Fetal Growth Restriction Prevention: Is There a Role for Aspirin, Heparin, Statins, and Others?

Joanne Stone1

  • 1Icahn School of Medicine at Mount Sinai New York, New York USA.

PubMed

Insights

Low-dose aspirin before 16 weeks is the most effective treatment for fetal growth restriction (FGR). Other therapies are investigational, but FGR shares pathways with preeclampsia, offering early intervention opportunities.

Area of Science:

  • Obstetrics and Gynecology
  • Perinatal Medicine
  • Maternal-Fetal Medicine

Background:

  • Fetal Growth Restriction (FGR) impacts up to 10% of pregnancies, contributing significantly to perinatal complications.
  • Placental dysfunction is a key factor in FGR, leading to adverse fetal outcomes and mortality.

Purpose of the Study:

  • To review current and emerging therapeutic strategies for preventing and treating placental-mediated FGR.
  • To identify the most evidence-based interventions for FGR management.

Main Methods:

  • Literature review of studies on FGR therapies.
  • Analysis of evidence for interventions including aspirin, heparin, and novel agents.
  • Exploration of shared pathophysiology between FGR and preeclampsia.

Main Results:

  • Low-dose aspirin initiated prior to 16 weeks of gestation demonstrates the strongest evidence of efficacy.
  • Interventions such as low-molecular-weight heparin, PDE-5 inhibitors, statins, nitric oxide donors, VEGF gene therapy, melatonin, and IGF-based strategies are currently investigational.
  • Shared pathophysiological mechanisms with preeclampsia suggest potential for early intervention.

Conclusions:

  • Early initiation of low-dose aspirin is a recommended therapy for FGR.
  • Further research is needed to develop targeted therapies for improving placental function and fetal outcomes in FGR.
  • Risk stratification is crucial for optimizing FGR management and improving perinatal results.

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