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Better prediction for FGR (fetal growth restriction) with the sFlt-1/PIGF ratio

机译:sFlt-1 / PIGF比值可更好地预测FGR(胎儿生长受限)

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摘要

The aim of this study was to check whether the sFlt-1/PIGF ratio, established as the biomarker for preeclampsia, reduces the false positive rate of late fetal growth restriction (FGR) detection by ultrasound biometry.This was a prospective case-control study, conducted at one regional maternity hospital in Romania. Study participants included singleton pregnancy women for whom the estimated fetal weight (EFW) at 28 to 35 weeks was < 10 percentiles and as controls, pregnant women with EFW >10 percentiles. All pregnancies were dated in the first trimester by crown-rump-length. We also recorded maternal characteristics, pregnancy and neonatal outcomes.The primary outcome measures were the relation between the sFlt-1/PIGF ratio and incidence of FGR. Secondary outcome was establishing a threshold for statistical significance of the marker and influence of other conditions (e.g., pre-eclampsia) on the accuracy of the marker in FGR prediction.Included in the study were 37 pregnant women and 37 controls.When we used ultrasound (US) biometry and maternal risk factors to estimate EFW <10 percentiles, the sensitivity was 44.4% with a specificity of 89% for an FPR (false positive result) of 10%. When we combined the US biometry and maternal risk factors with sFlt1/PIGF ratio, for a cut off of 38, the sensitivity was 84.21%, and the specificity was 84.31% for an FPR of 10%. The cut off value (36) did not change if we considered all cases of SGA, including those with associated preeclampsia or if we considered only FGR cases without associated preeclampsia.When associated with maternal factors and US biometry, the sFlt1/PIGF ratio enhanced the sensitivity for detecting late FGR.
机译:这项研究的目的是检查作为先兆子痫的生物标志物的sFlt-1 / PIGF比率是否可以降低超声生物测定法检测晚期胎儿生长受限(FGR)的假阳性率,这是一项前瞻性病例对照研究。在罗马尼亚的一家地区妇产医院进行。研究参与者包括单胎妊娠妇女,其在28至35周时的估计胎儿体重(EFW)为<10个百分点,作为对照,EFW> 10个百分点的孕妇。所有妊娠均在头三个月按冠臀长定型。我们还记录了母亲的特征,怀孕和新生儿结局。主要结局指标是sFlt-1 / PIGF比值与FGR发生率之间的关系。次要结果是确定标志物的统计显着性阈值以及其他条件(例如先兆子痫)对标志物在FGR预测中准确性的影响。该研究包括37名孕妇和37名对照。 (US)生物特征和孕产妇危险因素来估计EFW <10%,灵敏度为44.4%,FPR(假阳性结果)为10%的特异性为89%。当我们将美国生物统计学和产妇危险因素与sFlt1 / PIGF比率结合使用时,对于38的临界值,FPR为10%时,灵敏度为84.21%,特异性为84.31%。如果我们考虑所有SGA病例,包括伴有先兆子痫的病例,或者如果我们仅考虑不伴有先兆子痫的FGR病例,则临界值(36)不会改变。当与母亲因素和US生物特征学相关联时,sFlt1 / PIGF比值增强了检测晚期FGR的灵敏度。

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