Jones T H, Darne J F
University of Sheffield, Department of Medicine, UK.
Clin Endocrinol (Oxf). 1993 Feb;38(2):203-8. doi: 10.1111/j.1365-2265.1993.tb00994.x.
We determined whether or not self-administered subcutaneous human menopausal gonadotrophin (hMG) therapy is safe and effective in the stimulation of testicular growth and initiation of spermatogenesis in men with hypogonadotrophic hypogonadism where human chorionic gonadotrophin alone had failed.
Human menopausal gonadotrophin was self-administered subcutaneously in two dosage regimens to patients requiring (a) fertility (Group I), 37.5 IU twice daily (total weekly dose 525 IU) (n = 7) and (b) increased testicular size (Group II) 37.5 IU once daily (total weekly dose 265.5 IU) (n = 2). Patients were assessed on a monthly basis.
Nine patients with hypogonadotrophic hypogonadism were studied. Six patients had idiopathic isolated hypogonadotrophic hypogonadism, one Kallman's syndrome, one idiopathic isolated hypogonadotrophic hypogonadism secondary to trauma and one with panhypopituitarism secondary to radiotherapy for a hypothalamic pituitary tumour. Five of these patients had a history of unilateral or bilateral cryptorchidism.
Semen analysis and serum testosterone. Testicular size was assessed by use of a Prader orchidometer.
Six of seven patients (four with a history of cryptorchidism) requesting fertility attained sperm counts of > 10 million/ml. Three pregnancies have been achieved so far. One failure occurred in a patient with a previous history of cryptorchidism. In Group I patients (a) with an initial testicular volume of 4 ml or less (n = 4), mean size increased from 3.25 +/- 0.9 (SD) ml to 12.2 +/- 3.8 ml, (b) an initial testicular volume of > 4 ml mean size (n = 3) increased from 9.2 +/- 3.9 ml to 10.3 +/- 4 ml. In Group II (n = 2) testis size increased from a mean of 3.0 +/- 1.4 ml to 9.0 +/- 1.4 ml over a 6-months treatment period.
Self-administered subcutaneous human menopausal gonadotrophin is a safe and effective mode of therapy in increasing testicular size and inducing spermatogenesis in males with hypogonadotrophic hypogonadism.
我们确定了对于单独使用人绒毛膜促性腺激素治疗失败的低促性腺激素性性腺功能减退男性患者,自我皮下注射人绝经期促性腺激素(hMG)疗法在刺激睾丸生长和启动精子发生方面是否安全有效。
将人绝经期促性腺激素以两种剂量方案自我皮下注射给有如下需求的患者:(a)生育需求(第一组),每日两次,每次37.5国际单位(每周总剂量525国际单位)(n = 7);(b)增大睾丸体积(第二组),每日一次,37.5国际单位(每周总剂量265.5国际单位)(n = 2)。每月对患者进行评估。
对9例低促性腺激素性性腺功能减退患者进行了研究。6例患有特发性孤立性低促性腺激素性性腺功能减退,1例患有卡尔曼综合征,1例因创伤继发特发性孤立性低促性腺激素性性腺功能减退,1例因下丘脑 - 垂体肿瘤放疗继发全垂体功能减退。这些患者中有5例有单侧或双侧隐睾病史。
精液分析和血清睾酮。使用普拉德睾丸计评估睾丸大小。
7例有生育需求的患者中有6例(4例有隐睾病史)精子计数达到>1000万/毫升。到目前为止已实现3次妊娠。1例有隐睾病史的患者治疗失败。在第一组患者中,(a)初始睾丸体积为4毫升或更小的患者(n = 4),平均大小从3.25±0.9(标准差)毫升增加到12.2±3.