Capalbo Antonio, Treff Nathan, Cimadomo Danilo, Tao Xin, Ferrero Susanna, Vaiarelli Alberto, Colamaria Silvia, Maggiulli Roberta, Orlando Giovanna, Scarica Catello, Scott Richard, Ubaldi Filippo Maria, Rienzi Laura
Genera, Centers for Reproductive Medicine, Clinica Valle Giulia, Rome, Italy; Genetyx, Molecular Genetics Laboratory, Marostica, Italy.
Reproductive Medicine Associates of New Jersey, Basking Ridge, New Jersey.
Fertil Steril. 2017 Dec;108(6):1007-1015.e3. doi: 10.1016/j.fertnstert.2017.08.004. Epub 2017 Sep 15.
To test whether abnormally fertilized oocyte (AFO)-derived blastocysts are diploid and can be rescued for clinical use.
Longitudinal-cohort study from January 2015 to September 2016 involving IVF cycles with preimplantation genetic testing for aneuploidy (PGT-A). Ploidy assessment was incorporated whenever a blastocyst from a monopronuclear (1PN) or tripronuclear zygote (2PN + 1 smaller PN; 2.1 PN) was obtained.
Private IVF clinics and genetics laboratories.
PATIENT(S): A total of 556 women undergoing 719 PGT-A cycles.
INTERVENTION(S): Conventional chromosome analysis was performed on trophectoderm biopsies by quantitative polymerase chain reaction. For AFO-derived blastocysts, ploidy assessment was performed on the same biopsy with the use of allele ratios for hetorozygous SNPs analyzed by means of next-generation sequencing (1:1 = diploid; 2:1 = triploid; loss of heterozygosity = haploid). Balanced-diploid 1PN- and 2.1PN-derived blastocysts were transferred in the absence of normally fertilized transferable embryos.
MAIN OUTCOME MEASURE(S): Ploidy constitution and clinical value of AFO-derived blastocysts in IVF PGT-A cycles.
RESULT(S): Of the 5,026 metaphase II oocytes injected, 5.2% and 0.7% showed 1PN and 2.1PN, respectively. AFOs showed compromised embryo development (P<.01). Twenty-seven AFO-derived blastocysts were analyzed for ploidy constitution. The 1PN-derived blastocysts were mostly diploid (n = 9/13; 69.2%), a few were haploid (n = 3/13; 23.1%), and one was triploid (n = 1/13; 7.7%). The 2.1PN-derived blastocysts were also mostly diploid (n = 12/14; 85.7%), and the remainder were triploid. Twenty-six PGT-A cycles resulted in one or more AFO-derived blastocysts (n = 26/719; 3.6%). Overall, eight additional balanced-diploid transferable embryos were obtained from AFOs. In three cycles, the only balanced-diploid blastocyst produced was from an AFO (n = 3/719; 0.4%). Three AFO-derived live births were achieved: one from a 1PN zygote and two from 2.1PN zygotes.
CONCLUSION(S): Enhanced PGT-A technologies incorporating reliable ploidy assessment provide an effective tool to rescue AFO-derived blastocysts for clinical use.
检测异常受精的卵母细胞(AFO)来源的囊胚是否为二倍体,以及能否挽救用于临床。
2015年1月至2016年9月的纵向队列研究,涉及进行非整倍体植入前基因检测(PGT-A)的体外受精周期。每当获得来自单原核(1PN)或三原核合子(2PN + 1个较小原核;2.1PN)的囊胚时,进行倍性评估。
私立体外受精诊所和遗传学实验室。
共有556名接受719个PGT-A周期的女性。
通过定量聚合酶链反应对滋养外胚层活检组织进行常规染色体分析。对于AFO来源的囊胚,使用通过下一代测序分析的杂合单核苷酸多态性(SNP)的等位基因比率对同一活检组织进行倍性评估(1:1 = 二倍体;2:1 = 三倍体;杂合性缺失 = 单倍体)。在没有正常受精的可移植胚胎的情况下,移植平衡二倍体的1PN和2.1PN来源的囊胚。
IVF PGT-A周期中AFO来源的囊胚的倍性构成和临床价值。
在5026个注射的MII期卵母细胞中,分别有5.2%和0.7%显示为1PN和2.1PN。AFO显示胚胎发育受损(P<0.01)。对27个AFO来源的囊胚进行了倍性构成分析。1PN来源的囊胚大多为二倍体(n = 9/13;69.2%),少数为单倍体(n = 3/13;23.1%),一个为三倍体(n = 1/13;7.7%)。2.1PN来源的囊胚也大多为二倍体(n = 12/14;85.7%),其余为三倍体。26个PGT-A周期产生了一个或多个AFO来源的囊胚(n = 26/719;3.6%)。总体而言,从AFO中额外获得了8个平衡二倍体可移植胚胎。在三个周期中,产生的唯一平衡二倍体囊胚来自AFO(n = 3/719;0.4%)。实现了三例AFO来源的活产:一例来自1PN合子,两例来自2.1PN合子。
结合可靠倍性评估的增强型PGT-A技术为挽救AFO来源的囊胚用于临床提供了一种有效工具。