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Hypertensive disorders in pregnancy: screening by biophysical and biochemical markers at 11–13 weeks

Objective To examine the performance of screening for pre‐eclampsia (PE) and gestational hypertension (GH) by a combination of maternal factors and various biophysical and biochemical markers at 11–13 weeks' gestation. Methods This was a case–control study of 26 cases of early PE, 90 of late PE...

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Published in:Ultrasound in obstetrics & gynecology 2010-06, Vol.35 (6), p.662-670
Main Authors: Poon, L. C. Y., Akolekar, R., Lachmann, R., Beta, J., Nicolaides, K. H.
Format: Article
Language:English
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Summary:Objective To examine the performance of screening for pre‐eclampsia (PE) and gestational hypertension (GH) by a combination of maternal factors and various biophysical and biochemical markers at 11–13 weeks' gestation. Methods This was a case–control study of 26 cases of early PE, 90 of late PE, 85 of GH and 201 unaffected controls. Maternal history was recorded, the uterine artery with the lowest pulsatility index (L‐PI) and mean arterial pressure (MAP) were measured and stored plasma and serum were analyzed for placental growth factor (PlGF), inhibin‐A, activin‐A, tumor necrosis factor receptor‐1, matrix metalloproteinase‐9, pentraxin‐3 and P‐selectin. Results Multivariate logistic regression analysis demonstrated that significant prediction for early PE was provided by maternal factors, MAP, uterine artery L‐PI and serum PlGF. Significant prediction of late PE was provided by maternal factors, MAP, uterine artery L‐PI, PlGF, activin‐A and P‐selectin. For GH significant prediction was provided by maternal factors, MAP, uterine artery L‐PI and activin‐A. In screening by a combination of maternal factors, biophysical and biochemical markers the estimated detection rates, at a 5% false‐positive rate, were 88.5% (95% CI, 69.8–97.4%) for early PE, 46.7% (95% CI, 36.1–57.5%) for late PE and 35.3% (95% CI, 25.2–46.4%) for GH. Conclusion Combined biophysical and biochemical testing at 11–13 weeks could effectively identify women at high risk for subsequent development of hypertensive disorders in pregnancy. Copyright © 2010 ISUOG. Published by John Wiley & Sons, Ltd.
ISSN:0960-7692
1469-0705
1469-0705
DOI:10.1002/uog.7628