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Published on: November 20, 2015
Antenatal glucocorticoids increase early total thyroxine levels in premature infants
Camilia R Martin1, Linda J Van Marter, Elizabeth N Allred
1Department of Neonatology, Beth Israel Deaconess Medical Center, Division of Newborn Medicine, Boston, MA 02215, USA. cmartin1@bidmc.harvard.edu
Insights
Antenatal glucocorticoids, used to support preterm delivery, were associated with higher early total thyroxine (T4) levels in extremely premature infants. This finding suggests a potential influence on neonatal thyroid function.
Area of Science:
- Neonatalogy
- Endocrinology
- Obstetrics
Background:
- Hypothyroxinemia in premature infants is linked to severe adverse outcomes, including neurodevelopmental deficits and mortality.
- Understanding factors influencing thyroid function in preterm neonates is critical.
- Antenatal glucocorticoid exposure is common in threatened preterm deliveries, but its impact on neonatal thyroid function is understudied.
Purpose of the Study:
- To investigate the association between antenatal glucocorticoid exposure and early total thyroxine (T4) levels in extremely premature infants.
- To determine if antenatal glucocorticoids modify neonatal thyroid hormone levels shortly after birth.
Main Methods:
- A cohort of 521 infants born between 23-28 weeks gestational age was studied across four medical centers.
- Serum total T4 levels were measured in the first postnatal week, sourced from newborn screening programs.
- Antenatal glucocorticoid exposure was categorized as none, partial, or complete, with a complete course defined by specific betamethasone or dexamethasone dosing.
Main Results:
- Infants receiving a complete course of antenatal glucocorticoids exhibited significantly higher total T4 levels (0.8 microg/dl greater) compared to unexposed infants (p = 0.03).
- This association persisted after controlling for maternal, perinatal, and neonatal confounding factors.
- The observed increase in T4 levels was statistically significant, indicating a potential biological effect.
Conclusions:
- Complete antenatal glucocorticoid administration is associated with elevated total thyroxine levels in the first week of life for extremely premature infants.
- The relationship between antenatal glucocorticoids and neonatal thyroid function is not fully explained by known confounding variables.
- These findings suggest that antenatal glucocorticoids may directly influence early thyroid hormone regulation in preterm neonates.
Background:
Hypothyroxinemia is associated with adverse neonatal outcomes including white matter damage, cerebral palsy, poor neurodevelopment and death. It has become increasingly important to understand the natural history and modifiers of thyroid function in the premature infant. It is standard obstetrical practice to offer antenatal glucocorticoids to pregnant women with threatened preterm delivery. Few studies have investigated the effect of antenatal glucocorticoids on neonatal thyroid function.
Objective:
To examine the association between antenatal exposure to glucocorticoids and early total thyroxine (T4) levels among extremely premature infants.
Methods:
We studied 521 infants born at 4 medical centers. Entry criteria included a gestational age of 23-28 weeks and a serum thyroxine level obtained in the first postnatal week. Receipt of antenatal glucocorticoids was recorded as none, partial, or complete. A complete course consisted of two doses of betamethasone or four doses of dexamethasone within a 48-hour period between 2 and 7 days of delivery. Early total T4 levels were obtained from state-mandated newborn screening programs.
Results:
Controlling for potential maternal, perinatal and neonatal confounding variables, infants exposed to a complete course of antenatal glucocorticoids had total T4 levels 0.8 microg/dl higher than their peers who were not exposed to a complete course of antenatal glucocorticoids (p = 0.03).
Conclusions:
Extremely premature infants who received a complete course of antenatal glucocorticoids had significantly higher total thyroxine levels in the first postnatal week. Maternal, perinatal, and early neonatal variables did not completely explain this association. We speculate that antenatal glucocorticoids influence early neonatal thyroid function.
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