Sex Differences in 11-Oxygenated Androgen Patterns Across Adulthood

被引:58
作者
Davio, Angela [1 ]
Woolcock, Helen [2 ]
Nanba, Aya T. [1 ]
Rege, Juilee [2 ]
O'Day, Patrick [1 ]
Ren, Jianwei [1 ]
Zhao, Lili [3 ]
Ebina, Hiroki [5 ]
Auchus, Richard [1 ,4 ]
Rainey, William E. [1 ,2 ]
Turcu, Adina F. [1 ]
机构
[1] Univ Michigan, Div Metab Endocrinol & Diabet, 1150 W Med Ctr Dr,MSRB 2,5570B, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Mol & Integrat Physiol, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Sch Publ Hlth, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Dept Pharmacol, Ann Arbor, MI 48109 USA
[5] Tohoku Univ, Dept Pathol, Sendai, Miyagi, Japan
关键词
androgens; aging; 11-ketotestosterone; adrenal; adrenal cortex; 11-oxyandrogens; 19-CARBON STEROIDS; AGE; WOMEN; TESTOSTERONE; GENERATION; BIOMARKERS; TISSUE;
D O I
10.1210/clinem/dgaa343
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: The gonads are the major source of sex steroids during reproductive ages. The gonadal function declines abruptly in women and gradually in men. The adrenals produce 11-oxygenated androgens (11-oxyandrogens), which start rising during adrenarche. Following menopause, 11-oxyandrogens levels remain similar to reproductive ages. Objective: To compare the circulating 11-oxyandrogen concentrations in men and women across adult ages. Methods: We used mass spectrometry to measure testosterone (T), androstenedione (A4), 11 beta-hydroxytestosterone (11OHT), 11-ketotestosterone (11KT), 11 beta-hydroxyandrostenedione (11OHA4), 11-ketoandrostenedione (11KA4), cortisol, and cortisone in morning sera obtained from adults in outpatient setting. We performed double immunofluorescence of 3 beta-hydroxysteroid dehydrogenase type 2 and cytochrome b(5) in adrenal tissue from 19 men, age 23-78 years. Results: We included 590 patients (319 men), aged 18 to 97 years, and 84% white. 11KT and 11KA4 were stable across ages in women, but they declined in men (0.21 and 0.06 ng/dL/year, respectively; P < 0.05). 11OHA4 and 11OHT increased modestly with age in women (0.6 and 0.09 ng/dL/year, respectively; P < 0.01), and both remained stable across ages in men. As body mass index (BMI) increased, 11KA4 decreased in women, and 11KT increased in men, both suggesting higher 17 beta-hydroxysteroid dehydrogenase activity in obese individuals. A4 and T declined with age and A4 with BMI in both sexes; T declined with BMI in men. Adrenal androgenic enzyme expressions in aging men were similar to those observed in women. Conclusions: In contrast with traditional androgens, the production of 11OHA4 and 11OHT is sustained with aging in both sexes. The bioactive androgen 11 KT declines in aging men but not in women.
引用
收藏
页码:E2921 / E2929
页数:9
相关论文
共 28 条
[11]   DHEA and DHEA-S: A review [J].
Kroboth, PD ;
Salek, FS ;
Pittenger, AL ;
Fabian, TJ ;
Frye, RF .
JOURNAL OF CLINICAL PHARMACOLOGY, 1999, 39 (04) :327-348
[12]   Developmental and functional biology of the primate fetal adrenal cortex [J].
Mesiano, S ;
Jaffe, RB .
ENDOCRINE REVIEWS, 1997, 18 (03) :378-403
[13]   11-Oxygenated C19 Steroids Do Not Decline With Age in Women [J].
Nanba, Aya T. ;
Rege, Juilee ;
Ren, Jianwei ;
Auchus, Richard J. ;
Rainey, William E. ;
Turcu, Adina F. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2019, 104 (07) :2615-2622
[14]   AKR1C3-Mediated Adipose Androgen Generation Drives Lipotoxicity in Women With Polycystic Ovary Syndrome [J].
O'Reilly, Michael W. ;
Kempegowda, Punith ;
Walsh, Mark ;
Taylor, Angela E. ;
Manolopoulos, Konstantinos N. ;
Allwood, J. William ;
Semple, Robert K. ;
Hebenstreit, Daniel ;
Dunn, Warwick B. ;
Tomlinson, Jeremy W. ;
Arlt, Wiebke .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2017, 102 (09) :3327-3339
[15]   11-Ketotestosterone and 11-Ketodihydrotestosterone in Castration Resistant Prostate Cancer: Potent Androgens Which Can No Longer Be Ignored [J].
Pretorius, Elzette ;
Africander, Donita J. ;
Vlok, Mare ;
Perkins, Meghan S. ;
Quanson, Jonathan ;
Storbeck, Karl-Heinz .
PLOS ONE, 2016, 11 (07)
[16]   Androgen generation in adipose tissue in women with simple obesity -: a site-specific role for 17β-hydroxysteroid dehydrogenase type 5 [J].
Quinkler, M ;
Sinha, B ;
Tomlinson, JW ;
Bujalska, IJ ;
Stewart, PM ;
Arlt, W .
JOURNAL OF ENDOCRINOLOGY, 2004, 183 (02) :331-342
[17]   The human fetal adrenal: Making adrenal androgens for placental estrogens [J].
Rainey, WE ;
Rehman, KS ;
Carr, BR .
SEMINARS IN REPRODUCTIVE MEDICINE, 2004, 22 (04) :327-336
[18]   Dissecting human adrenal androgen production [J].
Rainey, WE ;
Carr, BR ;
Sasano, H ;
Suzuki, T ;
Mason, JI .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2002, 13 (06) :234-239
[19]   11-Ketotestosterone Is the Dominant Circulating Bioactive Androgen During Normal and Premature Adrenarche [J].
Rege, Juilee ;
Turcu, Adina F. ;
Kasa-Vubu, Josephine Z. ;
Lerario, Antonio M. ;
Auchus, Gabriela C. ;
Auchus, Richard J. ;
Smith, Joshua M. ;
White, Perrin C. ;
Rainey, William E. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2018, 103 (12) :4589-4598
[20]   Liquid Chromatography-Tandem Mass Spectrometry Analysis of Human Adrenal Vein 19-Carbon Steroids Before and After ACTH Stimulation [J].
Rege, Juilee ;
Nakamura, Yasuhiro ;
Satoh, Fumitoshi ;
Morimoto, Ryo ;
Kennedy, Michael R. ;
Layman, Lawrence C. ;
Honma, Seijiro ;
Sasano, Hironobu ;
Rainey, William E. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2013, 98 (03) :1182-1188