TY - JOUR
T1 - Early Appearance of Thyroid Autoimmunity in Children Followed from Birth for Type 1 Diabetes Risk
AU - behalf of the TEDDY Study Group
AU - Jonsdottir, Berglind
AU - Clasen, Joanna L.
AU - Vehik, Kendra
AU - Lernmark, Åke
AU - Lundgren, Markus
AU - Bonifacio, Ezio
AU - Schatz, Desmond
AU - Ziegler, Anette Gabriele
AU - Hagopian, William
AU - Rewers, Marian
AU - McIndoe, Richard
AU - Toppari, Jorma
AU - Krischer, Jeffrey
AU - Akolkar, Beena
AU - Steck, Andrea
AU - Veijola, Riitta
AU - Haller, Michael J.
AU - Elding Larsson, Helena
AU - Bautista, Kimberly
AU - Baxter, Judith
AU - Felipe-Morales, Daniel
AU - Frohnert, Brigitte I.
AU - Stahl, Marisa
AU - Garcia, Isabel Flores
AU - Gesualdo, Patricia
AU - Hays, Sierra
AU - Hoffman, Michelle
AU - Johnson, Randi
AU - Karban, Rachel
AU - Liu, Edwin
AU - Loaiza, Leila
AU - Norris, Jill
AU - O'Donnell, Holly
AU - Thorndahl, Loana
AU - Waugh, Kathleen
AU - Toppari, Jorma
AU - Simell, Olli G.
AU - Adamsson, Annika
AU - Ahonen, Suvi
AU - Åkerlund, Mari
AU - Anttila, Sirpa
AU - Hakola, Leena
AU - Hekkala, Anne
AU - Honkanen, Tiia
AU - Hurskainen, Teija
AU - Hyöty, Heikki
AU - Ilonen, Jorma
AU - Itoshima, Saori
AU - Jokipolvi, Minna
AU - Ziegler, Anette G.
N1 - Publisher Copyright:
© 2024 The Author(s).
PY - 2025/2/1
Y1 - 2025/2/1
N2 - Context: Autoantibodies to thyroid peroxidase (TPOAb) and thyroglobulin (TgAb) define preclinical autoimmune thyroid disease (AITD), which can progress to either clinical hypothyroidism or hyperthyroidism. Objective: We determined the age at seroconversion in children genetically at risk for type 1 diabetes. Methods: TPOAb and TgAb seropositivity were determined in 5066 healthy children with human leukocyte antigen (HLA) DR3- or DR4-containing haplogenotypes from The Environmental Determinants of Diabetes in the Young (TEDDY) study. Children seropositive on the cross-sectional initial screen at age 8 to 13 years had longitudinally collected samples (from age 3.5 months) screened retrospectively and prospectively for thyroid autoantibodies to identify age at seroconversion. The first-appearing autoantibody was related to sex, HLA genotype, family history of AITD, and subsequent thyroid dysfunction and disease. Results: The youngest appearance of TPOAb and TgAb was age 10 and 15 months, respectively. Girls had higher incidence rates of both autoantibodies. Family history of AITD was associated with a higher risk of TPOAb hazard ratio (HR) 1.90; 95% CI, 1.17-3.08; and TgAb HR 2.55; 95% CI, 1.91-3.41. The risk of progressing to hypothyroidism or hyperthyroidism was not different between TgAb and TPOAb, but children with both autoantibodies appearing at the same visit had a higher risk compared to TPOAb appearing first (HR 6.34; 95% CI, 2.72-14.76). Conclusion: Thyroid autoantibodies may appear during the first years of life, especially in girls, and in children with a family history of AITD. Simultaneous appearance of both autoantibodies increases the risk for hypothyroidism or hyperthyroidism.
AB - Context: Autoantibodies to thyroid peroxidase (TPOAb) and thyroglobulin (TgAb) define preclinical autoimmune thyroid disease (AITD), which can progress to either clinical hypothyroidism or hyperthyroidism. Objective: We determined the age at seroconversion in children genetically at risk for type 1 diabetes. Methods: TPOAb and TgAb seropositivity were determined in 5066 healthy children with human leukocyte antigen (HLA) DR3- or DR4-containing haplogenotypes from The Environmental Determinants of Diabetes in the Young (TEDDY) study. Children seropositive on the cross-sectional initial screen at age 8 to 13 years had longitudinally collected samples (from age 3.5 months) screened retrospectively and prospectively for thyroid autoantibodies to identify age at seroconversion. The first-appearing autoantibody was related to sex, HLA genotype, family history of AITD, and subsequent thyroid dysfunction and disease. Results: The youngest appearance of TPOAb and TgAb was age 10 and 15 months, respectively. Girls had higher incidence rates of both autoantibodies. Family history of AITD was associated with a higher risk of TPOAb hazard ratio (HR) 1.90; 95% CI, 1.17-3.08; and TgAb HR 2.55; 95% CI, 1.91-3.41. The risk of progressing to hypothyroidism or hyperthyroidism was not different between TgAb and TPOAb, but children with both autoantibodies appearing at the same visit had a higher risk compared to TPOAb appearing first (HR 6.34; 95% CI, 2.72-14.76). Conclusion: Thyroid autoantibodies may appear during the first years of life, especially in girls, and in children with a family history of AITD. Simultaneous appearance of both autoantibodies increases the risk for hypothyroidism or hyperthyroidism.
KW - autoimmune thyroid disease
KW - children
KW - thyroid autoimmunity
UR - http://www.scopus.com/inward/record.url?scp=85216511705&partnerID=8YFLogxK
U2 - 10.1210/clinem/dgae478
DO - 10.1210/clinem/dgae478
M3 - Article
C2 - 38996042
AN - SCOPUS:85216511705
SN - 0021-972X
VL - 110
SP - 498
EP - 510
JO - Journal of Clinical Endocrinology and Metabolism
JF - Journal of Clinical Endocrinology and Metabolism
IS - 2
ER -