Levels of Neonatal Thyroid Hormone in Preterm Infants and Neurodevelopmental Outcome at 5½ Years: Millennium Cohort Study

Author:

Delahunty Caroline1,Falconer Shona2,Hume Robert2,Jackson Lesley3,Midgley Paula4,Mirfield Marie2,Ogston Simon2,Perra Oliver2,Simpson Judith5,Watson Jennifer2,Willatts Peter6,Williams Fiona2,

Affiliation:

1. Wishaw General Hospital (C.D.), Wishaw ML2 0DP, Scotland, United Kingdom;

2. Clinical and Population Sciences and Education (S.F., R.H., M.M., S.O., O.P., J.W., F.W.), University of Dundee, Ninewells Hospital and Medical School Campus, Dundee DD2 4BF, Scotland, United Kingdom;

3. Neonatal Unit (L.J.), Southern General Hospital, Glasgow G51 4TF, Scotland, United Kingdom;

4. Neonatal Unit (P.M.), Royal Infirmary of Edinburgh, Edinburgh EH16 4SA, Scotland, United Kingdom;

5. Neonatal Unit (J.S.), Queen Mother’s Hospital, Glasgow G3 8SJ Scotland, United Kingdom;

6. Department of Psychology (P.W.), University of Dundee, Dundee DD1 4HN, Scotland, United Kingdom

Abstract

Context: Transient hypothyroxinemia is the commonest thyroid dysfunction of premature infants, and recent studies have found adverse associations with neurodevelopment. The validity of these associations is unclear because the studies adjusted for a differing range of factors likely to influence neurodevelopment. Objective: The aim was to describe the association of transient hypothyroxinemia with neurodevelopment at 5.5 yr corrected age. Design: We conducted a follow-up study of a cohort of infants born in Scotland from 1999 to 2001 ≤34 wk gestation. Main Outcome Measures: We measured scores on the McCarthy scale adjusted for 26 influences of neurodevelopment including parental intellect, home environment, breast or formula fed, growth retardation, and use of postnatal drugs. Results: A total of 442 infants ≤34 wk gestation who had serum T4 measurements on postnatal d 7, 14, or 28 and 100 term infants who had serum T4 measured in cord blood were followed up at 5.5 yr. Infants with hypothyroxinemia (T4 level ≤ 10th percentile on d 7, 14, or 28 corrected for gestational age) scored significantly lower than euthyroid infants (T4 level greater than the 10th percentile and less than the 90th percentile on all days) on all McCarthy scales, except the quantitative. After adjustment for confounders of neurodevelopment, hypothyroxinemic infants scored significantly lower than euthyroid infants on the general cognitive and verbal scales. Conclusions: Our findings do not support the view that the hypothyroxinemic state, in the context of this analysis, is harmless in preterm infants. Many factors contribute both to the etiology of hypothyroxinemia and neurodevelopment; strategies for correction of hypothyroxinemia should acknowledge its complex etiology and not rely solely on one approach.

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference36 articles.

1. Thyroid function in very low birth weight infants: effects on neonatal hypothyroidism screening.;Frank;J Pediatr,1996

2. Low thyroxinaemia occurs in the majority of very preterm newborns.;Rooman;Eur J Pediatr,1996

3. Normal and abnormal thyroid function in premature infants: the low T3 syndrome;Fisher;In: Hesch RD, ed. The low T3 syndrome. Vol 40. Proc of the Serono Symposia. London: Academic Press;,1981

4. The relation of transient hypothyroxinaemia in preterm infants to neurologic development at two years of age.;Reuss;N Engl J Med,1996

5. Transient hypothyroxinaemia associated with developmental delay in very preterm infants.;Meijer;Arch Dis Child,1992

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