在接受GnRH拮抗剂方案治疗的低预后妇女中,优势卵泡比例的增加与IVF/ICSI的不良结果有关:一项回顾性队列研究。

IF 3.8 3区 医学 Q1 REPRODUCTIVE BIOLOGY Journal of Ovarian Research Pub Date : 2024-08-31 DOI:10.1186/s13048-024-01502-4
Qijun Xie, Wei Jiang, Yi Wei, Danyu Ni, Nan Yan, Ye Yang, Chun Zhao, Rong Shen, Xiufeng Ling
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引用次数: 0

摘要

目的:本研究旨在探讨接受促性腺激素释放激素拮抗剂(GnRH-ant)方案的POSEIDON第3组和第4组患者中,不同优势卵泡比例(DFP)与体外受精或卵胞浆内单精子显微注射(IVF/ICSI)结果之间的相关性。此外,该研究还试图确定触发时机的最佳DFP阈值:对2016年至2022年期间接受GnRH-ant方案治疗控制性卵巢过度刺激(COH)的POSEIDON第3组(593人)和第4组(563人)患者进行了回顾性分析。这些患者根据其DFP分为两组,DFP定义为触发日≥18毫米优势卵泡与≥12毫米卵泡的比率(DFP≤40%和DFP≥40%)。统计分析包括受限立方样条线(RCS)和多变量逻辑回归,以评估DFP与IVF/ICSI结果之间的关系:各组患者的人口统计学特征相似。在 POSEIDON 第 3 组和第 4 组中,DFP > 40 与取回的卵母细胞数、裂解胚胎数和可用胚胎数显著减少有关。此外,在 GnRH-ant 周期之后,与 DFP ≤ 40 组相比,DFP > 40 组在新鲜胚胎移植(ET)中的临床妊娠率和活产率明显降低,而在首次冷冻解冻胚胎移植(FET)的妊娠结果中,两组间未观察到显著差异。在 POSEIDON 3 组中,DFP ≤ 40 亚组的累积临床妊娠率(CCPR)和累积活产率(CLRB)显著高于 DFP > 40 亚组,随着 DFP 水平的升高,CLRB 明显下降。然而,在 POSEIDON 第 4 组中,各组之间的 CCPR 和 CLRB 没有发现明显差异。逻辑回归分析发现,年龄和取卵数是影响第 4 组 CLRB 的关键因素:结论:对于 POSEIDON 第 3 组患者,保持 DFP ≤ 40 mm 对于通过避免延迟触发获得最佳实验室和妊娠结果至关重要。然而,对于波塞冬第 4 组患者而言,无论 DFP 如何,年龄仍是影响 CLRB 的关键因素,尽管 DFP≤40 的取卵数和可用胚胎数越高越好。
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Increasing dominant follicular proportion was associated with adverse IVF/ICSI outcomes in low-prognosis women undergoing GnRH antagonist protocol: a retrospective cohort study.

Purpose: This study aimed to examine the correlation between different dominant follicle proportions (DFPs) and outcomes of in-vitro fertilization or intracytoplasmic sperm injection (IVF/ICSI) among patients classified under POSEIDON Groups 3 and 4, who underwent gonadotropin-releasing hormone antagonist (GnRH-ant) protocols. Additionally, it sought to determine the optimal DFP threshold for trigger timing.

Methods: A retrospective analysis was performed on patients classified under POSEIDON Groups 3 (n = 593) and 4 (n = 563) who underwent GnRH-ant protocols for controlled ovarian hyperstimulation (COH) between 2016 and 2022. These patients were categorized into two groups based on their DFPs, defined as the ratio of ≥ 18-mm dominant follicles to ≥ 12-mm follicles on the trigger day (DFP ≤ 40% and DFP ≥ 40%). Statistical analyses, including restricted cubic spline (RCS) and multivariate logistic regression, were employed to assess the relationship between DFP and IVF/ICSI outcomes.

Results: Demographic characteristics of patients were similar across groups. In POSEIDON Groups 3 and 4, DFP > 40 was associated with a significant decrease in the number (No.) of oocytes retrieved, cleaved embryos, and available embryos. Moreover, following the GnRH-ant cycle, the clinical pregnancy and live birth rates in fresh embryo transfer (ET) were notably reduced in the DFP > 40 group compared with the DFP ≤ 40 group, whereas no significant differences were observed in the pregnancy outcomes of the first frozen-thawed embryo transfer (FET) between the groups. In POSEIDON Group 3, the cumulative clinical pregnancy rate (CCPR) and cumulative live birth rate (CLRB) were significantly higher in the DFP ≤ 40 subgroup than in the DFP > 40 subgroup, with a notable decrease in CLRB observed with increasing DFP levels. However, in POSEIDON Group 4, no significant differences in CCPR and CLRB were found between the groups. Logistic regression analysis identified age and the No. of oocytes retrieved as pivotal factors influencing CLRB in Group 4.

Conclusion: For patients in POSEIDON Group 3, maintaining a DFP ≤ 40 mm is crucial to achieve optimal laboratory and pregnancy outcomes by avoiding delayed triggering. However, for patients in POSEIDON Group 4, age remains a critical factor influencing CLRB regardless of DFP, although a higher No. of oocytes retrieved and available embryos with DFP ≤ 40 is beneficial.

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来源期刊
Journal of Ovarian Research
Journal of Ovarian Research REPRODUCTIVE BIOLOGY-
CiteScore
6.20
自引率
2.50%
发文量
125
审稿时长
>12 weeks
期刊介绍: Journal of Ovarian Research is an open access, peer reviewed, online journal that aims to provide a forum for high-quality basic and clinical research on ovarian function, abnormalities, and cancer. The journal focuses on research that provides new insights into ovarian functions as well as prevention and treatment of diseases afflicting the organ. Topical areas include, but are not restricted to: Ovary development, hormone secretion and regulation Follicle growth and ovulation Infertility and Polycystic ovarian syndrome Regulation of pituitary and other biological functions by ovarian hormones Ovarian cancer, its prevention, diagnosis and treatment Drug development and screening Role of stem cells in ovary development and function.
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