Maymon R, Jauniaux E, Bar J, Moroz C
Felsenstein Medical Research Center, Rabin Medical Center, Petach Tikva, Israel.
Am J Perinatol. 1998;15(11):607-12. doi: 10.1055/s-2007-994078.
High levels of placental isoferritin (PLF), which is an immunosuppressive cytokine, have been demonstrated in the sera of pregnant women. In the current study, 41 pregnant patients at high risk for placento-vascular complications, such as preeclamptic toxemia (PET) and/or intrauterine growth retardation (IUGR) were preselected if abnormal uterine artery Doppler measurements appeared at the time of the 20th-22nd gestational week scan. Concomitantly, venous blood was collected from each patient. PLF serum concentrations were determined by specific enzyme-linked immunoadsorbent assay (ELISA). The PLF levels were compared to 44 healthy pregnant women at midgestation with uneventful pregnancy outcomes. The aim of the current study was to evaluate the contribution of PLF measurement in this preselected group. Following delivery, two subgroups of abnormal uterine artery Doppler waveforms were retrospectively defined. Twenty-one (51%) patients had normal outcomes, whereas 20 (49%) had pathological outcomes mainly complicated by PET and/or IUGR. Significant differences in PLF serum levels were observed between the control group (84+/-64 U/mL; median 84 U/mL) compared with those of the study subgroup with normal outcome (31+/-19 U/mL; median 23 U/mL) and with the pathological outcome subgroup (19+/-8 U/mL; median 17 U/mL) (p<0.05). Nineteen percent of the normal subgroup compared with 45% of the pathological subgroup were found to have a serum PLF concentration <19 U/mL. This cutoff level was achieved based on receiver operating characteristic (ROC) curve. The combination of abnormal uterine artery waveforms followed by low serum PLF <19 U/mL increased the positive predictive value to 63%, as compared with up to 30% positive predictive value only for the abnormal Doppler waveforms. The current preliminary results concur with previous studies suggesting that low PLF levels may reflect abnormal placentation. The exact contribution of PLF and uterine artery Doppler waveforms in monitoring patients for placento-vascular complications should be the design of a future, larger, prospective study.
胎盘异铁蛋白(PLF)是一种免疫抑制细胞因子,已证实在孕妇血清中含量较高。在本研究中,41例有胎盘血管并发症高风险的孕妇,如先兆子痫(PET)和/或宫内生长受限(IUGR),若在妊娠第20 - 22周扫描时出现子宫动脉多普勒测量异常,则被预先选定。同时,采集每位患者的静脉血。通过特异性酶联免疫吸附测定(ELISA)法测定PLF血清浓度。将PLF水平与44例妊娠中期妊娠结局正常的健康孕妇进行比较。本研究的目的是评估在该预先选定的组中测量PLF的作用。分娩后,对子宫动脉多普勒波形异常的两个亚组进行回顾性定义。21例(51%)患者结局正常,而20例(49%)患者有病理结局,主要并发PET和/或IUGR。与结局正常的研究亚组(31±19 U/mL;中位数23 U/mL)和病理结局亚组(19±8 U/mL;中位数17 U/mL)相比,对照组(84±64 U/mL;中位数84 U/mL)的PLF血清水平存在显著差异(p<0.05)。正常亚组中有19%的患者血清PLF浓度<19 U/mL,而病理亚组中有45%的患者血清PLF浓度<19 U/mL。该临界值是根据受试者工作特征(ROC)曲线确定的。子宫动脉波形异常且血清PLF<19 U/mL,其阳性预测值增至63%,而仅异常多普勒波形的阳性预测值最高为30%。目前的初步结果与先前的研究一致,表明低PLF水平可能反映胎盘形成异常。PLF和子宫动脉多普勒波形在监测胎盘血管并发症患者中的确切作用,应是未来一项更大规模前瞻性研究的设计内容。