Preimplantation Genetic Testing for Couples with Balanced Chromosomal Rearrangements.

Sachin Shetty, Jiny Nair, Jnapti Johnson, Navya Shetty, Ajay Kumar J, Nirmala Thondehalmath, Deepanjali Ganesh, Vidyalakshmi R Bhat, Sajana M, Anjana R, Rajsekhar Nayak, Devika Gunasheela, Jayarama S Kadandale, Swathi Shetty
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Abstract

Background: Chromosomal rearrangements play an important role in infertility. Carriers of chromosomal rearrangements have a lower chance of producing normal or balanced gametes due to abnormal segregation of chromosomes at meiosis, which leads to recurrent spontaneous abortions and infertility. Preimplantation genetic testing for structural chromosome rearrangements (PGT-SR) is offered to couples who have balanced chromosomal rearrangements in order to select embryos with a balanced karyotype prior to implantation, thereby increasing the chances of pregnancy. The purpose of the current study was to assess the outcomes of PGT-SR in patients carrying various balanced chromosomal rearrangements and to assess their clinical pregnancy outcome after in vitro fertilization (IVF).

Methods: In this study, infertile couples with balanced chromosomal abnormalities undergoing PGT-SR were retrospectively analyzed at a single fertility center from January 2016 to December 2019.

Results: PGT-SR was performed on 87 embryos from 22 couples in whom one partner carried a balanced translocation or an inversion. Fifty-seven (65.5%) of these embryos had unbalanced or sporadic aneuploidies, 30 (34.5%) embryos were normal or chromosomally balanced, which were then transferred in 18 couples. A higher rate of unbalanced translocations in comparison to sporadic aneuploidies was observed in couples with reciprocal translocation. The live birth rate per embryo transfer was found to be 66.6% (12/18).

Conclusion: PGT-SR is a useful tool in selecting normal or balanced embryos for transfer in IVF, which could lead to a pregnancy by reducing the chance of miscarriages due to chromosome aneuploidy in couples with balanced chromosomal rearrangements.

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平衡染色体重排夫妇的胚胎植入前基因检测。
背景:染色体重排在不孕症中起重要作用。由于减数分裂时染色体分离异常,染色体重排携带者产生正常或平衡配子的机会较低,这导致复发性自然流产和不孕症。为染色体重排平衡的夫妇提供着床前基因检测(PGT-SR),以便在着床前选择具有平衡核型的胚胎,从而增加怀孕机会。本研究的目的是评估携带各种平衡染色体重排的患者PGT-SR的结果,并评估其体外受精(IVF)后的临床妊娠结局。方法:本研究回顾性分析2016年1月至2019年12月在同一生育中心接受PGT-SR治疗的染色体平衡异常不育夫妇。结果:对22对夫妻的87个胚胎进行了PGT-SR,其中一方携带平衡易位或反转。这些胚胎中57个(65.5%)存在不平衡或零星的非整倍体,30个(34.5%)胚胎正常或染色体平衡,然后将其移植到18对夫妇中。与零星的非整倍体相比,在反向易位的夫妇中观察到更高的不平衡易位率。每次胚胎移植的活产率为66.6%(12/18)。结论:PGT-SR是选择正常或平衡胚胎进行体外受精的有用工具,可以减少染色体重排平衡的夫妇因染色体非整倍体而流产的机会,从而导致妊娠。
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来源期刊
Journal of Reproduction and Infertility
Journal of Reproduction and Infertility Medicine-Reproductive Medicine
CiteScore
2.70
自引率
0.00%
发文量
44
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