Phase 1 Trial of 4 Thyroid Hormone Regimens for Transient Hypothyroxinemia in Neonates of <28 Weeks' Gestation

Author:

La Gamma Edmund F.1,van Wassenaer Aleid G.2,Ares Susana3,Golombek Sergio G.1,Kok Joke H.2,Quero Jose3,Hong Ting45,Rahbar Mohammad H.6,de Escobar Gabriella Morreale7,Fisher Delbert A.8,Paneth Nigel45

Affiliation:

1. Department of Neonatal-Perinatal Medicine, Regional Neonatal Center, Maria Fareri Children's Hospital at Westchester Medical Center, New York Medical College, Valhalla, New York

2. Department of Neonatology, Emma Children's Hospital-Academic Medical Center, Amsterdam, Netherlands

3. Neonatology Unit, University Hospital La Paz

4. Epidemiology

5. Pediatrics and Human Development, Michigan State University, East Lansing, Michigan

6. Center for Clinical and Translational Sciences, University of Texas Health Science Center at Houston, Houston, Texas

7. Instituto de Investigaciones Biomedicas, Autonomous University of Madrid and Center for Biomedical Research on Rare Diseases (CIBERER), Madrid, Spain; Departments of

8. Quest Diagnostics Nichols Institute, San Juan Capistrano, California

Abstract

BACKGROUND: Transiently low levels of thyroid hormones occur in ∼50% of neonates born 24–28 weeks' gestation and are associated with higher rates of cerebral palsy and cognitive impairment. Raising hormone levels shows promise for improving neurodevelopmental outcome. OBJECTIVE: To identify whether any of 4 thyroid hormone supplementation regimens could raise T4 and FT4 without suppressing TSH (biochemical euthyroidism). METHODS: Eligible subjects had gestational ages between 24\batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \({0}/{7}\) \end{document} and 27\batchmode \documentclass[fleqn,10pt,legalpaper]{article} \usepackage{amssymb} \usepackage{amsfonts} \usepackage{amsmath} \pagestyle{empty} \begin{document} \({6}/{7}\) \end{document} weeks and were randomized &lt;24 hours of birth to one of six study arms (n = 20–27 per arm): placebo (vehicle: 5% dextrose), potassium iodide (30 μg/kg/d) and continuous or bolus daily infusions of either 4 or 8 μg/kg/d of T4 for 42 days. T4 was accompanied by 1 μg/kg/d T3 during the first 14 postnatal days and infused with 1 mg/mL albumin to prevent adherence to plastic tubing. RESULTS: FT4 was elevated in the first 7 days in all hormone-treated subjects; however, only the continuous 8 μg/kg/d treatment arm showed a significant elevation in all treatment epochs (P &lt; .002 versus all other groups). TT4 remained elevated in the first 7 days in all hormone-treated subjects (P &lt; .05 versus placebo or iodine arms). After 14 days, both 8 μg/kg/d arms as well as the continuous 4 μg/kg/d arm produced a sustained elevation of the mean and median TT4, &gt;7 μg/dL (90 nM/L; P &lt; .002 versus placebo). The least suppression of THS was achieved in the 4 μg/kg/d T4 continuous infusion arm. Although not pre-hypothesized, the duration of mechanical ventilation was significantly lower in the continuous 4 μg/kg/d T4 arm and in the 8 μg/kg/d T4 bolus arm (P &lt; .05 versus remaining arms). ROP was significantly lower in the combined 4 thyroid hormone treatment arms than in the combined placebo and iodine arms (P &lt; .04). NEC was higher in the combined 8 μg/kg/d arms (P &lt; .05 versus other arms). CONCLUSIONS: Elevation of TT4 with only modest suppression of TSH was associated with trends suggesting clinical benefits using a continuous supplement of low-dose thyroid hormone (4 μg/kg/d) for 42 days. Future trials will be needed to assess the long-term neurodevelopmental effects of such supplementation.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

Reference59 articles.

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2. Centers for Disease Control and Prevention. Economic costs associated with mental retardation, cerebral palsy, hearing loss, and vision impairment: United States, 2003. MMWR Morb Mortal Wkly Rep. 2004;53(3):57–59

3. Hirtz D, Thurman DJ, Gwinn-Hardy K, Mohamed M, Chaudhuri AR, Zalutsky R. How common are the “common” neurologic disorders?Neurology. 2007;68(5):326–337

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