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Published on: November 20, 2015
The hypothalamic-pituitary-thyroid axis in preterm infants; changes in the first 24 hours of postnatal life
Nuala Murphy1, Robert Hume, Hans van Toor
1Department of Paediatrics, The Rotunda Hospital, Dublin, Ireland.
Insights
Extremely premature infants (24-27 weeks gestation) show a blunted thyroid-stimulating hormone (TSH) surge and altered thyroid hormone levels after birth, indicating a distinct hypothalamic-pituitary-thyroid axis response compared to more mature preterm infants.
Area of Science:
- Neonatal endocrinology
- Perinatal physiology
- Thyroid hormone metabolism
Background:
- Thyroid hormones are crucial for neonatal adaptation after birth.
- Preterm infants, especially those with very low gestational age, may exhibit altered thyroid function.
- The hypothalamic-pituitary-thyroid (HPT) axis undergoes significant changes in the transition from fetal to neonatal life.
Purpose of the Study:
- To measure key thyroid hormones and binding proteins in preterm infants during the first 24 hours of life.
- To compare thyroid hormone profiles across different gestational age groups (24-27, 28-30, and 31-34 weeks).
- To characterize the HPT axis response to birth in extremely preterm infants.
Main Methods:
- Serum samples collected at cord, 1, 7, and 24 hours postpartum.
- Assays performed for T4, free T4, TSH, T3, reverse T3 (rT3), T4 sulfate, and thyroxine-binding globulin.
- Infants stratified into three gestational age groups: 24-27 wk, 28-30 wk, and 31-34 wk.
Main Results:
- The TSH surge at 1 hour was markedly attenuated in the 24-27 wk group compared to older groups.
- T4 levels declined in the most immature group but increased in more mature groups over 24 hours.
- Free T4 and T3 showed minimal increases in the immature group, contrasting with sustained increases in older preterm infants.
- Higher cord levels of rT3 and T4 sulfate were observed in the most immature infants.
Conclusions:
- Infants born between 24-27 weeks gestation exhibit a severely attenuated or failed HPT axis response to delivery.
- This distinct endocrine response differentiates the extremely preterm group from more mature preterm infants.
- The findings highlight the unique physiological challenges and adaptations in the earliest preterm neonates.
Abstract:
The purpose of this study was to measure serum T4, free T4, TSH, T3, rT3, T4 sulfate, and thyroxine binding globulin at four time points within the first 24 h of life (cord and 1, 7, and 24 h) in infants between 24 and 34 wk gestation. The infants were subdivided into gestational age groups: 24-27 wk (n = 22); 28-30 wk (n = 26); and 31-34 wk (n = 24). The TSH surge in the first hour of postnatal life was markedly attenuated in infants of 24-27 wk gestation [8 compared with 20 (28-30 wk) and 23 mU/liter (31-34 wk)]. T4 levels in the most immature group declined over the first 24 h, whereas levels increased in the more mature groups [mean cord and 24-h levels: 65 and 59 (NS) vs. 70 and 84 (P < 0.002) vs. 98 and 125 (NS) nmol/liter]. Free T4 and T3 showed only small, transient increases in the most immature group and progressively larger and sustained increases in the other gestational groups. rT3 and T4 sulfate levels in cord serum were higher in the most immature infants, and in all groups levels decreased initially and then variably increased. The features of a severely attenuated or failed hypothalamic-pituitary-thyroid response to delivery critically define this 24- to 27-wk group as distinct from more mature preterm infants.
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