DHEA Dosage for Menopausal Women
For menopausal women experiencing vaginal dryness or sexual pain, vaginal DHEA (prasterone) is recommended at FDA-approved doses, while oral DHEA supplementation at 25-50mg daily may be considered for systemic symptoms, though evidence for oral supplementation is less robust.
Vaginal DHEA (Prasterone)
- Vaginal DHEA (prasterone) has received FDA approval for treating dyspareunia in postmenopausal women 1
- Several studies have shown prasterone to be effective at reducing dyspareunia in postmenopausal women 1
- A randomized controlled trial of 464 survivors of breast or gynecologic cancer showed that vaginal DHEA led to significant improvements in sexual desire, arousal, pain, and overall sexual function 1
Safety Considerations for Vaginal DHEA
- The FDA label for prasterone warns that exogenous estrogens are contraindicated in women with a history of breast cancer 1
- DHEA should be used with caution in survivors receiving aromatase inhibitor therapy, as vaginal DHEA increases levels of circulating androgens 1
- Overall, safety data for androgen-based therapy in survivors of hormonally mediated cancers are limited 1
Oral DHEA Supplementation
Research studies have used various doses of oral DHEA:
- 25mg daily: A 12-month study showed increased levels of androgens, estrogens, and neurosteroids with improvement in climacteric symptoms 2
- 50mg daily:
- 100mg daily: A 6-month study showed elevation of circulating DHEA and DHEA sulfate with gender-specific responses - men experienced decreased fat mass and increased muscle strength, while women showed increased total body mass 5
Endocrine Effects of Oral DHEA
- Oral DHEA supplementation increases serum levels of DHEA, DHEA sulfate, androstenedione, testosterone, and dihydrotestosterone 2, 6, 5
- It may also increase estradiol and estrone levels 2, 6
- These hormonal changes can potentially affect menopausal symptoms
Alternative Options for Menopausal Symptoms
If DHEA is not appropriate, consider:
For vaginal dryness and sexual pain:
For vasomotor symptoms:
Clinical Recommendation
Based on the available evidence:
- For vaginal symptoms: Use FDA-approved vaginal DHEA (prasterone) at prescribed doses
- For systemic symptoms: If oral supplementation is desired, start with 25mg daily and monitor for 3 months, with the option to increase to 50mg daily if needed and well-tolerated
- Monitor hormone levels, lipid parameters, and symptom improvement during treatment
- Discontinue if adverse effects occur or no benefit is observed after 3-6 months
Caution
DHEA supplementation should be avoided in women with:
- History of hormone-dependent cancers
- Active liver disease
- History of abnormal vaginal bleeding
- Previous venous thromboembolism or stroke
- Coronary heart disease 7