11-oxygenated C19 steroids Do not decline with age in women
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CONTEXT: The ovaries and adrenals are sources of androgens in women. Although dehydroepiandrosterone (DHEA), DHEA sulfate (DHEAS), and testosterone (T) all decline with age, these C19 steroids correlate poorly with parameters of androgen action in postmenopausal women. OBJECTIVE: To comprehensively compare the androgen profiles of pre- and postmenopausal women. METHODS: We quantified 19 steroids-including DHEA; DHEAS; T; androstenedione (A4); and the following adrenal-specific 11-oxygenated C19 steroids (11oxyandrogens): 11β-hydroxytestosterone (11OHT), 11-ketotestosterone (11KT), 11β-hydroxyandrostenedione (11OHA4), and 11-ketoandrostenedione (11KA4)-using liquid chromatography-tandem mass spectrometry in morning serum obtained from 100 premenopausal (age 20 to 40 years) and 100 postmenopausal (age ≥ 60 years) women. Double immunofluorescence of 3β-hydroxysteroid dehydrogenase type 2 (HSD3B2) with cytochrome b5 (CYB5A) or sulfotransferase 2A1 (SULT2A1) was performed in normal adrenal glands obtained from eight premenopausal and eight postmenopausal women. RESULTS: DHEA, DHEAS, A4, and T were significantly higher in pre- than in postmenopausal women (2.9, 2.8, 2.9, and 1.6-fold, respectively; P < 0.0001). In contrast, the 11-oxyandrogens did not decrease with aging, and the 11OHT/T and 11OHA4/A4 ratios showed strong positive correlations with age (r = 0.5 and 0.8, respectively; P < 0.0001). Double immunofluorescence analysis showed that with the involution of the zona reticularis in the old adrenals, the sharp zonal segregation of HSD3B2 and CYB5A becomes less distinct, and areas of HSD3B2 and CYB5A overlap are observed. CONCLUSIONS: Unlike DHEA, DHEAS, A4, and T, the 11oxyandrogens do not decline in aging women. Structural changes within the adrenal cortex might explain the evolution of androgen profiles in aging women.
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Unlike the classical androgens, the circulating levels of 11-oxygenated androgens do not decrease with age in women, suggested to be due to the involution of the zona reticularis with age and the appearance of areas co-expressing HSD3B2 and CYB5A.
“Significantly, a recent study has revealed that unlike the classical androgens, the circulating levels of 11-oxygenated androgens do not decrease with age in women, suggested to be due to the involution of the zona reticularis with age and the appearance of areas co-expressing HSD3B2 and CYB5A [289].”
From Human steroid biosynthesis, metabolism and excretion are differentially reflected by serum and urine steroid metabolomes: a comprehensive review (2019) · cites this paper as [289]
11KA4 is the next most abundant 11-oxygenated androgen precursor in circulation.
“11KA4 is the next most abundant 11-oxygenated androgen precursor in circulation (Table 2) [39,41,68,69,289].”
From Human steroid biosynthesis, metabolism and excretion are differentially reflected by serum and urine steroid metabolomes: a comprehensive review (2019) · cites this paper as [289]
Although multiple studies have measured circulating concentrations of 11-oxygenated androgens in healthy control groups, there are significant variations in the levels reported and no reference ranges have been established to date.
“However, although multiple studies have measured the circulating concentrations of 11-oxygenated androgens in healthy control groups, there are significant variations in the levels reported and as such, no reference ranges have been established to date [39,41,68,69,289].”
From Human steroid biosynthesis, metabolism and excretion are differentially reflected by serum and urine steroid metabolomes: a comprehensive review (2019) · cites this paper as [289]
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References 39 · Cited by 113
- Authors
- Nanba, A. T., Rege, J., Ren, J., Auchus, R. J., Rainey, W. E., & Turcu, A. F.
- Affiliations
- University of Michigan (US)
- Corresponding author
- Turcu, Adina F
- Venue
- The Journal of Clinical Endocrinology & Metabolism
- Publisher
- The Endocrine Society
- Published
- 2019-02-08
- Volume
- 104
- Issue
- 7
- Pages
- 2615-2622
- ISSN
- 0021-972X (ISSN-L)
- 1945-7197
- PMC
- PMC6525564
- OpenAlex
- W2913786411
- Cited by
- 113
- References
- 39
- Citations by year
- 2026: 13 · 2025: 17 · 2024: 16 · 2023: 16 · 2022: 13 · 2021: 14 · 2020: 15 · 2019: 9
- FWCI
- 10.32
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- The Journal of Clinical Endocrinology & Metabolism (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Glenn Foundation for Medical Research (N024780-00)
- National Institute of Diabetes and Digestive and Kidney Diseases (1K08DK109116)
- Claude D. Pepper Older Americans Independence Center, University of California San Francisco (AG-024824)
- Michigan Institute for Clinical and Health Research (UL1TR000433)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
- Health Sciences › Medicine › Reproductive Medicine › Ovarian function and disorders
- Keywords
- 11β-hydroxytestosterone, 11-ketotestosterone, 11β-hydroxyandrostenedione, 11-ketoandrostenedione, postmenopausal women, premenopausal women, adrenal zona reticularis, HSD3B2, cytochrome b5, dehydroepiandrosterone, DHEA sulfate, androstenedione, testosterone
- MeSH terms
- Adrenal Cortex, Adult, Aged, Aging, Androstenes, Female, Humans, Middle Aged, Oxygen, Progesterone Reductase, Sulfotransferases, Cytochromes b5, Postmenopause, Young Adult
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