Kafy Souzan, Tulandi Togas
Department of Obstetrics and Gynecology, McGill University, Montreal, Quebec, Canada.
Curr Opin Obstet Gynecol. 2007 Jun;19(3):248-52. doi: 10.1097/GCO.0b013e3280c60c9a.
To review recent advances in ovulation induction.
Aromatase inhibitors can replace clomiphene citrate as ovulation-inducing substances. The most widely used aromatase inhibitor for this purpose is letrozole and the optimal dose is 5 mg daily for 5 days. Compared to clomiphene citrate, it is associated with a thicker endometrium and a better pregnancy rate. It is as effective as gonadotropin but yet less expensive. The overall rates of congenital malformation among newborns conceived after infertility treatment with letrozole or clomiphene citrate are similar. When letrozole is combined with gonadotropin, it leads to lower gonadotropin requirements with pregnancy rates comparable to gonadotropin treatment alone. Another promising aromatase inhibitor is anastrazole. Recent evidence suggests that luteinizing hormone activity in human menopausal gonadotropin modifies follicular development so that fewer intermediate-sized follicles develop. Compared to the use of follicular stimulating hormone only, human menopausal gonadotropin is associated with less ovarian hyperstimulation.
Aromatase inhibitors are alternative drugs to clomiphene or gonadotropin for ovulation induction or superovulation.
回顾排卵诱导的最新进展。
芳香化酶抑制剂可替代枸橼酸氯米芬作为排卵诱导药物。为此目的最广泛使用的芳香化酶抑制剂是来曲唑,最佳剂量是每日5毫克,共5天。与枸橼酸氯米芬相比,它可使子宫内膜更厚,妊娠率更高。它与促性腺激素效果相当,但成本更低。使用来曲唑或枸橼酸氯米芬治疗不孕症后受孕的新生儿中,先天性畸形的总体发生率相似。当来曲唑与促性腺激素联合使用时,可降低促性腺激素的用量,妊娠率与单独使用促性腺激素治疗相当。另一种有前景的芳香化酶抑制剂是阿那曲唑。最近的证据表明,人绝经期促性腺激素中的促黄体生成素活性会改变卵泡发育,从而使中等大小卵泡的发育减少。与仅使用促卵泡生成素相比,人绝经期促性腺激素与较少的卵巢过度刺激相关。
芳香化酶抑制剂是用于排卵诱导或超排卵的枸橼酸氯米芬或促性腺激素的替代药物。