Segal S, Casper R F
Department of Obstetrics and Gynaecology, University of Toronto, Canada.
Fertil Steril. 1992 Jun;57(6):1254-8.
To compare the use of gonadotropin-releasing hormone agonist (GnRH-a) with human chorionic gonadotropin (hCG) for triggering the final stage of follicular maturation for in vitro fertilization (IVF).
In vitro fertilization outcome was determined in a randomized, prospective study.
The University of Toronto IVF program at The Toronto Hospital, Toronto General Division.
One hundred seventy-nine women in the IVF program were given a subcutaneous injection of leuprolide acetate (500 micrograms) or an intramuscular injection of hCG (5,000 IU) 34 to 36 hours before oocyte retrieval. Vaginal progesterone (P) suppositories (50 mg) were used two times a day for luteal phase support. A subgroup of 41 women had serum estradiol (E2) and P levels determined 2 and 7 days after embryo transfer (ET).
Pregnancy rates and luteal phase E2 and P were compared.
In the GnRH-a group, there were 18 pregnancies from 84 ETs (20%). In the hCG group, there were 19 pregnancies from 95 ETs (19%). Luteal phase E2 and P levels were significantly lower in the GnRH-a group compared with the hCG group, and 18% of the former group had an apparent short luteal phase.
Gonadotropin-releasing hormone agonist appears to be an effective alternative to hCG for inducing follicular maturation in IVF. The lower luteal phase E2 concentrations may potentially be beneficial in preventing ovarian hyperstimulation and for enhancing implantation. Better luteal phase support or a different dose of GnRH-a is needed to prevent luteal phase deficiency.
比较促性腺激素释放激素激动剂(GnRH-a)与人绒毛膜促性腺激素(hCG)用于触发体外受精(IVF)卵泡成熟最后阶段的效果。
在一项随机前瞻性研究中确定体外受精结果。
多伦多大学附属多伦多总医院的体外受精项目。
179名参与体外受精项目的女性在取卵前34至36小时接受皮下注射醋酸亮丙瑞林(500微克)或肌肉注射hCG(5000国际单位)。黄体期支持采用每天两次阴道用黄体酮(P)栓剂(50毫克)。41名女性亚组在胚胎移植(ET)后2天和7天测定血清雌二醇(E2)和P水平。
比较妊娠率及黄体期E2和P水平。
GnRH-a组84次ET中有18例妊娠(20%)。hCG组95次ET中有19例妊娠(19%)。GnRH-a组黄体期E2和P水平显著低于hCG组,且前一组中18%出现明显的黄体期缩短。
促性腺激素释放激素激动剂似乎是IVF中诱导卵泡成熟的一种有效替代hCG的方法。较低的黄体期E2浓度可能对预防卵巢过度刺激和增强着床有益。需要更好的黄体期支持或不同剂量的GnRH-a来预防黄体期缺陷。