Estradiol in elderly men
Open accessAbstract
The role of estrogens in male physiology has become more evident, as a consequence of the discovery of human models of estrogen deficiency such as estrogen resistance or aromatase deficiency. In males, testosterone is the major source of plasma estradiol, the main biologically active estrogen, only 20% of which is secreted by the testes. Plasma estrone, 5% of which is converted to plasma estradiol, originates from tissue aromatization of, mainly adrenal, androstenedione. The plasma concentration of estradiol in males is 2-3 ng/dl and its production rate in blood is 25-40 micrograms/24 h; both of these values are significantly higher than in postmenopausal women. Plasma levels of estradiol do not necessarily reflect tissue-level activity as peripherally formed estradiol is partially metabolized in situ; thus, not all enters the general circulation, with a fraction remaining only locally active. Of the factors influencing plasma estradiol levels, plasma testosterone is a major determinant. However, the age-associated decrease in testosterone levels is scarcely reflected in plasma estradiol levels, as a result of increasing aromatase activity with age and the age-associated increase in fat mass. Free and bioavailable estradiol levels do decrease modestly with age as does the ratio of free testosterone to free estradiol, the latter testifying to the age-associated increased aromatization of testosterone. Estradiol levels are highly significantly positively related to body fat mass and more specifically to subcutaneous abdominal fat, but not to visceral (omental) fat. Indeed, aromatase activity in omental fat is only one-tenth of the activity in gluteal fat. Estrogens in males play an important role in the regulation of the gonadotropin feedback, several brain functions, bone maturation, regulation of bone resorption and in lipid metabolism. Moreover, they affect skin metabolism and are an important factor determining sex interest in man.
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17β-estradiol can be produced locally from fat, brain, skeletal muscle, and testes by aromatization, which converts androstenedione and testosterone to 17β-estradiol.
“It can also be produced locally from fat, brain, skeletal muscle, and testes by aromatization, which converts androstenedione and testosterone to 17β-estradiol (116, 117).”
From From mitochondria to sarcopenia: role of 17β-estradiol and testosterone (2023) · cites this paper as [116]
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“Interestingly, recent studies suggest that SHBG may partially TABLE 2 Summary of the impact of perturbing circulating and WAT-derived sex steroids on metabolic disease and aging in mouse models.”
- Authors
- Vermeulen, A., Kaufman, J. M., Goemaere, S., & Van Pottelberg, I.
- Affiliations
- Ghent University Hospital (BE)
- Venue
- The Aging Male
- Publisher
- Informa UK Limited
- Published
- 2002-01
- Volume
- 5
- Issue
- 2
- Pages
- 98-102
- ISSN
- 1368-5538 (ISSN-L)
- 1473-0790
- OpenAlex
- W1999158243
- Cited by
- 452
- References
- 29
- Citations by year
- 2026: 8 · 2025: 12 · 2024: 17 · 2023: 19 · 2022: 20 · 2021: 23 · 2020: 19 · 2019: 14 · 2018: 23 · 2017: 17 · 2016: 16 · 2015: 27 · 2014: 25 · 2013: 16 · 2012: 23
- FWCI
- 9.93
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- The Aging Male (publishedVersion)
- PubMed (publishedVersion)
- Ghent University Academic Bibliography (Ghent University) (submittedVersion)
- Topics
- Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Estrogen and related hormone effects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Sexual Differentiation and Disorders
- Keywords
- estradiol, older men, male physiology, aromatase, testosterone, estrone, estrogen resistance, aromatase deficiency, fat mass, abdominal fat, gonadotropin feedback, bone metabolism, lipid metabolism, aging
- MeSH terms
- Adrenal Glands, Aged, Aged, 80 and over, Aging, Aromatase, Estradiol, Humans, Male, Middle Aged, Obesity, Testosterone
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