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Published on: March 25, 2016
Risk factors of primary thyroid dysfunction in early infants born to mothers with autoimmune thyroid disease
Junfen Fu1, Youjun Jiang, Li Liang
1Department of Endocrinology, The Children's Hospital of Zhejiang University School of Medicine, Hangzhou, China. fjf68@yahoo.com.cn
Insights
Maternal autoimmune thyroid disease during pregnancy significantly impacts infant thyroid function. Careful management of these conditions is crucial to prevent adverse neonatal outcomes.
Area of Science:
- Endocrinology
- Neonatal Health
- Immunology
Background:
- Maternal thyroid dysfunction during pregnancy can pose risks to infant health.
- Autoimmune thyroid diseases (AITD) like Graves' disease and Hashimoto thyroiditis are common in pregnant women.
Purpose of the Study:
- To determine if maternal thyroid status and alterations during gestation affect infant thyroid function.
- To identify risk factors for early infant thyroid dysfunction using logistic regression.
Main Methods:
- A cross-sectional study involving 78 neonates born to mothers with AITD and a control group of neonates from healthy mothers.
- Clinical and biochemical assessments of thyroid function, including antibody testing (TPOAb, TGAb, TRAb, TSAb) in mothers and infants.
- Multiple logistic regression analysis to evaluate maternal and infant risk factors.
Main Results:
- A high prevalence of subtle thyroid abnormalities (52.6%) was observed in infants of mothers with AITD, significantly higher than controls (0.54%).
- Maternal thyroid function during gestation, type of AITD, and neonatal TRAb levels were significantly correlated with infant thyroid dysfunction.
Conclusions:
- Maternal autoimmune thyroid disease during pregnancy adversely affects infant thyroid function.
- Effective management of maternal AITD throughout pregnancy is vital for preventing negative neonatal outcomes.
Aim:
To assess whether the state of maternal thyroid function and the pattern of thyroid alterations during gestation would affect the infants' thyroid function and to evaluate the risk factors affecting early infants' thyroid function by means of multiple logistic regression.
Methods:
In a cross-sectional study, 78 neonates born to mothers with Graves disease or Hashimoto thyroiditis were examined and followed clinically and biochemically. Neonates born to healthy mothers during the same period were set as controls. Tests of thyroid function, antithyroid peroxidase antibody (TPOAb), antithyroglobulin antibody (TGAb), anti-TSH receptor antibody (TRAb) and antithyroid-stimulating antibody (TSAb) were performed both in early infants and their mothers. All possible maternal and/or infantile risk factors for thyroid dysfunction during early infancy were analysed by means of multiple-factor logistical regression.
Results:
The overall prevalence of underlying subtle thyroid abnormalities in these 78 infants was 52.6%, which was significantly higher than that witnessed among infants from healthy mothers (5.4 per thousand, p<0.01). By using multiple logistic regression analysis, the state of maternal thyroid function in gestation, the type of autoimmune thyroid disease during pregnancy and the level of TRAb in the newborn were significantly correlated with the early infants' thyroid dysfunction.
Conclusion:
Maternal autoimmune thyroid disease during pregnancy will affect infant thyroid function. Therefore, appropriate management of maternal autoimmune thyroid disease throughout pregnancy is essential in the prevention of undesirable neonatal outcomes.
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