Follow-up of newborns with elevated screening T4 concentrations

Stephen H. LaFranchi, David B. Snyder, David E. Sesser, Michael R. Skeels, Nalini Singh, Gregory A. Brent, Jerald C. Nelson

Research output: Contribution to journalArticlepeer-review

119 Scopus citations

Abstract

Objective: To determine the type and incidence of hyperthyroxinemic disorders detected by follow-up of infants with elevated screening total T4 (TT4) values. Study design: Infants born in Oregon with a screening TT4 measurement >3 SD above the mean were offered enrollment. Serum TT4, free T4, total T3, free T3, and thyroid-stimulating hormone concentrations were measured in study infants and their mothers. Results: Over a 20-month period, 101 infants (51 boys) and their mothers enrolled in the study (of 241 eligible infants), from a total screening population of 80,884; 17 infants were identified with persistent hyperthyroxinemia (TT4 >16 μg/dL). Ten had thyroxine-binding globulin excess (1:8088), 5 had evidence for increased T4 binding but not thyroxine-binding globulin excess (1:16,177), and 2 had findings compatible with thyroid hormone resistance (1:40,442): the other 84 infants had transient hyperthyroxinemia. Sequence analysis revealed a point mutation in the thyroid hormone receptor-β gene in one infant with thyroid hormone resistance; no mutation was identified in the other infant. Conclusions: Although neonatal Graves' disease occurs in approximately 1 in 25,000 newborn infants, we did not detect any case among 80,884 infants, most likely because their mothers were receiving antithyroid drugs. Although the other hyperthyroxinemic disorders in the aggregate occur frequently (1:4758) and may benefit from detection, in general they do not require treatment.

Original languageEnglish (US)
Pages (from-to)296-301
Number of pages6
JournalJournal of Pediatrics
Volume143
Issue number3
DOIs
StatePublished - Sep 1 2003

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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