Wolfson Institute of Preventive Medicine, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, UK.
J Med Screen. 2012 Jun;19(2):60-7. doi: 10.1258/jms.2012.011114. Epub 2012 Apr 30.
To estimate the pre-eclampsia screening performance of placental growth factor (PlGF) and endoglin with second-trimester Quadruple test markers used for antenatal Down's syndrome screening.
A nested case-control study of 88 pregnant women with known early second-trimester Down's syndrome Quadruple test marker levels who subsequently developed pre-eclampsia and 275 unaffected controls. Frozen maternal serum samples were thawed and assayed for PlGF and endoglin. Monte Carlo simulation was used to estimate the pre-eclampsia screening performance of a pre-eclampsia detection algorithm using the Quadruple test markers with or without the addition of PlGF and/or endoglin.
Median PlGF was 33% lower (95% confidence interval 24-41%) and endoglin 31% (20-43%) higher in pre-eclampsia than in unaffected pregnancies. Adding PlGF to the Quadruple test markers increased the pre-eclampsia detection rate from 34% to 45% at a 5% false-positive rate - it increased it to 43% with endoglin and to 50% with both. The corresponding estimates for early pre-eclampsia (before 36 weeks' gestation) were a few percentage points higher (48%, 48% and 55% respectively). Including information on parity, pre-eclampsia in a previous pregnancy, family history (woman's mother) and assuming a pre-eclampsia prevalence of 2%, the detection rates for a 5% false-positive rate were 39% with the Quadruple test markers, 48% with addition of endoglin, 49% with addition of PlGF, and 54% with addition of both.
Adding PlGF to the Quadruple test Down's syndrome screening markers improves pre-eclampsia screening performance. There is a modest extra benefit in also adding the measurement of endoglin.
评估用于产前唐氏综合征筛查的中孕期四联试验标志物中胎盘生长因子(PlGF)和内皮下蛋白检测子痫前期的筛查性能。
一项巢式病例对照研究,纳入 88 例已知早孕期唐氏综合征四联试验标志物水平且随后发生子痫前期的孕妇(病例组)和 275 例未受影响的对照孕妇(对照组)。解冻冷冻的母血清样本,检测 PlGF 和内皮下蛋白。采用蒙特卡罗模拟方法,估计在使用四联试验标志物(添加或不添加 PlGF 和/或内皮下蛋白)的子痫前期检测算法的子痫前期筛查性能。
与未受影响的妊娠相比,子痫前期孕妇的 PlGF 中位数降低 33%(95%置信区间 24%-41%),内皮下蛋白中位数升高 31%(20%-43%)。将 PlGF 添加到四联试验标志物中,将子痫前期的检出率从 34%提高到 45%(假阳性率为 5%)-添加内皮下蛋白时提高到 43%,添加两者时提高到 50%。早发性子痫前期(36 周前)的相应估计值高几个百分点(分别为 48%、48%和 55%)。如果考虑到产妇年龄、前次妊娠子痫前期史、家族史(母亲),并假设子痫前期的患病率为 2%,则假阳性率为 5%时,四联试验标志物的检出率为 39%,添加内皮下蛋白为 48%,添加 PlGF 为 49%,添加两者为 54%。
将 PlGF 添加到四联试验唐氏综合征筛查标志物中可提高子痫前期的筛查性能。同时测量内皮下蛋白可适度提高其筛查性能。