The purpose of these studies was first to determine if vascular endothelial
growth factor (VEGF), a vascular permeability agent, is increased in the s
erum of women with preclinical and clinical preclampsia (PE), and second to
determine how these levels change after delivery. Twenty preeclamptic and
25 normotensive women at term consented to have blood taken pre- and post-d
elivery. Ten preeclamptic, 10 gestational hypertensive, and 28 normotensive
women had blood collected respectively at 12, 20, and 30 weeks gestation a
nd predelivery. Serum was extracted from all samples, and VEGF concentratio
ns were determined by radioimmunoassay. Predelivery, the median serum VEGF
concentration in the preeclamptic group was 51.7 ng/mL, and in the control
group the concentration was 13.9 ng/mL. (P<0.0001). Serum VEGF concentratio
ns fell within 24 hours of delivery in both groups, which resulted in media
n values of 3.8 ng/mL and 3.2 ng/mL respectively (P<0.3). At 12 and 20 week
s, there was no significant difference between the serum VEGF concentration
s in the 3 groups (P<0.3, 0.052 respectively). At 30 weeks, prior to the on
set of clinical PE, the serum VEGF levels in the eventual preeclamptic grou
p were elevated significantly compared with the gestational hypertensive an
d normotensive groups (P<0.001). Predelivery serum VEGF concentrations were
significantly elevated in the preecalmptic group and were similar to those
in the first study (P<0.0001). These findings suggest that VEGF may be imp
ortant in the pathophysiology of PE and has the potential to act as a precl
inical, marker for the condition.