Carmina E, Janni A, Lobo R A
Cattedra di Endocrinologia, Universita di Palermo, Italy.
J Clin Endocrinol Metab. 1994 Jan;78(1):126-30. doi: 10.1210/jcem.78.1.8288696.
GnRH agonists (GnRH-A) have been used for the treatment of hirsutism in women with ovarian hyperandrogenism. However, significant side-effects, including vasomotor symptoms and bone loss, have prevented the long term use of this therapy. In this study, we evaluated the effects of low dose (physiological) estrogen replacement on the side-effects and clinical and hormonal parameters of 22 hirsute women with ovarian hyperandrogenism when treated with a long-acting GnRH-A, Decapeptyl. Ten patients with Ferriman-Gallwey (FG) scores averaging 13.4 +/- 1.5 were randomly assigned to be treated with Decapeptyl alone (3.75 mg, im, every 28 days for 6 months), and 12 other patients with FG scores averaging 13.3 +/- 1 received Decapeptyl with estrogen (conjugated equine estrogens, 0.625 mg) for 21 days and medroxyprogesterone acetate (10 mg) for 10 days (days 12-21). After 6 months, LH was suppressed in both groups, whereas FSH was significantly reduced only in the group receiving GnRH-A with estrogen (2.5 +/- 4 vs. 4.8 +/- 0.6 IU/L; P < 0.01). Serum androgen levels were reduced in both groups, although the reduction of testosterone and unbound testosterone was greater in the group receiving hormonal replacement [1.73 +/- 0.3 vs. 2.57 +/- 0.4 nmol/L for testosterone (P < 0.05); 8.3 +/- 1 vs. 14.6 +/- 2.8 pmol/L for unbound testosterone (P < 0.05)]. The reduction in hirsutism scores was greater with hormonal replacement (FG scores, -4.1 +/- 0.3 vs. -2.5 +/- 0.3; P < 0.05), whereas the polycystic appearance of ovaries by ultrasound was decreased in both groups. Amenorrhea and vasomotor symptoms were observed only with GnRH-A alone. Serum osteocalcin rose significantly with GnRH-A alone, reflecting a change in bone turnover (0.49 +/- 0.05 to 0.64 +/- 0.09 nmol/L; P < 0.05), but was unchanged with hormonal replacement. Patients receiving hormonal replacement had treatment extended to 1 yr. A further improvement of hirsutism, with scores dropping into the normal range (4.9 +/- 0.7), as well as a normalization of ovarian morphology were evident at this time. In conclusion, low dose (physiological) estrogen replacement may enhance the effects of GnRH-A treatment, while preventing most of the side-effects encountered with GnRH-A alone. This may allow more prolonged treatment, which is necessary for hirsutism.
促性腺激素释放激素激动剂(GnRH-A)已被用于治疗卵巢雄激素过多症女性的多毛症。然而,包括血管舒缩症状和骨质流失在内的显著副作用阻碍了该疗法的长期使用。在本研究中,我们评估了低剂量(生理剂量)雌激素替代疗法对22例患有卵巢雄激素过多症的多毛女性在使用长效GnRH-A(曲普瑞林)治疗时的副作用、临床和激素参数的影响。10例费里曼-盖尔韦(FG)评分平均为13.4±1.5的患者被随机分配仅接受曲普瑞林治疗(3.75mg,肌肉注射,每28天一次,共6个月),另外12例FG评分平均为13.3±1的患者接受曲普瑞林联合雌激素(结合马雌激素,0.625mg)治疗21天,并联合醋酸甲羟孕酮(10mg)治疗10天(第12 - 21天)。6个月后,两组的促黄体生成素(LH)均受到抑制,而仅在接受GnRH-A联合雌激素治疗的组中促卵泡生成素(FSH)显著降低(2.5±4与4.8±0.6IU/L;P<0.01)。两组的血清雄激素水平均降低,尽管接受激素替代治疗的组中睾酮和游离睾酮的降低幅度更大[睾酮:1.73±0.3与2.57±0.4nmol/L(P<0.05);游离睾酮:8.3±1与14.6±2.8pmol/L(P<0.05)]。激素替代治疗使多毛症评分降低幅度更大(FG评分,-4.1±0.3与-2.5±0.3;P<0.05),而两组经超声检查卵巢的多囊样表现均有所减轻。仅单独使用GnRH-A时观察到闭经和血管舒缩症状。单独使用GnRH-A时血清骨钙素显著升高,反映了骨转换的变化(0.49±0.05至0.64±0.09nmol/L;P<0.05),但在激素替代治疗时未发生变化。接受激素替代治疗的患者治疗延长至1年。此时多毛症进一步改善,评分降至正常范围(4.9±0.7),且卵巢形态恢复正常。总之,低剂量(生理剂量)雌激素替代疗法可能增强GnRH-A治疗的效果,同时预防单独使用GnRH-A时遇到的大多数副作用。这可能允许进行更长时间的治疗,这对于多毛症治疗是必要的。