滤泡排出率(FORT)作为评估不良反应者经皮睾酮疗效的方法。

IF 1.9
Roser Solernou, Sara Peralta, Gemma Casals, Marta Guimera, Marina Solsona, Aina Borras, Dolores Manau, Francesc Fàbregues
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引用次数: 2

摘要

目的:卵泡输出率(FORT)是卵巢对促性腺激素反应性的有效定量和定性指标。经皮睾酮(TT)已被用作促性腺激素的辅助治疗,以改善不良反应者的卵巢反应(PR)。本研究的目的是分析TT是否可以改善卵泡对促性腺激素的敏感性。方法:本回顾性研究,在三级护理大学医院举行,包括90例PR患者,根据博洛尼亚标准。第1组患者(n = 46)在垂体抑制下,在促性腺激素刺激卵巢前经皮应用睾酮。第2组(n = 44)采用高剂量促性腺激素联合小剂量GnRH激动剂方案刺激卵巢。我们分析了卵巢刺激参数和体外受精结果。我们测定卵巢刺激前的卵泡计数(AFC) (3-8 mm),排卵前卵泡计数(PFC) (16-22 mm)和hCG给药当天。我们使用PFCx100/AFC比率计算FORT。结果:两组的基线特征和卵巢储备参数相似。1组的FORT和取卵量明显高于2组。妊娠率无显著差异。第1组FORT与AFC有显著相关性。结论:本研究提示TT对不良反应患者的潜在有益机制可能是基于增加窦卵泡对促性腺激素的敏感性。FORT是演示这一点的绝佳工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Follicular Output Rate (FORT) as a method to evaluate transdermal testosterone efficacy in poor responders.

The Follicular Output Rate (FORT) as a method to evaluate transdermal testosterone efficacy in poor responders.

The Follicular Output Rate (FORT) as a method to evaluate transdermal testosterone efficacy in poor responders.

Objective: Follicular Output Rate (FORT) is an efficient quantitative and qualitative marker of ovarian responsiveness to gonadotropins. Transdermal testosterone (TT) has been used as adjuvant therapy to gonadotrophins in order to improve ovarian response in poor responders (PR). The aim of this study was to analyze whether TT can improve follicular sensitivity to gonadotropins using FORT.

Methods: This retrospective study, held in a tertiary-care university hospital included 90 PR patients, according to the Bologna criteria. Patients in Group 1 (n = 46) received transdermal application of testosterone preceding gonadotrophin ovarian stimulation under pituitary suppression. In Group 2 (n = 44) ovarian stimulation was carried out with high-dose gonadotrophin in association with minidose GnRH agonist protocol. We analyzed ovarian stimulation parameters and IVF outcomes. We determined antral follicle count (AFC) (3-8 mm) before ovarian stimulation, pre-ovulatory follicle count (PFC) (16-22 mm) and the day of hCG administration. We calculated the FORT using the PFCx100/AFC ratio.

Results: Baseline characteristics and ovarian reserve parameters were similar in both groups. FORT and oocytes retrieved were significantly higher in group 1 vs group 2. There were no significant differences in pregnancy rates. In group 1 there was a significant correlation between FORT and AFC.

Conclusions: This study suggests that the potential beneficial mechanism of TT in poor responder patients may be based on increasing the antral follicle sensitivity to gonadotrophin. FORT is an excellent tool to demonstrate this.

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