No Association Between Transient Hypothyroxinemia of Prematurity and Neurodevelopmental Outcome in Young Adulthood

J Clin Endocrinol Metab. 2015 Dec;100(12):4648-53. doi: 10.1210/jc.2015-3078. Epub 2015 Oct 19.

Abstract

Context: Transient hypothyroxinemia of prematurity (THoP) has been associated with neurodevelopmental impairment in infancy and childhood. It is not known whether these relations persist into adulthood.

Objective: The objective was to examine whether there is an effect of THoP on intelligence quotient (IQ) score and motor functioning at a young adult age.

Design: This study was part of the 19-year follow-up of the Project On Preterm and Small-for-gestational-age birth (POPS) cohort, which included infants born very preterm (ie, <32 wk) and/or with a very low birth weight (ie, <1500 g).

Setting: This was a multicenter study.

Patients: There were 398 19-year-old participants of the POPS cohort, of whom 120 had THoP.

Exposure: T4 concentrations were obtained through the national neonatal screening program for congenital hypothyroidism. THoP was defined as a total T4 concentration < -3 SD of the daily mean (approximately 60 nmol/L).

Main outcome measures: Main outcome measures were IQ and motor functioning, measured with the digital Multicultural Capacities Test-Intermediate Level and a revised version of Touwen's examination of minor neurological dysfunction, respectively.

Results: THoP was not associated with IQ score (mean difference, 0 [95% confidence interval, -3.8 to 3.8] points) or motor function (mean difference, 0.6 [95% confidence interval, -1.3 to 2.5] points) after adjustment for demographic and perinatal characteristics.

Conclusions: No associations between THoP and neurodevelopmental outcome at age 19 years were found.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cohort Studies
  • Congenital Hypothyroidism / complications*
  • Congenital Hypothyroidism / epidemiology*
  • Developmental Disabilities / epidemiology*
  • Developmental Disabilities / etiology*
  • Female
  • Follow-Up Studies
  • Humans
  • Infant, Extremely Premature
  • Infant, Low Birth Weight
  • Infant, Newborn
  • Infant, Premature
  • Infant, Small for Gestational Age
  • Intelligence Tests
  • Male
  • Nervous System Diseases / epidemiology*
  • Nervous System Diseases / etiology*
  • Neuropsychological Tests
  • Psychomotor Performance
  • Thyroxine / blood
  • Thyroxine / deficiency*
  • Young Adult

Substances

  • Thyroxine