Department of Obstetrics and Feto-Maternal Medicine, Medical University of Vienna, Vienna, Austria.
Department of Statistics, Faculty of Arts and Sciences, Middle East Technical University, Ankara, Turkey; Department of Obstetrics and Gynecology, School of Medicine, Koç University, Istanbul, Turkey.
Am J Obstet Gynecol. 2021 Sep;225(3):305.e1-305.e14. doi: 10.1016/j.ajog.2021.03.041. Epub 2021 Apr 1.
Women with chronic hypertension are at increased risk for adverse maternal and perinatal outcomes. Maternal serum angiogenic markers, such as soluble fms-like tyrosine kinase 1 and placental growth factor, can be used to triage women with suspected preeclampsia. However, data about these markers in pregnant women with chronic hypertension are scarce.
We aimed to evaluate the predictive accuracy of maternal serum levels of soluble fms-like tyrosine kinase 1, placental growth factor, and their ratio for predicting adverse maternal and perinatal outcomes in women with chronic hypertension.
This was a retrospective analysis of prospectively collected data from January 2013 to October 2019 at the University of Vienna Hospital, Vienna, Austria. The inclusion criteria were pregnant women with chronic hypertension and suspected preeclampsia. The primary outcome of this study was the prognostic performance of angiogenic markers for the prediction of adverse maternal and perinatal outcomes in pregnant women with chronic hypertension. The accuracy of angiogenic markers for predicting adverse composite outcomes was assessed with a binomial logistic regression. The accuracy of each marker was assessed using receiver operating characteristics curves and area under the curve values. Area under the curve values were compared using De Long's test.
Of the 145 included women with chronic hypertension and suspected superimposed preeclampsia, 26 (17.9%) women developed complications (ie, composite adverse maternal or fetal outcomes) within 1 week of assessment (average gestational age at assessment, 29.9 weeks) and 35 (24.1%) developed complications at any time (average gestational age at assessment, 30.1 weeks). In women who developed complications at any time, the median maternal serum soluble fms-like tyrosine kinase-1 to placental growth factor ratio was 149.4 (interquartile range, 64.6-457.4) compared with 8.0 (interquartile range, 3.37-41.2) for women who did not develop complications (P<.001). The area under the curve values for the maternal serum soluble fms-like tyrosine kinase-1 to placental growth factor ratio Z-score (0.95; 95% confidence interval, 0.90-0.99) and placental growth factor level Z-score (0.94; 95% confidence interval, 0.88-0.99) for predicting complications within 1 week of assessment were very high. The area under the curve values for new-onset edema (0.61; 95% confidence interval, 0.52-0.70), proteinuria (0.62; 95% confidence interval, 0.52-0.71), high mean arterial pressure (0.52; 95% confidence interval, 0.50-0.54), and other symptoms of preeclampsia (0.57; 95% confidence interval, 0.49-0.65) were all significantly lower than for the angiogenic markers (P<.001 for all). Women who had an angiogenic imbalance and/or proteinuria had the highest rate of complications (28/57, 49.1%). The rate of complications in women with an angiogenic imbalance and/or proteinuria was significantly higher than in women with either proteinuria, other symptoms, or intrauterine growth restriction in the absence of an angiogenic imbalance (49.1% vs 16.7%; P=.039). The highest positive and negative predictive values for predicting adverse outcomes were demonstrated by an angiogenic imbalance and/or proteinuria criteria with a positive predictive value of 49.1% (95% confidence interval, 50.4%-57.9%) and a negative predictive value of 92% (95% confidence interval, 85.5%-95.8%). Longitudinal changes in measurements of the gestational age-corrected ratio of soluble fms-like tyrosine kinase-1 to placental growth factor up to the last measurement had a significantly higher area under the curve value than the last measurement alone (area under the curve, 0.95; 95% confidence interval, 0.92-0.99 vs 0.87; 95% confidence interval, 0.79-0.95; P=.024) CONCLUSION: Maternal serum angiogenic markers are superior to clinical assessment in predicting adverse maternal and perinatal outcomes in pregnant women with chronic hypertension. Repeated measurements of the ratio of soluble fms-like tyrosine kinase-1 to placental growth factor seems beneficial given the better predictive accuracy compared with a single measurement alone. The use of angiogenic makers should be implemented in clinical management guidelines for pregnant women with chronic hypertension.
