Abstract
Background: ADAM12 has been shown to be an efficient maternal serum marker for Down syndrome (DS) in the first trimester; but recent studies, using a second generation assay, have not confirmed these findings. We examined the efficiency of a second generation assay for ADAM12. Materials and Methods: ADAM12 concentrations were determined in 28 first trimester DS and 503 control pregnancies using a novel Research DelfiaR ADAM12 kit. Log10MoM distributions of ADAM12 and correlations with other markers were established. Population performance of screening was estimated by Monte Carlo simulation. Results: ADAM12 was significantly reduced in the first trimester in DS pregnancies with a log10MoM of -0.1621 (equivalent to 0.68 MoM) (p < 0.001). The reduction decreased with advancing gestational age. ADAM12 used with PAPP-A+hCGβ+NT (CUB screening) increased the detection rate (DR) from 86% to 89% for a false positive rate (FPR) of 5%. When used for a fixed DR of 90%, the addition of ADAM12 resulted in a 25% reduction of the FPR. Conclusion: ADAM12 is a moderately effective DS marker. It is not a cost-effective addition to CUB screening, but may be used to reduce the FPR in selected high-risk cases.
Original language | English |
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Journal | Prenatal Diagnosis |
Volume | 30 |
Issue number | 2 |
Pages (from-to) | 110-4 |
Number of pages | 5 |
ISSN | 0197-3851 |
DOIs | |
Publication status | Published - Feb 2010 |
Keywords
- ADAM Proteins
- ADAM12 Protein
- Adult
- Biomarkers
- Case-Control Studies
- Down Syndrome
- False Positive Reactions
- Female
- Humans
- Mass Screening
- Membrane Proteins
- Pregnancy
- Pregnancy Trimester, First
- Prenatal Care
- Comparative Study
- Journal Article