Kokeguchi Shoji, Okamoto Eri, Shibahara Hiroaki, Yamagami Kazuki, Furuhashi Kohyu, Enatsu Noritoshi, Shiotani Masahide
Medical Physics, Hanabusa Women's Clinic, Kobe, JPN.
Embryology, Hanabusa Women's Clinic, Kobe, JPN.
Cureus. 2025 Mar 27;17(3):e81281. doi: 10.7759/cureus.81281. eCollection 2025 Mar.
This study aimed to compare the outcomes of assisted reproductive technology (ART) between progestin-primed ovarian stimulation (PPOS) and antagonist protocols, using follitropin delta as the sole ovarian stimulation agent. While many comparative studies on PPOS and antagonist protocols exist, most utilize follitropin alpha or beta as stimulatory agents. Notably, no studies have reported on the use of follitropin delta in this context.
A retrospective analysis was conducted on ART cases initiated in 2022, including 529 PPOS cycles and 298 antagonist cycles. Subgroup analyses were performed based on anti-Müllerian hormone (AMH) levels, dividing patients into four groups: <1.2 ng/mL, 1.2≤ AMH <2.03 ng/mL, 2.03≤ AMH <5.0 ng/mL, and ≥5.0 ng/mL. Assessed outcomes included the number of retrieved oocytes, fertilization rates, cleavage rates, blastocyst formation rates (BL rates), and good-quality blastocyst formation rates (GBL rates), as well as the number of retrieved oocytes, fertilized embryos, cleavage-stage embryos, BL, and GBL. All cases were planned for complete blastocyst vitrification, including those in the antagonist group.
The mean patient age was 35.1 years in the PPOS group and 36.2 years in the antagonist group. Other baseline characteristics included the causes and duration of infertility, proportion of primary infertility, baseline hormone levels, BMI, duration and dosage of follitropin delta administration, and duration of medroxyprogesterone acetate (MPA) use. There were no significant differences in the background characteristics between the two groups. In AMH levels of 2.03 ng/mL and above, the two groups with AMH-based subgroups showed that the PPOS protocol demonstrated a significantly higher number of retrieved oocytes, BL, and GBL compared to the antagonist protocol.
While previous studies have indicated that no significant differences in outcomes between these protocols, the present study observed that the follitropin delta enhanced the formation of blastocysts and good-quality blastocysts. Further research is needed to determine whether these findings are specific to follitropin delta or extend to other recombinant follicle-stimulating hormone (rFSH) preparations.
本研究旨在比较以卵泡刺激素δ作为唯一卵巢刺激剂时,孕激素预处理卵巢刺激(PPOS)方案与拮抗剂方案在辅助生殖技术(ART)中的结局。虽然存在许多关于PPOS和拮抗剂方案的比较研究,但大多数研究使用卵泡刺激素α或β作为刺激剂。值得注意的是,尚无研究报道在这种情况下使用卵泡刺激素δ的情况。
对2022年启动的ART病例进行回顾性分析,包括529个PPOS周期和298个拮抗剂周期。根据抗苗勒管激素(AMH)水平进行亚组分析,将患者分为四组:<1.2 ng/mL、1.2≤AMH<2.03 ng/mL、2.03≤AMH<5.0 ng/mL和≥5.0 ng/mL。评估的结局包括取卵数、受精率、卵裂率、囊胚形成率(BL率)和优质囊胚形成率(GBL率),以及取卵数、受精胚胎数、卵裂期胚胎数、BL和GBL。所有病例均计划进行完全囊胚玻璃化冷冻,拮抗剂组的病例也不例外。
PPOS组患者的平均年龄为35.1岁,拮抗剂组为36.2岁。其他基线特征包括不孕原因和持续时间、原发不孕比例、基线激素水平、BMI、卵泡刺激素δ给药的持续时间和剂量以及醋酸甲羟孕酮(MPA)的使用时间。两组的背景特征无显著差异。在AMH水平为2.03 ng/mL及以上时,基于AMH的亚组分析显示,与拮抗剂方案相比,PPOS方案的取卵数、BL和GBL显著更高。
虽然先前的研究表明这些方案在结局上无显著差异,但本研究观察到卵泡刺激素δ可提高囊胚和优质囊胚的形成率。需要进一步研究以确定这些发现是否特定于卵泡刺激素δ,还是可扩展到其他重组促卵泡生成素(rFSH)制剂。