Keleştimur Fahrettin, Everest Hatice, Unlühizarci Kürşad, Bayram Fahri, Sahin Yilmaz
Department of Endocrinology, Erciyes University Medical School, Kayseri, Turkey.
Eur J Endocrinol. 2004 Mar;150(3):351-4. doi: 10.1530/eje.0.1500351.
To compare the clinical efficacy and safety of the combination of spironolactone (100 mg/day) plus finasteride (5 mg/day) and spironolactone (100 mg/day) alone in the treatment of hirsutism.
Sixty-five hirsute women were randomly assigned to one of these two treatment groups. Hirsutism score was measured according to the modified Ferriman-Gallwey scoring system. Baseline and post-treatment assessments were carried out in each subject by an investigator blinded to the therapy. Both groups had similar demographic properties at baseline. The serum levels of total and free testosterone, dehydroepiandrosterone sulphate and sex hormone-binding globulin were measured at the beginning and after 1 year of therapy. Blood chemistry and side-effects were evaluated during the study. Hirsutism scores were decreased significantly in both groups at the end of the year.
The mean percentage change in hirsutism scores from baseline in the spironolactone plus finasteride-treated group (51.3%) was significantly (P<0.005) higher than in the group treated with spironolactone alone (36.6%). Patients from both treatment groups experienced similar side-effects.
We have concluded that a combination of spironolactone plus finasteride is a safe and effective therapy in the treatment of hirsutism.
比较螺内酯(100毫克/天)联合非那雄胺(5毫克/天)与单用螺内酯(100毫克/天)治疗多毛症的临床疗效和安全性。
65名多毛女性被随机分配至这两个治疗组之一。根据改良的费里曼-盖尔维评分系统测量多毛症评分。由对治疗不知情的研究者对每位受试者进行基线和治疗后评估。两组在基线时的人口统计学特征相似。在治疗开始时及治疗1年后测量总睾酮、游离睾酮、硫酸脱氢表雄酮和性激素结合球蛋白的血清水平。在研究期间评估血液生化指标和副作用。两组的多毛症评分在年末均显著降低。
螺内酯联合非那雄胺治疗组的多毛症评分相对于基线的平均变化百分比(51.3%)显著高于(P<0.005)单用螺内酯治疗组(36.6%)。两个治疗组的患者出现的副作用相似。
我们得出结论,螺内酯联合非那雄胺是治疗多毛症的一种安全有效的疗法。