Zhao Shibin, Wang Congmin
Department of Reproductive Medicine, the Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Ann Palliat Med. 2023 Jan;12(1):133-140. doi: 10.21037/apm-22-1448.
We investigated the efficacy of progestin-primed ovarian stimulation (PPOS) and minimal stimulation using clomiphene citrate (CC) + gonadotropin (Gn) for in-vitro fertilization-embryo transfer (IVF-ET) in advanced maternal age (AMA) women with poor ovarian response (POR) according to the Patient-Oriented Strategies Encompassing Individualized Oocyte Number (POSEIDON) criteria.
A retrospective analysis was performed using the data of AMA patients who had received IVF-ET due to a low ovarian reserve. The enrolled patients were screened according to the POSEIDON group 4 criteria. 102 patients were included in the study, including 52 in the PPOS group and 50 in the minimal stimulation group (who received CC + Gn). The duration of Gn administration, Gn dose, estradiol (E2), and luteinizing hormone (LH) levels on the day of trigger, the cancellation rate of the oocyte retrieval cycle, the number of oocytes retrieved, the number of metaphase II (MII) oocytes, and IVF laboratory outcomes during ovarian stimulation were compared between the 2 groups.
No significant differences were found in terms of age, infertility, body mass index (BMI), and basal follicle-stimulating hormone, LH, E2, AFC, and AMH between the 2 groups (all P>0.05). The duration of ovarian stimulation [(9.43±2.44) vs. (7.48±3.09) days, P<0.05] was significantly longer and the total Gn dose [(2,423.22±738.66) vs. (1,579.68±728.86) IU, P<0.05] were significantly higher in the PPOS group than the minimal stimulation group. The LH value on the day of trigger in the PPOS group (3.28 mIU/mL) was significantly lower than that in the minimal stimulation group (5.57 mIU/mL) (P<0.05). The number of oocytes retrieved, normal fertilization rate, number of good-quality embryos on day 3, number of transferable embryos, and number of frozen blastocysts did not differ significantly between the 2 groups (all P>0.05). The proportion of MII oocytes was significantly higher in the PPOS group than the minimal stimulation group (94.05% vs. 81.40%, P<0.05).
For patients in the POSEIDON group 4, PPOS effectively blocked the premature LH surge and increased the proportion of mature oocytes. Thus, it is a feasible ovulation stimulation protocol for AMA women with POR.
我们根据以患者为导向的涵盖个体化卵母细胞数量的策略(POSEIDON)标准,研究了孕激素预处理的卵巢刺激(PPOS)和使用枸橼酸氯米芬(CC)+促性腺激素(Gn)的微刺激方案在卵巢反应不良(POR)的高龄产妇(AMA)行体外受精-胚胎移植(IVF-ET)中的疗效。
对因卵巢储备功能低下接受IVF-ET的AMA患者的数据进行回顾性分析。根据POSEIDON组4标准对纳入的患者进行筛选。102例患者纳入研究,其中PPOS组52例,微刺激组(接受CC+Gn)50例。比较两组在Gn给药持续时间、Gn剂量、扳机日的雌二醇(E2)和黄体生成素(LH)水平、取卵周期取消率、取卵数、中期II(MII)卵母细胞数以及卵巢刺激期间的IVF实验室结果。
两组在年龄、不孕情况、体重指数(BMI)以及基础卵泡刺激素、LH、E2、窦卵泡计数(AFC)和抗缪勒管激素(AMH)方面均无显著差异(均P>0.05)。PPOS组的卵巢刺激持续时间[(9.43±2.44)天对(7.48±3.09)天,P<0.05]显著长于微刺激组,总Gn剂量[(2423.22±738.66)IU对(1579.68±728.86)IU,P<0.05]也显著高于微刺激组。PPOS组扳机日的LH值(3.28 mIU/mL)显著低于微刺激组(5.57 mIU/mL)(P<0.05)。两组在取卵数、正常受精率、第3天优质胚胎数、可移植胚胎数和冷冻囊胚数方面均无显著差异(均P>0.05)。PPOS组的MII卵母细胞比例显著高于微刺激组(94.05%对81.40%,P<0.05)。
对于POSEIDON组4的患者,PPOS有效阻断了LH过早峰,并提高了成熟卵母细胞的比例。因此,它是POR的AMA女性可行的促排卵方案。