Pangalos Constantinos, Hagnefelt Birgitta, Lilakos Konstantinos, Konialis Christopher
Genomis Ltd, London, United Kingdom; InterGenetics-Diagnostic Genetic Centre, Athens, Greece.
InterGenetics-Diagnostic Genetic Centre , Athens , Greece.
PeerJ. 2016 Apr 26;4:e1955. doi: 10.7717/peerj.1955. eCollection 2016.
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.
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。