BMC Pregnancy and Childbirth · 2021 · 33 citations · 18 references
MedicineMaternal HealthObstetricsMaternal-fetal MedicineMolecular DiagnosticsPrenatal DiagnosisDna SequencingInvasive Prenatal TestingNoninvasive Prenatal TestingPrenatal AssessmentPrenatal Genetic DiagnosisPrenatal Molecular TestingCell-free Fetal Dna TestingMaternal Plasma Dna SequencingMolecular Prenatal DiagnosisNon-invasive Prenatal TestingNuchal Translucency ScreeningPrenatal Diagnostic TestingPrenatal ScreeningTwin Pregnancy Testing
BACKGROUND: The prenatal test of cell-free fetal DNA (cffDNA) is also known as noninvasive prenatal testing (NIPT) with high sensitivity and specificity. This study is to evaluate the performance of NIPT and its clinical relevance with various clinical indications. METHODS: A retrospective analysis was conducted on 14,316 pregnant women with prenatal indications, including advanced maternal age (≥35 years), maternal serum screening abnormalities, the thickened nuchal translucency (≥2.5 mm) and other ultrasound abnormalities, twin pregnancy/IVF-ET pregnancy, etc. The whole-genome sequencing (WGS) of maternal plasma cffDNA was employed in this study. RESULTS: A total of 189 (1.32%) positive NIPT cases were identified, and 113/189 (59.79%)cases were confirmed by invasive prenatal testing. Abnormal serological screening (53.14%) was the most common indication, followed by elderly pregnancy (23.02%). The positive prediction value for T21, T18, T13, sex chromosome abnormalities, other autosomal aneuploidy abnormalities, and CNV abnormalities were 91.84, 68.75,37.50, 66.67, 14.29, and 6.45%, respectively. The positive rate and the true positive rate of nuchal translucency (NT) thickening were the highest (4.17 and 3.33%), followed by the voluntary requirement group (3.49 and 1.90%) in the various prenatal screening indications. The cffDNA concentration was linearly correlated with gestational age (≥10 weeks) and the positive NIPT group's Z-score values. CONCLUSIONS: whole-genome sequencing of cffDNA has extremely high sensitivity and specificity for T21, high sensitivity for T18, sex chromosome abnormalities, and T13. It also provides evidence for other abnormal chromosomal karyotypes (CNV and non-21/18/13 autosomal aneuploidy abnormalities). The cffDNA concentration is closely related to the gestational age and determines the specificity of NIPT. Our results highlight NIPT's clinical significance, which is an effective prenatal screening tool for high-quality care of pregnancy.
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Rossa W. K. Chiu, K.C. Allen Chan, Yuan Gao et al. · Proceedings of the National Academy of Sciences · 2008 · 947 citations · Full text
Life Sciences, Genetics, Obstetrics +17
Anthony R. Gregg, Brian G. Skotko, Judith Benkendorf et al. · Genetics in Medicine · 2016 · 692 citations · Full text