Angiogenesis-Related Biomarkers (sFlt-1/PLGF) in the Prediction and Diagnosis of Placental Dysfunction: An Approach for Clinical Integration

Int J Mol Sci. 2015 Aug 13;16(8):19009-26. doi: 10.3390/ijms160819009.

Abstract

Placental dysfunction is involved in a group of obstetrical conditions including preeclampsia, intrauterine growth restriction, and placental abruption. Their timely and accurate recognition is often a challenge since diagnostic criteria are still based on nonspecific signs and symptoms. The discovering of the role of angiogenic-related factors (sFlt-1/PlGF) in the underlying pathophysiology of placental dysfunction, taking into account that angiogenesis-related biomarkers are not specific to any particular placental insufficiency-related disease, has marked an important step for improving their early diagnosis and prognosis assessment. However, sFlt-1/PlGF has not been yet established as a part of most guidelines. We will review the current evidence on the clinical utility of sFlt-1/PlGF and propose a new protocol for its clinical integration.

Keywords: PlGF; angiogenesis; intrauterine growth restriction; placental abruption; placental insufficiency; preeclampsia; sFlt-1.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Abruptio Placentae / diagnosis*
  • Abruptio Placentae / physiopathology
  • Biomarkers / analysis
  • Female
  • Fetal Growth Retardation / diagnosis*
  • Fetal Growth Retardation / physiopathology
  • Humans
  • Neovascularization, Pathologic / diagnosis*
  • Neovascularization, Pathologic / physiopathology
  • Placenta / blood supply*
  • Placenta / physiopathology
  • Placenta Growth Factor
  • Pre-Eclampsia / diagnosis*
  • Pre-Eclampsia / physiopathology
  • Pregnancy
  • Pregnancy Proteins / analysis*
  • Prognosis
  • Vascular Endothelial Growth Factor Receptor-1 / analysis*

Substances

  • Biomarkers
  • PGF protein, human
  • Pregnancy Proteins
  • Placenta Growth Factor
  • FLT1 protein, human
  • Vascular Endothelial Growth Factor Receptor-1