4.7 Article

Should Dehydroepiandrosterone Be Administered to Women?

Journal

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM
Volume 107, Issue 6, Pages 1679-1685

Publisher

ENDOCRINE SOC
DOI: 10.1210/clinem/dgac130

Keywords

DHEA; androstenedione; testosterone; hormonal therapies

Funding

  1. Veterans Affairs Merit Review Award [001]
  2. NIH NCI [K08CA222620]

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Androgen prohormones, such as DHEA, increase in early puberty, peak in the second and third decade, and decline thereafter. Studies have examined the potential benefits of DHEA therapy in various hormone-deficient states and in normal women. The data support small benefits in quality of life and mood for women with hormone deficiencies, but not for anxiety or sexual function. However, no consistent beneficial effects have been observed in menopausal symptoms, sexual function, cognition, or overall wellbeing in normal women. Local administration of DHEA may be beneficial for vulvovaginal atrophy, but caution is advised for long-term use due to the risks of androgenic and estrogenic side effects.
Context Androgen prohormones such as dehydroepiandrosterone (DHEA) increase in early puberty, peak in the second and third decade, and thereafter decline, independent of menopausal status. Investigators have examined their potential beneficial effects in normal women and those with DHEA-deficient states. Evidence Acquisition A review of the literature from 1985 to 2021 on the potential benefits and risks of androgen prohormones in women. Evidence Synthesis Studies have examined the potential benefit of DHEA therapy for anti-aging, sexual dysfunction, infertility, metabolic bone health, cognition, and wellbeing in hormone-deficient states such as primary adrenal insufficiency, hypopituitarism, and anorexia as well as administration to normal women across the lifespan. Conclusions Data support small benefits in quality of life and mood but not for anxiety or sexual function in women with primary or secondary adrenal insufficiency or anorexia. No consistent beneficial effects of DHEA administration have been observed for menopausal symptoms, sexual function, cognition, or overall wellbeing in normal women. Local administration of DHEA shows benefit in vulvovaginal atrophy. Use of DHEA to improve induction of ovulation response in women with diminished ovarian reserve is not recommended. Risks of high physiologic or pharmacologic use of DHEA include androgenic and estrogenic side effects which are of concern for long-term administration. Clinical Case A 49-year-old woman with Addison's disease who is on low dose estrogen with cyclic progesterone therapy for menopausal symptoms returns for follow-up. She is on a stable glucocorticoid replacement strategy of hydrocortisone 10 mg in the morning and 5 mg in the early afternoon and fludrocortisone 0.05 mg each morning. She has read on the internet that additional therapy with DHEA may help her overall quality of life and libido. She asks whether she should add this therapy to her regimen and at what dose.

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