Abstract

The aim of our study was to assess the predictive values for hypertensive complications of pregnancy of the multiples of median (MoM) of serum pregnancy associated plasma protein A (PAPP-A), measured in 128 pregnant patients between 11 and 14 weeks gestational age. The 5th and the 10th percentile for MoM PAPP-A were 0.27 and 0.33, respectively. The detection rate for pregnancy induced hypertension, mild preeclampsia, severe preeclampsia, all preeclampsia and all hypertensive complications was 0%, 9.09%, 0%, 7.69%, and 6.25% for MoM PAPP-A below the 5th percentile (for a false positive rate of 5%), and 33.33%, 9.09%, 0%, 7.69%, and 12.5% for MoM PAPP-A below the 10th percentile (for a false positive rate of 10%), respectively. The specificity ranged from 89.57% to 95.73%, the positive predictive value from 0% to 16.67%, and the negative predictive value from 87.70% to 98.36%.

Highlights

  • The aim of our study was to assess the predictive values for hypertensive complications of pregnancy of the multiples of median (MoM) of serum pregnancy associated plasma protein A (PAPP-A), measured in 128 pregnant patients between 11 and 14 weeks gestational age

  • Maternal serum concentrations are related to subsequent fetal growth and it can be used as a diagnostic test for adverse pregnancy outcomes, including intrauterine growth restriction, premature birth, preeclampsia, and stillbirth [1]

  • The plasmatic concentrations of PAPP-A are altered in pregnant patients who will develop preeclampsia (PE), the predictive value being high especially for the preterm type 2,3

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Summary

Experimental part Materials and methods

The study included 128 pregnant patients with gestational ages between 11 weeks and 13 weeks+6 days, who were examined by ultrasound, including uterine artery Doppler, and who had the plasmatic concentration of PAPP-A determined. Plasmatic PAPP-A was determined with the ELISA Sunrise device, Tecan, Switzerland, and Pregnancy Associated Plasma Protein A reactant, MBS026323, MyBioSource, Inc., USA

Results and discussions
Family history of DM
PE Total hypertension
Conclusions
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