Diagnosis of preeclampsia and fetal growth restriction with the sFlt-1/PlGF ratio: Diagnostic accuracy of the automated immunoassay Kryptor®

2017 ◽  
Vol 8 ◽  
pp. 31-36 ◽  
Author(s):  
Lisa Antonia Dröge ◽  
Alice Höller ◽  
Laura Ehrlich ◽  
Stefan Verlohren ◽  
Wolfgang Henrich ◽  
...  
Placenta ◽  
2021 ◽  
Vol 105 ◽  
pp. 70-77
Author(s):  
Nir Melamed ◽  
Liran Hiersch ◽  
Amir Aviram ◽  
Elad Mei-Dan ◽  
Sarah Keating ◽  
...  

BMJ Open ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. e022743 ◽  
Author(s):  
Debora Farias Batista Leite ◽  
Aude-Claire Morillon ◽  
Elias F Melo Júnior ◽  
Renato T Souza ◽  
Ali S Khashan ◽  
...  

IntroductionFetal growth restriction (FGR) is a relevant research and clinical concern since it is related to higher risks of adverse outcomes at any period of life. Current predictive tools in pregnancy (clinical factors, ultrasound scan, placenta-related biomarkers) fail to identify the true growth-restricted fetus. However, technologies based on metabolomics have generated interesting findings and seem promising. In this systematic review, we will address diagnostic accuracy of metabolomics analyses in predicting FGR.Methods and analysisOur primary outcome is small for gestational age infant, as a surrogate for FGR, defined as birth weight below the 10th centile by customised or population-based curves for gestational age. A detailed systematic literature search will be carried in electronic databases and conference abstracts, using the keywords ‘fetal growth retardation’, ‘metabolomics’, ‘pregnancy’ and ‘screening’ (and their variations). We will include original peer-reviewed articles published from 1998 to 2018, involving pregnancies of fetuses without congenital malformations; sample collection must have been performed before clinical recognition of growth impairment. If additional information is required, authors will be contacted. Reviews, case reports, cross-sectional studies, non-human research and commentaries papers will be excluded. Sample characteristics and the diagnostic accuracy data will be retrieved and analysed. If data allows, we will perform a meta-analysis.Ethics and disseminationAs this is a systematic review, no ethical approval is necessary. This protocol will be publicised in our institutional websites and results will be submitted for publication in a peer-reviewed journal.PROSPERO registration numberCRD42018089985.


2019 ◽  
Vol 17 ◽  
pp. S28-S29
Author(s):  
C. Villalaín ◽  
L. Valle ◽  
M. Mendoza ◽  
M. Vázquez-Fernández ◽  
A. Fernández Oliva ◽  
...  

2020 ◽  
Vol 20 ◽  
pp. 44-49 ◽  
Author(s):  
Elisa Simón ◽  
Ignacio Herraiz ◽  
Cecilia Villalaín ◽  
Paula Isabel Gómez-Arriaga ◽  
María Soledad Quezada ◽  
...  

2020 ◽  
Vol 56 (4) ◽  
pp. 549-556 ◽  
Author(s):  
M. S. Quezada ◽  
J. Rodríguez‐Calvo ◽  
C. Villalaín ◽  
P. I. Gómez‐Arriaga ◽  
A. Galindo ◽  
...  

Hypertension ◽  
2020 ◽  
Vol 75 (4) ◽  
pp. 918-926 ◽  
Author(s):  
Holger Stepan ◽  
Martin Hund ◽  
Theresa Andraczek

Placental dysfunction underlies a spectrum of perinatal pathologies, including preeclampsia and fetal growth restriction. Angiogenesis-related factors, including sFlt-1 (soluble fms-like tyrosine kinase 1) and PlGF (placental growth factor), play an important role in placental dysfunction; altered levels are detectable several weeks before onset of pregnancy complications. In vitro diagnostic tests for these biomarkers can improve early diagnosis and facilitate prediction of maternal and fetal outcomes. We assessed evidence for combining angiogenic biomarkers with other biomarkers or clinical parameters to predict maternal/fetal outcomes in pregnant women with placental dysfunction. Pooled information on placental perfusion (ultrasonography, mean arterial pressure), clinical characteristics, and biomarker levels (PlGF) can improve first-trimester prediction and preeclampsia diagnosis. Angiogenic factors (sFlt-1/PlGF ratio; PlGF alone) with or without clinical characteristics can facilitate second-/third-trimester prediction of early-onset and late-onset preeclampsia. A combination of increased sFlt-1/PlGF ratio and ultrasound can rule out early fetal growth restriction. The sFlt-1/PlGF ratio is also a reliable tool for discriminating between pregnancy-related hypertensive disorders, including superimposed preeclampsia and gestational hypertension. Analysis of angiogenic factors with or without uterine Doppler substantially improves sensitivity and specificity for predicting adverse outcomes and iatrogenic preterm delivery. We propose to extend the American College of Obstetricians and Gynecologists definition of preeclampsia in the future to include the combination of new-onset hypertension and new-onset of altered angiogenic factors (sFlt-1/PlGF ratio or PlGF alone). In summary, altered angiogenic biomarkers indicate placental dysfunction, and their implementation into clinical practice will help reduce the considerable burden of morbidity and mortality associated with adverse pregnancy outcomes as a consequence of angiogenic-placental syndrome.


2019 ◽  
Vol 54 (S1) ◽  
pp. 115-116
Author(s):  
M.S. Quezada ◽  
I. Herraiz ◽  
C. Villalain ◽  
E. Simón ◽  
P.I. Gómez‐Arriaga ◽  
...  

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