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本文引用的文献

1
Current controversies in prenatal diagnosis 2: should a fetal exome be used in the assessment of a dysmorphic or malformed fetus?产前诊断的当前争议2:胎儿外显子组是否应用于评估畸形或结构异常胎儿?
Prenat Diagn. 2016 Jan;36(1):15-9. doi: 10.1002/pd.4718. Epub 2015 Nov 22.
2
Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning Disability.ZIC1功能获得性突变与冠状缝早闭和学习障碍相关。
Am J Hum Genet. 2015 Sep 3;97(3):378-88. doi: 10.1016/j.ajhg.2015.07.007.
3
Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities.用于超声异常胎儿产前诊断的外显子组测序
Prenat Diagn. 2015 Oct;35(10):1010-7. doi: 10.1002/pd.4675. Epub 2015 Sep 11.
4
Reproductive genetic counseling challenges associated with diagnostic exome sequencing in a large academic private reproductive genetic counseling practice.在一家大型学术性私立生殖遗传咨询机构中,与诊断性外显子组测序相关的生殖遗传咨询挑战。
Prenat Diagn. 2015 Oct;35(10):1022-9. doi: 10.1002/pd.4674. Epub 2015 Sep 4.
5
Prenatal whole-exome sequencing: parental attitudes.产前全外显子测序:父母的态度。
Prenat Diagn. 2015 Oct;35(10):1030-6. doi: 10.1002/pd.4635. Epub 2015 Jul 6.
6
Exome sequencing positively identified relevant alterations in more than half of cases with an indication of prenatal ultrasound anomalies.外显子组测序在超过半数有产前超声异常迹象的病例中明确鉴定出相关变异。
Prenat Diagn. 2015 Nov;35(11):1073-8. doi: 10.1002/pd.4648. Epub 2015 Aug 3.
7
Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.序列变异解读的标准与指南:美国医学遗传学与基因组学学会和分子病理学协会的联合共识推荐
Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.
8
Dilemmas in Prenatal Chromosomal Diagnosis Revealed Through a Single Center's 30 Years' Experience and 90,000 Cases.通过单中心30年经验和9万例病例揭示的产前染色体诊断困境
Fetal Diagn Ther. 2015;38(3):218-32. doi: 10.1159/000368604. Epub 2015 Jan 30.
9
Exome sequencing for gene discovery in lethal fetal disorders--harnessing the value of extreme phenotypes.外显子组测序用于致死性胎儿疾病的基因发现——利用极端表型的价值
Prenat Diagn. 2015 Oct;35(10):1005-9. doi: 10.1002/pd.4464. Epub 2014 Aug 22.
10
Survival is affected by mutation type and molecular mechanism in vascular Ehlers-Danlos syndrome (EDS type IV).在血管型埃勒斯-当洛综合征(IV型EDS)中,生存受突变类型和分子机制的影响。
Genet Med. 2014 Dec;16(12):881-8. doi: 10.1038/gim.2014.72. Epub 2014 Jun 12.

靶向外显子组测序方法在超声异常胎儿中的首次应用揭示了相当一部分伴有相关基因缺陷的病例。

First applications of a targeted exome sequencing approach in fetuses with ultrasound abnormalities reveals an important fraction of cases with associated gene defects.

作者信息

Pangalos Constantinos, Hagnefelt Birgitta, Lilakos Konstantinos, Konialis Christopher

机构信息

Genomis Ltd, London, United Kingdom; InterGenetics-Diagnostic Genetic Centre, Athens, Greece.

InterGenetics-Diagnostic Genetic Centre , Athens , Greece.

出版信息

PeerJ. 2016 Apr 26;4:e1955. doi: 10.7717/peerj.1955. eCollection 2016.

DOI:10.7717/peerj.1955
PMID:27168972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4860337/
Abstract

Background. Fetal malformations and other structural abnormalities are relatively frequent findings in the course of routine prenatal ultrasonographic examination. Due to their considerable genetic and clinical heterogeneity, the underlying genetic cause is often elusive and the resulting inability to provide a precise diagnosis precludes proper reproductive and fetal risk assessment. We report the development and first applications of an expanded exome sequencing-based test, coupled to a bioinformatics-driven prioritization algorithm, targeting gene disorders presenting with abnormal prenatal ultrasound findings. Methods. We applied the testing strategy to14 euploid fetuses, from 11 on-going pregnancies and three products of abortion, all with various abnormalities or malformations detected through prenatal ultrasound examination. Whole exome sequencing (WES) was followed by variant prioritization, utilizing a custom analysis pipeline (Fetalis algorithm), targeting 758 genes associated with genetic disorders which may present with abnormal fetal ultrasound findings. Results. A definitive or highly-likely diagnosis was made in 6 of 14 cases (43%), of which 3 were abortuses (Ellis-van Creveld syndrome, Ehlers-Danlos syndrome and Nemaline myopathy 2) and 3 involved on-going pregnancies (Citrullinemia, Noonan syndrome, PROKR2-related Kallmann syndrome). In the remaining eight on-going pregnancy cases (57%), a ZIC1 variant of unknown clinical significance was detected in one case, while in seven cases testing did not reveal any pathogenic variant(s). Pregnancies were followed-up to birth, resulting in one neonate harboring the PROKR2 mutation, presenting with isolated minor structural cardiac abnormalities, and in seven apparently healthy neonates. Discussion. The expanded targeted exome sequencing-based approach described herein (Fetalis), provides strong evidence suggesting a definite and beneficial increase in our diagnostic capabilities in prenatal diagnosis of otherwise chromosomally balanced fetuses with troubling ultrasound abnormalities. Furthermore, the proposed targeted exome sequencing strategy, designed primarily as a diagnostic rather than a research discovery tool, overcomes many of the problems and limitations associated with clinical wide-scale WES testing in a prenatal setting.

摘要

背景。胎儿畸形和其他结构异常是常规产前超声检查中较为常见的发现。由于其显著的遗传和临床异质性,潜在的遗传病因往往难以捉摸,无法做出精确诊断使得无法进行恰当的生殖和胎儿风险评估。我们报告了一种基于外显子组测序的扩展检测方法的开发及首次应用,该方法结合了生物信息学驱动的优先级算法,针对产前超声检查发现异常的基因疾病。方法。我们将该检测策略应用于14例整倍体胎儿,这些胎儿来自11例正在进行的妊娠和3例流产产物,所有胎儿均通过产前超声检查发现有各种异常或畸形。全外显子组测序(WES)之后进行变异优先级排序,使用定制分析流程(Fetalis算法),针对758个与可能出现胎儿超声异常的遗传疾病相关的基因。结果。14例病例中有6例(43%)做出了明确或高度可能的诊断,其中3例为流产胎儿(埃利斯-范克里夫德综合征、埃勒斯-丹洛斯综合征和2型杆状体肌病),3例涉及正在进行的妊娠(瓜氨酸血症、努南综合征、与PROKR2相关的卡尔曼综合征)。在其余8例正在进行的妊娠病例(57%)中,1例检测到意义未明的ZIC1变异,而7例检测未发现任何致病变异。对这些妊娠进行随访直至分娩,结果1例携带PROKR2突变的新生儿出现孤立的轻微心脏结构异常,7例新生儿看起来健康。讨论。本文所述的基于外显子组测序的扩展靶向方法(Fetalis)提供了有力证据,表明在产前诊断染色体正常但超声异常令人担忧的胎儿时,我们的诊断能力有了明确且有益的提高。此外,所提出的靶向外显子组测序策略主要设计为诊断工具而非研究发现工具,克服了产前环境中临床大规模WES检测相关的许多问题和局限性。