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单基因疾病植入前基因检测中的不良预后参数。

Parameters of poor prognosis in preimplantation genetic testing for monogenic disorders.

作者信息

Van Der Kelen A, Santos-Ribeiro S, De Vos A, Verdyck P, De Rycke M, Berckmoes V, Tournaye H, Blockeel C, De Vos M, Hes F J, Keymolen K, Verpoest W

机构信息

Vrije Universiteit Brussel (VUB), Universitair Ziekenhuis Brussel (UZ Brussel), Centre for Medical Genetics, Brussels, Belgium.

Department of Obstetrics and Gynecology, IVIRMA Lisboa, Lisbon, Portugal.

出版信息

Hum Reprod. 2021 Aug 18;36(9):2558-2566. doi: 10.1093/humrep/deab136.

Abstract

STUDY QUESTION

What is the likelihood of success of a single cycle of preimplantation genetic testing for monogenic disorders (PGT-M), measured as the cumulative live birth rate (CLBR) and based on various patient demographics?

SUMMARY ANSWER

For all women aged ≤40 years, the CLBR was at least 10% when the number of oocytes was ≥7 (range 10-30%) or was at least 5% when the number of oocytes was ≥3 (range 5-17%).

WHAT IS KNOWN ALREADY

The number of oocytes is significantly associated with the number of embryos for genetic testing and the clinical outcome in PGT-M. Embryos diagnosed as affected or embryos that remain without diagnosis cannot be used for embryo transfer. The size of the group of embryos non-suitable for transfer varies between 25% and 81%, depending on the indication. Thus, PGT-M is more likely to be more severely impacted by suboptimal ovarian response, poor fertilization and suboptimal embryo development than conventional IVF/ICSI schemes without PGT.

STUDY DESIGN, SIZE, DURATION: This was a single-centre retrospective comparative cohort study, of cycles between January 2011 and December 2015. A total number of 2265 PGT-M cycles were compared to 2833 conventional ICSI cycles. The principal aim of our study was the identification of the parameters of poor CLBR in couples undergoing PGT-M using multiplex short tandem repeat (STR) markers on blastomere biopsy DNA. The secondary aim was to compare the parameters of poor CLBR of the PGT-M population to those of couples undergoing ICSI without PGT.

PARTICIPANTS/MATERIALS, SETTING, METHODS: The baseline characteristics of the PGT-M group were compared to the conventional ICSI group. A multiple regression analysis was applied to account for the following potential confounding factors: female age, number of previous ART cycles, number of oocytes/suitable embryos for transfer and dosage of gonadotrophins used for ovarian stimulation.

MAIN RESULTS AND THE ROLE OF CHANCE

The PGT-M group was younger (female age 32.0 vs 34.5 years), had a higher number of previous ART cycles (1.1 vs 0.9 cycles) and used more gonadotrophins (2367 vs 1984 IU). Per cycle, the PGT-M group had more retrieved oocytes (11.8 vs 8.3 oocytes), fewer suitable embryos for transfer (1.7 vs 2.8 embryos) and a lower CLBR (29.4% vs 35.0%). Multiple regression analysis showed that the CLBR in the PGT-M group was significantly influenced by female age, the number of previous ART cycles, the number of oocytes and the dose of ovarian stimulation. In both groups, the predicted CLBR increased with increasing numbers of oocytes and suitable embryos. At least two retrieved oocytes or one embryo per single PGT-M cycle could confer an estimated CLBR above 10%. By assessing female age and the number of retrieved oocytes together, it was shown that for all women aged ≤40 years, the predicted CLBR per single PGT-M cycle was ≥10% when the number of oocytes was ≥7 or was ≥5% when the number of oocytes was ≥3.

LIMITATIONS, REASONS FOR CAUTION: Despite the large sample size, the findings are confined by limited confounder adjustment and the lack of specific PGT-M comparators.

WIDER IMPLICATIONS OF THE FINDINGS

This study aimed to describe the likelihood of success of PGT-M treatment, measured as CLBR, based on various patient demographics. In a PGT-M program, couples need to be informed of the prognosis more specifically when it is futile. The table of predicted CLBRs presented in this study is a useful tool in counselling PGT-M couples for making reproductive choices.

STUDY FUNDING/COMPETING INTEREST(S): No funding was required and there are no competing interests.

TRIAL REGISTRATION NUMBER

N/A.

摘要

研究问题

单基因疾病植入前基因检测(PGT-M)单个周期的成功率如何,以累积活产率(CLBR)衡量,并基于各种患者人口统计学特征?

总结答案

对于所有年龄≤40岁的女性,当卵母细胞数量≥7时,CLBR至少为10%(范围为10 - 30%);当卵母细胞数量≥3时,CLBR至少为5%(范围为5 - 17%)。

已知信息

卵母细胞数量与用于基因检测的胚胎数量以及PGT-M的临床结局显著相关。被诊断为受影响的胚胎或未得到诊断的胚胎不能用于胚胎移植。不适合移植的胚胎组大小因适应证而异,在25%至81%之间。因此,与没有PGT的传统体外受精/卵胞浆内单精子注射(IVF/ICSI)方案相比,PGT-M更有可能受到卵巢反应欠佳、受精不良和胚胎发育欠佳的严重影响。

研究设计、规模、持续时间:这是一项单中心回顾性比较队列研究,研究对象为2011年1月至2015年12月期间的周期。共将2265个PGT-M周期与2833个传统ICSI周期进行了比较。我们研究的主要目的是使用卵裂球活检DNA上的多重短串联重复序列(STR)标记物,确定接受PGT-M的夫妇中CLBR较低的参数。次要目的是将PGT-M人群中CLBR较低的参数与未进行PGT的接受ICSI的夫妇的参数进行比较。

参与者/材料、设置、方法:将PGT-M组的基线特征与传统ICSI组进行比较。应用多元回归分析来考虑以下潜在混杂因素:女性年龄、既往ART周期数、用于移植的卵母细胞/合适胚胎数量以及用于卵巢刺激的促性腺激素剂量。

主要结果及机遇的作用

PGT-M组年龄更小(女性年龄32.0岁对34.5岁),既往ART周期数更多(1.1次对0.9次),使用的促性腺激素更多(2367IU对1984IU)。每个周期,PGT-M组回收的卵母细胞更多(11.8个对8.3个卵母细胞),适合移植的胚胎更少(1.7个对2.8个胚胎),CLBR更低(29.4%对35.0%)。多元回归分析表明,PGT-M组的CLBR受女性年龄、既往ART周期数、卵母细胞数量和卵巢刺激剂量的显著影响。在两组中,预测的CLBR均随着卵母细胞和合适胚胎数量的增加而增加。每个PGT-M周期至少回收2个卵母细胞或1个胚胎可使估计的CLBR高于10%。通过综合评估女性年龄和回收的卵母细胞数量,结果显示,对于所有年龄≤40岁的女性,当卵母细胞数量≥7时,单个PGT-M周期的预测CLBR≥10%;当卵母细胞数量≥3时,预测CLBR≥5%。

局限性、谨慎理由:尽管样本量较大,但研究结果受到有限的混杂因素调整和缺乏特定PGT-M对照的限制。

研究结果的更广泛影响

本研究旨在根据各种患者人口统计学特征描述PGT-M治疗的成功率,以CLBR衡量。在PGT-M项目中,当治疗无效时,需要更具体地告知夫妇预后情况。本研究中呈现的预测CLBR表是为PGT-M夫妇提供生殖选择咨询的有用工具。

研究资金/利益冲突:无需资金,不存在利益冲突。

试验注册号

无。

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