Background Collateral growth is induced by chemical signals from the i
schemic myocardium. We hypothesized that angiogenic growth factors are
produced by cardiac tissue; they are diffusible, more concentrated in
pericardial fluids, and are increased by myocardial ischemia. Methods
and Results With the use of an enzyme-linked immunosorbent assay, we
measured the concentrations of basic fibroblast growth factor (bFGF) a
nd vascular endothelial growth factor (VEGF) in pericardial fluids of
12 patients with unstable angina (group 1) and of 8 patients with noni
schemic heart diseases (group 2). The levels of protein in pericardial
fluids were quite comparable between the two groups (34+/-2 versus 32
+/-4 mg/mL). The concentration of bFGF in pericardial fluids in group
1 was 2036+/-357 pg/mL, significantly (P <.001) higher than the 289+/-
72 pg/mL in group 2. The amount of bFGF per milligram of protein was a
lso significantly (P <.05) higher in group 1 than in group 2 (67+/-15
versus 12+/-4 pg/mg). The concentration of VEGF in pericardial fluids
tended to be higher in group 1, but the difference was statistically i
nsignificant (39+/-7 versus 22+/-6 pg/mL). The amount of VEGF per mill
igram of protein was 1.2+/-0.3 pg/mg in group 1, similar to the 0.8+/-
0.4 pg/mg in group 2. Conclusions This finding provides new evidence t
hat bFGF plays an important role in mediating collateral growth in hum
ans.