COMPARING BLASTOCYST EUPLOIDY RATES BETWEEN PROGESTIN-PRIMED AND GONADOTROPHIN-RELEASING HORMONE ANTAGONIST PROTOCOLS IN ANEUPLOIDY GENETIC TESTING: A RETROSPECTIVE ANALYSIS

IF 3.5 2区 医学 Q1 OBSTETRICS & GYNECOLOGY Reproductive biomedicine online Pub Date : 2024-11-01 DOI:10.1016/j.rbmo.2024.104543
MURAT BERKKANOGLU , KEVIN COETZEE , HASAN BULUT , HANDE NALAN TORE , KEMAL OZGUR
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Abstract

Objective

This study aims to compare the euploidy rate of blastocysts following the progestin-primed ovarian stimulation (PPOS) protocol and the gonadotropin-releasing hormone antagonist protocol in women undergoing preimplantation genetic testing for aneuploidy (PGT-A).

Materials & Methods

This is a retrospective study. The data of the total of 269 women undergoing PGT-A were analyzed. They were divided into two groups. 1) The antagonist group (n:153): an antagonist given once daily from day 6 of ovarian stimulation till the day of the ovulation trigger; and 2) The PPOS (n:116) group: medroxyprogesteron from the first or sixth day of ovarian stimulation till the day of ovulation trigger. The primary outcome is the euploidy rate of blastocysts.

Results

Basal characteristics were similar in the two groups; a substantial similarity of the main outcome measures in the two treatment groups has also been found. The mean ages (±Std) were 34,9 ±4,7 for group 1 and 33,8 ±3,8 for group 2, respectively (p=0,102). The means of antral follicle counts (±Std) were 15,6 ±11,3 for group 1 and 14,7 ±8,2 for group 2, respectively (p=0,732). The means of duration of infertility (±Std) were 4,3 ±3,7 for group 1 and 4,4 ±3,8 for group 2, respectively (p=0,962). The means of body mass index (±Std) were 25,1 ±4,6 for group 1 and 25,3 ±4,7 for group 2, respectively (p=0,654). The rates of formation of euploid blastocysts per oocytes were 55,8% for group 1 and 55% for group 2 respectively (p=0,931). Further subgroup analysis also showed there were not significant differences between below and above 35 years old patient data. The euploidy rates under 35 years old were 67,1% for group 1 and 58,6% for group 2 (p=0,153) and over 35 years old were 40,2% for group 1 and 58,6% for group 2 (p=0,469) respectively.

Conclusion

There are some studies showing there is no significant difference in rate of euploidy between PPOS and antagonist protocols.1,2 But, there is a recent retrospective study showing that PPOS protocol could potentially reduce the euploidy rate in aging IVF patients when compared to the conventional GnRH-antagonist approach.3 However, in our study we found no significant difference in the rate of euploid embryo between the antagonist and the PPOS groups in general population and also at younger or older age groups. Therefore, our results encourage the use of PPOS protocol for candidates for preimplantation genetic testing. Since our study is also a retrospective study, randomized control studies investigating the effect of PPOS on the euploidy rate and on the live birth rate are warranted.
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在非整倍体基因检测中比较孕激素引发和促性腺激素释放激素拮抗剂方案的囊胚整倍体率:回顾性分析
目的比较非整倍体着床前基因检测(PGT-A)女性采用促性腺激素释放激素拮抗剂(促性腺激素释放激素拮抗剂)和孕激素诱导卵巢刺激(PPOS)方案后囊胚的整倍体率。材料,方法回顾性研究。分析了269名接受PGT-A的妇女的数据。他们被分成两组。1)拮抗剂组(n:153):拮抗剂从卵巢刺激第6天起至触发排卵当天每天1次;2) PPOS (n:116)组:甲羟孕酮从卵巢刺激的第1天或第6天起至触发排卵日止。主要结果是囊胚的整倍体率。结果两组患者基本特征相似;两个治疗组的主要结局指标也有很大的相似性。1组患者平均年龄(±Std)为34,9±4,7岁,2组患者平均年龄为33,8±3,8岁(p=0,102)。实验组的平均卵泡数(±Std)分别为15、6±11,3和14、7±8,2 (p= 0.732)。不孕症持续时间(±Std)均值1组为4,3±3,7,2组为4,4±3,8 (p=0,962)。对照组体重指数平均值(±Std)为25,1±4,6,对照组为25,3±4,7 (p=0,654)。每只卵母细胞形成整倍体囊胚的比例,组1为55.8%,组2为55% (p= 0.931)。进一步的亚组分析也显示35岁以下和35岁以上患者数据之间没有显著差异。35岁以下组的整倍体率分别为67.1%和58.6% (p=0,153), 35岁以上组的整倍体率分别为40.2%和58.6% (p=0,469)。结论有研究表明,PPOS与拮抗剂方案之间的整倍体率无显著差异。但是,最近有一项回顾性研究表明,与传统的gnrh拮抗剂方法相比,PPOS方案可能会降低老年IVF患者的整倍体率然而,在我们的研究中,我们发现拮抗剂和PPOS组在一般人群以及年轻人和老年人群体中的整倍体胚胎率没有显着差异。因此,我们的结果鼓励使用PPOS方案的候选人植入前基因检测。由于我们的研究也是一项回顾性研究,因此调查PPOS对整倍体率和活产率的影响的随机对照研究是有必要的。
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来源期刊
Reproductive biomedicine online
Reproductive biomedicine online 医学-妇产科学
CiteScore
7.20
自引率
7.50%
发文量
391
审稿时长
50 days
期刊介绍: Reproductive BioMedicine Online covers the formation, growth and differentiation of the human embryo. It is intended to bring to public attention new research on biological and clinical research on human reproduction and the human embryo including relevant studies on animals. It is published by a group of scientists and clinicians working in these fields of study. Its audience comprises researchers, clinicians, practitioners, academics and patients. Context: The period of human embryonic growth covered is between the formation of the primordial germ cells in the fetus until mid-pregnancy. High quality research on lower animals is included if it helps to clarify the human situation. Studies progressing to birth and later are published if they have a direct bearing on events in the earlier stages of pregnancy.
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