Role of soluble fms-like tyrosine kinase-1/placental growth factor ratio along with uterine artery Doppler for the prediction of pre-eclampsia – A case–control study

Sathya Jagdish, Kiruthiga T, Shruthi Prashanth, Jaya Vijayaraghavan, Sinduja Thirumanagalam Palanisamy
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Abstract

Background: Hypertensive disorders of pregnancy are becoming the leading cause of maternal morbidity and mortality worldwide and are responsible for 9–25% of deaths 1. They are believed to occur due to an imbalance between pro-angiogenic factors, like placental growth factor (PlGF) and anti-angiogenic factors, like soluble fms-like tyrosine kinase-1 (sFLT-1). Aims and Objectives: The aim of the study was to evaluate the role of the sFLT-1/PlGF ratio along with uterine artery Doppler for the prediction of pre-eclampsia (PE). Materials and Methods: The current study was a prospective case–control study conducted at Sri Ramachandra Medical College and Hospital, Chennai, from 2018 to 2020. Blood samples for sFLT-1 and PlGF and uterine artery Doppler were done in 100 pregnant mothers who are at 16–20-week gestation attending antenatal outpatient department in the Department of Obstetrics and Gynecology. Results: We found that the mean sFLT-1 in high-risk group was 826.17 ng/L (standard deviation [SD]±251.31) compared to 924.69 ng/L (SD±360.61) in low-risk groups. The mean PlGF in the high-risk group was 23.07 ng/L (SD±4.68) compared to 27.43 ng/L (SD±5.62) in low-risk group. The mean sFLT-1/PlGF ratio was increased in high-risk group of about 39.68 (SD±22.77) compared to 35 (SD±16.98) in low-risk group. Women with high resistance uterine artery Doppler have 8.5 odds of getting PE compared to those with normal uterine artery Doppler. Conclusion: According to our study, the sFLT-1/PlGF ratio carries more sensitivity (90%) and negative predictive value (74.19%) if we keep the value as 32.25 along with uterine Doppler rather than their individual values for the prediction of PE.
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可溶性酪氨酸激酶-1/胎盘生长因子比值与子宫动脉多普勒在预测先兆子痫中的作用--一项病例对照研究
背景:妊娠高血压疾病正成为全球孕产妇发病率和死亡率的主要原因,造成9%-25%的孕产妇死亡1。据认为,妊娠高血压是由于促血管生成因子(如胎盘生长因子(PlGF))和抗血管生成因子(如可溶性fms样酪氨酸激酶-1(sFLT-1))之间的失衡造成的:研究旨在评估 sFLT-1/PlGF 比值与子宫动脉多普勒在预测子痫前期(PE)中的作用:本研究是一项前瞻性病例对照研究,于 2018 年至 2020 年在钦奈 Sri Ramachandra 医学院和医院进行。我们对 100 名妊娠 16-20 周、在妇产科产前门诊就诊的孕产妇进行了 sFLT-1 和 PlGF 的血样采集以及子宫动脉多普勒检查:结果:我们发现高风险组的平均 sFLT-1 为 826.17 ng/L(标准差 [SD]±251.31),而低风险组为 924.69 ng/L(SD±360.61)。高风险组的 PlGF 平均值为 23.07 ng/L(标准差±4.68),而低风险组为 27.43 ng/L(标准差±5.62)。高风险组的 sFLT-1/PlGF 比率平均值增加了约 39.68(SD±22.77),而低风险组为 35(SD±16.98)。与子宫动脉多普勒正常的妇女相比,子宫动脉多普勒阻力大的妇女患 PE 的几率为 8.5:根据我们的研究,如果将 sFLT-1/PlGF 比值与子宫多普勒值保持在 32.25,则预测 PE 的灵敏度(90%)和阴性预测值(74.19%)均高于它们各自的值。
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