Department of Obstetrics and Feto-Maternal Medicine Medical University of Vienna Austria.
Department of Statistics Faculty of Arts and Sciences Middle East Technical University Ankara Turkey.
J Am Heart Assoc. 2021 Sep 7;10(17):e020631. doi: 10.1161/JAHA.120.020631. Epub 2021 Aug 28.
Background Women with chronic hypertension face a 5- to 6-fold increased risk of developing preeclampsia compared with normotensive women. Angiogenic markers, especially soluble fms-like kinase 1 (sFlt-1) and placental growth factor (PlGF), were identified as clinically useful markers predicting the development of preeclampsia, but data on the prediction of superimposed preeclampsia are scarce. Therefore, we aimed to evaluate the predictive value of the sFlt-1/PlGF ratio for delivery because of superimposed preeclampsia in women with chronic hypertension. Methods and Results This retrospective study included 142 women with chronic hypertension and suspected superimposed preeclampsia. Twenty-seven women (19.0%) delivered because of maternal indications only, 17 women (12.0%) because of fetal indications primarily, and 98 women (69.0%) for other reasons. Women who both delivered because of maternal indications and for fetal indications had a significantly higher sFlt-1/PlGF ratio (median 99.9 and 120.2 versus 7.3, respectively, <0.001 for both) and lower PlGF levels (median 73.6 and 53.3 versus 320.0 pg/mL, respectively, <0.001 for both) compared with women who delivered for other reasons. SFlt-1/PlGF ratio and PlGF were strong predictors for delivery because of superimposed preeclampsia, whether for maternal or fetal indications (<0.05). Half of women with angiogenic imbalance (sFlt-1/PlGF ratio ≥85 or PlGF levels <100 pg/mL) delivered because of maternal or fetal indications within 1.6 weeks (95% CI, 1.0-2.4 weeks). Conclusions Angiogenic marker imbalance in women with suspected superimposed preeclampsia can predict delivery because of maternal and fetal indications related to superimposed preeclampsia and is associated with a significantly shorter time to delivery interval.
背景 与正常血压女性相比,患有慢性高血压的女性发生子痫前期的风险增加 5-6 倍。血管生成标志物,特别是可溶性 fms 样激酶 1(sFlt-1)和胎盘生长因子(PlGF),被鉴定为预测子痫前期发展的有用临床标志物,但关于预测子痫前期重叠的标志物数据很少。因此,我们旨在评估 sFlt-1/PlGF 比值对患有慢性高血压且疑似子痫前期重叠的女性因子痫前期重叠而分娩的预测价值。
方法和结果 这项回顾性研究纳入了 142 名患有慢性高血压且疑似子痫前期重叠的女性。27 名女性(19.0%)因母体指征而分娩,17 名女性(12.0%)因胎儿指征主要而分娩,98 名女性(69.0%)因其他原因而分娩。因母体和胎儿指征均分娩的女性 sFlt-1/PlGF 比值明显更高(中位数分别为 99.9 和 120.2 与 7.3,均 <0.001),PlGF 水平明显更低(中位数分别为 73.6 和 53.3 与 320.0 pg/mL,均 <0.001),与因其他原因分娩的女性相比。sFlt-1/PlGF 比值和 PlGF 是子痫前期重叠的强有力预测因素,无论是母体或胎儿指征(<0.05)。半数血管生成失衡(sFlt-1/PlGF 比值≥85 或 PlGF 水平 <100 pg/mL)的女性在 1.6 周内(95%CI,1.0-2.4 周)因母体或胎儿指征而分娩。
结论 在疑似子痫前期重叠的女性中,血管生成标志物失衡可预测与子痫前期重叠相关的母体和胎儿指征的分娩,并与分娩间隔明显缩短相关。