Down syndrome maternal serum marker screening after 18 weeks' gestation |
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Authors: | Françoise Muller Sophie Dreux Jean-François Oury Dominique Luton Serge Uzan Michèle Uzan Michel Levardon Marc Dommergues |
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Affiliation: | 1. Service de Biochimie, Hôpital Ambroise Paré, Boulogne, France;2. Maternité, Hôpital Robert Debré, Paris, France;3. Maternité, Hôpital Tenon, Paris, France;4. Maternité, Hôpital Jean Verdier, Paris, France;5. Maternité, Hôpital Beaujon, Paris, France;6. Maternité, Hôpital Necker, Paris, France |
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Abstract: | ![]() Women having access to prenatal care late in pregnancy may still wish to benefit from maternal serum screening for Down syndrome. Therefore, we established reference values for α-feto protein (AFP) and free β-human chorionic gonadotrophin (β-hCG), and assessed the diagnostic value of maternal serum marker screening at 18–35 weeks' gestation based upon a series of 4072 sera from unaffected pregnancies and 118 sera from pregnant women with fetuses affected by Down syndrome. Using a 1/250 risk cut-off, a detection rate of 72.9% (95% CI = 71.5–74.3%) was achieved with a false-positive rate of 7.51% (95% CI = 6.71–8.3%). This was not significantly different from the percentages observed in our 14–17 weeks routine screening (50 596 patients): 71.9% (95% CI = 71.5–72.3%) and 6.48% (95% CI = 6.28–6.68%), respectively. Detection and screen-positive rates were, respectively, 51.3% (95% CI = 35.6–67.0%) and 5.95% (95% CI = 5.12–6.68%) in women aunder 35 years of age, and 84.8% (95% CI = 76.9–92.7%) and 24% (95% CI = 20.7–27.3%) in women aged 35 years and over. In conclusion, maternal serum marker screening is feasible at 18 weeks' gestation and later, which may be of interest in selected cases. Copyright © 2002 John Wiley & Sons, Ltd. |
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Keywords: | prenatal diagnosis trisomy 21 amniocentesis maternal serum markers Down syndrome screening |
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