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子痫前期的血管生成生物标志物。

Angiogenic Biomarkers in Preeclampsia.

机构信息

Division of Maternal Fetal Medicine, San Gabriel Valley Perinatal Medical Group, Pomona Valley Hospital Medical Center, Pomona, California.

出版信息

Obstet Gynecol. 2024 Apr 1;143(4):515-523. doi: 10.1097/AOG.0000000000005532. Epub 2024 Feb 13.

Abstract

Preeclampsia contributes disproportionately to maternal and neonatal morbidity and mortality throughout the world. A critical driver of preeclampsia is angiogenic imbalance, which is often present weeks to months before overt disease. Two placenta-derived angiogenic biomarkers, soluble fms-like tyrosine kinase 1 (sFlt-1) and placental growth factor (PlGF), have proved useful as diagnostic and prognostic tests for preeclampsia. Recently, the U.S. Food and Drug Administration approved the sFlt-1/PlGF assay to aid in the prediction of preeclampsia with severe features among women with hypertensive disorders of pregnancy at 24-34 weeks of gestation. In this narrative review, we summarize the body of work leading to this approval and describe how the sFlt-1/PlGF ratio may be implemented in clinical practice as an adjunctive measure to help optimize care and to reduce adverse outcomes in preeclampsia.

摘要

子痫前期在全球范围内不成比例地导致孕产妇和新生儿发病率和死亡率升高。子痫前期的一个关键驱动因素是血管生成失衡,这种失衡通常在明显疾病出现前数周到数月就存在。两种胎盘来源的血管生成生物标志物,可溶性 fms 样酪氨酸激酶 1(sFlt-1)和胎盘生长因子(PlGF),已被证明可作为子痫前期的诊断和预后检测手段。最近,美国食品和药物管理局批准了 sFlt-1/PlGF 检测,以帮助预测 24-34 孕周妊娠高血压疾病女性中严重特征的子痫前期。在本叙述性综述中,我们总结了促成这一批准的研究工作,并描述了 sFlt-1/PlGF 比值如何作为辅助措施在临床实践中实施,以帮助优化护理并减少子痫前期的不良结局。

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