59 children (15 more cases than expected by chance alone, p = 0.02), and with CDA in 125 children (26 cases above expected, p = 0.01). The risk of developing IA or CDA after thyroid autoimmunity varied by which thyroid autoantibody appeared first: TPOAb-first was associated with both IA (HR 1.92, 95% CI 1.09, 3.40) and CDA (1.69, 95% CI 1.03, 2.76), whereas TGAb-first was not associated with the risk of either. IA and CDA are frequently found in connection to thyroid autoimmunity in children and young adolescents. The relationships of thyroid autoimmunity with IA and CDA depend on which thyroid autoantibody appears first.
(Less)
- author
- organization
- publishing date
- 2026-01-23
- type
- Contribution to journal
- publication status
- epub
- subject
- in
- American Journal of Epidemiology
- publisher
- Oxford University Press
- external identifiers
-
- pmid:41574899
- ISSN
- 0002-9262
- DOI
- 10.1093/aje/kwag016
- language
- English
- LU publication?
- yes
- additional info
- Published by Oxford University Press on behalf of the Johns Hopkins Bloomberg School of Public Health 2026.
- id
- 04f7a1d1-4663-48b8-b5a7-4fce75b4ba2c
- date added to LUP
- 2026-01-24 17:16:28
- date last changed
- 2026-01-26 07:37:28
@article{04f7a1d1-4663-48b8-b5a7-4fce75b4ba2c,
abstract = {{<p>We aimed to determine if thyroid autoimmunity is associated with a child's risk for subsequent development of islet or celiac autoantibodies. Children at high genetic risk of type 1 diabetes were followed for thyroid autoimmunity (thyroid peroxidase antibodies [TPOAb] and thyroglobulin antibodies [TGAb]), islet autoimmunity (IA), and celiac disease autoimmunity [CDA] in The Environmental Determinants of Diabetes in the Young (TEDDY) study. Out of 5482 children tested for thyroid autoimmunity, IA, and CDA, 39% developed at least one autoantibody. At age 14 years, thyroid autoimmunity co-occurred with IA in 59 children (15 more cases than expected by chance alone, p = 0.02), and with CDA in 125 children (26 cases above expected, p = 0.01). The risk of developing IA or CDA after thyroid autoimmunity varied by which thyroid autoantibody appeared first: TPOAb-first was associated with both IA (HR 1.92, 95% CI 1.09, 3.40) and CDA (1.69, 95% CI 1.03, 2.76), whereas TGAb-first was not associated with the risk of either. IA and CDA are frequently found in connection to thyroid autoimmunity in children and young adolescents. The relationships of thyroid autoimmunity with IA and CDA depend on which thyroid autoantibody appears first.</p>}},
author = {{Clasen, Joanna L and Jonsdottir, Berglind and Vehik, Kendra and Lynch, Kristian F and Parikh, Hemang M and Koskenniemi, Jaakko J and Lernmark, Åke and Agardh, Daniel and Hagopian, William A and Rewers, Marian J and Toppari, Jorma and Ziegler, Anette-Gabriele and Akolkar, Beena and Krischer, Jeffrey P and Haller, Michael and Larsson, Helena Elding}},
issn = {{0002-9262}},
language = {{eng}},
month = {{01}},
publisher = {{Oxford University Press}},
series = {{American Journal of Epidemiology}},
title = {{Thyroid autoimmunity and the subsequent development of islet and celiac autoimmunity in the TEDDY study}},
url = {{http://dx.doi.org/10.1093/aje/kwag016}},
doi = {{10.1093/aje/kwag016}},
year = {{2026}},
}
