Prediction of in-vitro developmental competence of early cleavage-stage mouse embryos with compact time-lapse equipment
Abstract
Single blastocyst transfer is regarded as an efficient way to achieve high pregnancy rates and to avoid multiple pregnancies. Risk of cancellation of transfer due to a lack of available embryos may be reduced by early prediction of blastocyst development. Time-lapse investigation of mouse embryos shows that the time of the first and second cleavage (to the 2- and 3-cell stages, respectively) has a strong predictive value for further development in vitro, while cleavage from the 3-cell to the 4-cell stage has no predictive value. In humans, embryo fragmentation during preimplantation development has been associated with lower pregnancy rates and a higher incidence of developmental abnormalities. Analysis of time-lapse records shows that most fragmentation is reversible in the mouse and is resorbed in an average of 9
h. Daily or bi-daily microscopic checks of embryo development, applied routinely in human IVF laboratories, would fail to detect 36 or 72% of these fragmentations, respectively. Fragmentation occurring in a defined time frame has a strong predictive value for in-vitro embryo development. The practical compact system used in the present trial, based on the ‘one camera per patient’ principle, has eliminated the usual disadvantages of time-lapse investigations and is applicable for the routine follow-up of in-vitro embryo development.
Keywords: blastocyst, early cleavage, fragmentation, in-vitro culture, microwell culture dish, time-lapse monitoring
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Csaba Pribenszky obtained a DVM degree (1998) and a PhD degree (2005) in the field of assisted reproductive technologies in Budapest, Hungary. Together with Mikos Molnar, he developed and patented the concept of ‘stress for stress tolerance’, utilizing sub-lethal hydrostatic pressure stress treatment to gametes, embryos, other cells and tissues in order to improve cell survival during subsequent procedures (e.g. cryopreservation, SCNT). His current focus is the application of the above method to human oocyte vitrification and the effect of different environmental factors on in-vitro embryo developmental dynamics and embryo fragmentation.
PII: S1472-6483(09)00284-3
doi:10.1016/j.rbmo.2009.12.007
© 2009 Reproductive Healthcare Ltd. Published by Elsevier Inc All rights reserved.
