Department of Clinical Genetics, Aarhus University Hospital, Aarhus, Denmark.
Center for Fetal Diagnostics, Aarhus University Hospital/Aarhus University, Aarhus, Denmark.
Acta Obstet Gynecol Scand. 2021 May;100(5):884-892. doi: 10.1111/aogs.14052. Epub 2021 Feb 24.
In Denmark, non-invasive prenatal testing (NIPT) has been used since 2013. We aimed to evaluate the early clinical use of NIPT in Danish public and private healthcare settings before NIPT became an integrated part of the national guidelines on prenatal screening and diagnosis in 2017.
NIPT data were collected between March 2013 and June 2017 from national public registries and private providers. Results from follow-up samples (chorionic villi, amniotic fluid, postnatal blood or fetal tissue) were included from The Danish Cytogenetics Central Registry and indications and outcome from The Danish Fetal Medicine Database.
A total of 3936 NIPT results were included in the study from public hospitals (n = 3463, 88.0%) and private clinics (n = 473, 12.0%). The total number of prenatal tests was 19 713 during the study period: 20% were NIPT analyses (n = 3936) and 80% invasive procedures (n = 15 777). Twenty-five percent of NIPTs in the private clinics were performed before gestational week 11 , whereas NIPT in public settings was used only after combined first trimester screening (P < .001). Regardless of indication, the national public sensitivity was 96.9% (95% CI 82.0%-99.8%) for trisomy 21, 100% (95% CI 46.3%-100%) for trisomy 18, 100% (95% CI 5.5%-100%) for trisomy 13, and 87.0% (95% CI 74.5%-92.4%) for any fetal chromosomal aberration. Forty-seven true-positive NIPT results included cases of common aneuplodies (trisomy 21, n = 31; trisomy 18, n = 5; and trisomy 13, n = 1), sex chromosomal aberrations (n = 7) and atypical chromosomal aberrations (n = 3). One false-negative NIPT result occurred (trisomy 21). Of 47 cases, 21 (45%) cases with a true-positive NIPT result resulted in live births by choice; 11 of these children had Down and 4 had Edwards syndrome.
The total number of NIPT analyses was low compared with the number of invasive procedures in the implementation period. In contrast to the generally high termination rate after a positive result following invasive testing in Denmark, a high proportion of true-positive NIPT results from the public setting resulted in live births. NIPT may be an important risk-free alternative to invasive testing for a minority of women in the public setting who wish to use prenatal genetic testing for information only and not for reproductive decision-making.
在丹麦,自 2013 年以来,非侵入性产前检测(NIPT)已被使用。我们旨在评估 2017 年 NIPT 成为国家产前筛查和诊断指南的一部分之前,在丹麦公共和私人医疗保健环境中 NIPT 的早期临床应用。
NIPT 数据于 2013 年 3 月至 2017 年 6 月从国家公共登记处和私人提供者处收集。来自丹麦细胞遗传学中央登记处的后续样本(绒毛膜绒毛、羊水、产后血液或胎儿组织)的结果以及丹麦胎儿医学数据库的适应症和结果都包括在内。
本研究共纳入 3936 例 NIPT 结果,分别来自公立医院(n=3463,88.0%)和私立诊所(n=473,12.0%)。研究期间进行的产前检查总数为 19713 次:20%为 NIPT 分析(n=3936),80%为侵入性程序(n=15777)。25%的私立诊所的 NIPT 是在妊娠 11 周之前进行的,而公共环境中的 NIPT 仅在联合早孕期筛查后使用(P<0.001)。无论适应症如何,国家公共检测的敏感性为 21 三体综合征 96.9%(95%CI 82.0%-99.8%)、18 三体综合征 100%(95%CI 46.3%-100%)、13 三体综合征 100%(95%CI 5.5%-100%)和任何胎儿染色体异常 87.0%(95%CI 74.5%-92.4%)。47 例阳性 NIPT 结果包括常见的非整倍体(21 三体,n=31;18 三体,n=5;13 三体,n=1)、性染色体异常(n=7)和非典型染色体异常(n=3)。1 例 NIPT 结果为假阴性。在 47 例中,21 例(45%)阳性 NIPT 结果的活产是出于选择;其中 11 例患儿患有唐氏综合征,4 例患儿患有爱德华氏综合征。
在实施期间,NIPT 分析的总数与侵入性程序的数量相比很低。与丹麦在侵入性检测后阳性结果通常高终止率形成对比的是,公共环境中阳性 NIPT 结果的很大一部分导致了活产。对于希望仅使用产前遗传检测获得信息而不进行生殖决策的公共环境中的少数女性来说,NIPT 可能是一种重要的无风险替代侵入性检测的方法。