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早黄体期内分泌谱受触发卵母细胞最终成熟的方式和黄体期支持治疗的影响,这些治疗方法在重组卵泡刺激素-促性腺激素释放激素拮抗剂体外受精周期中使用。

Early luteal phase endocrine profile is affected by the mode of triggering final oocyte maturation and the luteal phase support used in recombinant follicle-stimulating hormone-gonadotropin-releasing hormone antagonist in vitro fertilization cycles.

机构信息

Center for Reproductive Medicine, Dutch-Speaking Free University, Brussels, Belgium.

出版信息

Fertil Steril. 2013 Sep;100(3):742-7. doi: 10.1016/j.fertnstert.2013.05.028. Epub 2013 Jun 24.

DOI:10.1016/j.fertnstert.2013.05.028
PMID:23806846
Abstract

OBJECTIVE

To assess endocrine differences during early luteal phase according to mode of triggering final oocyte maturation with or without luteal phase support (LPS).

DESIGN

A prospective randomized study.

SETTING

University center for reproductive medicine.

PATIENT(S): Four oocyte donors each underwent four consecutive cycles.

INTERVENTION(S): To avoid interpatient variation, each donor underwent the same stimulation regimen. However, different modes of triggering final oocyte maturation and LPS were administered: A) 10,000 IU hCG and standard LPS; B) GnRH agonist (GnRHa; 0.2 mg triptorelin), and 35 hours later 1,500 IU hCG, and standard LPS; C) GnRH agonist (0.2 mg triptorelin) and standard LPS; and D) GnRH agonist (0.2 mg triptorelin) without LPS.

MAIN OUTCOME MEASURE(S): Blood sampling was performed on the day of ovulation trigger, ovulation trigger + 1 day, and ovum pick-up + 5 days. Serum E2, FSH, LH, and P were measured.

RESULT(S): The early luteal phase steroid levels following GnRHa trigger and modified luteal phase support (B) were similar to those seen after hCG trigger (A). However, significant differences were seen between groups A and B compared with C and D, as well as between groups C and D.

CONCLUSION(S): Administration of a single bolus of GnRHa effectively induced LH and FSH surges in oocyte donors stimulated with recombinant FSH and cotreated with a GnRH antagonist. However, gonadotropin and steroid levels differed significantly according to the type of luteal phase support used after GnRHa trigger.

EUROPEAN COMMUNITY CLINICAL TRIAL SYSTEM (EUDRACT) NUMBER: 2009-009429-26.

摘要

目的

根据是否有黄体支持(LPS)来评估促黄体生成素峰期早期的内分泌差异。

设计

前瞻性随机研究。

地点

大学生殖医学中心。

患者

每位供卵者接受了四个连续周期的治疗。

干预措施

为避免个体间的差异,每位供卵者都接受了相同的刺激方案。然而,采用了不同的触发卵母细胞成熟和 LPS 的方式:A)10000IU hCG 和标准 LPS;B)GnRH 激动剂(GnRHa;0.2mg 曲普瑞林),35 小时后给予 1500IU hCG 和标准 LPS;C)GnRH 激动剂(0.2mg 曲普瑞林)和标准 LPS;D)GnRH 激动剂(0.2mg 曲普瑞林)而没有 LPS。

主要观察指标

排卵诱导日、排卵诱导后 1 天和取卵日进行采血。检测血清 E2、FSH、LH 和 P。

结果

GnRHa 触发和改良黄体支持(B)后的早黄体期类固醇水平与 hCG 触发(A)后的水平相似。然而,与 C 和 D 相比,A 和 B 之间、C 和 D 之间存在显著差异。

结论

在接受重组 FSH 刺激和 GnRH 拮抗剂治疗的供卵者中,单次给予 GnRH 激动剂可有效诱导 LH 和 FSH 激增。然而,根据 GnRHa 触发后使用的黄体支持类型,促性腺激素和类固醇水平存在显著差异。

欧洲共同体临床试验系统(EUDRACT)编号:2009-009429-26。

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