Cited by 118Sexual Differentiation and DisordersAdrenal Hormones and DisordersNeonatal Respiratory Health Research

How safe is long-term prenatal glucocorticoid treatment?

Seckl, Jonathan R.·1997·JAMA: The Journal of the American Medical Association

Abstract

GLUCOCORTICOIDS are commonly used in obstetric practice, both for maternal immunosuppression and for shortterm treatment of the fetus, usually to accelerate lung maturation when there is threatened preterm delivery. The immediate benefits of short-term prepartum glucocorticoid therapy in maturing the fetal lung and reducing neonatal mortality are clearly supported by controlled studies.1,2Recently, long-term prenatal therapy of fetuses potentially affected with congenital adrenal hyperplasia (CAH) has been advocated,3,4but the safety of this experimental therapy has not been established in rigorously controlled trials. See also p 1073. Congenital adrenal hyperplasia is a recessively inherited disease in which a disordered steroidogenic enzyme, usually P450c21 (21-hydroxylase), diverts adrenal steroid synthesis away from cortisol toward androgens.5In utero, low fetal plasma cortisol levels stimulate increased corticotropin (ACTH) secretion, which in turn stimulates further adrenal steroidogenesis, resulting in even more androgen synthesis. In an XY male fetus, these adrenal androgens have

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Crossref · 10.1001/jama.1997.03540370067039

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  • Since the mid-1980s, prenatal treatment with high doses of dexamethasone has been proposed for pregnant women with a fetus at risk for classic CAH using a protocol of 20 μg/kg/day, maximum 1.5 mg/day, aiming to prevent prenatal virilization of the external genitalia in affected girls.

    “Since the mid-1980's, prenatal treatment with high doses of Dex has been proposed for to pregnant women with a fetus at risk for classic CAH using a treatment protocol of 20 µg/kg/day, maximum 1.5 mg/day, with the aim of preventing prenatal virilization of the external genitalia in affected girls (313,317,440).”

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Authors
Seckl, J. R.
Affiliations
Western General Hospital (GB)
Corresponding author
Seckl, Jonathan R.
Venue
JAMA: The Journal of the American Medical Association
Published
1997-04-02
Volume
277
Issue
13
Pages
1077
ISSN
  • 0002-9955 (ISSN-L)
  • 0098-7484
OpenAlex
W2087015880
Cited by
118
References
4
Citations by year
2026: 1 · 2025: 1 · 2024: 2 · 2023: 1 · 2021: 1 · 2020: 1 · 2019: 2 · 2018: 3 · 2016: 2 · 2015: 4 · 2014: 1 · 2013: 2 · 2012: 4
FWCI
3.53
Type
journal article
Language
en
Open access
closed
Locations
  • JAMA (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (5r01dk042154-09)
  • National Institute of Diabetes and Digestive and Kidney Diseases (DK-37922, DK 42154, R01DK037922)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Sexual Differentiation and Disorders
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Neonatal Respiratory Health Research
Keywords
antenatal glucocorticoids, congenital adrenal hyperplasia, 21-hydroxylase deficiency, long-term safety, fetal lung maturation, preterm birth, neonatal mortality, maternal immunosuppression, ACTH stimulation test
MeSH terms
Adrenal Hyperplasia, Congenital, Animals, Clinical Trials as Topic, Dexamethasone, Ethics, Medical, Female, Fetal Diseases, Glucocorticoids, Humans, Male, Pregnancy, Prenatal Exposure Delayed Effects, Rats

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