Diana Stein, embryologist for over 30 years and Lab Director of Laniado Hospital-Sanz Medical Center (Israel) and a MIRI® Time-Lapse user, had an initial impression after a quick look of the embryo status morning of Day 2 to transfer the embryo on the right, based on its more advanced and slightly better morphology.
However, after review of its time-lapse video she decided to replace it with the one on the left due to Direct Cleavage of the embryo from 2 to 5 cells. Embryo on right continued to develop and was vitrified on Day 4.
Patient delivered a healthy baby girl from D2 replacement of embryo on left. Diana considered this as one of her many “ah-hah” moments.
Limitations of Conventional Embryo Scoring
Conventional embryo classification only scores embryo morphology at a few predefined time points during its pre-implantation development, with the consequent lack of information about what happened between the analyzed time points. There might be unusual cleavage patterns missed out with the conventional scoring that could help in assessing the embryo’s ability to implant. Thus, continual monitoring through time-lapse provides one strategy to collect a complete picture of embryo developmental kinetics.
What are you missing with standard observation at fixed times?
With a time-lapse incubator, you are able to review and annotate accordingly all important events as the embryo develops. Although “abnormal” cleavage events may occur not only at any time but multiple times in the embryos development most occur between standard observation checks. Examples typically seen between D1 and D2 in the embryos development are:
These “abnormal” events may cause chromosomal abnormalities in the affected embryo which are correlated with decreased implantation, decreased pregnancy rates and spontaneous abortion.
Direct Cleavage (DCL)
A retrospective analysis by Rubio, et. al (2012) demonstrates that direct cleavage from two to three cells, or also known as DC2-3, have a statistically significantly lower implantation rate than embryos with a normal cleavage pattern. Around 14% of the total embryonic cohort (715 cases out of 5,225 studied) underwent direct cleavage, making this as a relevant and important morphokinetic parameter for clinical use.1
Reverse Cleavage (RCL)
Cleavage-stage embryos that were observed to reduce in cell number are said to undergo a process referred to as reverse cleavage or blastomere fusion. In the majority of cases, two blastomeres of an embryo fuse resulting in a hybrid cell containing two nuclei.
In a study by Liu et. al (2014), about 27.4% of embryos underwent Reverse Cleavage during the first three cleavage cycles.2
Numerous studies have shown that multinucleation impairs embryo viability. Hence, in many embryo grading systems, multinucleation detection is an important parameter. However, in conventional scoring multinucleation may occur at different times during the developmental period and can disappear in a very short period of time.3 With time-lapse microscopy it is possible to evaluate multinucleation at optimal timepoints such as midpoints between cell division events.
1Rubio, I., Kuhlmann, R., Agerholm, I., Kirk, J., Herrero, J., Escriba, M.-J., . . . Meseguer, M. (2012). Limited implantation success of direct-cleaved human zygotes: a time-lapse study.
2Liu, Y., Chapple, V., Roberts, P., & Matson, P. (2014). Prevalence, consequence, and significance of reverse cleavage by human embryos viewed with the use of the Embryoscope time-lapse video system.
3Ergin, E. G., Caliskan, E., Yalcinkaya, E., Oztel, Z., Cokelez, K., Ozay, A., & Ozornek, H. (2014). Frequency of embryo multinucleation detected by time-lapse system and its impact on pregancy outcome. Eurofertil IVF Center, Istanbul, Turkey: Fertility and Sterility® Vol. 102, No. 4.