Quality of Blastocysts Created by Embryo Splitting: A Time-Lapse Monitoring and Chromosomal Aneuploidy Study

(Pages: 367-374)
Marjan Omidi, Ph.D, 1Mohammad Ali Khalili, Ph.D, 1,2,*Iman Halvaei, Ph.D, 3Fatemeh Montazeri, Ph.D, 4Seyed Mehdi Kalantar, Ph.D, 4
Research and Clinical Center for Infertility, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
Department of Reproductive Biology, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
Department of Anatomical Sciences, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran
Abortion Research Center, Yazd Institute of Reproductive Sciences, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
Research and Clinical Center for Infertility, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
Department of Reproductive Biology, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
Department of Anatomical Sciences, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran
Abortion Research Center, Yazd Institute of Reproductive Sciences, Shahid Sadoughi University of Medical Sciences, Yazd, Iran
*Corresponding Address: P.O.Box; 89195-999 Research and Clinical Center for Infertility Yazd Reproductive Sciences Institute Shahid Sadoughi University of Medical Sciences Yazd Iran Email:khalili59@hotmail.com
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Omidi M, Khalili MA, Halvaei I, Montazeri F, Kalantar SM. Quality of blastocysts created by embryo splitting: a time-lapse monitoring and chromosomal aneuploidy study. Cell J. 2020; 22(3): 367-374. doi: 10.22074/cellj.2020.6717.

Abstract

Objective

The aim of this study was to screen the potential of human embryos to develop into expanding blastocysts following in vitro embryo splitting and then assess the quality of the generated blastocysts based on chromosomal characteristics and using morphokinetics.

Materials and Methods

In this experimental study, a total of 82 good quality cleavage-stage donated embryos (8- 14 cells) were used (24 embryos were cultured to the blastocyst stage as controls and 58 embryos underwent in vitro splitting). After in vitro splitting, the blastomere donor and blastomere recipient embryos were named twin A and twin B, respectively. Morphokinetics and morphological parameters were evaluated using a time-lapse system in the blastocysts developed from twin embryos. Aneuploidy of chromosomes 13, 15, 16, 18, 21, 22, X and Y were analyzed in the twin blastocysts.

Results

Following in vitro splitting, of the 116 resulting twin embryos, 80 (69%) developed to the expanded blastocyst (EBL) stage compared to 21 (87.5%) embryos in the control group (P>0.05). The morphokinetics analysis suggested that the developmental time-points were influenced by the in vitro splitting. Moreover, the blastocysts developed from A and B twins had impaired morphology compared to controls. Regarding chromosome abnormalities, there was no significant difference in the rate of aneuploidy or mosaicism between the different groups.

Conclusion

This study showed that while no chromosomal abnormalities were seen, in vitro embryo splitting may affect the embryo morphokinetics.