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本文引用的文献

1
sFlt-1/PlGF for prediction of early-onset pre-eclampsia: STEPS (Study of Early Pre-eclampsia in Spain).sFlt-1/PlGF 用于预测早发型子痫前期:STEPs(西班牙子痫前期研究)。
Ultrasound Obstet Gynecol. 2017 Sep;50(3):373-382. doi: 10.1002/uog.17373.
2
Screening for pre-eclampsia using sFlt-1/PlGF ratio cut-off of 38 at 30-37 weeks' gestation.在妊娠30至37周时,使用可溶性fms样酪氨酸激酶-1(sFlt-1)/胎盘生长因子(PlGF)比值截断值38进行子痫前期筛查。
Ultrasound Obstet Gynecol. 2017 Jan;49(1):73-77. doi: 10.1002/uog.17301. Epub 2016 Dec 5.
3
sFlt-1/PlGF ratio test for pre-eclampsia: an economic assessment for the UK.用于子痫前期的可溶性血管内皮生长因子受体-1/胎盘生长因子比值检测:英国的经济评估
Ultrasound Obstet Gynecol. 2016 Dec;48(6):765-771. doi: 10.1002/uog.15997. Epub 2016 Nov 8.
4
Influence of the sFlt-1/PlGF Ratio on Clinical Decision-Making in Women with Suspected Preeclampsia.可溶性血管内皮生长因子受体-1/胎盘生长因子比值对疑似子痫前期女性临床决策的影响
PLoS One. 2016 May 31;11(5):e0156013. doi: 10.1371/journal.pone.0156013. eCollection 2016.
5
Predictive Value of the sFlt-1:PlGF Ratio in Women with Suspected Preeclampsia.sFlt-1:PlGF 比值在疑似子痫前期妇女中的预测价值。
N Engl J Med. 2016 Jan 7;374(1):13-22. doi: 10.1056/NEJMoa1414838.
6
Competing-risks model in screening for pre-eclampsia by maternal factors and biomarkers at 35-37 weeks' gestation.孕35 - 37周时,基于母体因素和生物标志物筛查子痫前期的竞争风险模型
Ultrasound Obstet Gynecol. 2016 Jul;48(1):72-9. doi: 10.1002/uog.15812. Epub 2016 May 30.
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Is It Possible to Differentiate Chronic Kidney Disease and Preeclampsia by means of New and Old Biomarkers? A Prospective Study.能否通过新旧生物标志物鉴别慢性肾病和先兆子痫?一项前瞻性研究。
Dis Markers. 2015;2015:127083. doi: 10.1155/2015/127083. Epub 2015 Oct 8.
8
Doppler Assessment of Uterine Blood Flow in Pre-eclampsia: A Review.子痫前期子宫血流的多普勒评估:综述
Hypertens Pregnancy. 2015 Nov;34(4):400-421. doi: 10.3109/10641955.2015.1074244. Epub 2015 Sep 21.
9
The definition of severe and early-onset preeclampsia. Statements from the International Society for the Study of Hypertension in Pregnancy (ISSHP).重度早发型子痫前期的定义。来自国际妊娠高血压研究学会(ISSHP)的声明。
Pregnancy Hypertens. 2013 Jan;3(1):44-7. doi: 10.1016/j.preghy.2012.11.001. Epub 2012 Nov 30.
10
Is the imbalance between pro-angiogenic and anti-angiogenic factors associated with preeclampsia?促血管生成和抗血管生成因子失衡与子痫前期有关吗?
Clin Chim Acta. 2015 Jul 20;447:34-8. doi: 10.1016/j.cca.2015.05.004. Epub 2015 May 13.

sFlt-1/PlGF 比值评估用于预测和改善子痫前期的临床管理:在一家专业围产护理中心的经验。

Evaluation of sFlt-1/PlGF Ratio for Predicting and Improving Clinical Management of Pre-eclampsia: Experience in a Specialized Perinatal Care Center.

机构信息

Department of Biochemistry, Nantes University Hospital, France.

Department of Gynecology and Obstetrics, Nantes University Hospital, Nantes, France.

出版信息

Ann Lab Med. 2018 Mar;38(2):95-101. doi: 10.3343/alm.2018.38.2.95.

DOI:10.3343/alm.2018.38.2.95
PMID:29214752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5736685/
Abstract

BACKGROUND

Management of pregnant women at high risk of pre-eclampsia (PE) requires frequent monitoring, with referral to specialized perinatal care centers. Reliable tests are necessary to improve prediction of PE and related complications and to assess disease severity and progression. An imbalance in two biomarkers, soluble fms-like tyrosine kinase 1 (sFlt-1) and placental growth factor (PlGF), is involved in PE pathogenesis. The sFlt-1 to PlGF ratio is increased in pregnant women before the onset of PE. An elevated ratio is highly predictive of PE, whereas the diagnosis of PE can be ruled out within one week for low ratios. The main objective of this study was to assess whether a low sFlt-1/PlGF ratio, below a cutoff of 38, can predict the absence of PE within one week.

METHODS

We performed a prospective, monocentric, observational study to evaluate serum sFlt-1/PlGF ratio (Roche Diagnostics Cobas e411 system) for predicting -PE in a group of 67 high-risk pregnant women (20-37 gestation weeks).

RESULTS

Among the 67 patients included, 53 had a sFlt-1/PlGF ratio lower than 38; none developed subsequent PE leading to a negative predictive value of 100%. Eight patients developed clinical PE. The positive predictive value was 21% at one week and 18% at four weeks, in accordance with previous studies.

CONCLUSIONS

The serum sFlt-1/PlGF ratio showed highly predictive performances for ruling out PE. Using these biomarkers in routine management of PE may improve clinical care and avoid inappropriate hospitalization, which has a significant economic impact.

摘要

背景

子痫前期(PE)高危孕妇的管理需要频繁监测,并转至专门的围产期护理中心。需要可靠的测试来提高对 PE 及相关并发症的预测能力,并评估疾病的严重程度和进展。两种生物标志物(可溶性 fms 样酪氨酸激酶 1(sFlt-1)和胎盘生长因子(PlGF))的失衡与 PE 的发病机制有关。在 PE 发病前,孕妇的 sFlt-1/PlGF 比值升高。比值升高高度提示存在 PE,而比值较低则可在一周内排除 PE 的诊断。本研究的主要目的是评估 sFlt-1/PlGF 比值是否低于 38(cutoff 值)是否可预测一周内无 PE。

方法

我们进行了一项前瞻性、单中心、观察性研究,以评估 67 名高危孕妇(20-37 孕周)的血清 sFlt-1/PlGF 比值(罗氏诊断 Cobas e411 系统)预测 PE 的能力。

结果

在 67 名纳入患者中,有 53 名患者的 sFlt-1/PlGF 比值低于 38,无一例随后发生导致阴性预测值为 100%的 PE。8 名患者发生临床 PE。一周和四周时的阳性预测值分别为 21%和 18%,与以往研究一致。

结论

血清 sFlt-1/PlGF 比值对排除 PE 具有高度预测性能。在 PE 的常规管理中使用这些生物标志物可能会改善临床护理并避免不必要的住院治疗,从而产生重大的经济影响。