Key result
Direct intramyocardial injection of phVEGF165 significantly increased maximal vasodilatation flow to the ischemic region in a porcine model compared to controls (2.16 vs 1.31; p<0.05).
Why the study?
Does direct intramyocardial injection of naked DNA encoding VEGF improve myocardial perfusion in a porcine model of chronic myocardial ischemia?
Population
36 pigs
Comparison
Direct intramyocardial injection of 500 microg… vs Direct intramyocardial injection of 200 microg…
Design
Preclinical
Authors
Loading...
Positive porcine data remain hypothesis-generating; leaves open human translation of intramyocardial VEGF gene therapy.
Does direct intramyocardial injection of naked DNA encoding VEGF improve myocardial perfusion in a porcine model of chronic myocardial ischemia?
Absolute Event Rate: 2.16% vs 1.31%
p-value: p=< 0.05
Direct intramyocardial transfection of naked DNA encoding VEGF is safe and enhances collateral formation and myocardial perfusion in a porcine model of chronic myocardial ischemia.
Tio et al. (1999) studied chronic myocardial ischemia (n=36). phVEGF165 (naked DNA encoding VEGF) vs. pCMVbeta (plasmid DNA encoding beta-galactosidase) was evaluated on Maximal vasodilatation flow to the ischemic region (p=< 0.05). Direct intramyocardial injection of phVEGF165 significantly increased maximal vasodilatation flow to the ischemic region in a porcine model compared to controls (2.16 vs 1.31; p<0.05).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: