Department of Gynecological Endocrinology and Fertility Disorders, University Clinics of Heidelberg, Vossstr. 9, D-69115 Heidelberg, Germany.
Reprod Biomed Online. 2013 Jun;26(6):528-30. doi: 10.1016/j.rbmo.2013.03.011. Epub 2013 Mar 26.
Morphokinetic analysis of early human embryos in combination with trophectoderm biopsy and chromosomal enumeration by array technology has been shown to identify embryos with single and/or multiple aneuploidies. In a time-lapse imaging study, aneuploid embryos showed a delayed initiation of blastocyst formation and also reached the full blastocyst stage later compared with euploid embryos. Based on these findings, a model for a risk factor classification for aneuploidy of human embryos has been established. However, time values that allow differentiation between different risk classes have to be considered carefully as timings that are prognostic for one clinic may not apply directly to another clinic. Thus, risk models may need to be verified in specific IVF settings. Further studies are needed to verify that time-lapse imaging does allow subselection of embryos with a high aneuploidy risk and thus does hold the chance to restrict invasive biopsy procedures to those embryos where there is uncertainty regarding the chromosomal status.
早期人类胚胎的形态动力学分析结合滋养外胚层活检和染色体计数的阵列技术已被证明可以识别具有单倍体和/或多倍体非整倍体的胚胎。在延时成像研究中,与整倍体胚胎相比,非整倍体胚胎的囊胚形成起始延迟,并且达到完全囊胚阶段的时间也较晚。基于这些发现,已经建立了人类胚胎非整倍体风险因素分类的模型。然而,允许区分不同风险类别的时间值必须仔细考虑,因为对一个诊所具有预后意义的时间值可能并不直接适用于另一个诊所。因此,风险模型可能需要在特定的 IVF 环境中进行验证。需要进一步的研究来验证延时成像确实可以选择具有高非整倍体风险的胚胎,从而有机会将有创活检程序限制在那些对染色体状态不确定的胚胎上。