Division of Maternal-Fetal Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Am J Obstet Gynecol. 2012 Nov;207(5):407.e1-7. doi: 10.1016/j.ajog.2012.08.010. Epub 2012 Aug 10.
The purpose of this study was to examine whether longitudinally sampled maternal angiogenic concentrations predict preeclampsia.
Plasma sFlt-1 and placental growth factor (PlGF) concentrations in healthy pregnant women were quantified at 10, 17, 25, and 35 weeks' gestation. Preeclampsia was diagnosed with criteria from the American College of Obstetricians and Gynecologists.
In the first trimester, sensitivity/specificity for PlGF and sFlt-1 were 55/43% and 57/40%, respectively, and did not improve appreciably as the pregnancy progressed. Among pregnancies that later experienced preeclampsia, median PlGF was lower beginning in the second trimester, but sFlt-1 was not higher until the third trimester. Analyte positive predictive values approached 10% in the third trimester. Negative predictive values were >90% for the entire pregnancy.
Prediction of preeclampsia in early pregnancy was not possible with the use of maternal angiogenic protein concentrations. Even in late pregnancy, positive predictive values were not useful clinically. Negative predictive values are similarly unlikely to prove useful as a tool with which to a rule out suspected disease.
本研究旨在探讨是否可以通过纵向取样的母体血管生成浓度预测子痫前期。
在 10、17、25 和 35 周妊娠时定量检测健康孕妇的血浆可溶性血管内皮生长因子受体 1(sFlt-1)和胎盘生长因子(PlGF)浓度。子痫前期的诊断采用美国妇产科医师学会的标准。
在早孕期,PlGF 和 sFlt-1 的灵敏度/特异性分别为 55/43%和 57/40%,且随着妊娠的进展并未显著提高。在随后发生子痫前期的妊娠中,中位数 PlGF 从孕中期开始降低,但 sFlt-1 直到孕晚期才升高。在孕晚期,分析物的阳性预测值接近 10%。整个孕期的阴性预测值均>90%。
使用母体血管生成蛋白浓度无法预测早孕期的子痫前期。即使在孕晚期,阳性预测值在临床上也没有用处。阴性预测值也不太可能作为排除疑似疾病的工具证明有用。