Loading…

The significance of maternal blood pregnancy-associated plasma protein A (PAPP-A) and free beta-subunit of human chorionic gonadotropin (β-hCG) levels for the risk assessment of fetal trisomy 18 during the first prenatal testing between 11 and 13+6 weeks of pregnancy

OBJECTIVE: The aim of the study was to evaluate the significance of the maternal blood level of pregnancy-associated plasmaprotein A (PAPP-A) and free beta-subunit of human chorionic gonadotropin (β-hCG), to estimate the risk of fetal trisomy18 and their correlation with the assessment of nuchal tra...

Full description

Saved in:
Bibliographic Details
Published in:Ginekologia polska 2020, Vol.91 (12), p.748-754
Main Authors: Ziolkowska, Katarzyna, Tobola-Wrobel, Kinga, Dydowicz, Piotr, Zurawski, Sebastian, Pietryga, Marek, Wysocka, Ewa
Format: Article
Language:English
Subjects:
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:OBJECTIVE: The aim of the study was to evaluate the significance of the maternal blood level of pregnancy-associated plasmaprotein A (PAPP-A) and free beta-subunit of human chorionic gonadotropin (β-hCG), to estimate the risk of fetal trisomy18 and their correlation with the assessment of nuchal translucency (NT) during the first prenatal testing. MATERIAL AND METHODS: Examinations of 93 pregnant women between 11 and 13+6 weeks of pregnancy were conducted,which included determination of β-hCG and PAPP-A concentrations in the maternal serum and ultrasound assessment offetal nuchal translucency. Concentrations of biochemical parameters were expressed as multiples of median (MoM) for theappropriate gestational age. The risk assessment of trisomy 18 was analyzed using Astraia software. Pregnant women witha high (≥ 1:300) risk of trisomy 18 were offered a genetic amniocentesis with an examination of fetal karyotype. Twentycases were healthy and 23 with trisomy 18. RESULTS: PAPP-A and β-hCG MoM values < 0.3 were found in 61% cases of fetal trisomy 18. In 26% of cases, PAPP-A andβ-hCG MoM values < 0.2 were NT-independent risk factors for trisomy 18. There were no significant differences betweengroups with normal fetal karyotype (40%) and trisomy 18 (35%) in PAPP-A and β-hCG MoM 0.2–0.5 range. CONCLUSIONS: Maternal free β-hCG MoM was found to change parallelly to fetal NT widening in case of trisomy 18 diagnosis.Maternal β-hCG and PAPP-A MoM results presented less then 0.2 might be used independently of NT widening infetus for trisomy 18 risk evaluation. Above 0.2 for PAPP-A and β-hCG MoMs, fetal NT measurement was an requirment.
ISSN:0017-0011
2543-6767
DOI:10.5603/GP.a2020.0126