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全基因组 NIPS 检测到的常见三体以外的染色体异常的起源和临床相关性:TRIDENT 研究结果。

Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study.

机构信息

Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.

Department of Clinical Genetics, Academic Medical Center, Amsterdam, Amsterdam, The Netherlands.

出版信息

Genet Med. 2018 Apr;20(5):480-485. doi: 10.1038/gim.2017.132. Epub 2017 Sep 28.

Abstract

PurposeNoninvasive prenatal screening (NIPS) using cell-free DNA in maternal blood is highly sensitive for detecting fetal trisomies 21, 18, and 13. Using a genome-wide approach, other chromosome anomalies can also be detected. We report on the origin, frequency, and clinical significance of these other chromosome aberrations found in pregnancies at risk for trisomy 21, 18, or 13.MethodsWhole-genome shallow massively parallel sequencing was used and all autosomes were analyzed.ResultsIn 78 of 2,527 cases (3.1%) NIPS was indicative of trisomy 21, 18, or 13, and in 41 (1.6%) of other chromosome aberrations. The latter were of fetal (n = 10), placental (n = 22), maternal (n = 1) or unknown (n = 7). One case lacked cytogenetic follow-up. Nine of the 10 fetal cases were associated with an abnormal phenotype. Thirteen of the 22 (59%) placental aberrations were associated with fetal congenital anomalies and/or poor fetal growth (<p10), which was severe (<p2.3) in six cases.ConclusionGenome-wide NIPS in pregnancies at risk for trisomy 21, 18, or 13, reveals a chromosomal aberration other than trisomy 21, 18 or 13 in about one-third of the abnormal cases. The majority involves a fetal or placental chromosome aberration with clinical relevance for pregnancy management.

摘要

目的

利用母体血液中的游离细胞 DNA 进行非侵入性产前筛查(NIPS)对于检测 21 三体、18 三体和 13 三体的胎儿具有高度敏感性。采用全基因组方法,还可以检测到其他染色体异常。我们报告了在 21 三体、18 三体或 13 三体风险妊娠中发现的这些其他染色体畸变的起源、频率和临床意义。

方法

使用全基因组浅度大规模平行测序,并分析所有常染色体。

结果

在 2527 例 NIPS 中,有 78 例(3.1%)提示 21 三体、18 三体或 13 三体,41 例(1.6%)提示其他染色体异常。后者分别为胎儿(n=10)、胎盘(n=22)、母体(n=1)或未知(n=7)来源。1 例病例缺乏细胞遗传学随访。10 例胎儿病例中,有 9 例与异常表型相关。22 例(59%)胎盘异常与胎儿先天性畸形和/或胎儿生长不良(<p10)有关,其中 6 例为严重不良(<p2.3)。

结论

在 21 三体、18 三体或 13 三体风险妊娠中进行全基因组 NIPS,在约三分之一的异常病例中揭示了除 21 三体、18 三体或 13 三体以外的染色体异常。大多数涉及具有妊娠管理临床意义的胎儿或胎盘染色体异常。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ea/5929118/cdda6583a415/gim2017132f1.jpg

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