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单胎妊娠中借助可溶性血管内皮生长因子受体-1/胎盘生长因子比值对先兆子痫进行诊断及预后评估的研究进展

Update on the Diagnosis and Prognosis of Preeclampsia with the Aid of the sFlt-1/ PlGF Ratio in Singleton Pregnancies.

作者信息

Herraiz Ignacio, Llurba Elisa, Verlohren Stefan, Galindo Alberto

机构信息

Fetal Medicine Unit, Maternal and Child Health and Development Network (SAMID-RD12/0026/0016), Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), Department of Obstetrics and Gynecology, Hospital Universitario 12 de Octubre, Universidad Complutense de Madrid, Madrid, Spain.

出版信息

Fetal Diagn Ther. 2018;43(2):81-89. doi: 10.1159/000477903. Epub 2017 Jul 19.

Abstract

Preeclampsia (PE) is involved in a group of obstetrical conditions closely related by the presence of placental dysfunction (PD), which also includes intrauterine growth restriction and placental abruption. The timely and accurate recognition and management of PE are often challenging because diagnostic criteria are still based on nonspecific signs and symptoms and because common severity criteria correlate poorly with adverse maternal and fetal outcomes. The discovery of the role of angiogenesis-related factors - soluble fms-like tyrosine kinase-1 (sFlt-1) and placental growth factor (PlGF) - in the underlying pathophysiology of PD has marked an important step for improving its early diagnosis and prognosis assessment before gestational week 34. Nowadays, an sFlt-1/PlGF ratio cutoff level of ≤38 is widely accepted for ruling out PE in patients with suspicion of the disease, and its use is cost-effective. However, the evidence is more limited regarding the management and prognosis of women with an abnormally high sFlt-1/PlGF ratio. This review summarizes the current evidence of the clinical application of the sFlt-1/PlGF ratio for the diagnosis and prognosis assessment of PE and points out the next challenges for these biomarkers, including their role as target for the development and monitoring of new therapies.

摘要

子痫前期(PE)涉及一组因胎盘功能障碍(PD)而密切相关的产科病症,胎盘功能障碍还包括胎儿生长受限和胎盘早剥。PE的及时准确识别与管理往往具有挑战性,这是因为诊断标准仍基于非特异性体征和症状,且常见的严重程度标准与孕产妇和胎儿不良结局的相关性较差。血管生成相关因子——可溶性fms样酪氨酸激酶-1(sFlt-1)和胎盘生长因子(PlGF)——在PD潜在病理生理学中的作用的发现,标志着在孕34周前改善其早期诊断和预后评估方面迈出了重要一步。如今,sFlt-1/PlGF比值截止水平≤38已被广泛接受用于排除疑似该病患者的PE,且其使用具有成本效益。然而,关于sFlt-1/PlGF比值异常升高的女性的管理和预后的证据更为有限。本综述总结了sFlt-1/PlGF比值在PE诊断和预后评估中的临床应用的当前证据,并指出了这些生物标志物未来面临的挑战,包括它们作为新疗法开发和监测靶点的作用。

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