The sFlt1/PlGF ratio predicts faster fetal deterioration in early fetal growth restriction: A historical cohort study

Abstract Introduction The velocity of fetal deterioration in fetal growth restriction is extremely variable, which makes monitoring and counseling very challenging. The soluble fms‐like tyrosine kinase to placental growth factor (sFlt1/PlGF) ratio provides a readout of the vasoactive environment tha...

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Main Authors: Catarina R. Palma dos Reis, Sofia Brás, Tânia Meneses, Ana S. Cerdeira, Manu Vatish, Ana T. Martins
Format: Article
Language:English
Published: Wiley 2023-05-01
Series:Acta Obstetricia et Gynecologica Scandinavica
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Online Access:https://doi.org/10.1111/aogs.14546
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author Catarina R. Palma dos Reis
Sofia Brás
Tânia Meneses
Ana S. Cerdeira
Manu Vatish
Ana T. Martins
author_facet Catarina R. Palma dos Reis
Sofia Brás
Tânia Meneses
Ana S. Cerdeira
Manu Vatish
Ana T. Martins
author_sort Catarina R. Palma dos Reis
collection DOAJ
description Abstract Introduction The velocity of fetal deterioration in fetal growth restriction is extremely variable, which makes monitoring and counseling very challenging. The soluble fms‐like tyrosine kinase to placental growth factor (sFlt1/PlGF) ratio provides a readout of the vasoactive environment that correlates with preeclampsia and fetal growth restriction and that could be useful to predict fetal deterioration. Previous studies showed a correlation between higher sFlt1/PlGF ratios and lower gestational ages at birth, although it is unclear whether this is due to the increased incidence of preeclampsia. Our goal was to evaluate whether the sFlt1/PlGF ratio predicts faster fetal deterioration in early fetal growth restriction. Material and methods This was a historical cohort study in a tertiary maternity hospital. Data from singleton pregnancies with early fetal growth restriction (diagnosed before 32 gestational weeks) confirmed after birth monitored between January 2016 and December 2020 were retrieved from clinical files. Cases of chromosomal/fetal abnormalities, infection and medical terminations of pregnancy were excluded. The sFlt1/PlGF ratio was acquired at diagnosis of early fetal growth restriction in our unit. The correlation of log10 sFlt1/PlGF with latency to delivery/fetal demise was assessed with linear, logistic (positive sFlt1/PlGF if >85) and Cox regression excluding deliveries for maternal conditions and controlling for preeclampsia, gestational age at time of ratio test, maternal age and smoking during pregnancy. Receiver‐operating characteristic (ROC) analysis tested the performance of sFlt1/PlGF ratio in predicting delivery for fetal reasons in the following week. Results 125 patients were included. Mean sFlt1/PlGF ratio was 91.2 (SD 148.7) and 28% of patients had a positive ratio. A higher log10 sFlt1/PlGF ratio predicted shorter latency for delivery/fetal demise in linear regression after controlling for confounders, β = −3.001, (−3.713 to −2.288). Logistic regression with ratio positivity confirmed these findings (latency for delivery 5.7 ± 3.32 weeks for ratios ≤85 vs 1.9 ± 1.52 weeks for ratios >85); β = −0.698 (−1.064 to −0.332). Adjusted Cox regression showed that a positive ratio confers a significantly positive hazard ratio (HR) for earlier delivery/fetal demise, HR 9.869 (5.061–19.243). ROC analysis showed an area under the curve of 0.847 (SE ± 0.06). Conclusions sFlt1/PlGF ratio is correlated with faster fetal deterioration in early fetal growth restriction, independently of preeclampsia.
