Chafetz Ilana, Kuhnreich Ido, Sammar Marei, Tal Yossi, Gibor Yair, Meiri Hamutal, Cuckle Howard, Wolf Myles
Diagnostic Technologies Ltd, Haifa, Israel.
Am J Obstet Gynecol. 2007 Jul;197(1):35.e1-7. doi: 10.1016/j.ajog.2007.02.025.
The purpose of this study was to evaluate first-trimester serum placental protein 13 (PP13) as a screening test for preeclampsia and intrauterine growth restriction (IUGR).
We performed a prospective, nested case-control study in the Massachusetts General Hospital Obstetric Maternal Study. PP13 was measured by solid-phase sandwich enzyme-linked immunosorbent assay in serum samples that were collected at the first prenatal visit (9-12 weeks of gestation) from women who subsequently experienced preeclampsia (n = 47), IUGR (n = 42), or preterm delivery (n = 46). Women with uncomplicated term deliveries served as control subjects (n = 290) and were matched to cases by gestational age when serum was collected and for the duration of specimen storage.
The median first-trimester PP13 level was 132.5 pg/mL in the control subjects. Median PP13 levels were significantly lower among women who had preeclampsia (27.2 pg/mL; P < .001), IUGR (86.6 pg/mL; P < .001), and preterm delivery (84.9 pg/mL; P = .007). When PP13 was expressed as multiples of the gestational age-specific medians among the control subjects, the multiples of the medians were 0.2 for preeclampsia, 0.6 for IUGR, and 0.6 for preterm delivery (P < .001 for each disorder compared with control subjects). Receiver operating characteristic analysis yielded areas under the curve of 0.91, 0.65, and 0.60 for preeclampsia, IUGR, and preterm delivery, respectively. At a 90% specificity rate, the corresponding sensitivities were 79%, 33%, and 28%, respectively.
The screening of maternal PP13 levels in the first trimester is a promising diagnostic tool for the prediction of preeclampsia with high sensitivity and specificity.
本研究旨在评估孕早期血清胎盘蛋白13(PP13)作为子痫前期和胎儿生长受限(IUGR)筛查试验的价值。
我们在马萨诸塞州总医院产科孕产妇研究中进行了一项前瞻性巢式病例对照研究。采用固相夹心酶联免疫吸附测定法,对在首次产前检查(妊娠9 - 12周)时收集的血清样本中的PP13进行检测,这些孕妇随后发生了子痫前期(n = 47)、胎儿生长受限(n = 42)或早产(n = 46)。足月顺产无并发症的孕妇作为对照(n = 290),根据血清采集时孕周以及样本储存时长与病例进行匹配。
对照组孕早期PP13水平中位数为132.5 pg/mL。子痫前期孕妇(27.2 pg/mL;P < 0.001)、胎儿生长受限孕妇(86.6 pg/mL;P < 0.001)和早产孕妇(84.9 pg/mL;P = 0.007)的PP13水平中位数显著较低。当将PP13表示为对照组中孕周特异性中位数的倍数时,子痫前期的中位数倍数为0.2,胎儿生长受限为0.6,早产为0.6(每种疾病与对照组相比,P < 0.001)。受试者工作特征分析得出,子痫前期、胎儿生长受限和早产的曲线下面积分别为0.91、0.65和0.60。在特异性为90%时,相应的敏感度分别为79%、33%和28%。
孕早期筛查母体PP13水平是一种有前景的诊断工具,可用于预测子痫前期,具有高敏感性和特异性。