易位携带者性别对胚胎植入前基因检测夫妇临床结果的影响。

IF 1.6 4区 医学 Q4 GENETICS & HEREDITY
Zhiping Zhang, Jiayao Chen, Lei Zhang, Ruiyang Wei, Zhen Liu, Dunmei Zhao, Xingyu Bi, Lixia Liang, Xueluo Zhang, Dan Su, Xueqing Wu
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引用次数: 0

摘要

简介:本研究探讨了携带者对染色体结构异常夫妇可转移囊胚率和活产结局的影响。方法:将夫妇分为反向易位组、罗伯逊易位组和倒位组,回顾性分析临床资料。植入前进行染色体结构重排(PGT-SR)基因检测,并比较妊娠结局。结果:男性和女性携带者的胚胎整倍体率在反向易位组和倒位组之间差异不显著,但在三组之间差异显著。在罗伯逊易位组中,男性携带者的胚胎整倍体率高于女性携带者。反向易位和罗伯逊易位的男性携带者精子密度显著低于同一组的女性携带者,而反转组的差异不显著。不论染色体结构异常携带者的性别如何,pgt后胚胎移植的临床结果是相似的。具有罗伯逊易位的女性携带者比男性携带者产生染色体异常胚胎的风险更高。无论染色体结构重排类型和携带者性别如何,PGT-SR周期后的妊娠、活产和累计活产率相似。结论:本研究结果为遗传咨询提供了有价值的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Influence of the Sex of Translocation Carrier on Clinical Outcomes of Couples Undergoing Preimplantation Genetic Testing.

Influence of the Sex of Translocation Carrier on Clinical Outcomes of Couples Undergoing Preimplantation Genetic Testing.

Introduction: This study investigated the impact of the carrier on transferable blastocyst rate and live birth outcomes in couples with structural chromosomal abnormalities.

Methods: Couples were grouped into reciprocal translocation, Robertsonian translocation, or inversions groups, and clinical data were retrospectively analyzed. Preimplantation genetic testing for chromosomal structural rearrangements (PGT-SR) was conducted, and pregnancy outcomes were compared.

Results: Embryo euploidy rates between male and female carriers differed nonsignificantly in the reciprocal translocation and inversion groups but significantly among the three groups. In the Robertsonian translocation group, male carriers had a higher embryo euploidy rate than that of female carriers. Sperm density of male carriers with reciprocal and Robertsonian translocation was significantly lower than that of the female carrier in the same group, whereas the difference was non-significant in the inversion group. The clinical outcomes of embryo transfer post-PGT were similar regardless of the sex of carriers with structural chromosomal abnormalities. Female carriers with Robertsonian translocations displayed a higher risk of producing embryos with chromosomal abnormalities than male carriers. Pregnancy, live birth, and cumulative live birth rates following a PGT-SR cycle were similar, irrespective of chromosomal structural rearrangement type, and carrier sex.

Conclusion: Our findings offer valuable information for genetic counseling.

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来源期刊
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
4.20
自引率
0.00%
发文量
241
审稿时长
14 weeks
期刊介绍: Molecular Genetics & Genomic Medicine is a peer-reviewed journal for rapid dissemination of quality research related to the dynamically developing areas of human, molecular and medical genetics. The journal publishes original research articles covering findings in phenotypic, molecular, biological, and genomic aspects of genomic variation, inherited disorders and birth defects. The broad publishing spectrum of Molecular Genetics & Genomic Medicine includes rare and common disorders from diagnosis to treatment. Examples of appropriate articles include reports of novel disease genes, functional studies of genetic variants, in-depth genotype-phenotype studies, genomic analysis of inherited disorders, molecular diagnostic methods, medical bioinformatics, ethical, legal, and social implications (ELSI), and approaches to clinical diagnosis. Molecular Genetics & Genomic Medicine provides a scientific home for next generation sequencing studies of rare and common disorders, which will make research in this fascinating area easily and rapidly accessible to the scientific community. This will serve as the basis for translating next generation sequencing studies into individualized diagnostics and therapeutics, for day-to-day medical care. Molecular Genetics & Genomic Medicine publishes original research articles, reviews, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented.
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