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从染色体异常到个体基因突变——流产后绒毛组织遗传学研究在寻找流产原因中的意义。

From chromosomal aberrations to mutations in individual genes - the significance of genetic studies of chorions after miscarriage in the search for causes of miscarriages.

机构信息

Diagnostyka GENESIS sp. z o.o, Poznan, Poland.

Department of Medical Genetics, Poznan University of Medical Sciences, Poznan, Poland.

出版信息

J Matern Fetal Neonatal Med. 2024 Dec;37(1):2364249. doi: 10.1080/14767058.2024.2364249. Epub 2024 Jul 28.

Abstract

OBJECTIVE

To determine the frequency of chromosomal aberrations in chorions after a miscarriage. The second was to examine selected euploid chorions using a next-generation sequencing (NGS) panel designed to assess 43 genes associated with pregnancy loss.

MATERIALS AND METHODS

The 1244 chorions were tested by targeted quantitative fluorescent PCR (QF-PCR, 827 chorions) and microarray-based comparative genomic hybridization (aCGH, 417 chorions). Then, 9 euploid chorions were examined using a designed NGS panel.

RESULTS

Trisomies were the most common chromosomal aberration identified in the spontaneous miscarriage samples. The second chromosomal abnormality in the aCGH group and the third most common in the QF-PCR group was monosomy X. Structural aberrations were the third most common aberration in the samples screened by aCGH (7.7% of chorions). In 19% of 647 couples who submitted chorions for analysis after pregnancy loss, the chromosomal abnormality in the chorion originated from a woman with a balanced chromosomal rearrangement. This discovery was statistically significant compared to patients with normal chorions. Using the designed NGS panel, we identified a potentially pathogenic de novo variant in the gene in two euploid chorions. Additionally, among the patients who experienced miscarriages and were screened using the NGS panel, we identified variants in the , , and genes that could be associated with a predisposition to pregnancy loss.

CONCLUSION

Numerical aberrations are the most common cause of miscarriages, but structural chromosomal aberrations also account for a significant proportion of abnormal results. Our findings indicate that couples with structural chromosomal abnormalities in material post-miscarriage are at increased risk of carrying balanced chromosomal abnormalities. Moreover, NGS-based analyses can uncover previously unidentified causes of miscarriages in the chorionic villi.

摘要

目的

确定自然流产后绒毛染色体异常的频率。第二项是使用下一代测序 (NGS) 面板检查选定的整倍体绒毛,该面板旨在评估与妊娠丢失相关的 43 个基因。

材料和方法

通过靶向定量荧光 PCR (QF-PCR,827 个绒毛) 和基于微阵列的比较基因组杂交 (aCGH,417 个绒毛) 测试 1244 个绒毛。然后,使用设计的 NGS 面板检查 9 个整倍体绒毛。

结果

三体是自发流产样本中最常见的染色体异常。aCGH 组中的第二种染色体异常和 QF-PCR 组中的第三种最常见的是单体 X。结构异常是 aCGH 筛选样本中第三种最常见的异常 (绒毛的 7.7%)。在 647 对因妊娠丢失而提交绒毛进行分析的夫妇中,19%的绒毛的染色体异常来自携带平衡染色体重排的女性。与具有正常绒毛的患者相比,这一发现具有统计学意义。使用设计的 NGS 面板,我们在两个整倍体绒毛中鉴定出 基因的潜在致病性新生变异。此外,在使用 NGS 面板筛选的经历流产的患者中,我们鉴定出 基因中的变体,这些变体可能与妊娠丢失的易感性有关。

结论

数值异常是流产的最常见原因,但结构染色体异常也占异常结果的很大比例。我们的发现表明,在流产后物质中存在结构染色体异常的夫妇携带平衡染色体异常的风险增加。此外,基于 NGS 的分析可以揭示绒毛中以前未识别的流产原因。

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