Serum levels of vascular endothelial growth factor in preeclamptic and normotensive pregnancy

Citation
A. Hunter et al., Serum levels of vascular endothelial growth factor in preeclamptic and normotensive pregnancy, HYPERTENSIO, 36(6), 2000, pp. 965-969
Citations number
23
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
HYPERTENSION
ISSN journal
0194911X → ACNP
Volume
36
Issue
6
Year of publication
2000
Pages
965 - 969
Database
ISI
SICI code
0194-911X(200012)36:6<965:SLOVEG>2.0.ZU;2-F
Abstract
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.