Open AccessSelection of high‐quality and viable blastocysts based on timing of morula compaction and blastocyst formation
Author(s) -
Harada Yoshihisa,
Maeda Tomoyo,
Fukunaga Emi,
Shiba Reiko,
Okano Shinichiro,
Kinutani Masayuki,
Horiuchi Toshitaka
Publication year - 2020
Publication title -
reproductive medicine and biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.005
H-Index - 22
eISSN - 1447-0578
pISSN - 1445-5781
DOI - 10.1002/rmb2.12302
Subject(s) - blastocyst , pronucleus , intracytoplasmic sperm injection , andrology , blastomere , blastocyst transfer , embryo , pregnancy , medicine , embryo transfer , zygote , gynecology , in vitro fertilisation , biology , embryogenesis , genetics
Purpose The time‐lapse system is a device that allows continuous monitoring without removing embryos from the incubator. Using a time‐lapse system, we retrospectively investigated cleavage speed time points as potential indicators for selecting high‐quality viable blastocysts. Methods This study included 963 zygotes of two pronuclei retrieved from 196 patients between January 2015 and December 2016. All embryos in culture were monitored by time‐lapse after intracytoplasmic sperm injection. Of 492 blastocysts developed in vitro, 128 vitrified‐warmed single blastocyst transfers were classified into pregnancy and non‐pregnancy groups, and the parameters were compared. Results In the pregnancy group, timing of both morula compaction and regular blastocyst formation was significantly faster than in the non‐pregnancy group. Furthermore, the optimal cutoff values for compacted morula (94.9 hours) and regular blastocyst (113.9 hours) were determined using the receiver operator characteristic curve analysis. Embryos that formed compacted morulae within 94.9 hours and developed into regular blastocysts within 113.9 hours were associated with a significantly higher pregnancy rate than those that did not (44.4% vs 16.0%). Conclusion The timing of morula compaction and regular blastocyst formation is important as an indicator of high‐quality blastocysts to increase odds for pregnancy after embryo transfer.