Liu Yanli, Shen Junhan, Yang Rujing, Zhang Yuchao, Jia Liting, Guan Yichun
Department of Reproductive Medicine, The Third Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Neonatal Screening Center, The Third Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Int J Endocrinol. 2022 Mar 19;2022:9707081. doi: 10.1155/2022/9707081. eCollection 2022.
In total, 456 PGT cycles, including 283 PGT-SR cycles and 173 PGT-A cycles, were assessed through comprehensive chromosome screening (CCS) from January 2017 to June 2020 at the Department of Reproductive Medicine of the Third Affiliated Hospital of Zhengzhou University. Trophectoderm (TE) biopsies were sequenced using next-generation sequencing (NGS). The incidence of de novo chromosome abnormalities was calculated, and the relationships between de novo chromosome abnormality rates and maternal age, number of oocytes retrieved, and parameters of cleavage-stage embryos and blastocyst-stage embryos were investigated.
The incidence of de novo chromosome abnormalities was 28.0% (318/1,135) in the PGT-SR cycles and 36.3% (214/590) in the PGT-A cycles, which increased with maternal age in both PGT-SR cycles ( = 0.018) and PGT-A cycles ( < 0.001). The incidence of de novo chromosome abnormalities was related to TE grade ( < 0.001), internal cell mass grade ( = 0.002), and development speed (day 5 vs. day 7: < 0.001) of blastocyst-stage embryos. The incidence of de novo chromosomal abnormalities was irrelevant to the number of oocytes retrieved and the parameters of the embryo at the cleavage stage.
Blastocysts with higher morphology scores and faster progression had a lower incidence of de novo chromosome abnormalities, especially complex chromosome abnormalities. De novo chromosome abnormalities may negatively affect the morphological grading of blastocysts. Our findings will provide valuable information to the fertility doctor for embryo selection in non-PGT cycles.
2017年1月至2020年6月,郑州大学第三附属医院生殖医学科对总共456个植入前基因诊断(PGT)周期进行了评估,其中包括283个PGT-SR周期和173个PGT-A周期。采用下一代测序(NGS)技术对滋养外胚层(TE)活检样本进行测序。计算新发染色体异常的发生率,并研究新发染色体异常率与母亲年龄、获卵数以及卵裂期胚胎和囊胚期胚胎参数之间的关系。
PGT-SR周期中,新发染色体异常的发生率为28.0%(318/1135);PGT-A周期中,该发生率为36.3%(214/590)。在PGT-SR周期(P = 0.018)和PGT-A周期(P < 0.001)中,新发染色体异常的发生率均随母亲年龄的增加而升高。新发染色体异常的发生率与囊胚期胚胎的TE等级(P < 0.001)、内细胞团等级(P = 0.002)以及发育速度(第5天与第7天:P < 0.001)有关。新发染色体异常的发生率与获卵数和卵裂期胚胎参数无关。
形态学评分较高且发育进程较快的囊胚,新发染色体异常的发生率较低,尤其是复杂染色体异常。新发染色体异常可能对囊胚的形态学分级产生负面影响。我们的研究结果将为生殖医生在非PGT周期中进行胚胎选择提供有价值的信息。