Biotransformation of oral dehydroepiandrosterone in elderly men:: Significant increase in circulating estrogens

被引:113
作者
Arlt, W
Haas, J
Callies, F
Reincke, M
Hübler, D
Oettel, M
Ernst, M
Schulte, HM
Allolio, B
机构
[1] Med Univ Hosp Wuerzburg, Dept Endocrinol, D-97080 Wurzburg, Germany
[2] Jenapharm GmbH & Co KG, Jena, Germany
[3] Inst Hormone & Fertil Res, D-2000 Hamburg, Germany
关键词
D O I
10.1210/jc.84.6.2170
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The most abundant human steroids, dehydroepiandrosterone (DHEA) and its sulfate ester DHEAS, may have a multitude of beneficial effects, but decline with age. DHEA possibly prevents immunosenescence, and as a neuroactive steroid it may influence processes of cognition and memory. Epidemiological studies revealed an inverse correlation between DHEAS levels and the incidence of cardiovascular disease in men, but not in women. To define a suitable dose for DHEA substitution in elderly men we studied pharmacokinetics and biotransformation of orally administered DHEA in 14 healthy male volunteers (mean age, 58.8 +/- 5.1 yr; mean body mass index, 25.5 +/- 1.5 kg/m(2)) with serum DHEAS concentrations below 4.1 mu mol/L (1500 ng/mL). Diurnal blood sampling was performed on 3 occasions in a single dose, randomized, cross-over design (oral administration of placebo, 50 mg DHEA, or 100 mg DHEA). The intake of 50 mg DHEA led to an increase in serum DHEAS to mean levels of young adult men, whereas 100 mg DHEA induced supraphysiological concentrations [placebo vs. 50 mg DHEA vs. 100 mg DHEA; area under the curve (AUC) 0-12 h (mean +/- SD) for DHEA, 108 +/- 22 vs. 252 +/- 45 vs. 349 +/- 72 nmol/L h; AUC 0-12 h for DHEAS, 33 +/- 9 vs. 114 +/-. 19 vs. 164 +/- 36 mu mol/L h]. Serum testosterone and dihydrotestosterone remained unchanged after DHEA administration, In contrast, 17 beta-estradiol and estrone significantly increased in a dose-dependent manner to concentrations still within the upper normal range for men [placebo vs. 50 mg DHEA vs. 100 mg DHEA; AUC 0-12 h for 17 beta-estradiol, 510 +/- 198 vs. 635 +/- 156 vs. 700 +/- 209 pmol/L.h (P < 0.0001); AUC 0-12 h for estrone, 1443 +/- 269 vs. 2537 +/- 434 vs. 3254 +/- 671 pmol/L.h (P < 0.0001)]. In conclusion, 50 mg DHEA seems to be a suitable substitution dose in elderly men, as it leads to serum DHEAS concentrations usually measured in young healthy adults. The DHEA-induced increase in circulating estrogens may contribute to beneficial effects of DHEA in men.
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页码:2170 / 2176
页数:7
相关论文
共 34 条
[1]  
ADAMS JB, 1980, CANCER RES, V40, P3815
[2]   Oral dehydroepiandrosterone for adrenal androgen replacement:: Pharmacokinetics and peripheral conversion to androgens and estrogens in young healthy females after dexamethasone suppression [J].
Arlt, W ;
Justl, HG ;
Callies, F ;
Reincke, M ;
Hübler, D ;
Oettel, M ;
Ernst, M ;
Schulte, HM ;
Allolio, B .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (06) :1928-1934
[3]   DEHYDROEPIANDROSTERONE SULFOTRANSFERASE IN THE DEVELOPING HUMAN FETUS - QUANTITATIVE BIOCHEMICAL AND IMMUNOLOGICAL CHARACTERIZATION OF THE HEPATIC, RENAL, AND ADRENAL ENZYMES [J].
BARKER, EV ;
HUME, R ;
HALLAS, A ;
COUGHTRIE, MWH .
ENDOCRINOLOGY, 1994, 134 (02) :982-989
[4]  
BARRETTCONNOR E, 1987, NEW ENGL J MED, V317, P711
[5]   A PROSPECTIVE-STUDY OF DEHYDROEPIANDROSTERONE SULFATE, MORTALITY, AND CARDIOVASCULAR-DISEASE [J].
BARRETTCONNOR, E ;
KHAW, KT ;
YEN, SSC .
NEW ENGLAND JOURNAL OF MEDICINE, 1986, 315 (24) :1519-1524
[6]   ENDOGENOUS SEX-HORMONES AND CARDIOVASCULAR-DISEASE IN MEN - A PROSPECTIVE POPULATION-BASED STUDY [J].
BARRETTCONNOR, E ;
KHAW, KT .
CIRCULATION, 1988, 78 (03) :539-545
[7]  
Baulieu EE, 1996, J ENDOCRINOL, V150, pS221
[8]   Relationships of dehydroepiandrosterone sulfate in the elderly with functional, psychological, and mental status, and short-term mortality: A French community-based study [J].
Berr, C ;
Lafont, S ;
Debuire, B ;
Dartigues, JF ;
Baulieu, EE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (23) :13410-13415
[9]   Dehydroepiandrosterone stimulates the estrogen response element [J].
Bruder, JM ;
Sobek, L ;
Oettel, M .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1997, 62 (5-6) :461-466
[10]   POSTMENOPAUSAL STEROID REPLACEMENT WITH MICRONIZED DEHYDROEPIANDROSTERONE - PRELIMINARY ORAL BIOAVAILABILITY AND DOSE PROPORTIONALITY STUDIES [J].
BUSTER, JE ;
CASSON, PR ;
STRAUGHN, AB ;
DALE, D ;
UMSTOT, ES ;
CHIAMORI, N ;
ABRAHAM, GE .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1992, 166 (04) :1163-1170