Department of Urology, West China Hospital of Sichuan University, 37#Guoxuexiang street, Chengdu 610041, Sichuan, China.
Int Urol Nephrol. 2012 Apr;44(2):393-9. doi: 10.1007/s11255-011-0065-0. Epub 2011 Oct 12.
To demonstrate the efficacy of hormone treatment on the patients with hypogonadotropic hypogonadism (HH), we summarized our more than 10 years experience.
A total of 242 male patients (age range 15-52 years old) with HH including two Kallmann syndrome treated at the andrology outpatient clinics of university hospital in the past 10 years were reviewed retrospectively. The patients were divided into three groups based on the different treatment strategy. There were 84 patients treated with human chorionic gonadotropin (hCG) (group 1, hCG treatment group), 74 patients treated with hCG plus human menopause gonadotropin (hMG) (group 2, hCG + hMG treatment group), and 84 patients treated with testosterone (group 3, T treatment group). Sex characteristics, testicular volume, and sperm production were determined before and after the treatments. The therapeutic effects in the three groups were analyzed statistically.
In total, 42 patients of group 1 (50.0%) and 56 of group 2 (75.7%) had their testicular volumes increased after 6-18 months treatment, from 2.0 ± 1.1 to 6.8 ± 3.2 mL and 2.1 ± 1.1 to 8.8 ± 3.9 mL, respectively. Only six patients of group 3 had their testicular volumes increased but no statistically significant. Among the patients with testes growth, 34 patients of group 1 and 48 patients of group 2 achieved spermatogenesis, and three of them made their wives pregnant naturally. During the follow-up after treatment, there were 36 patients finally defined as delayed puberty, and 204 patients defined as idiopathic hypogonadotropic hypogonadism.
For the hormonal treatment of HH, testosterone therapy could not stimulate testes growth and spermatogenesis, but HCG therapy and hCG/hMG combination therapy both are effective, while hCG/hMG combination therapy could achieve better therapeutic effects.
为了展示激素治疗对低促性腺激素性性腺功能减退症(HH)患者的疗效,我们总结了 10 多年的经验。
回顾性分析了过去 10 年在大学医院男科门诊就诊的 242 例 HH 患者(年龄 15-52 岁),包括 2 例 Kallmann 综合征患者。根据不同的治疗策略,将患者分为 3 组。84 例患者接受人绒毛膜促性腺激素(hCG)治疗(第 1 组,hCG 治疗组),74 例患者接受 hCG 加人绝经促性腺激素(hMG)治疗(第 2 组,hCG + hMG 治疗组),84 例患者接受睾酮治疗(第 3 组,T 治疗组)。治疗前后测定患者的性特征、睾丸体积和精子生成情况。对 3 组患者的治疗效果进行统计学分析。
第 1 组有 42 例(50.0%)、第 2 组有 56 例(75.7%)患者的睾丸体积在 6-18 个月治疗后增大,从 2.0 ± 1.1 增加到 6.8 ± 3.2 ml 和 2.1 ± 1.1 增加到 8.8 ± 3.9 ml,差异有统计学意义。只有第 3 组的 6 例患者睾丸体积增大,但差异无统计学意义。在睾丸增大的患者中,第 1 组有 34 例、第 2 组有 48 例患者出现精子生成,其中 3 例自然受孕。治疗后随访中,最终有 36 例患者被定义为青春期延迟,204 例患者被定义为特发性低促性腺激素性性腺功能减退症。
对于 HH 的激素治疗,睾酮治疗不能刺激睾丸生长和精子发生,但 hCG 治疗和 hCG/hMG 联合治疗均有效,且 hCG/hMG 联合治疗效果更好。