Characterizing the steroidal milieu in amniotic fluid of mid-gestation: a GC-MS study
Abstract
Intact steroid hormone biosynthesis is essential for growth and development of the human fetus and embryo. In the present study, gas chromatography-mass spectrometry was employed to characterize the steroidal milieu in amniotic fluid (n = 65; male: female = 35: 30) of mid-gestation (median: 18.8th week, range: 16.0th - 24.6th week) by a comprehensive targeted steroid hormone metabolomics approach. The levels of 52 steroids including pregnenolone and 17-OH-pregnenolone metabolites, dehydroepiandrosterone (DHEA) and its metabolites, progesterone and 17-OH-progesterone metabolites, sex hormones as well as corticosterone and cortisol metabolites were measured. The dominating steroids were the group of pregnenolone and 17-OH-pregnenolone metabolites (mean ± SD: 138.0 ± 59.3 ng/mL), followed by the group of progesterone and 17-OH-progesterone metabolites (107.3 ± 44.3 ng/mL), and thereafter DHEA and its metabolites (97.1 ± 56.5 ng/mL). With respect to sex steroids, only testosterone showed a significantly higher value in male fetuses (p < 0.0001). Of all estrogen metabolites, estriol showed by far the highest concentrations (33.2 ± 26.1 ng/mL). Interestingly, cortisol metabolites were clearly present (59.6 ± 13.6 ng/mL) though fetal de novo synthesis of cortisol is assumed to start from gestational 28th week onwards. Our comprehensive characterization of the steroidal milieu in amniotic fluid of mid-gestation shows presence of all relevant classes of steroid hormones and provides reference data. We conclude that the steroidal milieu in amniotic fluid mirrors the steroidome of the feto-placental unit.
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There may be additional substances in dried blood spots that interfere with immunoassays (matrix effect).
“There may be additional substances in dried blood spots that interfere with immunoassays (matrix effect)(287).”
From Congenital Adrenal Hyperplasia—Current Insights in Pathophysiology, Diagnostics, and Management (2022) · cites this paper as [287]
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- Authors
- Wang, R., Hartmann, M. F., Tiosano, D., & Wudy, S. A.
- Affiliations
- Justus-Liebig-Universität Gießen (DE)
- Rambam Health Care Campus (IL)
- Corresponding author
- Wudy, S.A.
- Venue
- The Journal of Steroid Biochemistry and Molecular Biology
- Publisher
- Elsevier BV
- Published
- 2019-10
- Volume
- 193
- Pages
- 105412
- ISSN
- 0960-0760 (ISSN-L)
- OpenAlex
- W2884071010
- Cited by
- 22
- References
- 58
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 1 · 2023: 4 · 2022: 5 · 2021: 2 · 2020: 2 · 2019: 4
- FWCI
- 1.08
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Steroid Biochemistry and Molecular Biology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Deutsche Forschungsgemeinschaft
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolomics and Mass Spectrometry Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Steroid Chemistry and Biochemistry
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
- Keywords
- amniotic fluid, steroid hormones, second trimester, 17-hydroxypregnenolone, dehydroepiandrosterone, progesterone metabolites, 17-hydroxyprogesterone, sex steroids, testosterone, estriol, cortisol metabolites, fetal steroidogenesis, fetoplacental unit
- MeSH terms
- Adult, Amniotic Fluid, Female, Gestational Age, Humans, Male, Gas Chromatography-Mass Spectrometry, Pregnancy, Steroids, Young Adult
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