Liu Yali, Lin Jiaying, Chen Li, Mao Xiaoyan, Wang Li, Chen Qiuju, Yu Sha, Kuang Yanping
Department of Assisted Reproduction, Shanghai Ninth People's Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China.
Front Physiol. 2022 Aug 19;13:965210. doi: 10.3389/fphys.2022.965210. eCollection 2022.
Progestin is an alternative to gonadotropin-releasing hormone (GnRH) analogues in the follicular phase to suppress the premature luteinizing hormone (LH) surge in women with polycystic ovary syndrome (PCOS). However, progestin-primed ovarian stimulation (PPOS) is always accompanied by increased pituitary suppression and gonadotropin consumption. Previous studies suggested that letrozole appeared to have the potential to reduce the total gonadotropin dose required for ovarian stimulation. A retrospective cohort study was performed to evaluate the efficacy of PPOS with or without letrozole in infertile women with PCOS. This retrospective cohort study included 448 women with PCOS who underwent controlled ovarian stimulation (COS) with human menopausal gonadotropin (hMG) and medroxyprogesterone acetate (MPA) (n = 224) or hMG and MPA cotreatment with LE (n = 224) from January 2018 to March 2021 after propensity-score matching. The primary outcome measure was the hMG dose. The secondary outcomes were the durations of ovarian stimulation, the implantation rate, the number of oocytes retrieved and viable embryos, oocyte maturity and fertilization rates, the percentage of women with profound pituitary suppression (luteinizing hormone [LH] <1.0 IU/L on the trigger day). The hMG doses (1949.89 ± 725.03 IU vs 2017.41 ± 653.32 IU > 0.05) and durations of ovarian stimulation (9.03 ± 1.79 days vs 9.21 ± 2.18 days > 0.05) were similar between the two groups. The implantation rate was significantly higher in the study group (MPA + hMG + LE) than in the control group (MPA + hMG) (42.22 vs 34.69%, < 0.05). The numbers of oocytes and embryos retrieved were similar between the two groups. Interestingly, letrozole cotreatment was associated with decreased oocyte maturity and fertilization rates in comparison with standard PPOS protocols even though mature and fertilized oocyte yields were comparable. Compared with those in the control group, the LH values on the trigger day were significantly higher in the study group, together with significantly reduced pituitary suppression. Letrozole combined with PPOS cannot reduce hMG consumption in PCOS patients undergoing IVF treatment and shows no beneficial effect on cycle characteristics of COS. However, letrozole supplementation manifests as a superior implantation rate to that of the standard PPOS protocol in women with PCOS.
在卵泡期,孕激素是促性腺激素释放激素(GnRH)类似物的替代物,用于抑制多囊卵巢综合征(PCOS)女性过早出现的促黄体生成素(LH)峰。然而,孕激素预处理的卵巢刺激(PPOS)总是伴随着垂体抑制增加和促性腺激素消耗增多。既往研究表明,来曲唑似乎有可能降低卵巢刺激所需的促性腺激素总剂量。进行了一项回顾性队列研究,以评估PPOS联合或不联合来曲唑在PCOS不孕女性中的疗效。这项回顾性队列研究纳入了448例PCOS女性,她们在2018年1月至2021年3月经过倾向得分匹配后,接受了人绝经期促性腺激素(hMG)和醋酸甲羟孕酮(MPA)(n = 224)或hMG与MPA联合来曲唑(LE)(n = 224)的控制性卵巢刺激(COS)。主要结局指标是hMG剂量。次要结局包括卵巢刺激持续时间、着床率、获取的卵母细胞和存活胚胎数量、卵母细胞成熟率和受精率、促性腺激素深度抑制(扳机日促黄体生成素[LH]<1.0 IU/L)女性的比例。两组的hMG剂量(1949.89±725.03 IU对2017.41±653.32 IU,>0.05)和卵巢刺激持续时间(9.03±1.79天对9.21±2.18天,>0.05)相似。研究组(MPA+hMG+LE)的着床率显著高于对照组(MPA+hMG)(42.22%对34.69%,<0.05)。两组获取的卵母细胞和胚胎数量相似。有趣的是,与标准PPOS方案相比,联合来曲唑治疗与卵母细胞成熟率和受精率降低有关,尽管成熟和受精的卵母细胞产量相当。与对照组相比,研究组扳机日的LH值显著更高,同时垂体抑制显著减轻。来曲唑联合PPOS不能降低接受体外受精治疗的PCOS患者的hMG消耗量,且对COS的周期特征无有益影响。然而,在PCOS女性中,补充来曲唑的着床率优于标准PPOS方案。