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Are Perinatal Events Risk Factors for Childhood Thyroid Autoimmunity?
Berglind Jonsdottir1, Markus Lundgren1, Sara Wallengren1
1Department of Clinical Sciences, Malmö, Lund University, Skåne University Hospital, Malmö, Sweden.
Insights
Thyroid autoimmunity affects nearly 7% of children, with prematurity linked to thyroglobulin antibodies. A family history of autoimmune diseases significantly increases the risk for developing thyroid autoimmunity in children.
Area of Science:
- Pediatric Endocrinology
- Immunology
- Genetics
Background:
- Thyroid autoimmunity in children may be triggered by environmental and genetic factors.
- Research on perinatal risk factors for childhood thyroid autoimmunity is limited.
Purpose of the Study:
- To investigate the contribution of perinatal factors, family history of autoimmune diseases, and HLA-DQ genotypes to childhood thyroid autoimmunity within the Diabetes Prediction in Skåne (DiPiS) study.
Main Methods:
- Analysis of autoantibodies (TPOAb, TGAb) and HLA-DQ genotypes in 1,874 ten-year-old children.
- Prospective data collection on perinatal events and family history of autoimmunity via questionnaires.
Main Results:
- Thyroid autoimmunity detected in 6.9% of children, more prevalent in girls.
- Prematurity showed a positive association with thyroglobulin antibodies (TGAb).
- Family history of autoimmune diseases significantly elevated the risk for various thyroid autoantibodies.
Conclusions:
- Thyroid autoimmunity is present in 6.9% of children in the DiPiS cohort.
- A link between prematurity and TGAb was observed, but no general association with other perinatal factors.
- Family history of autoimmune diseases is a significant risk factor for childhood thyroid autoimmunity.
Background:
Environmental and genetic factors possibly trigger thyroid autoimmunity. Studies on perinatal risk factors for childhood thyroid autoimmunity are sparse.
Objectives:
The aim was to investigate if perinatal factors, family history of autoimmune diseases, and HLA-DQ genotypes contribute to thyroid autoimmunity in the Diabetes Prediction in Skåne (DiPiS) study.
Methods:
Samples from 1,874 ten-year-old children were analyzed for autoantibodies to thyroid peroxidase (TPOAb), thyroglobulin (TGAb), and HLA-DQ genotypes. Information on perinatal events and family history of autoimmunity was gathered prospectively in questionnaires.
Results:
Thyroid autoimmunity was found in 6.9% of the children (TPOAb 4.4%, TGAb 5.8%, both autoantibodies 3.3%) and was overrepresented in girls. Prematurity was positively related to TGAb (OR: 2.4, p = 0.003, p = 0.021). Autoimmune diseases in the family increased the risk of thyroid autoimmunity: TPOAb (OR: 2.2, p = 0.012), any autoantibody (OR: 1.7, p = 0.04), and both autoantibodies (OR: 2.2, p = 0.024). A first-degree relative (FDR) with thyroid disease increased the risk for TPOAb (OR: 2.4, p = 0.03) and both autoantibodies (OR: 2.6, p = 0.03), a FDR or sibling with celiac disease increased the risk for both autoantibodies (OR: 3.7, p = 0.03, and OR: 4.8, p = 0.003), a FDR or sibling with diabetes increased the risk for thyroid autoantibody (OR: 3.0, p = 0.01, and OR: 5.4, p = 0.032), and a father with rheumatic disease increased the risk for TPOAb (OR: 15.2, p = 0.017), TGAb (OR: 11.3, p = 0.029), any autoantibody (OR: 9.6, p = 0.038), and both autoantibodies (OR: 20, p = 0.01).
Conclusions:
Thyroid autoimmunity was found in 6.9% of the 10-year-old children who were being followed for their risk of type 1 diabetes. No relation to perinatal factors was found, with the exception of a possible association between prematurity and TGAb. Family history of autoimmune diseases increased the risk of thyroid autoimmunity.
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