Antiandrogen Therapy in Dermatology

    James C. Shaw
    From the encyclopedia
    Spironolactone →

    powerful topical and oral anti-androgen used mostly by women

    Cyproterone →

    a synthetic anti-androgen and weak progestogen that inhibits DHT binding to androgen receptor

    Finasteride →

    Frontline, gold standard treatment for combatting androgenic alopecia

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    Studysummary This review discusses the use of antiandrogen therapy in dermatology, covering treatments for conditions like acne, hirsutism, and androgenic alopecia but reports no new clinical findings.
    Our plain-language summary. Not medical advice or a treatment recommendation. Consult a qualified healthcare professional before changing treatment. Full disclaimer
    The 1996 document reviews the use of antiandrogens in dermatology, particularly for treating acne, hirsutism, and androgenetic alopecia in women. It details the effectiveness and potential risks of various treatments, including spironolactone, cyproterone acetate, flutamide, corticosteroids, oral contraceptives, finasteride, gonadotropin-releasing hormone agonists, cimetidine, and ketoconazole. Spironolactone and cyproterone acetate are noted for their benefits in treating acne and hirsutism, with the latter not available in the U.S. due to concerns about liver toxicity and tumor development. Flutamide is effective but carries a significant risk of hepatotoxicity. Corticosteroids are used empirically, and oral contraceptives are important for hormonal treatment, with newer formulations being safer. Finasteride shows potential for treating hirsutism and androgenetic alopecia, but more studies are needed. Ketoconazole has antiandrogenic effects but is limited by side effects at effective doses. The document concludes that antiandrogens can be valuable for treating women with androgen-mediated skin diseases, provided that an androgen-secreting tumor is excluded.
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