Hormonal effects of danazol and medical oophorectomy in endometriosis.

Obstetrics and gynecology · 1983 · vol. 62(4) , pp. 480–5 · PMID:6350956 · W2407804280
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Danazol suppressed estrogen to follicular phase levels and testosterone to levels that may inhibit endometrial proliferation, while GnRH-a caused greater estrogen suppression without androgenic effects.

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Abstract

The hormonal effects of danazol and of a long-acting gonadotropin-releasing hormone analogue (GnRH-a) were studied in women with endometriosis and those with oophorectomy. During danazol treatment, total serum concentrations of estrone and estradiol, and free, dialyzable estradiol were reduced to the low follicular phase range for premenopausal women. Corresponding estrogen levels were suppressed to a significantly greater degree (P less than .02) at the end of GnRH-a administration, to concentrations which were twofold to fourfold lower than with danazol therapy and similar to values in the oophorectomized women. Sex hormone binding globulin was markedly suppressed (P less than .001) throughout danazol treatment, resulting in a threefold elevation (P less than .01) of free testosterone. These data suggest that danazol may affect endometriosis by mechanisms other than by inducing a pseudomenopause. The increased tissue availability of testosterone may be responsible for acne and hirsutism observed in some women during danazol treatment and may inhibit proliferation of the ectopic endometrium. Medical oophorectomy using GnRH-a may have improved effects on endometriosis without the androgenic side effects of danazol.

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Condition tags

endometriosis

MeSH descriptors

Castration Danazol Endometriosis Pregnadienes Danazol Endometriosis Endometriosis Endometriosis Estradiol Estradiol Estrone Estrone Female Gonadotropin-Releasing Hormone Gonadotropin-Releasing Hormone Gonadotropin-Releasing Hormone Humans Pregnadienes Sex Hormone-Binding Globulin Sex Hormone-Binding Globulin

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Papers in the corpus that this work cites (lower rings, blue) and that cite this one (upper rings, green). Dot size scales with the paper's in-corpus citation count — bigger dot = more influential within the endo/adeno field. Click a dot to open that paper. [ expand to 2 hops ] — adds papers reached through this work's immediate citers/citees. Heavier; up to 60 extra dots.

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