Di Bisceglie C, Brocato L, Tagliabue M, Bertagna A, Gianotti L, Ghigo E, Manieri C
Division of Endocrinology and Metabolic Diseases, Department of Internal Medicine, University of Turin, Turin, Italy.
J Endocrinol Invest. 2003 Mar;26(3):206-10. doi: 10.1007/BF03345158.
The aim of this study was to verify the effect of goserelin, a GnRH agonist, in women with post-menopausal virilization. Six patients with post-menopausal virilization and increase in 17-hydroxyprogesterone (17-OHP), total (TT) and free testosterone (FT) levels underwent single subcutaneous administration of goserelin, 3.6 mg. Serum 17-OHP, TT, FT, LH, FSH, E2, delta4 and 3alpha-andro-stanediol glucuronide levels were measured before and 4, 8 and 18 days after goserelin administration. Goserelin administration was followed by progressive inhibition of FSH and LH, which fell to premenopausal levels on day 18, and progressive normalization of androgen parameters. The low E2 levels recorded at baseline were further reduced by goserelin administration. Four patients then underwent ovariectomy while in two patients, rejecting surgical treatment, goserelin treatment was protracted up to 6 and 12 months, respectively, with remission of hyperandrogenism. This study shows that in post-menopausal patients with virilization GnRH agonist allows to confirm the diagnosis of gonadotropin-dependent ovarian hyperandrogenism: its administration induces inhibition of gonadotropin levels, normalization of androgen parameters, and remission of virilization when the treatment is protracted in patients waiting for surgery.
本研究的目的是验证促性腺激素释放激素(GnRH)激动剂戈舍瑞林对绝经后出现男性化症状女性的疗效。6例绝经后出现男性化症状且17-羟孕酮(17-OHP)、总睾酮(TT)和游离睾酮(FT)水平升高的患者接受了3.6 mg戈舍瑞林的单次皮下注射。在注射戈舍瑞林前以及注射后4天、8天和18天测量血清17-OHP、TT、FT、促黄体生成素(LH)、促卵泡生成素(FSH)、雌二醇(E2)、δ4和3α-雄烷二醇葡萄糖醛酸苷水平。注射戈舍瑞林后,FSH和LH逐渐受到抑制,在第18天降至绝经前水平,雄激素参数也逐渐恢复正常。戈舍瑞林给药使基线时记录的低E2水平进一步降低。4例患者随后接受了卵巢切除术,而另外2例患者拒绝手术治疗,戈舍瑞林治疗分别延长至6个月和12个月,雄激素过多症状得到缓解。本研究表明,对于绝经后出现男性化症状的患者,GnRH激动剂可用于确诊促性腺激素依赖性卵巢雄激素过多症:给药可抑制促性腺激素水平,使雄激素参数恢复正常,并且在等待手术的患者中延长治疗时间可使男性化症状缓解。