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双胎妊娠子痫前期的孕晚期筛查:胎儿医学基金会算法、罗氏和奎德分诊法的比较性能

Third-Trimester Screening for Preeclampsia in Twins: Comparative Performance of Fetal Medicine Foundation Algorithm, Roche, and Quidel Triages.

作者信息

Walter Adeline, Geipel Annegret, Simonini Corinna, Strizek Brigitte, Sharabi-Nov Adi, Kugler Nadav, Svirsky Ran, Segal Jacob, Mor-Shalom Marina, Valinsky Lea, Naser Shaden, Abu Hamed Ramzia, Meiri Hamutal, Cuckle Howard, Maymon Ron

机构信息

Department of Obstetrics and Prenatal Medicine, University Hospital Bonn, Bonn, Germany.

BMBF Bundesministerium für Bildung und Forschung, DLR Deutsches Zentrum für Luft- und Raumfahrt, Cologne, Germany.

出版信息

Fetal Diagn Ther. 2025 Jul 28:1-13. doi: 10.1159/000546981.

Abstract

INTRODUCTION

We aimed to compare three preeclampsia screening methods in the third trimester: (a) Fetal Medicine Foundation (FMF) multi-marker algorithm (maternal factors, biophysical markers, serum placental growth factor [PlGF], and soluble fms-like tyrosine kinase-1 [sFLT-1]); (b) Roche triage (sFLT-1/PlGF), on fresh and stored samples; and (c) Quidel triage (PlGF) on stored samples.

METHODS

Women with two live fetuses were enrolled at a twin clinic at 11-13 weeks' gestation. They visited the clinic every 2-4 weeks until delivery for examination. Blood testing was conducted at enrollment in the first trimester at 11-13 weeks' gestation, and at 20-22 and 32-34 weeks' gestations. Here we evaluated the screening characteristics in the third trimester and the detection rate (DR), false-positive rate (FPR), and positive and negative predictive values (PPV and NPV) and compared the screening efficacy based on recommended cutoffs and area under the receiver operation characteristic curve (AUROC).

RESULTS

Third-trimester analysis included 146 women with twin pregnancies, of which 24 (16.4%) had preeclampsia. Preeclampsia prediction was conducted by three methods. (1) A prospective prediction was conducted on fresh samples using the FMF algorithm risk assessment in the third trimester for twin pregnancies, which had a DR of 79.2% and a FPR of 5.3%, with PPV and NPV of 76.0% and 95.5%, respectively. (2) Roche triage was tested on fresh samples prospectively using soluble fms-like tyrosine kinase-1 (sFLT-1) versus placental growth factor (PlGF), with a cutoff ratio >38, had a DR of 62.5% and a FPR of 22.1%, with PPV and NPV of 37.5% and 90.7%, respectively. In addition, we repeated the testing with Roche's Triage using stored samples and the same sFLT-1/PlGF ratio>38. (3) Quidel triage was performed retrospectively using stored samples, acting according to the definition of high risk according to PlGF <12 pg/mL and medium risk according to PlGF 12-100 pg/mL, and subsequently combined the high and medium risk groups into one. The AUROC for the FMF algorithm was 0.91 (95% CI: 0.82-0.99), which was statistically significantly higher (p < 0.0001) compared to the Roche triage of fresh samples at 0.74 (0.61-0.84) and stored samples at 0.76 (0.65-0.86). The AUROC for Quidel triage was 0.75 (0.64-0.86).

CONCLUSIONS

In twin pregnancy, the third-trimester FMF multi-marker algorithm is more effective for preeclampsia screening than Roche or Quidel triages. It is up to medical centers or professional societies to decide which preeclampsia screening method to adopt, according to local resources. This study describes the strength and limitations of each screening method.

摘要

引言

我们旨在比较孕晚期的三种子痫前期筛查方法:(a)胎儿医学基金会(FMF)多指标算法(母体因素、生物物理指标、血清胎盘生长因子[PlGF]和可溶性fms样酪氨酸激酶-1[sFLT-1]);(b)罗氏分诊法(sFLT-1/PlGF),用于新鲜样本和储存样本;(c)Quidel分诊法(PlGF),用于储存样本。

方法

怀有双活胎的女性在孕11 - 13周时在一家双胎诊所登记入组。她们每2 - 4周就诊一次直至分娩进行检查。在孕早期11 - 13周登记时、孕20 - 22周和孕32 - 34周时进行血液检测。在此,我们评估了孕晚期的筛查特征、检测率(DR)、假阳性率(FPR)以及阳性和阴性预测值(PPV和NPV),并根据推荐的临界值和受试者操作特征曲线下面积(AUROC)比较了筛查效果。

结果

孕晚期分析纳入了146例双胎妊娠女性,其中24例(16.4%)患有子痫前期。采用三种方法进行子痫前期预测。(1)在孕晚期对双胎妊娠新鲜样本使用FMF算法风险评估进行前瞻性预测,其检测率为79.2%,假阳性率为5.3%,阳性预测值和阴性预测值分别为76.0%和95.5%。(2)前瞻性地对新鲜样本使用罗氏分诊法,检测可溶性fms样酪氨酸激酶-1(sFLT-1)与胎盘生长因子(PlGF),临界比值>38,检测率为62.5%,假阳性率为22.1%,阳性预测值和阴性预测值分别为37.5%和90.7%。此外,我们使用罗氏分诊法对储存样本以相同的sFLT-1/PlGF比值>38重复检测。(3)使用储存样本对Quidel分诊法进行回顾性分析,根据PlGF<12 pg/mL定义为高风险,PlGF 12 - 100 pg/mL定义为中度风险,随后将高风险和中度风险组合为一组。FMF算法的AUROC为0.91(95%CI:0.82 - 0.99),与新鲜样本罗氏分诊法的0.74(0.61 - 0.84)和储存样本罗氏分诊法的0.76(0.65 - 0.86)相比,差异有统计学意义(p<0.0001)。Quidel分诊法的AUROC为0.75(0.64 - 0.86)。

结论

在双胎妊娠中,孕晚期FMF多指标算法对子痫前期筛查比罗氏或Quidel分诊法更有效。根据当地资源,由医疗中心或专业协会决定采用哪种子痫前期筛查方法。本研究描述了每种筛查方法的优势和局限性。

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