4.7 Article

Similar Pro- and Antiangiogenic Profiles Close to Delivery in Different Clinical Presentations of Two Pregnancy Syndromes: Preeclampsia and Fetal Growth Restriction

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Publisher

MDPI
DOI: 10.3390/ijms24020972

Keywords

ischemic placental syndrome; preeclampsia; fetal growth restriction; soluble endoglin (sEng); soluble fms-like tyrosine kinase-1 (sFlt-1); placental growth factor (PlGF); sFlt-1; PlGF and sFlt-1*sEng; PlGF ratios; pregnancy adverse outcomes

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The study evaluated serum levels of anti- and pro-angiogenic substances in pregnancies complicated by different clinical subsets of placental ischemic syndrome. Lower placental growth factor levels and higher soluble endoglin levels were found in all subgroups compared to the control group. The highest levels of sFlt-1 were found in patients with preeclampsia, suggesting its role in the development of the disease. The elevated sFlt-1/PlGF ratio in fetal growth restriction (FGR) indicates its potential as a diagnostic and prognostic marker.
The purpose of this study was to evaluate serum levels of anti- and pro-angiogenic substances measured using enzyme-linked immunosorbent assays and their ratios in pregnancies complicated by different clinical subsets of placental ischemic syndrome: preeclampsia and/or fetal growth restriction. A prospective case-control study was performed consisting of 77 singleton pregnancies complicated by preeclampsia, preeclampsia with concurrent fetal growth restriction (FGR), and isolated normotensive FGR pairwise matched by gestational age with healthy pregnancies. The entire study cohort was analyzed with respect to adverse pregnancy outcomes that occurred. In all investigated subgroups, placental growth factor (PlGF) was lower and soluble endoglin (sEng), the soluble fms-like tyrosine kinase-1-sFlt-1/PlGF and sFlt-1*sEng/PlGF ratios were higher than in the control group. The differences were most strongly pronounced in the PE with concurrent FGR group and in the sFlt-1/PlGF ratio. The highest sFlt-1 values in preeclamptic patients suggest that this substance may be responsible for reaching the threshold needed for PE to develop as a maternal manifestation of ischemic placental disease. The FGR is characterized by an elevated maternal sFlt-1/PlGF ratio, which boosts at the moment of indicated delivery due to fetal risk. We concluded that angiogenic imbalance is reflective of placental disease regardless of its clinical manifestation in the mother, and may be used as support for the diagnosis and prognosis of FGR.

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