Key result
Maternal serum PCSK9 levels were significantly lower in pregnant women carrying fetuses with open neural tube defects, with a second-trimester cutoff of 71.9 ng/ml yielding 84.6% sensitivity.
Why the study?
The study was conducted to evaluate maternal serum PCSK9 levels in pregnant women carrying a fetus diagnosed with open neural tube defects.
Are maternal serum PCSK9 levels associated with fetal open neural tube defects?
Case-Control (n=82)
Are maternal serum PCSK9 levels associated with fetal open neural tube defects?
Answers are grounded in this paper and cite their sources.
Maternal serum PCSK9 levels are lower in pregnancies with fetal open neural tube defects and may serve as an additional screening biomarker.
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.
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Erol et al. (2021) conducted a case-control in Fetal open neural tube defects (NTDs) (n=82). Maternal serum PCSK9 levels vs. Age-matched pregnant women with no specified risk factors was evaluated on Maternal serum PCSK9 levels in the first and second trimesters (p=0.010). Maternal serum PCSK9 levels were significantly lower in pregnant women carrying fetuses with open neural tube defects, with a second-trimester cutoff of 71.9 ng/ml yielding 84.6% sensitivity.
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