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Division of Endocrinology and Metabolic Diseases (C.N., F.T., G.G.S., M.M., R.C., P.M.), University of Verona, I37126 Verona; Laboratory of Clinical Chemistry (R.D.), Ospedale Maggiore, I-37126 Verona; Laboratory of Clinical Chemistry (A.F.), Ospedale San Bortolo, I-36100 Vicenza, Italy
Address correspondence and requests for reprints to: Dr. Paolo Moghetti, Divisione di Endocrinologia e Malattie del Metabolismo, Ospedale Maggiore, I-37126 Verona, Italy. E-mail: moghetti{at}iol.it
Assay by ultrasensitive methods of serum prostate-specific antigen (PSA) recently demonstrated that many women have detectable levels of this molecule. Interestingly, serum PSA concentrations were higher in hirsute than in nonhirsute subjects, suggesting that, also in females, PSA may be regulated by androgens.
To establish the potential for this assay as a biochemical marker of
androgen action in women, we studied 40 hirsute subjects recruited in a
double-blind, placebo-controlled, 6-month trial assessing the effects
of 3 different antiandrogen drugs: spironolactone, flutamide, or
finasteride. In each subject, serum PSA, free
testosterone, and 3
-androstanediol glucuronide were determined at
baseline and at the end of treatments.
At baseline, PSA concentrations were higher in these 40 women than in 19 nonhirsute healthy controls (12.9 ± 1.5 vs. 4.9 ± 0.7 pg/mL, P = 0.03) and significantly correlated with serum free testosterone (r = 0.37, P < 0.005). After treatments, the 29 hirsute subjects given active drugs showed significant reduction of serum PSA levels (7.2 ± 1.4 vs. 14.7 ± 3.0 pg/mL, P = 0.002). This phenomenon was correlated to baseline PSA values. No change was found in the placebo group.
In conclusion, serum PSA is increased in many hirsute women. A 6-month course of antiandrogen treatments with spironolactone, flutamide, or finasteride determines a reduction of PSA levels in these subjects. These results suggest that serum PSA is a biochemical marker of androgen action in tissues of female subjects.
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