TY - JOUR
T1 - Assisted oocyte activation effects on the morphokinetic pattern of derived embryos
AU - Martínez, Meritxell
AU - Durban, Mercè
AU - Santalo Pedro, Josep
AU - Rodríguez, Ana
AU - Vassena, Rita
N1 - Publisher Copyright:
© 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC part of Springer Nature.
PY - 2021/2
Y1 - 2021/2
N2 - Objective: Assisted oocyte activation (AOA) can restore fertilization rates after IVF/ICSI cycles with fertilization failure. AOA is an experimental technique, and its downstream effects remain poorly characterized. Clarifying the relationship between AOA and embryo, morphokinetics could offer complementary insights into the quality and viability of the embryos obtained with this technique. The aim of this study is to compare the preimplantation morphokinetic development of embryos derived from ICSI-AOA (experimental group) vs. ICSI cycles (control group). Methods: A retrospective cohort study was carried out with 141 embryos from fresh oocyte donation cycles performed between 2013 and 2017; 41 embryos were derived from 7 ICSI-AOA cycles and 100 embryos from 18 ICSI cycles. Morphokinetic development of all embryos was followed using a time-lapse system. Results: We show that embryos from both groups develop similarly for most milestones, with the exception of the time of second polar body extrusion (tPB2) and the time to second cell division (t3). Conclusions: We conclude that ionomycin mediated AOA does not seem to affect the morphokinetic pattern of preimplantation embryo development, despite the alterations found in tPB2 and t3, which could directly reflect the use of a Ca
2+ ionophore as a transient and quick non-physiologic increase of free intracytoplasmic Ca
2+.
AB - Objective: Assisted oocyte activation (AOA) can restore fertilization rates after IVF/ICSI cycles with fertilization failure. AOA is an experimental technique, and its downstream effects remain poorly characterized. Clarifying the relationship between AOA and embryo, morphokinetics could offer complementary insights into the quality and viability of the embryos obtained with this technique. The aim of this study is to compare the preimplantation morphokinetic development of embryos derived from ICSI-AOA (experimental group) vs. ICSI cycles (control group). Methods: A retrospective cohort study was carried out with 141 embryos from fresh oocyte donation cycles performed between 2013 and 2017; 41 embryos were derived from 7 ICSI-AOA cycles and 100 embryos from 18 ICSI cycles. Morphokinetic development of all embryos was followed using a time-lapse system. Results: We show that embryos from both groups develop similarly for most milestones, with the exception of the time of second polar body extrusion (tPB2) and the time to second cell division (t3). Conclusions: We conclude that ionomycin mediated AOA does not seem to affect the morphokinetic pattern of preimplantation embryo development, despite the alterations found in tPB2 and t3, which could directly reflect the use of a Ca
2+ ionophore as a transient and quick non-physiologic increase of free intracytoplasmic Ca
2+.
KW - AOA
KW - ICSI
KW - Ionomycin
KW - Oocyte donation
KW - Time-lapse
KW - Humans
KW - Time-Lapse Imaging
KW - Polar Bodies/metabolism
KW - Reproductive Techniques, Assisted
KW - Pregnancy
KW - Sperm Injections, Intracytoplasmic
KW - Fertilization in Vitro
KW - Oocytes/growth & development
KW - Embryo Transfer
KW - Embryonic Development/genetics
KW - Adult
KW - Female
KW - Oocyte Donation
KW - Pregnancy Rate
KW - FERTILIZATION FAILURE
KW - CHILDREN BORN
KW - INTRACYTOPLASMIC SPERM INJECTION
KW - CALCIUM IONOPHORE
KW - OSCILLATIONS
KW - MORPHOLOGY
KW - PROGRAM
UR - http://www.scopus.com/inward/record.url?scp=85098766164&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/82bbaeb9-2db3-3f7d-bdd0-a71c0dbfc071/
U2 - 10.1007/s10815-020-02025-9
DO - 10.1007/s10815-020-02025-9
M3 - Article
C2 - 33405007
SN - 1058-0468
VL - 38
SP - 531
EP - 537
JO - Journal of Assisted Reproduction and Genetics
JF - Journal of Assisted Reproduction and Genetics
IS - 2
ER -