Impact of Clomiphene Citrate on the Steroid Profile in Dysmetabolic
Men with Low Testosterone Levels
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Published:2021-08
Issue:08
Volume:53
Page:520-528
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ISSN:0018-5043
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Container-title:Hormone and Metabolic Research
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language:en
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Short-container-title:Horm Metab Res
Author:
Pelusi Carla1, Fanelli Flamina1, Baccini Margherita1, De Pergola Giovanni2, Triggiani Vincenzo3, Mezzullo Marco1, Fazzini Alessia1, Di Dalmazi Guido1, Petrovic Biljana4, Paterini Paola4, Labate Antonio Maria Morselli1, Pagotto Uberto1, Giagulli Vito Angelo35
Affiliation:
1. Division of Endocrinology and Diabetes Prevention and Care, IRCCS
Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy 2. Nutrition Outpatient Clinic, Clinical Oncology Unit, University of
Bari, Bari, Italy 3. Interdisciplinary Department of Medicine, Internal Medicine,
Geriatrics, Endocrinology and Rare Diseases, University of Bari, Bari,
Italy 4. Center for Applied Biomedical Research, Department of Medical &
Surgical Sciences (DIMEC), Alma Mater Studiorum University of Bologna, Bologna,
Italy 5. Outpatients Clinic of Endocrinology and Metabolic Disease, Conversano
Hospital, Bari, Italy
Abstract
AbstractClomiphene citrate (CC) in male hypogonadism increases testosterone (T) and
estrogen levels by stimulating pituitary gonadotropin release. Our group
confirmed these hormonal changes in a randomized, cross-over, double-blind trial
of CC versus placebo in addition to metformin, conducted in 21 obese
dysmetabolic men with low T levels. However, we hypothesize that based on its
mechanism of action, CC may directly or indirectly affect adrenal
steroidogenesis. The aim of this sub-study was to better understand the changes
in steroid levels and metabolism induced by CC treatment. We assessed
17α-hydroxypregnelone (17αOH-P5), dehydroepiandrosterone (DHEA),
progesterone (P4), 17α-hydroxyprogesterone (17αOH-P4),
androstenedione (A), T, dihydrotestosterone (DHT), estrone (E1),
17β-estradiol (E2), 11-deoxycortisol (11 S), cortisol (F), and
cortisone (E) by LC-MS/MS, and corticosteroid binding globulin (CBG) by
ELISA, before and after each treatment. In addition, free-F and steroid
product/precursor ratios were calculated. We observed a significant
change in serum levels induced by CC compared with placebo for 17αOH-P4,
DHT, T, E2, E1, F, E, and CBG, but not free-F. In addition, compared to placebo,
CC induced higher 17αOH-P4/P4, E2/E1,
17αOH-P4/17αOH-P5, A/17αOH-P4,
T/A, E1/A, F/11 S, and F/E ratios.
Therefore, besides the CC stimulating effect on testis steroidogenesis, our
study showed increased F, E, but not free-F, levels, indicating changes in
steroid metabolism rather than adrenal secretion stimulation. The steroid
profiling also revealed the CC stimulation of the Δ5 rather than the
Δ4 pathway, thus indicating considerable testicular involvement in the
increased androgen secretion.
Funder
Italian Research Project of Relevant Interest Emilia-Romagna Region–University Program grant for Young Investigators
“Alessandro Liberati”
Publisher
Georg Thieme Verlag KG
Subject
Biochemistry, medical,Clinical Biochemistry,Endocrinology,Biochemistry,General Medicine,Endocrinology, Diabetes and Metabolism
Cited by
1 articles.
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