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非侵入性植入前遗传学检测非整倍体和遗传物质之谜:一篇综述文章。

Non-Invasive Preimplantation Genetic Testing for Aneuploidy and the Mystery of Genetic Material: A Review Article.

机构信息

Department of Human Reproduction, Division of Obstetrics and Gynecology, University Medical Center Ljubljana, 1000 Ljubljana, Slovenia.

Faculty of Medicine, University of Ljubljana, 1000 Ljubljana, Slovenia.

出版信息

Int J Mol Sci. 2022 Mar 25;23(7):3568. doi: 10.3390/ijms23073568.

Abstract

This review focuses on recent findings in the preimplantation genetic testing (PGT) of embryos. Different preimplantation genetic tests are presented along with different genetic materials and their analysis. Original material concerning preimplantation genetic testing for aneuploidy (PGT-A) was sourced by searching the PubMed and ScienceDirect databases in October and November 2021. The searches comprised keywords such as 'preimplantation', 'cfDNA'; 'miRNA', 'PGT-A', 'niPGT-A', 'aneuploidy', 'mosaicism', 'blastocyst biopsy', 'blastocentesis', 'blastocoel fluid', 'NGS', 'FISH', and 'aCGH'. Non-invasive PGT-A (niPGT-A) is a novel approach to the genetic analysis of embryos. The premise is that the genetic material in the spent embryo culture media (SECM) corresponds to the genetic material in the embryo cells. The limitations of niPGT-A are a lower quantity and lesser quality of the cell-free genetic material, and its unknown origin. The concordance rate varies when compared to invasive PGT-A. Some authors have also hypothesized that mosaicism and aneuploid cells are preferentially excluded from the embryo during early development. Cell-free genetic material is readily available in the spent embryo culture media, which provides an easier, more economic, and safer extraction of genetic material for analysis. The sampling of the SECM and DNA extraction and amplification must be optimized. The origin of the cell-free media, the percentage of apoptotic events, and the levels of DNA contamination are currently unknown; these topics need to be further investigated.

摘要

本文综述了胚胎植入前遗传学检测(PGT)的最新研究进展。介绍了不同的胚胎植入前遗传学检测方法,以及不同的遗传物质及其分析方法。原始资料来源于 2021 年 10 月和 11 月在 PubMed 和 ScienceDirect 数据库中搜索的有关胚胎非整倍体(PGT-A)的植入前遗传学检测。搜索关键词包括“preimplantation”、“cfDNA”、“miRNA”、“PGT-A”、“niPGT-A”、“aneuploidy”、“mosaicism”、“blastocyst biopsy”、“blastocentesis”、“blastocoel fluid”、“NGS”、“FISH”和“aCGH”。非侵入性 PGT-A(niPGT-A)是一种新型的胚胎遗传分析方法。其前提是胚胎培养废弃液(SECM)中的遗传物质与胚胎细胞中的遗传物质相对应。niPGT-A 的局限性在于游离遗传物质的数量较少、质量较差,且其来源未知。与侵袭性 PGT-A 相比,niPGT-A 的一致性率存在差异。一些作者还假设,嵌合体和非整倍体细胞在早期发育过程中会优先从胚胎中被排除。游离遗传物质在胚胎培养废弃液中很容易获得,为分析提供了一种更简单、更经济、更安全的遗传物质提取方法。需要优化 SECM 的采样、DNA 提取和扩增。游离培养液的来源、凋亡事件的百分比以及 DNA 污染的水平目前尚不清楚,这些问题需要进一步研究。

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