Oral dehydroepiandrosterone supplementation modulates spontaneous and growth hormone-releasing hormone-induced growth hormone and insulin-like growthfactor-1 secretion in early and late postmenopausal women
Ad. Genazzani et al., Oral dehydroepiandrosterone supplementation modulates spontaneous and growth hormone-releasing hormone-induced growth hormone and insulin-like growthfactor-1 secretion in early and late postmenopausal women, FERT STERIL, 76(2), 2001, pp. 241-248
Objective: To evaluate the effects of dehydroepiandrosterone (DHEA) supplem
entation on the growth hormone-releasing hormone-growth hormone (GHRH-GH) a
xis in lean and obese postmenopausal women.
Design: Prospective study.
Setting: Postmenopausal women in a clinical research environment.
Patient(s): Thirty-one postmenopausal women were divided in two groups by a
ge (50 to 55 and 60 to 65 years). Within each group, lean and obese patient
s were considered.
Intervention(s): All patients underwent hormonal evaluations before and at
the third and sixth month of therapy (50 mg of DHEA orally each day) and a
GHRH test (I mug/kg) before and at the sixth month of treatment. Ultrasound
and bone mass density (BMD) examinations were performed before and after t
he sixth month of therapy.
Main Outcome Measure(s): Plasma dehydroepiandrosterone (DHEA), dehydroepian
drosterone sulfate (DHEAS), E-1, E-2, androstenedione (A), testosterone (T)
, osteocalcin, GH, insulin-like growth factor 1 (IGF-1) concentrations.
Result(s): The levels of all of the steroids that derived from DHEA metabol
ism (E-1, E-2, A, T, DHEAS) and osteocalcin were increased in plasma under
DHEA supplementation. The supplementation protocol also increased the level
s of GH and IGF-1. However, GHRH-induced GH and IGF-1 responses were not mo
dified by DHEA supplementation.
Conclusion(s): Administration of DHEA significantly affects several endocri
ne parameters in early and late postmenopausal women independently from bod
y mass index. Our data support the hypothesis that DHEA treatment acts simi
larly to estrogen-progestin replacement therapy on the GHRH-GH-IGF-I axis.
This suggests that DHEA is more than a more than a simple "diet supplement"
or "antiaging product"; rather it should be considered an effective hormon
al replacement treatment. (C) 2001 by American Society for Reproductive Med
icine.