» Articles » PMID: 31423415

The Frequency of Chromosomal Euploidy Among 3PN Embryos

Overview
Date 2019 Aug 20
PMID 31423415
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Background: The evaluation of embryo morphology is one of the most important parameters used to evaluate developmental timing, also providing an indication of chromosomal failure or degeneration. The first step in the evaluation of a fertilization event is determining the number and shape of the pronuclei (PN). Normally fertilized eggs possess two even PN. However, some embryos which develop from abnormally fertilized zygotes may be tri-pronuclear zygotes (3PN).

Methods: Thirty embryos were collected from 12 women who underwent fertilization (IVF) at Dr. Cipto Mangunkusumo General Hospital in Jakarta, Indonesia. Embryos were cultured until the blastocyst stage on days 5-6. The blastomere biopsy was performed by piercing the zona pellucida with a laser under a microscope. Chromosomal numerical abnormalities were analyzed using Next Generation Sequencing (NGS).

Results: Among the 30 embryos with 3PN zygotes, 33.3% had a normal chromosomal array, with 22 pairs of autosomes and 2 pairs of sex chromosomes. While the rest of sample population detected as abnormal chromosome (66.7%), with the highest percentage of abnormality was triploidy 43.3%, followed by mosaicism 13.4% and aneuploidy 10%.

Conclusion: This was a preliminary study revealed not all morphologically 3PN embryos are genetically abnormal.

Citing Articles

The Identification of Molecular Ploidy Status of Abnormal Pronuclear Zygotes Reveals a Significant Number of Euploid Blastocysts Available for Conception.

McCallie B, Haywood M, Henry L, Lee R, Schoolcraft W, Katz-Jaffe M Biomedicines. 2025; 13(1).

PMID: 39857635 PMC: 11760476. DOI: 10.3390/biomedicines13010051.


The impact of low oocyte maturity ratio on blastocyst euploidy rate: a matched retrospective cohort study.

Ou Z, Du J, Liu N, Fang X, Wen X, Li J Contracept Reprod Med. 2024; 9(1):41.

PMID: 39187878 PMC: 11346022. DOI: 10.1186/s40834-024-00303-w.


Machine learning in time-lapse imaging to differentiate embryos from young vs old mice†.

Yang L, Leynes C, Pawelka A, Lorenzo I, Chou A, Lee B Biol Reprod. 2024; 110(6):1115-1124.

PMID: 38685607 PMC: 11180621. DOI: 10.1093/biolre/ioae056.


Evaluating the developmental potential of 2.1PN-derived embryos and associated chromosomal analysis.

Wang J, Xiong S, Hao X, Gao Y, Xia F, Liao H J Assist Reprod Genet. 2024; 41(6):1597-1603.

PMID: 38613651 PMC: 11224204. DOI: 10.1007/s10815-024-03113-w.


The utility of human two plus one small pronucleated zygotes (2.1PN) based on clinical outcomes and the focused ploidy analysis.

Hattori H, Okuyama N, Ashikawa K, Sakuraba Y, Igarashi H, Kyono K J Assist Reprod Genet. 2024; 41(6):1589-1596.

PMID: 38613650 PMC: 11224203. DOI: 10.1007/s10815-024-03114-9.


References
1.
Munne S, Cohen J . Chromosome abnormalities in human embryos. Hum Reprod Update. 1999; 4(6):842-55. DOI: 10.1093/humupd/4.6.842. View

2.
SACHS A, Politch J, Jackson K, Racowsky C, Hornstein M, Ginsburg E . Factors associated with the formation of triploid zygotes after intracytoplasmic sperm injection. Fertil Steril. 2000; 73(6):1109-14. DOI: 10.1016/s0015-0282(00)00521-5. View

3.
Magli M, Jones G, Gras L, Gianaroli L, Korman I, Trounson A . Chromosome mosaicism in day 3 aneuploid embryos that develop to morphologically normal blastocysts in vitro. Hum Reprod. 2000; 15(8):1781-6. DOI: 10.1093/humrep/15.8.1781. View

4.
Feng H, Hershlag A . Fertilization abnormalities following human in vitro fertilization and intracytoplasmic sperm injection. Microsc Res Tech. 2003; 61(4):358-61. DOI: 10.1002/jemt.10349. View

5.
Porter R, Han T, Tucker M, Graham J, Liebermann J, Scott Sills E . Estimation of second polar body retention rate after conventional insemination and intracytoplasmic sperm injection: in vitro observations from more than 5000 human oocytes. J Assist Reprod Genet. 2003; 20(9):371-6. PMC: 3455839. DOI: 10.1023/a:1025481011680. View