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Maternal Third-Trimester TRAb Is Associated with Neonatal Thyroid Dysfunction and 24-Month Offspring
Jianing Zhang1, Yu Wang2, Guoyu Sun1
1Children's Medical Center, Peking University First Hospital, Beijing, China.
Maternal Graves' disease (GD) is linked to neonatal thyroid issues and potential neurodevelopmental delays in children. Higher maternal thyroid-stimulating hormone receptor antibodies (TRAbs) in the third trimester correlate with these outcomes, but neonatal thyroid function may not be the primary driver.
Area of Science:
- Endocrinology
- Neonatal Health
- Developmental Pediatrics
Background:
- Maternal Graves' disease (GD) is associated with neonatal thyroid dysfunction.
- The impact of maternal GD on offspring neurodevelopment is not well understood.
- Investigating the link between maternal thyroid factors and neonatal outcomes is crucial.
Purpose of the Study:
- To examine the associations between maternal GD-related thyroid factors and neonatal thyroid function.
- To assess the relationship between maternal GD and offspring neurodevelopment at 24 months.
- To explore the potential mediating role of neonatal thyroid function in this association.
Main Methods:
- A single-center bidirectional cohort study included pregnant women with GD and their offspring.
- Maternal thyroid variables (TSH, free T4, TRAbs) and antithyroid drug exposure were collected.
- Neonatal thyroid function and 24-month neurodevelopmental screening were assessed; logistic regression and mediation analysis were used.
Main Results:
- Maternal third-trimester TRAbs were linked to neonatal thyroid dysfunction (OR=1.59).
- Higher maternal TRAbs (OR=1.15) and neonatal TSH (OR=1.11) were associated with abnormal neurodevelopmental screening at 24 months.
- Neonatal TSH did not significantly mediate the association between maternal TRAbs and neurodevelopmental outcomes.
Conclusions:
- Elevated maternal third-trimester TRAbs are associated with neonatal thyroid dysfunction and abnormal neurodevelopmental screening in offspring of mothers with GD.
- The observed association with neurodevelopmental outcomes is not primarily explained by neonatal thyroid function alone.
- Further research is needed to elucidate the mechanisms linking maternal GD to offspring neurodevelopment.
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