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Published on: August 25, 2014
Thyroid function in preterm infants and neurodevelopment at 2 years
Fiona L R Williams1, Alice Lindgren2, Jennifer Watson3
1Division of Population Health & Genomics, School of Medicine, University of Dundee, Dundee, UK f.l.r.williams@dundee.ac.uk.
Insights
Mild thyroid dysfunction in preterm infants is linked to lower neurodevelopmental scores at two years. Many affected infants are missed by current screening, highlighting a need for improved detection methods.
Area of Science:
- Neonatal Medicine
- Endocrinology
- Developmental Pediatrics
Background:
- Postnatal thyroid dysfunction is common in preterm infants.
- The impact of mild thyroid dysfunction on neurodevelopment is not well understood.
Purpose of the Study:
- To investigate the relationship between thyroid function and neurodevelopment in preterm infants.
- To identify if mild thyroid dysfunction affects cognitive and motor outcomes.
Main Methods:
- A cohort analysis of 1275 infants born before 31 weeks' gestation.
- Thyroid function tests (TSH, TBG, T4) were measured in dried blood spots.
- Neurodevelopment was assessed at 2 years using the Bayley-III Scales.
Main Results:
- Infants in the top decile for thyroid-stimulating hormone showed reduced cognitive and motor scores.
- Infants in the bottom decile for thyroxine levels had significantly lower motor scores.
- No infants were identified as hypothyroid by routine screening.
Conclusions:
- Consistent mild thyroid dysfunction in preterm infants is associated with poorer neurodevelopmental outcomes.
- Current screening protocols may not detect many infants with mild thyroid dysfunction.
- Further research is needed to optimize screening and management for thyroid dysfunction in preterm infants.
Objectives:
Postnatal thyroid dysfunction is common in preterm infants but the relationship between mild dysfunction and neurodevelopment is unclear. Our aim is to describe the relationship between thyroid function and neurodevelopment.
Design:
Cohort analysis.
Patients:
1275 infants born under 31 weeks' gestation; there were no exclusion criteria.
Setting:
The infants were part of a UK daily iodine supplementation trial.
Main Outcomes:
Thyroid-stimulating hormone, thyroid-binding globulin and total thyroxine levels were measured in dried blood spots on postnatal days 7, 14, 28 and the equivalent of 34 weeks' gestation. Neurodevelopment was measured using the Bayley-III Scales of infant development at 2 years of age.
Results:
No infant was identified as hypothyroid through routine screening. The 3% of infants consistently in the top decile of gestationally age-adjusted thyroid-stimulating hormone levels had a reduction in cognitive score of 7 Bayley units when compared with those not in the top decile (95% CI -13 to -1). A reduction in motor composite score of 6 units (95% CI -12 to <-0.1) and fine motor score of 1 unit (95% CI -2 to -0.1) was also identified. The 0.7% of infants consistently in the bottom decile of age-adjusted thyroxine levels had a reduction in motor composite score of 14 units (95% CI -25 to -2) and its two subset scores, fine and gross motor, of 2 units (95% CI respectively -4.5 to <-0.1 and -4.3 to -0.3).
Conclusions:
Preterm infants with consistent 'mild' thyroid dysfunction score less on neurodevelopmental tests at 2 years of age. Many of these infants will not be detected by current clinical protocols or screening programmes.
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