Placental growth factor (PlGF) is an angiogenic molecule produced by the placenta and implicated in the pathogenesis of preeclampsia (PE) and intrauterine growth restriction (IUGR). We have evaluated utility and applicability of the PlGF test in a clinical setting of pregnancies at risk of PE or complicated by IUGR in order to assess its relationship with pregnancy outcomes. Seventy-three pregnancies were enrolled between 19 and 35 weeks: 57 pregnancies at risk of PE and 16 at diagnosis of IUGR. Maternal circulating PlGF levels were measured by the Triage PlGF test (Alere, San Diego, CA). Pregnancy outcomes were evaluated in relation to three categories of plasma PlGF levels: very low (<12 pg/ml), low (12–100 pg/ml) and normal (≥100 pg/ml). Uterine artery Doppler velocimetry (UADV) pulsatility index (PI) was measured in the same patients on the day of maternal sampling. Pregnancies at risk with very low plasma PlGF levels had significantly lower gestational age at delivery than patients with low or normal PlGF. The rate of emergency C-section was significantly higher in the group with PlGF <12 pg/ml. IUGR pregnancies with very low and low PlGF delivered earlier than patients with normal PlGF. All IUGR with very low and low PlGF had UADV PI > 95th percentile. Our data indicate that PlGF may provide useful information to identify fetuses requiring increased surveillance and possibly urgent delivery in pregnancies at risk of adverse outcomes. Furthermore, in IUGR, PlGF can predict adverse pregnancy outcomes that may be secondary to placental insufficiency

Cetin, I., Mazzocco, M., Giardini, V., Cardellicchio, M., Calabrese, S., Algeri, P., et al. (2017). PlGF in a clinical setting of pregnancies at risk of preeclampsia and/or intrauterine growth restriction. THE JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE, 30(2), 144-149 [10.3109/14767058.2016.1168800].

PlGF in a clinical setting of pregnancies at risk of preeclampsia and/or intrauterine growth restriction

GIARDINI, VALENTINA;ALGERI, PAOLA;VERGANI, PATRIZIA
Ultimo
2017

Abstract

Placental growth factor (PlGF) is an angiogenic molecule produced by the placenta and implicated in the pathogenesis of preeclampsia (PE) and intrauterine growth restriction (IUGR). We have evaluated utility and applicability of the PlGF test in a clinical setting of pregnancies at risk of PE or complicated by IUGR in order to assess its relationship with pregnancy outcomes. Seventy-three pregnancies were enrolled between 19 and 35 weeks: 57 pregnancies at risk of PE and 16 at diagnosis of IUGR. Maternal circulating PlGF levels were measured by the Triage PlGF test (Alere, San Diego, CA). Pregnancy outcomes were evaluated in relation to three categories of plasma PlGF levels: very low (<12 pg/ml), low (12–100 pg/ml) and normal (≥100 pg/ml). Uterine artery Doppler velocimetry (UADV) pulsatility index (PI) was measured in the same patients on the day of maternal sampling. Pregnancies at risk with very low plasma PlGF levels had significantly lower gestational age at delivery than patients with low or normal PlGF. The rate of emergency C-section was significantly higher in the group with PlGF <12 pg/ml. IUGR pregnancies with very low and low PlGF delivered earlier than patients with normal PlGF. All IUGR with very low and low PlGF had UADV PI > 95th percentile. Our data indicate that PlGF may provide useful information to identify fetuses requiring increased surveillance and possibly urgent delivery in pregnancies at risk of adverse outcomes. Furthermore, in IUGR, PlGF can predict adverse pregnancy outcomes that may be secondary to placental insufficiency
Articolo in rivista - Articolo scientifico
IUGR; preeclampsia; pregnancy outcomes; uterine artery Doppler velocimetry; Pediatrics, Perinatology and Child Health; Obstetrics and Gynecology
English
2017
30
2
144
149
none
Cetin, I., Mazzocco, M., Giardini, V., Cardellicchio, M., Calabrese, S., Algeri, P., et al. (2017). PlGF in a clinical setting of pregnancies at risk of preeclampsia and/or intrauterine growth restriction. THE JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE, 30(2), 144-149 [10.3109/14767058.2016.1168800].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/111140
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