Imani Babak, Eijkemans Marinus J C, Faessen Gerry H, Bouchard Philippe, Giudice Linda C, Fauser Bart C J M
Division of Reproductive Medicine, Department of Obstetrics and Gynecology, Erasmus University Medical Center Rotterdam, Rotterdam, The Netherlands.
Fertil Steril. 2002 Jan;77(1):83-90. doi: 10.1016/s0015-0282(01)02928-4.
To predict the FSH response (threshold) dose in normogonadotropic, anovulatory infertile women undergoing gonadotropin induction of ovulation.
Prospective longitudinal clinical study.
Specialist academic fertility unit.
PATIENT(S): Normogonadotropic, oligoamenorrheic, infertile women who were resistant to clomiphene citrate or in whom clomiphene citrate therapy had failed.
INTERVENTION(S): Daily exogenous FSH administration in a low-dose, step-up regimen.
MAIN OUTCOME MEASURE(S): The FSH dose on the day of ovarian response (follicle growth > 10 mm in diameter).
RESULT(S): Multivariate analysis was used to devise the following equation to predict the individual FSH response dose (75 to >187 IU/d) before initiation of therapy: [4 body mass index (in kg/m(2))] + [32 clomiphene citrate resistance (yes = 1 or no = 0)] + [7 initial free insulin-like growth factor-I (in ng/mL)] + [6 initial serum FSH level (in IU/L)] - 51. The SE of the predicted dose is 35 IU.
CONCLUSION(S): The individual FSH response dose for gonadotropin induction of ovulation in anovulatory infertile women can be predicted on the basis of initial screening characteristics. The prediction model developed in this study may increase the safety and efficiency of low-dose gonadotropin protocols (step-up and step-down) by correctly determining the appropriate starting dose for a given patient.
预测接受促性腺激素诱导排卵的性腺功能正常、无排卵的不孕女性的促卵泡生成素(FSH)反应(阈值)剂量。
前瞻性纵向临床研究。
专业学术性生育单位。
对枸橼酸氯米芬耐药或枸橼酸氯米芬治疗失败的性腺功能正常、月经过少的不孕女性。
采用低剂量递增方案每日给予外源性FSH。
卵巢出现反应当天(卵泡直径>10mm)的FSH剂量。
采用多变量分析得出以下方程,用于在治疗开始前预测个体FSH反应剂量(75至>187IU/d):[4×体重指数(kg/m²)]+[32×枸橼酸氯米芬耐药情况(是=1或否=0)]+[7×初始游离胰岛素样生长因子-I(ng/mL)]+[6×初始血清FSH水平(IU/L)]-51。预测剂量的标准误为35IU。
可根据初始筛查特征预测无排卵不孕女性促性腺激素诱导排卵时的个体FSH反应剂量。本研究中开发的预测模型通过正确确定特定患者的合适起始剂量,可能会提高低剂量促性腺激素方案(递增和递减)的安全性和有效性。