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Contingent first-trimester screening for aneuploidies with cell-free DNA in a Danish clinical setting

Authors :
Miltoft, Caroline Borregaard
Rode, Line
Ekelund, Charlotte Kvist
Sundberg, Karin
Kjaergaard, Susanne
Zingenberg, Helle
Tabor, Ann
Miltoft, Caroline Borregaard
Rode, Line
Ekelund, Charlotte Kvist
Sundberg, Karin
Kjaergaard, Susanne
Zingenberg, Helle
Tabor, Ann
Source :
Miltoft , C B , Rode , L , Ekelund , C K , Sundberg , K , Kjaergaard , S , Zingenberg , H & Tabor , A 2018 , ' Contingent first-trimester screening for aneuploidies with cell-free DNA in a Danish clinical setting ' , Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology , vol. 51 , no. 4 , pp. 470-479 .
Publication Year :
2018

Abstract

OBJECTIVES: The primary aim was to compare the screening performance for Trisomy 21, of standard combined first trimester screening with referral to invasive testing at a cut-off at 1 in 300, with a contingent testing, consisting of referral to invasive testing at a 1 in 100 cut-off and referral to cell-free DNA (cfDNA) testing for a risk between 1 in 100 and 1 in 1000.METHODS: Singleton pregnant women with a combined first trimester risk ≥ 1 in 1000 were consecutively recruited from two Danish hospitals between August 2014 and May 2015. First trimester combined screening was based on maternal and gestational age, nuchal translucency thickness, and levels of PAPP-A and ß-hCG. Blood samples for cfDNA testing were analysed using the Harmony Prenatal Test® giving risks for Trisomy 21, 18 and 13, and sex chromosomal aneuploidies. The cfDNA analysis was blinded from the combined risk assessment, karyotype results and pregnancy outcome. Pregnancy outcome and pre- and postnatal karyotypes were obtained from the Danish Fetal Medicine Database.RESULTS: Among 6449 women who had a combined first trimester screening, 869 (13.5%) had a risk ≥ 1 in 1000 and 597 were included for cfDNA testing. Among these there were 15 cases of Trisomy 21, one case of Trisomy 18 and two cases of Trisomy 13. The sensitivity for Trisomy 21 was 100% using both screening scenarios, while specificity increased significantly from 97.0% to 98.8% (p < 0.001) using the contingent approach. The sensitivity for Trisomy 21, 18 and 13 increased from 94.4% to 100% with overlapping confidence intervals, while specificity increased significantly from 97.1% to 98.9% (p < 0.0001). In seven pregnancies, the risk of a sex chromosomal aneuploidy was increased with cfDNA testing but discordant with the karyotype, corresponding to a false-positive rate of 1.2%.CONCLUSIONS: In a clinical setting with an efficient combined first trimester screening, a contingent screening offering women with

Details

Database :
OAIster
Journal :
Miltoft , C B , Rode , L , Ekelund , C K , Sundberg , K , Kjaergaard , S , Zingenberg , H & Tabor , A 2018 , ' Contingent first-trimester screening for aneuploidies with cell-free DNA in a Danish clinical setting ' , Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology , vol. 51 , no. 4 , pp. 470-479 .
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1322702942
Document Type :
Electronic Resource