血管生成生物标志物用于疑似先兆子痫单胎妊娠的随访。

IF 1.6 Q3 OBSTETRICS & GYNECOLOGY
Minerva obstetrics and gynecology Pub Date : 2023-10-01 Epub Date: 2022-06-22 DOI:10.23736/S2724-606X.22.05083-7
Cristina Gómez Fernández, Ana Otero Naveiro, Andrea Raña Mayán, Rebeca Álvarez Fernández, Rebeca Pérez Fernández, Eugenio Paz Fernández
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引用次数: 0

摘要

背景:先兆子痫(PE)是一种妊娠期高血压疾病,也是全球孕产妇和胎儿发病率和死亡率的主要原因之一。虽然根本原因尚不清楚,但妊娠早期的异常胎盘形成被认为是更严重和早发型的主要触发事件。胎盘功能不全的后果是母体循环中血管生成因子的失衡。目的是评估血管生成生物标志物sFlt-1/PlGF在先兆子痫诊断、随访和预后中的作用。方法:这是一项回顾性队列研究,包括2018年1月至2019年2月期间转诊至我院的65例疑似先兆子痫的连续单胎妊娠。PE定义为早发性(20-33+6周)和晚发性(≥34周)。主要自变量是sFlt-1/PlGF,分别在早发或晚发PE女性中分类为低。结果:14名参与者(4名早发,10名晚发)证实了PE。要求测定122 sFlt-1/PIGF比值。预测PE的最佳sFlt-1/PlGF≥86,灵敏度为93%,特异性为96%(AUC 0.95;CI 95%0.90-1.0;P结论:该生物标志物被证明可用于诊断PE和评估其预后。诊断为PE的患者并发症发生率较高,其新生儿出生体重较低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Angiogenic biomarkers for the follow-up of singleton pregnancies with suspected preeclampsia.

Background: Preeclampsia (PE) is a hypertensive disorder of pregnancy and one of the leading causes of maternal and fetal morbidity and mortality worldwide. While the underlying cause of remains unknown, abnormal placentation in early stages of pregnancy is thought to be a main triggering event for the more severe and early-onset forms. A consequence of placental insufficiency is an imbalance of angiogenic factors in the maternal circulation. The objective was to assess the utility of the angiogenic biomarker sFlt-1/PlGF for the diagnosis, follow-up and prognosis of preeclampsia.

Methods: This was a retrospective cohort study based including 65 consecutive singleton pregnancies with suspected preeclampsia referred to our hospital between January 2018 and February 2019. PE was defined as early-onset (20-33+6 weeks) and late-onset (≥34 weeks). The main independent variable was sFlt-1/PlGF classified in women with early or late onset PE, respectively, as low when <38 or <38, intermediate when 38-84 or 38-109, and high when ≥85 or ≥110.

Results: PE was confirmed in 14 (4 early-onset, 10 late-onset) of the participants. 122 sFlt-1/PIGF ratio determinations were requested. The optimal sFlt-1/PlGF to predict PE was ≥86 with a sensitivity of 93% and a specificity of 96% (AUC 0.95; CI 95% 0.90-1.0; P<0.001). A multilevel logistic model for the diagnosis of PE was adjusted for age, Body Mass Index, diabetes, proteinuria and mean arterial pressure. Women were 16.5 times (P=0.013) more likely to develop PE if they had intermediate sFlt-1/PlGF levels and 451 times (P<0.001) more likely if they had high biomarker levels compared to those with levels below 38. The probability of PE was 3.73 times (P=0.046) greater in those with maternal and/or fetal complications.

Conclusions: The biomarker proved useful to diagnose PE and assess its prognosis. Patients diagnosed with PE had a higher frequency of complications and their newborns were of lower birth weight.

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来源期刊
Minerva obstetrics and gynecology
Minerva obstetrics and gynecology OBSTETRICS & GYNECOLOGY-
CiteScore
2.90
自引率
11.10%
发文量
191
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