OBJECTIVE The purpose of this study was to investigate the clinical signifi
cance of vascular endothelial growth factor (VEGF) in acute myocardial infa
rction (AMI). We also examined the involvement of peripheral blood mononucl
ear cells (PBMCs), which are a possible source of VEGF in AMI.
BACKGROUND VEGF is a potent endothelial cell-specific mitogen and could aff
ect the outcome of AMI.
METHODS Thirty patients with AMI were used for this study. Serum and PBMCs
were isolated from peripheral blood on days 1, 7, 14 and 21 after the onset
of AMI. PBMCs were cultured at a density of 5 x 10(6) cells/ml for 24 h. V
EGF levels in serum and the culture media were measured by enzyme-linked im
munosorbent assay using a specific anti-human VEGF antibody.
RESULTS Serum VEGF levels elevated gradually after the onset of AMI and rea
ched a peak on day 14. VEGF levels in the culture medium of PBMCs after inc
ubation for 24 h (PBMC-VEGF) were maximally elevated 7 days after the onset
, Maximum serum VEGF levels showed significant positive correlations with m
aximum creatine phosphokinase (CPK) levels (r = +0.70, p < 0.001), but maxi
mum PBMC-VEGF levels did not correlate with maximum CPK levels. Patients sh
owing improvement in left ventricular systolic function during the course o
f AMI showed significantly higher PBMC-VEGF levels than patients without im
provement.
CONCLUSIONS The extent of myocardial damage contributes to the elevation of
serum VEGF levels in AMI. VEGF produced by PBMCs may play an important rol
e in the improvement of left ventricular function by promoting angiogenesis
and reendothelialization after AMI. (C) 2000 by the American College of Ca
rdiology.