Han May Phoo, Ferreira Ana Elizabeth Gomes de Melo Tavares, Elhindi James, McLennan Andrew C, Scott Fergus
Discipline of Women's Health, University of New South Wales, Randwick, Australia.
Sydney Ultrasound for Women, Sydney, Australia.
Prenat Diagn. 2025 Feb;45(2):147-154. doi: 10.1002/pd.6742. Epub 2025 Jan 3.
Genome-wide non-invasive prenatal testing (gwNIPT) has screening limitations for detectable genetic conditions and cannot detect microdeletions/microduplications (MD) or triploidy. Nuchal translucency (NT) increases with gestation and with genetic or structural abnormalities. This study aims to determine the utility of NT measurement in detecting genetic abnormalities not identified by gwNIPT and the optimal NT threshold value.
A 4-year retrospective study of singleton pregnancies undergoing first-line gwNIPT aneuploidy screening where invasive prenatal testing by CVS/or amniocentesis was subsequently undertaken. Population proportions for static and multiple of the median (MoM) NT cut-offs were derived from all 11-14 weeks ultrasound examinations.
Among 919 pregnancies with gwNIPT and invasive testing, 338 had a single genetic abnormality. There were 9 false negative GwNIPT results and a further 26 undetectable abnormalities (18 MD, 8 triploidy) in this cohort. Twelve had a dual chromosomal abnormality, four of which returned a low-risk gwNIPT. Thirty-three "missed cases" also had a 13-week scan, to which the various NT threshold values (3.0 mm, 1.6 MoM, 3.5 mm, and 1.9 MoM) were applied. In only 3 (9%) cases did the NT exceed 3.0 mm with similar detection rates (DR) for all higher cut-offs. Static and MoM-based NT cut-offs had similar positive predictive values (PPV).
Enlarged NT measurement is a poor predictor of genetic abnormalities not identified by gwNIPT. When applied, the fixed NT cut-off of 3.5 mm provides a low FPR with a similar DR to lower cut-off thresholds, resulting in a higher PPV.
全基因组无创产前检测(gwNIPT)在可检测的遗传疾病方面存在筛查局限性,无法检测微缺失/微重复(MD)或三倍体。颈项透明层(NT)会随着孕周增加以及遗传或结构异常而增厚。本研究旨在确定NT测量在检测gwNIPT未识别的遗传异常中的效用以及最佳NT阈值。
对接受一线gwNIPT非整倍体筛查的单胎妊娠进行了一项为期4年的回顾性研究,随后进行了绒毛取样(CVS)/羊膜穿刺术的侵入性产前检测。静态和中位数倍数(MoM)NT截断值的人群比例来自所有11 - 14周的超声检查。
在919例接受gwNIPT和侵入性检测的妊娠中,338例存在单一遗传异常。该队列中有9例假阴性的gwNIPT结果以及另外26例无法检测到的异常(18例MD,8例三倍体)。12例有双重染色体异常,其中4例返回了低风险的gwNIPT结果。33例“漏诊病例”也进行了13周的扫描,并应用了各种NT阈值(3.0毫米、1.6 MoM、3.5毫米和1.9 MoM)。只有3例(9%)的NT超过3.0毫米,所有更高截断值的检测率(DR)相似。基于静态和MoM的NT截断值具有相似的阳性预测值(PPV)。
增大的NT测量对于gwNIPT未识别的遗传异常预测效果不佳。应用时,3.5毫米的固定NT截断值具有较低的假阳性率(FPR),与较低截断阈值的DR相似,从而导致更高的PPV。