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卵裂期胚胎性别选择后废弃囊胚进行常染色体非整倍体的再分析。

Reanalysis of discarded blastocysts for autosomal aneuploidy after sex selection in cleavage-stage embryos.

作者信息

Ebrahimian Neda, Montazeri Fatemeh, Sadeghi Mohammad Reza, Kalantar Seyed Mehdi, Gilany Kambiz, Khalili Mohannad Ali

机构信息

Research and Clinical Center for Infertility, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.

Abortion Research Center, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.

出版信息

Clin Exp Reprod Med. 2020 Dec;47(4):293-299. doi: 10.5653/cerm.2019.03426. Epub 2020 Nov 19.

DOI:10.5653/cerm.2019.03426
PMID:33227189
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7711103/
Abstract

OBJECTIVE

The goal of the present study was to investigate the rate of chromosomal aneuploidies in surplus embryos after sex determination at the cleavage stage. Then, the same chromosomal aneuploidies were evaluated in blastocysts after extended culture.

METHODS

Sixty-eight surplus embryos were biopsied at the cleavage stage and incubated for an additional 3 days to allow them to reach the blastocyst stage. The embryos were reanalyzed via fluorescence in situ hybridization (FISH) to examine eight chromosomes (13, 15, 16, 18, 21, 22, X, and Y) in both cleavage-stage embryos and blastocysts.

RESULTS

Although the total abnormality rate was lower in blastocysts (32.35%) than in cleavage-stage embryos (45.58%), the difference was not significant (p=0.113). However, when we restricted the analysis to autosomal abnormalities, we observed a significant difference in the abnormality rate between the cleavage-stage embryos (44.11%) and the blastocysts (17.64%, p=0.008). A higher rate of sex chromosomal abnormalities was also observed in cleavage-stage embryos (29.4%) than in blastocysts (14.70%, p=0.038).

CONCLUSION

The data indicated that embryo biopsy should be conducted at the blastocyst stage rather than the cleavage stage. The results also emphasized that examination of common chromosomal aneuploidies apart from sex selection cycles can be conducted in the blastocyst stage with the FISH method.

摘要

目的

本研究的目的是调查卵裂期性别鉴定后多余胚胎的染色体非整倍体率。然后,在延长培养后的囊胚中评估相同的染色体非整倍体情况。

方法

68个多余胚胎在卵裂期进行活检,并再培养3天使其发育至囊胚期。通过荧光原位杂交(FISH)对卵裂期胚胎和囊胚中的8条染色体(13、15、16、18、21、22、X和Y)进行重新分析。

结果

尽管囊胚的总异常率(32.35%)低于卵裂期胚胎(45.58%),但差异不显著(p=0.113)。然而,当我们将分析限制在常染色体异常时,我们观察到卵裂期胚胎(44.11%)和囊胚(17.64%,p=0.008)的异常率存在显著差异。卵裂期胚胎的性染色体异常率(29.4%)也高于囊胚(14.70%,p=0.038)。

结论

数据表明胚胎活检应在囊胚期而非卵裂期进行。结果还强调,除性别选择周期外,可在囊胚期采用FISH方法检测常见染色体非整倍体情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b44/7711103/08e0d10cb6a3/cerm-2019-03426f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b44/7711103/6904d6b53367/cerm-2019-03426f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b44/7711103/08e0d10cb6a3/cerm-2019-03426f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b44/7711103/6904d6b53367/cerm-2019-03426f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b44/7711103/08e0d10cb6a3/cerm-2019-03426f2.jpg

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Genome Res. 2019 Mar;29(3):367-382. doi: 10.1101/gr.239830.118. Epub 2019 Jan 25.
2
Pregnancy rates after pre-implantation genetic screening for aneuploidy are only superior when trophectoderm biopsy is performed on hatching embryos.进行胚胎植入前遗传学筛查以排除非整倍体后,只有在孵化胚胎上进行滋养外胚层活检时,妊娠率才会更高。
J Assist Reprod Genet. 2019 Apr;36(4):621-628. doi: 10.1007/s10815-019-01400-5. Epub 2019 Jan 15.
3
Developmental and cytogenetic assessments of preimplantation embryos derived from in-vivo or in-vitro matured human oocytes.
对源自体内或体外成熟的人类卵母细胞的植入前胚胎进行发育和细胞遗传学评估。
Eur J Med Genet. 2018 Apr;61(4):235-241. doi: 10.1016/j.ejmg.2017.12.006. Epub 2017 Dec 8.
4
ESHRE PGD Consortium data collection XIV-XV: cycles from January 2011 to December 2012 with pregnancy follow-up to October 2013.ESHRE PGD 联盟数据收集 XIV-XV:2011 年 1 月至 2012 年 12 月的周期,随访至 2013 年 10 月。
Hum Reprod. 2017 Oct 1;32(10):1974-1994. doi: 10.1093/humrep/dex265.
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The quality of sperm preparation medium affects the motility, viability, and DNA integrity of human spermatozoa.精子制备培养基的质量会影响人类精子的活力、生存能力和DNA完整性。
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Diagnosis and clinical management of embryonic mosaicism.胚胎嵌合体的诊断与临床处理。
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