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CYPROTERONE ACETATE
Cyproterone acetate
blocks the binding of DHT dihydrotestosterone to its receptors. In a study
conducted by Peereboom-Wynia JD; van der Willigen AH; van Joost T; Stolz E
(Acta Derm Venereol 1989; 69 (5): 395-8) showed that female test subjects
who were treated with cyproterone acetate exhibited a statistically
significant increase in anagen hairs as well as a statistically
significant decrease in telogen hairs as compared to the control group. In men, cyproterone acetate competitively inhibits the effect of androgens from both the testis and the adrenal cortex. The sex drive and virility are also reduced and the function of the testis inhibited. These changes are reversible after discontinuation of the therapy. This drug can have some serious effects on male's sex drive and is sometimes prescribed for people undergoing male-female sex change. Recently, a study by
Gruber DM, Sator MO, Joura EA, Kokoschka EM, Heinze G, Huber JC. (Arch
Dermatol. 1998 Apr;134(4):459-63. Related Articles, Links) concluded that
topically applied cyproterone acetate in combination with liposomes are as
effective as oral antiandrogen medication in acne treatment while reducing
the risk of adverse effects and avoiding high serum cyproterone acetate
concentrations. This suggests that topical cyproterone may be effective in
treating hairloss in some patients by working as an androgen receptors
blocker.
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