TY - JOUR
T1 - Postmenopausal dehydroepiandrosterone administration increases free insulin-like growth factor-I and decreases high-density lipoprotein
T2 - A six- month trial
AU - Casson, Peter R.
AU - Santoro, Nanette
AU - Elkind-Hirsch, Karen
AU - Carson, Sandra A.
AU - Hornsby, Peter J.
AU - Abraham, Guy
AU - Buster, John E.
PY - 1998/7
Y1 - 1998/7
N2 - Objective: To determine the effect of administering 6 months of oral postmenopausal DHEA therapy on serum DHEA, DHEAS, and T levels and on physiologic endpoints including lipoproteins and insulin-like growth factor- I ([GF-I). Design: Randomized, double-blind, parallel trial. Setting: Academic referral practice. Patient(s): Thirteen normal-weight or overweight, healthy, nonsmoking, postmenopausal women. Intervention(s): Administration of oral micronized DHEA (25 mg/d). Main Outcome Measure(s): Monthly fasting 23 hours postdose levels of serum DHEA, DHEAS, T, lipoproteins, IGF-I, IGF binding protein-3 (IGFBP-3), and liver function tests. Morphometric indices by dual-energy x-ray absorptiometry scan (percent body fat; lean body mass), immune indices, and insulin sensitivity. Result(s): Levels of DHEA, DHEAS, and T all rose into premenopausal ranges, but after 6 months, levels of DHEA and T did not differ from baseline or placebo. At 3 months, the ratio of IGF- I to IGFBP-3 rose by 36.1% ± 12.7%, but it fell to placebo values by 6 months. High-density lipoprotein and apolipoprotein A1 levels declined. Conclusion(s): Patients appeared to tolerate 6 months of DHEA therapy well. Given the small study size, no statistically significant differences in morphometric indices, immune indices, or insulin-sensitizing properties were observed, but significant attenuation of bioavailability occurred. Supplementation with DHEA increased IGF-I/IGFBP-3 levels at 3 months and decreased high-density lipoprotein and apolipoprotein A1 levels at 6 months.
AB - Objective: To determine the effect of administering 6 months of oral postmenopausal DHEA therapy on serum DHEA, DHEAS, and T levels and on physiologic endpoints including lipoproteins and insulin-like growth factor- I ([GF-I). Design: Randomized, double-blind, parallel trial. Setting: Academic referral practice. Patient(s): Thirteen normal-weight or overweight, healthy, nonsmoking, postmenopausal women. Intervention(s): Administration of oral micronized DHEA (25 mg/d). Main Outcome Measure(s): Monthly fasting 23 hours postdose levels of serum DHEA, DHEAS, T, lipoproteins, IGF-I, IGF binding protein-3 (IGFBP-3), and liver function tests. Morphometric indices by dual-energy x-ray absorptiometry scan (percent body fat; lean body mass), immune indices, and insulin sensitivity. Result(s): Levels of DHEA, DHEAS, and T all rose into premenopausal ranges, but after 6 months, levels of DHEA and T did not differ from baseline or placebo. At 3 months, the ratio of IGF- I to IGFBP-3 rose by 36.1% ± 12.7%, but it fell to placebo values by 6 months. High-density lipoprotein and apolipoprotein A1 levels declined. Conclusion(s): Patients appeared to tolerate 6 months of DHEA therapy well. Given the small study size, no statistically significant differences in morphometric indices, immune indices, or insulin-sensitizing properties were observed, but significant attenuation of bioavailability occurred. Supplementation with DHEA increased IGF-I/IGFBP-3 levels at 3 months and decreased high-density lipoprotein and apolipoprotein A1 levels at 6 months.
KW - Androgen replacement
KW - DHEA
KW - DHEAS
KW - Menopause
UR - http://www.scopus.com/inward/record.url?scp=0032124833&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0032124833&partnerID=8YFLogxK
U2 - 10.1016/S0015-0282(98)00121-6
DO - 10.1016/S0015-0282(98)00121-6
M3 - Article
C2 - 9660430
AN - SCOPUS:0032124833
SN - 0015-0282
VL - 70
SP - 107
EP - 110
JO - Fertility and sterility
JF - Fertility and sterility
IS - 1
ER -