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体外受精治疗中胚胎嵌合体和非整倍体靶向染色体区域的临床见解及文献综述

Clinical Insights Regarding the Targeted Chromosomal Region for Mosaicism and Aneuploidy in Embryos in IVF Treatment and Literature Review.

作者信息

Doroftei Bogdan, Savuca Alexandra, Anton Nicoleta, Maftei Radu, Cretu Ana-Maria, Bivoleanu Anca Roxana, Doroftei Mara, Ilea Ciprian

机构信息

Origyn Fertility Center, Palace Street No. 3C, 700032 Iasi, Romania.

Department of Mother and Child Care, University of Medicine and Pharmacy "Grigore T. Popa", University Street No. 16, 700115 Iasi, Romania.

出版信息

Diagnostics (Basel). 2025 May 29;15(11):1375. doi: 10.3390/diagnostics15111375.

Abstract

: Given the common occurrence of mosaicism and aneuploidy in IVF embryos, our study aimed to retrospectively identify whether specific chromosomal regions or individual chromosomes are predominantly affected in our clinic. Understanding these patterns can improve embryo selection, reduce miscarriage risks, and enhance genetic counseling. At the same time, due to the limited data on potential comorbidities in affected children, our findings aim to support both clinicians and patients in making informed decisions. : The retrospective clinical study included 461 PGT-A biopsies from our clinic database (September 2023-December 2024) to determine whether specific chromosome regions or individual chromosomes (C) are more likely to be mosaic or aneuploid. : Among the 461 embryos analyzed in our clinic, the incidence rate of mosaicism was 16.70% whereas the aneuploidy rate was 32.10%. Our results showed that mosaicism tends to target a specific chromosomal region in embryos, namely the chromosome 1 to 9 region, in particular chromosomes 7, 1, 9. On the other hand, aneuploidy targets the chromosomal region chromosome 16 to 22, particularly chromosomes 16, 19, and 22. : Our data suggest that mosaicism and aneuploidy affect the genome in an uneven manner and are often concentrated in specific chromosomal regions, with mosaicism primarily affecting the C1-C9 region and aneuploidy targeting the C16-C22 region. These data highlight the need for further research to understand these patterns and the impact of IVF methods on chromosomal targeting. Comparative studies could also be helpful in genetic counseling by clarifying the implications of the levels of mosaicism in the newborn.

摘要

鉴于试管婴儿胚胎中嵌合体和非整倍体现象普遍存在,我们的研究旨在回顾性地确定在我们的诊所中,特定染色体区域或个别染色体是否受到主要影响。了解这些模式可以改善胚胎选择、降低流产风险并加强遗传咨询。同时,由于受影响儿童潜在合并症的数据有限,我们的研究结果旨在支持临床医生和患者做出明智的决策。:这项回顾性临床研究纳入了我们诊所数据库(2023年9月至2024年12月)中的461例植入前基因检测-非整倍体(PGT-A)活检样本,以确定特定染色体区域或个别染色体(C)是否更有可能出现嵌合或非整倍体情况。:在我们诊所分析的461个胚胎中,嵌合体的发生率为16.70%,而非整倍体率为32.10%。我们的结果表明,嵌合体倾向于在胚胎中靶向特定染色体区域,即1号至9号染色体区域,尤其是7号、1号、9号染色体。另一方面,非整倍体靶向16号至22号染色体区域,特别是16号、19号和22号染色体。:我们的数据表明,嵌合体和非整倍体以不均衡的方式影响基因组,并且通常集中在特定染色体区域,嵌合体主要影响C1-C9区域,而非整倍体靶向C16-C22区域。这些数据凸显了进一步研究以了解这些模式以及试管婴儿方法对染色体靶向影响的必要性。比较研究也有助于遗传咨询,通过阐明新生儿嵌合水平的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06bb/12155553/ebe4f38cbd1d/diagnostics-15-01375-g001.jpg

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