第2天卵裂球对称性对囊胚等级和倍性状态的影响

Diana Chieh Xing Tain, M. Lim, B. L. Ng, E. Hammond, P. Wong
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引用次数: 2

摘要

以往的研究表明,非整倍体率与卵裂期的细胞不对称有关。回顾性研究了4细胞期卵裂球对称性对囊胚等级和倍性状态的影响。采用慢移成像技术(Embryoscope, Vitrolife)对2017年191例接受非整倍体植入前基因检测的患者的732个第5/6天囊胚进行了分析。在第2天4个细胞的第一张图像上,通过在每个卵裂球上垂直绘制的2条线的平均直径制表来测量卵裂球的对称性。对称定义为[公式:见文]卵裂球直径差的25%。在第5/6天进行滋养外胚层(TE)活检,随后使用Next Generation Sequencing (VeriSeq Protocol, Illumina)进行染色体评估。囊胚等级分为“好”(内细胞质量(ICM)和TE,分别为AA)、“好/好”(AB, BA)、“好”(BB)和“差”(囊胚早期2级或TE等级为C)。采用卡方检验测量囊胚对称性对囊胚等级和倍性状态的意义。对称胚和非对称胚的囊胚质量无显著差异(表1:p[公式:见文]0.10)。此外,对称胚和非对称胚的整倍体率(42.5% vs. 45.3%)和嵌合率(22.1% vs. 16.2%)无显著差异(p[公式:见文]0.24)。综上所述,4细胞期卵裂球不对称的存在不影响胚胎发育成囊胚的高质量囊胚形成率和整倍体率。然而,本研究排除了未发育到囊胚期的胚胎,以及在第2天分裂模式不稳定、直接分裂和反向分裂的胚胎,这两者都有可能影响倍性的结果。不对称的4细胞胚胎具有高质量整倍体囊胚发育的潜力,可以考虑在没有对称4细胞胚胎的情况下进行第2天的胚胎移植。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Influence of Day 2 Blastomere Symmetry on Blastocyst Grade and Ploidy Status
Previous studies have suggested that aneuploidy rates are co-related with cell asymmetry at the cleavage stage. A retrospective study was carried out to determine the significance of blastomere symmetry at the 4-cell stage on blastocyst grade and ploidy status. 732 Day 5/6 blastocysts from 191 patients undergoing Pre-implantation Genetic Testing for Aneuploidy were analysed with time-lapse imaging (Embryoscope, Vitrolife) during 2017. Blastomere symmetry was measured at the first image of 4-cells on Day 2 by tabulating the mean diameter of 2 lines drawn perpendicularly on each blastomere. Symmetry was defined as the blastomere diameter difference of [Formula: see text] 25%. Trophectoderm (TE) biopsy was performed on Day 5/6 followed by chromosomal evaluation using Next Generation Sequencing (VeriSeq Protocol, Illumina). Blastocyst grade was classified as either “Good” (inner cell mass (ICM) and TE, AA respectively), “Fair/Good” (AB, BA), “Fair” (BB) and “Poor” (early blastocyst grade 2 or TE grading of C). The significance of blastomere symmetry on blastocyst grade and ploidy status was measured using chi-square tests. There was no significance difference in resulting blastocyst quality for symmetrical and asymmetrical embryos (Table 1: p [Formula: see text] 0.10). Furthermore, there was no significance difference in the euploid rate (42.5% vs. 45.3%) or mosaic rate (22.1% vs. 16.2%) between symmetrical and asymmetrical embryos (p [Formula: see text] 0.24). In conclusion, the presence of asymmetrical blastomeres at the 4-cell stage do not impact the good quality blastocyst formation rate and euploidy rate for embryos that progress into blastocysts. However, this study excludes embryos that do not develop to the blastocyst stage and those with erratic division patterns, direct cleavage and reverse cleavage on Day 2, both of which have potential to influence ploidy result. Asymmetrical 4-cell embryos have the potential for high quality euploid blastocyst progression and can be considered for day 2 embryo transfer in the absence of symmetrical 4-cell embryos.
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