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孕 11-13 周时通过母体因素和生物标志物筛查子痫前期。

Screening for pre-eclampsia by maternal factors and biomarkers at 11-13 weeks' gestation.

机构信息

King's College Hospital, London, UK.

King's College London, London, UK.

出版信息

Ultrasound Obstet Gynecol. 2018 Aug;52(2):186-195. doi: 10.1002/uog.19112. Epub 2018 Jul 11.

Abstract

OBJECTIVE

To examine the performance of screening for early, preterm and term pre-eclampsia (PE) at 11-13 weeks' gestation by maternal factors and combinations of mean arterial pressure (MAP), uterine artery (UtA) pulsatility index (PI), serum placental growth factor (PlGF) and serum pregnancy-associated plasma protein-A (PAPP-A).

METHODS

The data for this study were derived from three previously reported prospective non-intervention screening studies at 11 + 0 to 13 + 6 weeks' gestation in a combined total of 61 174 singleton pregnancies, including 1770 (2.9%) that developed PE. Bayes' theorem was used to combine the prior distribution of gestational age at delivery with PE, obtained from maternal characteristics, with various combinations of biomarker multiples of the median (MoM) values to derive patient-specific risks of delivery with PE at < 37 weeks' gestation. The performance of such screening was estimated.

RESULTS

In pregnancies that developed PE, compared to those without PE, the MoM values of UtA-PI and MAP were increased and those of PAPP-A and PlGF were decreased, and the deviation from normal was greater for early than late PE for all four biomarkers. Combined screening by maternal factors, UtA-PI, MAP and PlGF predicted 90% of early PE, 75% of preterm PE and 41% of term PE, at a screen-positive rate of 10%; inclusion of PAPP-A did not improve the performance of screening. The performance of screening depended on the racial origin of the women; on screening by a combination of maternal factors, MAP, UtA-PI and PlGF and using a risk cut-off of 1 in 100 for PE at < 37 weeks in Caucasian women, the screen-positive rate was 10% and detection rates for early, preterm and term PE were 88%, 69% and 40%, respectively. With the same method of screening and risk cut-off in women of Afro-Caribbean racial origin, the screen-positive rate was 34% and detection rates for early, preterm and term PE were 100%, 92% and 75%, respectively.

CONCLUSION

Screening by maternal factors and biomarkers at 11-13 weeks' gestation can identify a high proportion of pregnancies that develop early and preterm PE. © 2018 Crown copyright. Ultrasound in Obstetrics & Gynecology © 2018 ISUOG.

摘要

目的

通过母体因素和平均动脉压(MAP)、子宫动脉(UtA)搏动指数(PI)、血清胎盘生长因子(PlGF)和血清妊娠相关血浆蛋白-A(PAPP-A)的组合,研究 11-13 周妊娠时筛查早期、早产和足月子痫前期(PE)的表现。

方法

本研究的数据来自三个之前报道的前瞻性非干预性筛查研究,共纳入 61174 例单胎妊娠,在 11+0 至 13+6 周妊娠时进行,其中 1770 例(2.9%)发生 PE。贝叶斯定理用于将来自母体特征的分娩时胎龄的先验分布与从母体特征中获得的 PE 与各种生物标志物中位数倍数(MoM)值的组合相结合,以得出在<37 周妊娠时发生 PE 的患者特定风险。评估了这种筛查的性能。

结果

与未发生 PE 的妊娠相比,发生 PE 的妊娠的 UtA-PI 和 MAP 的 MoM 值增加,PAPP-A 和 PlGF 的 MoM 值降低,并且对于所有四种生物标志物,早期 PE 的偏离正常值大于晚期 PE。母体因素、UtA-PI、MAP 和 PlGF 的联合筛查预测了 90%的早期 PE、75%的早产 PE 和 41%的足月 PE,筛查阳性率为 10%;包含 PAPP-A 并没有改善筛查的性能。筛查的性能取决于女性的种族起源;在白种女性中,采用母体因素、MAP、UtA-PI 和 PlGF 的组合筛查,并将<37 周时 PE 的风险截断值设定为 1/100,筛查阳性率为 10%,早期、早产和足月 PE 的检出率分别为 88%、69%和 40%。在 Afro-Caribbean 种族起源的女性中,采用相同的筛查方法和风险截断值,筛查阳性率为 34%,早期、早产和足月 PE 的检出率分别为 100%、92%和 75%。

结论

11-13 周妊娠时通过母体因素和生物标志物筛查可识别出很大比例发生早期和早产 PE 的妊娠。©2018 英国皇家妇产科医师学院版权所有。超声医学与妇产科 ©2018 国际妇产科超声学会。

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