Abstract
BackgroundTo study whether maternal serum hyperglycosylated human chorionic gonadotropin (hCG-h) improves first trimester prediction of pre-eclampsia when combined with placental growth factor (PlGF), pregnancy-associated plasma protein-A (PAPP-A) and maternal risk factors.MethodsGestational-age-adjusted concentrations of hCG, hCG-h, PlGF and PAPP-A were analysed in serum samples by time-resolved immunofluorometric assays at 8–13 weeks of gestation. The case–control study included 98 women who developed pre-eclampsia, 25 who developed gestational hypertension, 41 normotensive women with small-for-gestational-age (SGA) infants and 177 controls.ResultsOf 98 women with pre-eclampsia, 24 women developed preterm pre-eclampsia (diagnosis < 37 weeks of gestation) and 13 of them had early-onset pre-eclampsia (diagnosis < 34 weeks of gestation). They had lower concentrations of PlGF, PAPP-A and proportion of hCG-h to hCG (%hCG-h) than controls. In receiver-operating characteristics (ROC) curve analysis, the area under the curve (AUC) for the combination of PlGF, PAPP-A, %hCG-h, nulliparity and mean arterial blood pressure was 0.805 (95% confidence interval, CI, 0.699–0.912) for preterm pre-eclampsia and 0.870 (95% CI 0.750–0.988) for early-onset pre-eclampsia. Without %hCG-h the AUC values were 0.756 (95% CI 0.651–0.861) and 0.810 (95% CI 0.682–0.938) respectively. For prediction of gestational hypertension, the AUC for %hCG-h was 0.708 (95% CI 0.608–0.808), but for other markers the AUC values were not significant. None of the AUC values were significant for the prediction of SGA infants in normotensive women.ConclusionsFirst trimester maternal serum %hCG-h tended to improve prediction of preterm and early-onset pre-eclampsia when combined with PlGF, PAPP-A and maternal risk factors.
Highlights
To study whether maternal serum hyperglycosylated human chorionic gonadotropin improves first trimester prediction of pre-eclampsia when combined with placental growth factor (PlGF), pregnancy-associated plasma protein-A (PAPP-A) and maternal risk factors
We have recently shown that the proportion of human chorionic gonadotropin (hCG)-h to total hCG (%Hyperglycosylated hCG (hCG-h)) at 8– 13 weeks of gestation predicts pre-eclampsia with moderate accuracy, i.e. with 56% sensitivity at 90% specificity [12]
The aim of this study was to investigate whether a combination of first-trimester serum %hCG-h with PlGF, PAPP-A and maternal clinical risk factors improves the diagnostic accuracy for prediction of pre-eclampsia
Summary
To study whether maternal serum hyperglycosylated human chorionic gonadotropin (hCG-h) improves first trimester prediction of pre-eclampsia when combined with placental growth factor (PlGF), pregnancy-associated plasma protein-A (PAPP-A) and maternal risk factors. Pre-eclampsia occurs in 2–8% of all pregnancies. It is a significant cause of maternal morbidity and mortality, especially in developing countries. There has been no therapy for pre-eclampsia other than delivery [1]. Several recent studies suggest that early-onset (diagnosis before 34 weeks of gestation) and severe forms of pre-eclampsia might be prevented by daily low-dose aspirin when started by the 16th week of gestation in mothers at risk [2, 3]. Early prediction of pre-eclampsia has become important
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