Ontology highlight
ABSTRACT: Context
Ovarian and adrenal steroidogenesis underlie endocrine-metabolic dysfunction in polycystic ovary syndrome (PCOS). Adipocytes express aldo-keto reductase 1C3 and type 1 11β-hydroxysteroid dehydrogenase, which modulate peripheral androgen and cortisol production.Objectives
To compare serum adrenal steroids, including 11-oxygenated androgens (11-oxyandrogens), cortisol, and cortisone between normal-weight women with PCOS and body mass index- and age-matched ovulatory women with normal-androgenic profiles (controls), and assess whether adrenal steroids associate with abdominal adipose deposition.Design
Prospective, cross-sectional, cohort study.Setting
Academic medical center.Patients
Twenty normal-weight women with PCOS and 20 body mass index-/age-matched controls.Interventions
Blood sampling, IV glucose tolerance testing, and total-body dual-energy x-ray absorptiometry.Main outcome measures
Clinical characteristics, hormonal concentrations, and body fat distribution.Results
Women with PCOS had higher serum total/free testosterone (T) and androstenedione (A4) levels and a greater android/gynoid fat mass than controls (androgens P < .001; android/gynoid fat mass ratio, P = .026). Serum total/free T and A4 levels correlated positively with android/gynoid fat mass ratio in all women combined (P < .025, all values). Serum 11ß-hydroxyA4, 11-ketoA4, 11ß-hydroxyT, 11-ketoT, cortisol, and cortisone levels were comparable between female types and unrelated to body fat distribution. Serum 11-oxyandrogens correlated negatively with % total body fat, but lost significance adjusting for cortisol. Serum cortisol levels, however, correlated inversely with android fat mass (P = .021), with a trend toward reduced serum cortisol to cortisone ratio in women with PCOS vs controls (P = .075), suggesting diminished 11β-hydroxysteroid dehydrogenase activity.Conclusion
Reduced cortisol may protect against preferential abdominal fat mass in normal-weight PCOS women with normal serum 11-oxyandrogens.
SUBMITTER: Dumesic DA
PROVIDER: S-EPMC10315644 | biostudies-literature | 2023 Jul
REPOSITORIES: biostudies-literature
Dumesic Daniel A DA Turcu Adina F AF Liu Haiping H Grogan Tristan R TR Abbott David H DH Lu Gwyneth G Dharanipragada Devyani D Chazenbalk Gregorio D GD
Journal of the Endocrine Society 20230607 8
<h4>Context</h4>Ovarian and adrenal steroidogenesis underlie endocrine-metabolic dysfunction in polycystic ovary syndrome (PCOS). Adipocytes express aldo-keto reductase 1C3 and type 1 11β-hydroxysteroid dehydrogenase, which modulate peripheral androgen and cortisol production.<h4>Objectives</h4>To compare serum adrenal steroids, including 11-oxygenated androgens (11-oxyandrogens), cortisol, and cortisone between normal-weight women with PCOS and body mass index- and age-matched ovulatory women w ...[more]