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Re: Maternal, Infant, and Delivery Factors Associated with Neonatal Thyroid Hormone Status
 

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Published: 6 years ago
 
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Re: Maternal, Infant, and Delivery Factors Associated with Neonatal Thyroid Hormone Status


 online.liebertpub.com/doi/abs/10.1089/thy.2007.0180

Maternal, Infant, and Delivery Factors Associated with Neonatal Thyroid Hormone Status

To cite this article:
Julie Herbstman, Benjamin J. Apelberg, Frank R. Witter, Susan Panny, and Lynn R. Goldman. Thyroid. January 2008, 18(1): 67-76. doi:10.1089/thy.2007.0180.

Published in Volume: 18 Issue 1: January 28, 2008
Online Ahead of Print: December 6, 2007

Author information

Julie Herbstman
Columbia University Mailman School of Public Health, New York, New York.
Benjamin J. Apelberg
Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.
Frank R. Witter
Johns Hopkins School of Medicine, Baltimore, Maryland.
Susan Panny
Maryland Department of Health and Mental Hygiene, Baltimore, Maryland.
Lynn R. Goldman
Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland.

ABSTRACT

Background: Thyroid function is dynamic during the perinatal period with many factors potentially influencing maternal, fetal and neonatal TSH and thyroid hormone levels. We sought to identify the impact of numerous maternal, fetal and delivery attributes on thyroid parameters in newborns.

Methods: This was a cross sectional study of 300 newborns. Detailed information was obtained from medical records and multiple characteristics from the record were tested as predictors of cord blood serum total T4, free T4 and TSH and infant T4 levels from the Maryland newborn screening program.

Main outcome: Outcomes are levels of thyroid stimulating hormone (TSH), thyroxine (T4), and free T4 in newborn cord serum and total T4 in postnatal heelstick bloodspot samples.

Results: Multivariate models identified a number of variables that are independently associated with thyroid hormone levels: higher birth order (lower cord TSH); older maternal age (lower cord total T4); pregnancy-induced hypertension and/or preeclampsia (lower cord total T4 and free T4); gestational diabetes (higher cord free T4); sexually transmitted disease during pregnancy (lower cord TSH); alcohol use during pregnancy (lower cord TSH); thyroid condition/medications (higher bloodspot total T4, both neonatal and subsequent); Asian ancestry (higher cord TSH); male sex (higher TSH and lower neonatal bloodspot total T4); and C-section (lower cord TSH). Gestational age was independently associated with lower cord TSH, higher cord total T4, and higher neonatal and subsequent bloodspot total T4.

Conclusions: Fetal and newborn thyroid hormone levels during the perinatal period are dynamic and influenced by several biological and delivery related factors. Efforts to identify fetal thyroid disruptors in late gestation must carefully consider these factors.

 

 
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