Adrenal steroid metabolites and bone status in patients with adrenal incidentalomas and hypercortisolism

EBioMedicine. 2023 Sep:95:104733. doi: 10.1016/j.ebiom.2023.104733. Epub 2023 Aug 3.

Abstract

Background: Autonomous cortisol secretion (ACS), resulting from cortisol-producing adenomas (CPA), causes endogenous steroid-induced osteoporosis (SIOP). However, the risk of endogenous SIOP cannot be explained by cortisol excess alone, and how other steroid metabolites affect bone status is unclear.

Methods: ACS was diagnosed as serum cortisol ≥1.8 μg/dL after the 1-mg dexamethasone suppression test (DST-cortisol). Using liquid chromatography tandem mass spectrometry, 21 plasma steroid metabolites were measured in 73 patients with ACS and 85 patients with non-functioning adrenal tumors (NFAT). Expression of steroidogenic enzymes and relevant steroid metabolites were analyzed in some of CPA tissues.

Findings: Discriminant and principal component analyses distinguished steroid profiles between the ACS and NFAT groups in premenopausal women. Premenopausal women with ACS exhibited higher levels of a mineralocorticoid metabolite, 11-deoxycorticosterone (11-DOC), and lower levels of androgen metabolites, dehydroepiandrosterone-sulfate, and androsterone-glucuronide. In premenopausal women with ACS, DST-cortisol negatively correlated with trabecular bone score (TBS). Additionally, 11-DOC negatively correlated with lumbar spine-bone mineral density, whereas androsterone-glucuronide positively correlated with TBS. The CPA tissues showed increased 11-DOC levels with increased expression of CYP21A2, essential for 11-DOC synthesis. Adrenal non-tumor tissues were atrophied with reduced expression of CYB5A, required for androgen synthesis.

Interpretation: This study demonstrates that unbalanced production of adrenal steroid metabolites, derived from both adrenal tumor and non-tumor tissues, contributes to the pathogenesis of endogenous SIOP in premenopausal women with ACS.

Funding: JSPS KAKENHI, Secom Science and Technology Foundation, Takeda Science Foundation, Japan Foundation for Applied Enzymology, AMED-CREST, JSTA-STEP, JST-Moonshot, and Ono Medical Research Foundation.

Keywords: Adrenal incidentalomas; Autonomous cortisol secretion; Cortisol-producing adenomas; Steroid metabolites; Steroid-induced osteoporosis.

MeSH terms

  • Adrenal Gland Neoplasms* / complications
  • Adrenal Gland Neoplasms* / metabolism
  • Androgens
  • Androsterone
  • Cushing Syndrome*
  • Female
  • Glucuronides
  • Humans
  • Hydrocortisone
  • Osteoporosis*
  • Steroid 21-Hydroxylase
  • Steroids

Substances

  • Hydrocortisone
  • Androgens
  • Androsterone
  • Glucuronides
  • Steroids
  • CYP21A2 protein, human
  • Steroid 21-Hydroxylase

Supplementary concepts

  • Adrenal incidentaloma