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Sperm Chromatin Condensation Defect Accelerates the Kinetics of Early Embryonic Development but Does Not Modify ICSI Outcome

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2023 Jan 8
PMID 36613835
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Abstract

The origin and quality of gametes are likely to influence the kinetics of embryonic development. The purpose of the study was to assess the impact of sperm nuclear quality, and in particular sperm chromatin condensation, on the kinetics of early embryo development after intracytoplasmic sperm injection (ICSI). Our study included 157 couples who benefitted from ICSI for male factor infertility. Chromatin condensation and DNA fragmentation were assessed in spermatozoa prior to ICSI. Above the 20% threshold of sperm condensation defect, patients were included in the abnormal sperm chromatin condensation (ASCC) group; below the 20% threshold, patients were included in the normal sperm chromatin condensation (NSCC) group. After ICSI, the oocytes were placed in the time-lapse incubator. The kinetics of the cohort's embryonic development have been modeled. The fading times of pronuclei and the time to two blastomeres (t2, first cleavage) and four blastomeres (t4, third cleavage) differed significantly between the NSCC and ASCC groups, with earlier events occurring in the ASCC group. On the other hand, the state of sperm chromatin condensation did not seem to have an impact on live birth rates or the occurrence of miscarriages. The kinetics of early embryonic development was accelerated in males with a sperm chromatin condensation defect without compromising the chances of pregnancy or promoting miscarriage. However, our study highlights the paternal contribution to early embryonic events and potentially to the future health of the conceptus.

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References
1.
Esbert M, Pacheco A, Soares S, Amoros D, Florensa M, Ballesteros A . High sperm DNA fragmentation delays human embryo kinetics when oocytes from young and healthy donors are microinjected. Andrology. 2018; 6(5):697-706. DOI: 10.1111/andr.12551. View

2.
Aguilar J, Motato Y, Escriba M, Ojeda M, Munoz E, Meseguer M . The human first cell cycle: impact on implantation. Reprod Biomed Online. 2014; 28(4):475-84. DOI: 10.1016/j.rbmo.2013.11.014. View

3.
Del Gallego R, Remohi J, Meseguer M . Time-lapse imaging: the state of the art†. Biol Reprod. 2019; 101(6):1146-1154. DOI: 10.1093/biolre/ioz035. View

4.
Chamayou S, Patrizio P, Storaci G, Tomaselli V, Alecci C, Ragolia C . The use of morphokinetic parameters to select all embryos with full capacity to implant. J Assist Reprod Genet. 2013; 30(5):703-10. PMC: 3663978. DOI: 10.1007/s10815-013-9992-2. View

5.
Lin M, Lee R, Li S, Lu C, Sun F, Hwu Y . Sperm chromatin structure assay parameters are not related to fertilization rates, embryo quality, and pregnancy rates in in vitro fertilization and intracytoplasmic sperm injection, but might be related to spontaneous abortion rates. Fertil Steril. 2007; 90(2):352-9. DOI: 10.1016/j.fertnstert.2007.06.018. View