TY - JOUR
T1 - Perspectives on the Use of Placental Growth Factor (PlGF) in the Prediction and Diagnosis of Pre-Eclampsia
T2 - Recent Insights and Future Steps
AU - Creswell, Lyndsay
AU - O’gorman, Neil
AU - Palmer, Kirsten Rebecca
AU - Costa, Fabricio da Silva
AU - Rolnik, Daniel Lorber
N1 - Funding Information:
Associarte Professor Kirsten Rebecca Palmer reports grants from National Health and Medical Research Council, nonfinancial support from ThermoFisher, outside the submitted work. Professor Fabricio da Silva Costa reports non-financial support from ThermoFisher, during the conduct of the study. The authors report no other conflicts of interest.
Publisher Copyright:
© 2023 Creswell et al.
PY - 2023
Y1 - 2023
N2 - Pre-eclampsia (PE) is a complex multisystem disease of pregnancy that is becoming increasingly recognized as a state of angiogenic imbalance characterized by low concentrations of placental growth factor (PlGF) and elevated soluble fms-like tyrosine kinase (sFlt-1). PlGF is a protein highly expressed by the placenta with vasculogenic and angiogenic properties, which has a central role in spiral artery remodeling and the development of a low-resistance placental capillary network. PlGF concentrations are significantly lower in women with preterm PE, and these reduced levels have been shown to precede the clinical onset of disease. Subsequently, the clinical utility of maternal serum PlGF has been extensively studied in singleton gestations from as early as 11 to 13 weeks’ gestation, utilizing a validated multimarker prediction model, which performs superiorly to the National Institute for Health and Care Excellence (NICE) and American College of Obstetricians and Gynecologists (ACOG) guidelines in the detection of preterm PE. There is extensive research highlighting the role of PlGF-based testing utilizing commercially available assays in accelerating the diagnosis of PE in symptomatic women over 20 weeks’ gestation and predicting time-to-delivery, allowing individualized risk stratification and appropriate antenatal surveillance to be determined. “Real-world” data has shown that interpretation of PlGF-based test results can aid clinicians in improving maternal outcomes and a growing body of evidence has implied a role for sFlt-1/PlGF in the prognostication of adverse pregnancy and perinatal events. Subsequently, PlGF-based testing is increasingly being implemented into obstetric practice and is advocated by NICE. This literature review aims to provide healthcare professionals with an understanding of the role of angiogenic biomarkers in PE and discuss the evidence for PlGF-based screening and triage. Prospective studies are warranted to explore if its implementation significantly improves perinatal outcomes, explore the value of repeat PlGF testing, and its use in multiple pregnancies.
AB - Pre-eclampsia (PE) is a complex multisystem disease of pregnancy that is becoming increasingly recognized as a state of angiogenic imbalance characterized by low concentrations of placental growth factor (PlGF) and elevated soluble fms-like tyrosine kinase (sFlt-1). PlGF is a protein highly expressed by the placenta with vasculogenic and angiogenic properties, which has a central role in spiral artery remodeling and the development of a low-resistance placental capillary network. PlGF concentrations are significantly lower in women with preterm PE, and these reduced levels have been shown to precede the clinical onset of disease. Subsequently, the clinical utility of maternal serum PlGF has been extensively studied in singleton gestations from as early as 11 to 13 weeks’ gestation, utilizing a validated multimarker prediction model, which performs superiorly to the National Institute for Health and Care Excellence (NICE) and American College of Obstetricians and Gynecologists (ACOG) guidelines in the detection of preterm PE. There is extensive research highlighting the role of PlGF-based testing utilizing commercially available assays in accelerating the diagnosis of PE in symptomatic women over 20 weeks’ gestation and predicting time-to-delivery, allowing individualized risk stratification and appropriate antenatal surveillance to be determined. “Real-world” data has shown that interpretation of PlGF-based test results can aid clinicians in improving maternal outcomes and a growing body of evidence has implied a role for sFlt-1/PlGF in the prognostication of adverse pregnancy and perinatal events. Subsequently, PlGF-based testing is increasingly being implemented into obstetric practice and is advocated by NICE. This literature review aims to provide healthcare professionals with an understanding of the role of angiogenic biomarkers in PE and discuss the evidence for PlGF-based screening and triage. Prospective studies are warranted to explore if its implementation significantly improves perinatal outcomes, explore the value of repeat PlGF testing, and its use in multiple pregnancies.
KW - aspirin
KW - biomarkers
KW - PlGF
KW - pre-eclampsia
KW - prediction
KW - pregnancy complications
KW - prevention
KW - screening
KW - sFlt-1
UR - http://www.scopus.com/inward/record.url?scp=85148451720&partnerID=8YFLogxK
U2 - 10.2147/IJWH.S368454
DO - 10.2147/IJWH.S368454
M3 - Review Article
C2 - 36816456
AN - SCOPUS:85148451720
SN - 1179-1411
VL - 15
SP - 255
EP - 271
JO - International Journal of Women's Health
JF - International Journal of Women's Health
ER -