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First‐trimester Down syndrome screening using additional serum markers with and without nuchal translucency and cell‐free DNA
Author(s) -
Johnson J,
Pastuck M,
Metcalfe A,
Connors G,
Krause R,
Wilson D,
Cuckle H
Publication year - 2013
Publication title -
prenatal diagnosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.956
H-Index - 97
eISSN - 1097-0223
pISSN - 0197-3851
DOI - 10.1002/pd.4194
Subject(s) - cell free fetal dna , down syndrome , nuchal translucency , pregnancy associated plasma protein a , medicine , obstetrics , gestation , nuchal translucency measurement , gynecology , fetus , first trimester , aneuploidy , pregnancy , trisomy , human chorionic gonadotropin , prenatal diagnosis , biology , chromosome , genetics , psychiatry , gene
Objective This study aimed to evaluate serum‐only four‐marker first trimester (1T‐Quad) Down syndrome screening, alone or contingently to select 10–20% with highest risk for nuchal translucency (NT) or cell‐free (cf)DNA. Methods Stored maternal serum samples (−80 °C) from 90 pregnancies with fetal Down syndrome and 1607 controls were retrieved and measured for placental growth factor, α‐fetoprotein, pregnancy‐associated plasma protein and free β‐human chorionic gonadotropin. Samples were from singleton pregnancies (9–13 + 6 weeks), and NT was measured between 11 and 13 + 6 weeks. Markers were expressed in multiples of the normal median (MoM) for gestation. Gaussian models were fitted to the distribution of log MoMs by using observed parameters, standardized maternal age distribution (mean 27, SD 5.5) and published cfDNA results. Results The model‐predicted detection rate (DR) for 1T‐Quad was 74% [5% false‐positive rate (FPR)]. When used contingently to select for NT, the DR was 89% at 5%. When used to select for cfDNA, the DR was 91% (FPR < 0.05%). Conclusion The 1T‐Quad test can achieve a similar DR to a second‐trimester Quad test. When used contingently to select for NT, the DR is similar to the Combined test. Used contingently to select for cfDNA would achieve even higher detection. © 2013 John Wiley & Sons, Ltd.