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基于新一代测序的三种不同结构重排的比较:对胚胎植入前遗传学检测至生殖结局的染色体异常评估。

Evaluation of chromosomal abnormalities from preimplantation genetic testing to the reproductive outcomes: a comparison between three different structural rearrangements based on next-generation sequencing.

机构信息

IVF Center, Department of Obstetrics and Gynecology, Sun Yat-sen Memorial Hospital, Sun Yat-sen University, 107 Yan Jiang West Road, Guangzhou, 510120, Guangdong, China.

出版信息

J Assist Reprod Genet. 2021 Mar;38(3):709-718. doi: 10.1007/s10815-020-02053-5. Epub 2021 Jan 6.

Abstract

PURPOSE

The aim of this study was to determine factors affecting the chromosome imbalance in blastocysts and reproductive outcomes by a comparison between the reciprocal translocation (REC), inversion (INV), and Robertsonian translocation (ROB) carriers.

METHODS

Couples with one partner carrying translocation or inversion underwent preimplantation genetic testing for chromosomal structural rearrangement (PGT-SR) cycles, including 215 PGT-SR cycles performed in subsequent 164 frozen-thawed embryo transfer cycles and 61 prenatal diagnoses of fetuses and 59 normal live birth babies. A total of 899 samples were processed by whole-genome amplification followed by next-generation sequencing (NGS). Karyotype and chromosome microarray analyses were used to confirm the PGT results from the amniotic fluid samples.

RESULTS

A total of 843 blastocysts from 124 REC, 21 INV, and 35 ROB carriers were diagnosed by PGT-SR. The percentage of unbalanced blastocysts was significantly higher in REC than in INV and ROB carriers (64.31% vs. 28.05% vs. 37.02%). Stratification analysis of female carrier age and gonadotropin doses showed no significant increase in unbalanced chromosomal abnormalities in the three groups. Also, the different breakpoints in chromosomal arms did not affect the rate of unbalanced chromosomes in the embryos. Logistic regression indicated blastocyst quality as a statistically significant risk factor associated with unbalanced chromosomal abnormalities from translocation carriers (P < 0.001). The source of abnormalities in the three groups showed significant differences such that the abnormalities in REC mostly originated from parental translocation but the abnormalities in INV were mainly de novo variations. 164 blastocysts were transferred, and there were no significant differences in the clinical pregnancy rate and miscarriage rate. A total of 59 healthy babies were born, and there were no significant differences in the gender ratio and birth height, except the birth weight of boys between INV and ROB groups (P = 0.02). The results of amniocentesis revealed that more fetuses have normal chromosomal karyotypes than balanced carriers, particularly in the REC group.

CONCLUSIONS

Reciprocal translocation carriers have more risk of unbalanced rearrangement, but embryonic chromosome abnormalities of inversion carriers come mainly from de novo variations. This is the first study specifically comparing three different PGT-SRs using the NGS method and evaluating their reproductive outcomes. Our findings will provide the reciprocal translocation, inversion, and Robertsonian translocation carrier couples with more accurate genetic counseling on the reproductive risk of chromosomal imbalance.

摘要

目的

本研究旨在通过比较相互易位(REC)、倒位(INV)和罗氏易位(ROB)携带者,确定影响囊胚染色体不平衡和生殖结局的因素。

方法

携带易位或倒位的夫妇接受胚胎植入前染色体结构重排(PGT-SR)检测,包括 215 个 PGT-SR 周期,这些周期随后在 164 个冷冻-解冻胚胎移植周期和 61 个胎儿产前诊断和 59 个正常活产婴儿中进行。总共处理了 899 个样本,通过全基因组扩增和下一代测序(NGS)进行。核型和染色体微阵列分析用于确认羊水样本的 PGT 结果。

结果

124 名 REC、21 名 INV 和 35 名 ROB 携带者的 843 个囊胚通过 PGT-SR 进行了诊断。REC 携带者的非平衡囊胚百分比明显高于 INV 和 ROB 携带者(64.31%比 28.05%比 37.02%)。对女性携带者年龄和促性腺激素剂量的分层分析显示,三组中染色体异常的非平衡率均无显著增加。此外,染色体臂不同的断点并不影响胚胎中不平衡染色体的比例。逻辑回归表明,囊胚质量是与易位携带者染色体不平衡异常相关的统计学上显著的危险因素(P<0.001)。三组的异常来源存在显著差异,即 REC 组的异常主要来自父母易位,但 INV 组的异常主要是新生变异。164 个囊胚进行了转移,临床妊娠率和流产率无显著差异。共出生 59 名健康婴儿,除 INV 和 ROB 组之间的男孩出生体重(P=0.02)外,性别比例和出生身高无显著差异。羊膜穿刺术的结果显示,正常染色体核型的胎儿多于平衡携带者,尤其是在 REC 组。

结论

相互易位携带者发生非平衡重排的风险更高,但 INV 携带者的胚胎染色体异常主要来自新生变异。这是首次使用 NGS 方法比较三种不同 PGT-SR 并评估其生殖结局的研究。我们的研究结果将为 REC、INV 和 ROB 携带者夫妇提供更准确的染色体不平衡生殖风险的遗传咨询。

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