Endocrine responses to chronic androstenedione intake in 30- to 56-year-old men

In young men, chronic ingestion of 100 mg androstenedione (ASD), three times per day, does not increase serum total testosterone but does increase serum estrogen and ASD concentrations. We investigated the effects of ASD ingestion in healthy 30- to 56-yr-old men. In a double-blind, randomly assigned...

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Veröffentlicht in:The journal of clinical endocrinology and metabolism 2000-11, Vol.85 (11), p.4074-4080
Hauptverfasser: BROWN, Gregory A, VUKOVICH, Matthew D, MARTINI, Emily R, KOHUT, Marian L, FRANKE, Warren D, JACKSON, David A, KING, Douglas S
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container_end_page 4080
container_issue 11
container_start_page 4074
container_title The journal of clinical endocrinology and metabolism
container_volume 85
creator BROWN, Gregory A
VUKOVICH, Matthew D
MARTINI, Emily R
KOHUT, Marian L
FRANKE, Warren D
JACKSON, David A
KING, Douglas S
description In young men, chronic ingestion of 100 mg androstenedione (ASD), three times per day, does not increase serum total testosterone but does increase serum estrogen and ASD concentrations. We investigated the effects of ASD ingestion in healthy 30- to 56-yr-old men. In a double-blind, randomly assigned manner, subjects consumed 100 mg ASD three times daily (n = 28), or placebo (n = 27) for 28 days. Serum ASD, dihydrotestosterone (DHT), free and total testosterone, estradiol, prostate-specific antigen (PSA), and lipid concentrations were measured at week 0 and each week throughout the supplementation period. Serum total testosterone and PSA concentrations did not change with supplementation. Elevated serum concentrations of ASD (300%), free testosterone (45%), DHT (83%), and estradiol (68%) were observed during weeks 1-4 in ASD (P < 0.05). There was no relationship between age and changes in serum ASD (r2 = 0.024), free testosterone (r2 = 0.00), or estradiol (r2 = 0.029) concentrations with ASD, whereas the serum DHT response to ASD ingestion was related to age (r2 = 0.244; P < 0.05). Serum concentrations of high-density lipoprotein cholesterol were decreased by 10% during the supplementation period (P < 0.05). These results suggest that the ingestion of 100 mg ASD, three times per day, does not increase serum total testosterone or PSA concentrations but does elicit increases in ASD, free testosterone, estradiol, and DHT and decreases serum high-density lipoprotein cholesterol concentrations.
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We investigated the effects of ASD ingestion in healthy 30- to 56-yr-old men. In a double-blind, randomly assigned manner, subjects consumed 100 mg ASD three times daily (n = 28), or placebo (n = 27) for 28 days. Serum ASD, dihydrotestosterone (DHT), free and total testosterone, estradiol, prostate-specific antigen (PSA), and lipid concentrations were measured at week 0 and each week throughout the supplementation period. Serum total testosterone and PSA concentrations did not change with supplementation. Elevated serum concentrations of ASD (300%), free testosterone (45%), DHT (83%), and estradiol (68%) were observed during weeks 1-4 in ASD (P &lt; 0.05). There was no relationship between age and changes in serum ASD (r2 = 0.024), free testosterone (r2 = 0.00), or estradiol (r2 = 0.029) concentrations with ASD, whereas the serum DHT response to ASD ingestion was related to age (r2 = 0.244; P &lt; 0.05). Serum concentrations of high-density lipoprotein cholesterol were decreased by 10% during the supplementation period (P &lt; 0.05). 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Serum concentrations of high-density lipoprotein cholesterol were decreased by 10% during the supplementation period (P &lt; 0.05). These results suggest that the ingestion of 100 mg ASD, three times per day, does not increase serum total testosterone or PSA concentrations but does elicit increases in ASD, free testosterone, estradiol, and DHT and decreases serum high-density lipoprotein cholesterol concentrations.</description><subject>Administration, Oral</subject><subject>Adult</subject><subject>Affect</subject><subject>Age Factors</subject><subject>Androstenedione - administration &amp; dosage</subject><subject>Androstenedione - blood</subject><subject>Androstenedione - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Cholesterol - blood</subject><subject>Cholesterol, HDL - blood</subject><subject>Cholesterol, LDL - blood</subject><subject>Double-Blind Method</subject><subject>Estradiol - blood</subject><subject>Genital system. 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Reproduction</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pharmacology. 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source MEDLINE; Oxford University Press Journals; EZB Electronic Journals Library
subjects Administration, Oral
Adult
Affect
Age Factors
Androstenedione - administration & dosage
Androstenedione - blood
Androstenedione - pharmacology
Biological and medical sciences
Cholesterol - blood
Cholesterol, HDL - blood
Cholesterol, LDL - blood
Double-Blind Method
Estradiol - blood
Genital system. Reproduction
Humans
Male
Medical sciences
Middle Aged
Pharmacology. Drug treatments
Placebos
Prostate-Specific Antigen - blood
Testosterone - blood
Time Factors
title Endocrine responses to chronic androstenedione intake in 30- to 56-year-old men
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