Neonatal Hypothyroxinemia: Effects of Iodine Intake and Premature Birth1

Author:

Ares Susana1,Escobar-Morreale Héctor F.2,Quero José1,Durán Socorro2,Presas María Jesus2,Herruzo Rafael3,Morreale de Escobar Gabriella2

Affiliation:

1. Unidad de Neonatología, Hospital La Paz, Instituto Nacional de Salud (S.A., J.Q.), Madrid, Spain

2. Unidad de Endocrinología Molecular, Instituto de Investigaciones Biomédicas y Facultad de Medicina, Consejo Superior de Investigaciones Científicas and Universidad Autónoma (H.F.E.-M., S.D., M.J.P., G.M.d.E.), Madrid, Spain

3. Unidad de Medicina Preventiva, Facultad de Medicina de la Universidad Autónoma (R.H.), Madrid, Spain

Abstract

Abstract We have investigated the effects of iodine (I) intake on urinary I excretion in preterm (PT) babies up to 2 months after birth and its effect on serum T4, free T4 (FT4), T3, TSH, and thyroglobulin (Tg) levels compared to those in term (T) newborns. Very premature and very sick infants were in negative I balance for the first weeks after birth. Later, these same infants, as well as the other PT and T newborns, were in positive balance; 75–80% of the ingested I was not accounted for in the urine. The urinary I levels of PT and T neonates cannot be equated to their I intakes. T4, FT4, and T3 levels in PT and T neonates increased with postmenstrual age, whereas Tg decreased and TSH did not change. Serum FT4, T3, Tg, and TSH levels in PT neonates were affected negatively, independently from age, by a low I intake. PT birth also affected T4, FT4, and Tg negatively, independently from I intake and postmenstrual age, for at least 6–8 weeks after birth. Care should be taken to avoid I deficiency in PT neonates. However, even when I intake is adequate, PT newborns are hypothyroxinemic compared to T babies during an important period of brain development. This suggests the possible convenience of interventions that might mimic the intrauterine hormone environment and accelerate maturation.

Publisher

The Endocrine Society

Subject

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

Reference41 articles.

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2. Maternal-fetal transfer of thyroxine in congenital hypothyroidism due to a total organification defect of thyroid agenesis.;Vulsma;N Engl J Med,1989

3. Congenital hypothyroidism, as studied in rats: crucial role of maternal thyroxine but not of 3,5,3′-triiodothyronine in the protection of the fetal brain.;Calvo;J Clin Invest,1990

4. Ontogenesis of pituitary-thyroid function and metabolism in man, sheep and rat.;Fisher;Recent Prog Horm Res,1977

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