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An Ex vivo Culture System to Study Thyroid Development
Published on: June 6, 2014
Developmental trends in cord and postpartum serum thyroid hormones in preterm infants
Fiona L R Williams1, Judith Simpson, Caroline Delahunty
1Community Health Sciences, University of Dundee, Ninewells Hospital and Medical School, Dundee DD1 9SY, Scotland, United Kingdom.
Insights
Thyroid hormone levels in preterm infants show distinct postnatal trends. Extremely preterm infants (23-27 weeks) exhibit reversed T4 trends, indicating hypothyroidism.
Area of Science:
- Neonatal endocrinology
- Pediatric thyroidology
- Perinatal medicine
Background:
- Thyroid hormone levels undergo significant changes during the transition from fetal to neonatal life.
- Preterm infants, especially those born extremely early, may experience altered thyroid hormone dynamics due to physiological immaturity.
Purpose of the Study:
- To delineate postnatal thyroid hormone (T4, FT4, TSH, T3, rT3, T4 sulfate) trends in preterm infants across different gestational ages (23-34 weeks).
- To compare these trends with those observed in term infants and cord blood levels.
Main Methods:
- Longitudinal study measuring serum thyroid hormone levels at birth and on days 7, 14, and 28 in preterm infants (n=540) and term infants (n=812).
- Gestational age groups for preterm infants: 23-27, 28-30, and 31-34 weeks.
Main Results:
- Preterm infants showed variable postnatal changes in TSH, rT3, T4-binding globulin, T3, and T4 sulfate compared to cord levels.
- Term infants presented with hyperthyroxinemia relative to cord and adult levels.
- Postnatal T4 increases were blunted or reversed in preterm infants, with the 23-27 week group showing significant hypothyroxinemia.
Conclusions:
- The 23-27 week gestational age group exhibits unique hypothyroxinemia, despite FT4 levels being within the expected range for their gestational age.
- Thyroid hormone regulation is significantly impacted by gestational immaturity, necessitating careful monitoring in extremely preterm neonates.
Abstract:
The purpose of this study was first to clarify postnatal trends in sera T(4), free T(4) (FT(4)), T(4)-binding globulin, TSH, T(3), rT(3), and T(4) sulfate levels in cord and at 7, 14, and 28 d in groups of preterm infants at 23-27 wk (n = 101), 28-30 wk (n = 196), and 31-34 (n = 253) wk gestation, and second to compare these trends to those of term infants and also with cord sera levels of equivalent gestational ages (n = 812; 23-42 wk gestation). In all preterm groups, TSH and rT(3) decrease to below, T(4)-binding globulin increases to within, and T(3) and T(4) sulfate increase to above cord levels of equivalent gestational age. Term infants are hyperthyroxinemic relative to cord and nonpregnant adult levels of T(4). Postnatal T(4) increases are attenuated in 31- to 34-wk infants, absent in 28- to 30-wk infants (although levels are equivalent to gestational age), and crucially reversed in 23- to 27-wk infants. This immature group is hypothyroxinemic relative to other groups and to cord levels of equivalent gestational age. Compared with term infants, postnatal FT(4) increases are lower in 31- to 34-wk infants, attenuated in 28- to 30-wk infants, and absent in 23- to 27-wk infants. The 23- to 27-wk group is distinctive; they are hypothyroxinemic on T(4) levels, yet FT(4) levels are within the cord levels of equivalent gestational age.
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