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Updated: Jul 13, 2026

Fetal Echocardiography and Pulsed-wave Doppler Ultrasound in a Rabbit Model of Intrauterine Growth Restriction
Published on: June 29, 2013
Increased expression of vascular endothelial growth factor in cardiac structures of fetus with hydrops as compared to
Helen Brandenburg1, Margot M Bartelings, Lambertus J Wisse
1Department of Obstetrics and Gynecology, Erasmus Medical Center, University of Rotterdam, Rotterdam, The Netherlands. h.brrandenburg@erasmusmc.nl
Objective:
The hypothesis that severe fetal hydrops is caused by an excess of vascular endothelial growth factor (VEGF), mainly produced in the fetal heart, is tested.
Methods:
Immunohistochemical VEGF-stained postmortem biopsies from the right ventricle and right atrium of 8 hydropic fetuses were compared to those of 8 nonhydropic fetuses. The endocardium, myocardium, epicardium, endothelium, and vascular smooth muscle cells were scored on intensity of VEGF-staining. The Mann-Witney test was used to test for significancy (p < 0.05) of the differences in staining. Increased vascularization as a result of VEGF was measured in both groups by standard randomization count.
Results:
The endocardium, epicardium and endothelium of the coronary vessels showed significantly (p < 0.05) more intense VEGF-staining in the hydrops group than in the control group. The atria showed more intense staining than the ventricles in both groups. The hydropic fetuses showed a significantly increased number of coronary vessels in the myocardium. These vessels contained more blood cells than the coronary vessels in nonhydropic fetuses.
Conclusion:
The fetal heart appears to be a major source of excess VEGF in fetal hydrops.
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