Daily testosterone and gonadotropin levels are similar in azoospermic and nonazoospermic normal men administered weekly testosterone: implications for male contraceptive development
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Date
Authors
Matsumoto, Alvin M.
Bremner, William J.
Amory, John K.
Anawalt, Bradley D.
Journal Title
Journal ISSN
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Publisher
American Society of Andrology
Abstract
Weekly intramuscular administration of testosterone esters such as
testosterone enanthate (TE) suppresses gonadotropins and spermatogenesis
and has been studied as a male contraceptive. For unknown reasons,
however, some men fail to achieve azoospermia with such regimens. We
hypothesized that either 1) daily circulating serum fluoroimmunoreactive
gonadotropins were higher or testosterone levels were lower during the
weekly injection interval, or 2) monthly circulating bioactive
gonadotropin levels were higher in nonazoospermic men. We therefore
analyzed daily testosterone and fluoroimmunoreactive gonadotropin levels
as well as pooled monthly bioactive and fluoroimmunoreactive gonadotropin
levels in normal men receiving chronic TE injections and correlated these
levels with sperm production. After a 3-month control period, 51 normal
men were randomly assigned to receive intramuscular TE at 25 mg (n = 10),
50 mg (n = 9), 100 mg (n = 10), 300 mg (n = 10), or placebo (n = 12)
weekly for 6 months. After 5 months of testosterone administration,
morning testosterone and fluoroimmunoreactive follicle-stimulating hormone
(FSH) and luteinizing hormone (LH) levels were measured daily for a 1-week
period between TE injections. In addition, fluoroimmunoreactive and
bioactive FSH and LH levels were measured in pooled monthly blood samples
drawn just before the next TE injection. In the 100-mg and 300-mg TE
groups, mean monthly fluoroimmunoreactive FSH and LH levels were
suppressed by 86%-97%, bioactive FSH and LH levels by 62%-80%, and roughly
half the subjects became azoospermic. In the 1-week period of month 6,
daily testosterone levels between TE injections were within the normal
range in men receiving placebo, or 25 or 50 mg of weekly TE, but were
significantly elevated in men receiving 100 or 300 mg of weekly TE. At no
point during treatment, however, were there significant differences in
daily testosterone or fluoroimmunoreactive gonadotropin levels, or monthly
bioactive gonadotropin levels between men achieving azoospermia and those
with persistent spermatogenesis. This study, therefore, demonstrates that
neither monthly nor daily differences in serum testosterone, or
fluoroimmunoreactive or bioactive gonadotropins explain why some men fail
to completely suppress their sperm counts to zero with weekly TE
administration. Innate differences in the testicle's ability to maintain
spermatogenesis in a low-gonadotropin environment may explain persistent
spermatogenesis in some men treated with androgen-based contraceptive
regimens.
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Citation
J Androl. 2001 Nov-Dec;22(6):1053-60
