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Integrated ultrasound and biochemical screening for trisomy 21 using fetal nuchal translucency, absent fetal nasal bone, free β‐hCG and PAPP‐A at 11 to 14 weeks
Author(s) -
Cicero Simona,
Bindra Renu,
Rembouskos Georgios,
Spencer Kevin,
Nicolaides Kypros H.
Publication year - 2003
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.588
Subject(s) - nasal bone , trisomy , fetus , medicine , gestational age , gestation , obstetrics , pregnancy , andrology , surgery , biology , genetics
Abstract Background Screening for trisomy 21 by a combination of maternal age, fetal nuchal translucency (NT) thickness and maternal serum free β‐hCG and pregnancy‐associated plasma protein‐A (PAPP‐A) at 11 to 14 weeks of gestation is associated with a detection rate of 90% for a false‐positive rate of 5%. Recent evidence suggests that in about 70% of fetuses with trisomy 21, the nasal bone is not visible at the 11th‐ to 14th‐week scan (Cicero et al. , 2001). The aim of this study was to examine whether fetal NT thickness and the level of maternal serum biochemical markers is independent of the presence or absence of the nasal bone, and to estimate the performance of a screening test that integrates the two sonographic and the two biochemical markers. Methods This was a retrospective case‐control study comprising 100 trisomy 21 and 400 chromosomally normal singleton pregnancies at 11 to 14 weeks of gestation. Ultrasound examination was carried out for measurement of fetal NT and assessment of the presence or absence of the fetal nasal bone. Maternal serum free β‐hCG and PAPP‐A were measured using the Kryptor rapid random‐access immunoassay analyser (Brahms Diagnostica GmbH, Berlin). The distribution of fetal NT, maternal serum free β‐hCG and PAPP‐A in trisomy 21 fetuses with absent and present nasal bone was examined. Results The nasal bone was absent in 69 and present in 31 of the trisomy 21 fetuses. There were no significant differences in median maternal age, median gestational age, NT delta, free β‐hCG MoM and PAPP‐A MoM in trisomy 21 fetuses with and without a visible nasal bone. For a false‐positive rate of 5%, it was estimated that screening with the four markers in combination with maternal age would be associated with a detection rate of 97%. For a false‐positive rate of 0.5%, the detection rate was 90.5%. Conclusions An integrated sonographic and biochemical test at 11 to 14 weeks can potentially identify about 90% of trisomy 21 fetuses for a false‐positive rate of 0.5%. Copyright © 2003 John Wiley & Sons, Ltd.