Lannoo L, Van Den Bogaert K, Belmans A, Brison N, Dehaspe L, De Langhe E, Vancoillie L, Parijs I, Vermeesch J R, Devriendt K, Van Calsteren K
Department of Obstetrics and Gynaecology, University Hospitals Leuven, Leuven, Belgium.
Department of Development and Regeneration, KU Leuven, Leuven, Belgium.
Prenat Diagn. 2025 May;45(5):581-590. doi: 10.1002/pd.6778. Epub 2025 Mar 20.
To investigate maternal characteristics, underlying factors and perinatal outcome in pregnancies with persistent uninterpretable prenatal cfDNA screening in a general obstetric population (GOP).
This study included pregnant individuals with persistent uninterpretable prenatal cfDNA screening results from December 2020 to December 2022. Prenatal cfDNA screening results were classified as uninterpretable due to low quality score (LQS) or low fetal fraction (LFF). Maternal autoimmune screening and a third prenatal cfDNA screening were performed later in pregnancy. Data on maternal characteristics and perinatal outcome were analyzed.
Among 123 pregnant individuals with failed prenatal cfDNA screening, 68% were due to LFF and 32% to LQS. Obesity and autoimmune diseases were significantly overrepresented. A third prenatal cfDNA screening at 24 weeks was informative in 77.1% cases, with a higher success-rate in the LFF group (87.8%). Maternal autoimmune screening revealed unknown triple positivity for antiphospholipid antibodies in 2.4%. Abnormal perinatal outcome was registered in 69.9% of patients, with higher rates of adverse perinatal outcome in the LFF group.
Persistent uninterpretable prenatal cfDNA screening indicates a higher risk for adverse perinatal outcomes, especially in cases with LFF. Maternal autoimmune screening should be considered to identify high-risk pregnancies. A third prenatal cfDNA screening later in pregnancy can help stratify truly high-risk pregnancies and allows patients with initially uninterpretable results to make an informed decision about diagnostic testing.
在普通产科人群(GOP)中,调查产前cfDNA筛查持续无法解读的妊娠中的母体特征、潜在因素和围产期结局。
本研究纳入了2020年12月至2022年12月期间产前cfDNA筛查结果持续无法解读的孕妇。产前cfDNA筛查结果因质量分数低(LQS)或胎儿游离DNA比例低(LFF)而被归类为无法解读。在妊娠后期进行了母体自身免疫筛查和第三次产前cfDNA筛查。分析了母体特征和围产期结局的数据。
在123例产前cfDNA筛查失败的孕妇中,68%是由于LFF,32%是由于LQS。肥胖和自身免疫性疾病的比例明显过高。24周时进行的第三次产前cfDNA筛查在77.1%的病例中提供了有效信息,在LFF组中的成功率更高(87.8%)。母体自身免疫筛查显示2.4%的孕妇抗磷脂抗体呈未知的三联阳性。69.9%的患者出现围产期异常结局,LFF组不良围产期结局的发生率更高。
产前cfDNA筛查持续无法解读表明围产期不良结局的风险较高,尤其是在LFF的病例中。应考虑进行母体自身免疫筛查以识别高危妊娠。妊娠后期进行的第三次产前cfDNA筛查有助于对真正的高危妊娠进行分层,并使最初结果无法解读的患者能够对诊断检测做出明智的决定。