A comparison of the maternal levels of serum proprotein convertase subtilisin/kexin type 9 in pregnant women with the complication of fetal open neural tube defects

It was aimed to evaluate the levels of maternal serum proprotein convertase subtilisin/kexin type 9 (PCSK9) in pregnant women with a fetus diagnosed with open neural tube defects (NTDs). This case‐control study included 38 pregnant women carrying fetuses with open NTDs and 44 age‐matched, pregnant w...

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Veröffentlicht in:Congenital anomalies 2021-09, Vol.61 (5), p.169-176
Hauptverfasser: Erol, Seyit Ahmet, Tanacan, Atakan, Firat Oguz, Esra, Anuk, Ali Taner, Goncu Ayhan, Sule, Neselioglu, Salim, Sahin, Dilek
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container_end_page 176
container_issue 5
container_start_page 169
container_title Congenital anomalies
container_volume 61
creator Erol, Seyit Ahmet
Tanacan, Atakan
Firat Oguz, Esra
Anuk, Ali Taner
Goncu Ayhan, Sule
Neselioglu, Salim
Sahin, Dilek
description It was aimed to evaluate the levels of maternal serum proprotein convertase subtilisin/kexin type 9 (PCSK9) in pregnant women with a fetus diagnosed with open neural tube defects (NTDs). This case‐control study included 38 pregnant women carrying fetuses with open NTDs and 44 age‐matched, pregnant women with no specified risk factors. Comparisons were made of the groups in respect of demographic and clinical data and PCSK9 levels. To examine the performance of PCSK9 levels in the prediction of fetal open NTDs, receiver operating characteristic (ROC) curve analysis was used. In the first and second trimesters, PCSK9 levels were determined to be lower in the NTD group than in the control group (p = 0.010 and p = 0.015, respectively). In the first trimester, the lower PCSK9 levels in the NTD group were not statistically significant (p = 0.575). In the second trimester, the ROC curve value with the best balance of sensitivity/specificity for PCSK9 was 71.9 ng/ml (84.6% sensitivity, 51.7% specificity) and in the first and second trimester combined, 74.4 ng/ml (81.6% sensitivity, 45.5% specificity) (p = 0.015, p = 0.036, respectively). PCSK9 may be involved in the etiopathogenesis of open NTDs at the critical steps of fetal neuronal differentiation. Although it has limitations, PCSK9 may be used as an additional biomarker for the screening of NTDs.
doi_str_mv 10.1111/cga.12432
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identifier ISSN: 0914-3505
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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Biomarkers
Birth defects
Case-Control Studies
Defects
Female
Fetus
Fetuses
Humans
Kexin
Neural tube defects
Neural Tube Defects - diagnosis
Neural Tube Defects - etiology
open neural tube defects
Pregnancy
Pregnant Women
Proprotein Convertase 9 - blood
proprotein convertase subtilisin/kexin type 9
Proprotein convertases
Risk analysis
Risk factors
Sensitivity
Statistical analysis
Subtilisin
title A comparison of the maternal levels of serum proprotein convertase subtilisin/kexin type 9 in pregnant women with the complication of fetal open neural tube defects
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