患有慢性高血压的女性发生不良母婴和围产期结局的风险增加。母体血清血管生成标志物,如可溶性 fms 样酪氨酸激酶 1 和胎盘生长因子,可用于对疑似子痫前期的女性进行分类。然而,关于患有慢性高血压的孕妇这些标志物的数据很少。
我们旨在评估母体血清可溶性 fms 样酪氨酸激酶 1、胎盘生长因子及其比值对预测慢性高血压孕妇不良母婴和围产期结局的预测准确性。
这是一项回顾性分析,纳入了 2013 年 1 月至 2019 年 10 月在奥地利维也纳大学医院前瞻性收集的数据。纳入标准为患有慢性高血压和疑似子痫前期的孕妇。本研究的主要结局是血管生成标志物对预测慢性高血压孕妇不良母婴和围产期结局的预后表现。采用二项逻辑回归评估血管生成标志物对不良复合结局的预测准确性。采用受试者工作特征曲线和曲线下面积值评估每个标志物的准确性。采用 De Long 检验比较曲线下面积值。
在 145 名患有慢性高血压和疑似并发子痫前期的孕妇中,26 名(17.9%)孕妇在评估后 1 周内发生并发症(即复合不良母婴或胎儿结局)(平均孕龄为 29.9 周),35 名(24.1%)在任何时间发生并发症(平均孕龄为 30.1 周)。在任何时间发生并发症的女性中,母体血清可溶性 fms 样酪氨酸激酶 1 与胎盘生长因子比值中位数为 149.4(四分位距,64.6-457.4),而无并发症的女性中位数为 8.0(四分位距,3.37-41.2)(P<.001)。母体血清可溶性 fms 样酪氨酸激酶 1 与胎盘生长因子比值 Z 分数(0.95;95%置信区间,0.90-0.99)和胎盘生长因子水平 Z 分数(0.94;95%置信区间,0.88-0.99)对预测评估后 1 周内并发症的曲线下面积值非常高。新发水肿(0.61;95%置信区间,0.52-0.70)、蛋白尿(0.62;95%置信区间,0.52-0.71)、平均动脉压升高(0.52;95%置信区间,0.50-0.54)和其他子痫前期症状(0.57;95%置信区间,0.49-0.65)的曲线下面积值均明显低于血管生成标志物(均 P<.001)。存在血管生成失衡和/或蛋白尿的女性并发症发生率最高(28/57,49.1%)。存在血管生成失衡和/或蛋白尿的女性并发症发生率明显高于仅存在蛋白尿、其他症状或无血管生成失衡的胎儿宫内生长受限的女性(49.1%比 16.7%;P=.039)。以血管生成失衡和/或蛋白尿标准预测不良结局的阳性和阴性预测值最高,阳性预测值为 49.1%(95%置信区间,50.4%-57.9%),阴性预测值为 92%(95%置信区间,85.5%-95.8%)。与仅最后一次测量相比,直到最后一次测量为止,校正胎龄的可溶性 fms 样酪氨酸激酶 1 与胎盘生长因子比值的纵向变化的曲线下面积值更高(曲线下面积,0.95;95%置信区间,0.92-0.99 比 0.87;95%置信区间,0.79-0.95;P=.024)。
母体血清血管生成标志物在预测慢性高血压孕妇不良母婴和围产期结局方面优于临床评估。与单独单次测量相比,重复测量可溶性 fms 样酪氨酸激酶 1 与胎盘生长因子比值似乎具有更好的预测准确性。血管生成标志物的使用应纳入慢性高血压孕妇的临床管理指南。