首页> 外文期刊>Fertility and Sterility: Official Journal of the American Fertility Society, Pacific Coast Fertility Society, and the Canadian Fertility and Andrology Society >Letrozole administration during the luteal phase after ovarian stimulation impacts corpus luteum function: a randomized, placebo-controlled trial.
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Letrozole administration during the luteal phase after ovarian stimulation impacts corpus luteum function: a randomized, placebo-controlled trial.

机译:卵巢刺激后黄体期给予来曲唑影响黄体功能:一项随机,安慰剂对照的试验。

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OBJECTIVE: To investigate the effect of letrozole-an oral aromatase inhibitor-on E(2), P, and LH levels when administered during the luteal phase after oocyte retrieval in IVF/intracytoplasmic sperm injection (ICSI) cycles. DESIGN: Prospective, randomized, placebo controlled trial. SETTING: University-affiliated private reproductive medicine center. PATIENT(S): Thirty oocyte donors undergoing standardized controlled ovarian hyperstimulation (COH) protocols. INTERVENTION(S): Patients were randomized after successful egg retrieval to receive either 2.5 mg of letrozole (Femara; Novartis, Barcelona, Spain) or a placebo (folic acid tablets). All donors were under intrauterine device (IUD) contraception. MAIN OUTCOME MEASURE(S): Serum E(2), P, and LH the day of hCG administration and days +4, +7 and +10 after ovum pick-up. RESULT(S): Donors had a comparable serum E(2) level on the day of hCG administration (1,858 vs. 2,143 pg/mL). Interestingly, levels dramatically dropped 4 days after egg retrieval, reaching a statistically significant lower level in those receiving letrozole (279 vs. 1,586 pg/mL). Again, at the next time points serum E(2) levels were significantly lower (day +7: 240 vs. 855 pg/mL and day +10: 40 vs. 448 pg/mL). No significant differences were observed in P levels, but LH serum concentrations were lower in the control group on day +7 (0.18 vs. 0.02 mIU/mL and day +10 (0.40 vs. 0.16 mIU/mL), when serum E(2) levels were higher. CONCLUSION(S): The administration of 2.5 mg of letrozole during the luteal phase has an impact on corpus luteum (CL) function. It reduces serum E(2) levels, which allows a faster recovery of LH concentration. This may be of interest not only for egg donors, but also in patients at high risk of ovarian hyperstimulation syndrome (OHSS) who freeze all their embryos or who cancel hCG administration to reduce the potential risk that high E(2) levels pose.
机译:目的:探讨来曲唑(一种口服芳香酶抑制剂)对IVF /胞浆内精子注射(ICSI)周期中卵母细胞取出后黄体期给予黄体素E(2),P和LH的影响。设计:前瞻性,随机,安慰剂对照试验。地点:大学附属的私人生殖医学中心。患者:30名卵母细胞捐献者正在接受标准化的控制性卵巢过度刺激(COH)协议。干预:成功取卵后,将患者随机分组,接受2.5 mg来曲唑(Femara; Novartis,巴塞罗那,西班牙)或安慰剂(叶酸片)。所有捐献者均接受宫内节育器(IUD)避孕。主要观察指标:给予hCG当天,取卵后+ 4,+ 7和+10天的血清E(2),P和LH。结果:在给予hCG的当天,供血者的血清E(2)水平相当(1,858 vs. 2,143 pg / mL)。有趣的是,取卵后4天该水平急剧下降,在接受来曲唑的那些中达到统计学上显着的较低水平(279对1,586 pg / mL)。同样,在下一个时间点,血清E(2)水平显着降低(第+7天:240对855 pg / mL,第+10天:40对448 pg / mL)。当血清E(2)时,对照组的L水平在+7天(0.18 vs. 0.02 mIU / mL和+10天(0.40 vs. 0.16 mIU / mL))的P水平无明显差异,但对照组的LH血清浓度较低。结论:在黄体期施用2.5 mg来曲唑对黄体(CL)功能有影响,可降低血清E(2)水平,从而可以更快地恢复LH浓度。这不仅可能对卵子捐献者感兴趣,而且对于卵巢过度刺激综合症(OHSS)的高风险患者也是如此,他们冷冻了所有胚胎或取消了hCG给药以降低高E(2)水平带来的潜在风险。

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