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Updated: Jul 13, 2026

A Versatile, Behavioral Method to Investigate Thyroid Hormone Effects on Cerebellar Function
Published on: October 6, 2023
Thyroid function and dysfunction in premature infants
1David Geffen School of Medicine at UCLA, Harbor UCLA Medical Center, Torrance, CA 90509, USA. fisherd1@cox.net
Insights
Advances in premature infant care have increased survival rates for very low birth weight (VLBW) infants. However, these infants often experience transient hypothyroxinemia of prematurity (THOP), impacting neurological development, with supplementation trials yielding inconclusive results.
Area of Science:
- Neonatology
- Endocrinology
- Perinatal Medicine
Background:
- Significant advances in neonatal care have reduced mortality in premature infants, particularly very low birth weight (VLBW) infants.
- Increased survival of extremely preterm infants (<24 weeks gestation) leads to a larger population requiring intensive care.
- VLBW infants exhibit unique thyroid function patterns, including transient central hypothyroidism and non-thyroidal illness (NTI) syndrome.
Purpose of the Study:
- To investigate the roles of thyroid system immaturity and NTI in transient hypothyroxinemia of prematurity (THOP).
- To clarify the impact of THOP on subsequent neurological deficits in VLBW infants.
- To evaluate the effectiveness of thyroxine supplementation in VLBW infants.
Main Methods:
- Observational studies analyzing thyroid hormone levels (TSH, T4, T3, free T4, reverse T3, TBG) in VLBW infants.
- Review of existing thyroxine supplementation trials.
- Planned and ongoing research studies.
Main Results:
- VLBW infants show decreased TSH and T4 responses to parturition, with low total T4 and TSH, and variable free T4 in early postnatal weeks.
- A high prevalence of morbidity is observed, often correlating with reduced thyroid hormone levels, mimicking NTI.
- Previous thyroxine supplementation trials have produced inconclusive results regarding benefits.
Conclusions:
- The etiologies of THOP and its impact on neurological outcomes in VLBW infants require further elucidation.
- The precise role of thyroid system immaturity versus NTI in THOP remains unclear.
- Further research, including ongoing trials, is necessary to determine optimal management and potential benefits of thyroxine supplementation.
Abstract:
During the past four decades major advances in the management of premature infants have led to progressive reduction in mortality. During this period mortality in very low birth weight infants (VLBW, <1500 grams and <30 weeks gestation age) has decreased, and more than 50% of infants less than 24 weeks gestation age now survive, increasing the population of VLBW infants in intensive care nursery environments. Thyroid function in these infants is characterized by decreased TSH and T4 responses to parturition, low serum total T4 and TSH levels and variable free T4 concentrations during the first 2-4 postnatal weeks of life. These features reflect a state of transient hypothalamic-pituitary or central hypothyroidism. There is a high prevalence of morbidity in these infants, as well, often associated with further reductions in serum total T4, T3, TBG and TSH concentrations and variable levels of free T4 and reverse T3, resembling the non-thyroidal illness (NTI) syndrome in adults. The etiologic roles of thyroid system immaturity and NTI in the transient hypothyroxinemia of prematurity (THOP) and the impact of THOP on the subsequent neurological deficits in VLBW infants remains unclear. Several thyroxine supplementation trials have been conducted with inconclusive results. Further studies are planned or in progress.
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