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spelling doaj-art-5feaec00299f415e993f58ecaabeab672025-08-20T02:36:39ZengWileyActa Obstetricia et Gynecologica Scandinavica0001-63491600-04122023-05-01102563564310.1111/aogs.14546The sFlt1/PlGF ratio predicts faster fetal deterioration in early fetal growth restriction: A historical cohort studyCatarina R. Palma dos Reis0Sofia Brás1Tânia Meneses2Ana S. Cerdeira3Manu Vatish4Ana T. Martins5Maternidade Dr. Alfredo da Costa Lisbon PortugalMaternidade Dr. Alfredo da Costa Lisbon PortugalMaternidade Dr. Alfredo da Costa Lisbon PortugalNuffield Department of Women's & Reproductive Health University of Oxford Oxford UKNuffield Department of Women's & Reproductive Health University of Oxford Oxford UKMaternidade Dr. Alfredo da Costa Lisbon PortugalAbstract Introduction The velocity of fetal deterioration in fetal growth restriction is extremely variable, which makes monitoring and counseling very challenging. The soluble fms‐like tyrosine kinase to placental growth factor (sFlt1/PlGF) ratio provides a readout of the vasoactive environment that correlates with preeclampsia and fetal growth restriction and that could be useful to predict fetal deterioration. Previous studies showed a correlation between higher sFlt1/PlGF ratios and lower gestational ages at birth, although it is unclear whether this is due to the increased incidence of preeclampsia. Our goal was to evaluate whether the sFlt1/PlGF ratio predicts faster fetal deterioration in early fetal growth restriction. Material and methods This was a historical cohort study in a tertiary maternity hospital. Data from singleton pregnancies with early fetal growth restriction (diagnosed before 32 gestational weeks) confirmed after birth monitored between January 2016 and December 2020 were retrieved from clinical files. Cases of chromosomal/fetal abnormalities, infection and medical terminations of pregnancy were excluded. The sFlt1/PlGF ratio was acquired at diagnosis of early fetal growth restriction in our unit. The correlation of log10 sFlt1/PlGF with latency to delivery/fetal demise was assessed with linear, logistic (positive sFlt1/PlGF if >85) and Cox regression excluding deliveries for maternal conditions and controlling for preeclampsia, gestational age at time of ratio test, maternal age and smoking during pregnancy. Receiver‐operating characteristic (ROC) analysis tested the performance of sFlt1/PlGF ratio in predicting delivery for fetal reasons in the following week. Results 125 patients were included. Mean sFlt1/PlGF ratio was 91.2 (SD 148.7) and 28% of patients had a positive ratio. A higher log10 sFlt1/PlGF ratio predicted shorter latency for delivery/fetal demise in linear regression after controlling for confounders, β = −3.001, (−3.713 to −2.288). Logistic regression with ratio positivity confirmed these findings (latency for delivery 5.7 ± 3.32 weeks for ratios ≤85 vs 1.9 ± 1.52 weeks for ratios >85); β = −0.698 (−1.064 to −0.332). Adjusted Cox regression showed that a positive ratio confers a significantly positive hazard ratio (HR) for earlier delivery/fetal demise, HR 9.869 (5.061–19.243). ROC analysis showed an area under the curve of 0.847 (SE ± 0.06). Conclusions sFlt1/PlGF ratio is correlated with faster fetal deterioration in early fetal growth restriction, independently of preeclampsia.https://doi.org/10.1111/aogs.14546fetal deteriorationfetal growth restrictionsFlt1/PlGF ratio
spellingShingle Catarina R. Palma dos Reis
Sofia Brás
Tânia Meneses
Ana S. Cerdeira
Manu Vatish
Ana T. Martins
The sFlt1/PlGF ratio predicts faster fetal deterioration in early fetal growth restriction: A historical cohort study
Acta Obstetricia et Gynecologica Scandinavica
fetal deterioration
fetal growth restriction
sFlt1/PlGF ratio
title The sFlt1/PlGF ratio predicts faster fetal deterioration in early fetal growth restriction: A historical cohort study
title_full The sFlt1/PlGF ratio predicts faster fetal deterioration in early fetal growth restriction: A historical cohort study
title_fullStr The sFlt1/PlGF ratio predicts faster fetal deterioration in early fetal growth restriction: A historical cohort study
title_full_unstemmed The sFlt1/PlGF ratio predicts faster fetal deterioration in early fetal growth restriction: A historical cohort study
title_short The sFlt1/PlGF ratio predicts faster fetal deterioration in early fetal growth restriction: A historical cohort study
title_sort sflt1 plgf ratio predicts faster fetal deterioration in early fetal growth restriction a historical cohort study
topic fetal deterioration
fetal growth restriction
sFlt1/PlGF ratio
url https://doi.org/10.1111/aogs.14546
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