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Early Appearance of Thyroid Autoimmunity in Children Followed from Birth for Type 1 Diabetes Risk

  • behalf of the TEDDY Study Group
  • The Children's Hospital Iceland
  • University Hospital Malmö
  • University of South Florida College of Medicine
  • Center for Regenerative Therapies Dresden
  • University of Florida College of Medicine
  • Helmholtz Zentrum München German Research Center for Environmental Health
  • Technical University of Munich
  • Institute for Diabetes Research
  • Pacific Northwest Diabetes Research Institute
  • Barbara Davis Center for Childhood Diabetes
  • Medical College of Georgia
  • Turku University Hospital
  • University of Turku and Turku University Hospital
  • National Institutes of Health
  • Oulu University Hospital
  • Tampere University Hospital
  • Lunds University Hospital
  • Tampere University
  • University of Oulu
  • National Institute for Health and Welfare
  • University of Florida
  • Ludwig-Maximilians-Universität München
  • Lund University
  • University of Pittsburgh School of Medicine
  • University of South Florida, Tampa
  • Children's Hospital Oakland Research Institute
  • University of Copenhagen
  • Copenhagen University Hospital

Research output: Contribution to journalArticlepeer-review

5 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)498-510
Number of pages13
JournalJournal of Clinical Endocrinology and Metabolism
Volume110
Issue number2
DOIs
StatePublished - 1 Feb 2025
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • autoimmune thyroid disease
  • children
  • thyroid autoimmunity

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