Longevity PapersAbout
← All papers
RESEARCH PAPER / 2025-10-04

Female Adipose Tissue Sex Steroid Biosynthesis.

Natalia Hetemäki, Tomi S Mikkola, Hanna Savolainen-Peltonen

Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland. · pubmed

Abstract

Estrogens, including estradiol and estrone, and androgens, including testosterone, are locally produced in adipose tissue throughout a woman's lifespan. Already in fertile-aged women, subcutaneous and visceral adipose tissue produce notable amounts of estrogens despite ongoing ovarian estrogen synthesis. After menopause, adipose tissue becomes the most important producer of estrogens. A decrease in circulating estrogen concentrations coincides with a relative increase in the amount of visceral adipose tissue and an increased risk for metabolic disorders. Furthermore, local adipose tissue biosynthesis of sex steroids may regulate the distribution of adipose tissue between the subcutaneous and visceral depots. Further studies are needed to characterize the relation of local adipose tissue sex steroid milieu to local and circulating markers of adipose tissue and metabolic dysfunction. This can shed more light on the increasing adiposity and metabolic burden associated with menopause. Here, we discuss the roles estrogens and androgens play in adipose tissue distribution and function before and after menopause, and highlight the role of local sex steroid biosynthesis, or intracrinology, in determining local tissue sex steroid environments.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

The paper discusses the role of sex steroid biosynthesis in adipose tissue and its implications for metabolic dysfunction in women, particularly post-menopause. This research is relevant as it addresses hormonal changes and their impact on metabolic health, which are critical factors in aging and longevity.

Author of this paper? Send a correction.