Key result
Gene electro transfer of a plasmid encoding vascular endothelial growth factor significantly improved perfusion in the ischemic swine heart compared to injection alone or no treatment.
Why the study?
Does gene electro transfer of a plasmid encoding vascular endothelial growth factor improve perfusion and reduce cardiomyopathy in an ischemic swine heart model?
Does gene electro transfer of a plasmid encoding vascular endothelial growth factor improve perfusion and reduce cardiomyopathy in an ischemic swine heart model?
Absolute Event Rate: 19% vs 64.3%
p-value: p=<0.03
Gene electro transfer of a VEGF plasmid safely increases gene expression and perfusion in an ischemic swine heart model, though it did not significantly improve echocardiographic parameters over a 2-week period.
Hypothesis-generating for VEGF gene electrotransfer in ischemic heart disease; prospective human trials needed before clinical adoption.
Myocardial ischemia can damage heart muscle and reduce the heart's pumping efficiency. This study used an ischemic swine heart model to investigate the potential for gene electro transfer of a plasmid encoding vascular endothelial growth factor for improving perfusion and, thus, for reducing cardiomyopathy following acute coronary syndrome. Plasmid expression was significantly greater in gene electro transfer treated tissue compared to injection of plasmid encoding vascular endothelial growth factor alone. Higher gene expression was also seen in ischemic versus non-ischemic groups with parameters 20 Volts (p<0.03), 40 Volts (p<0.05), and 90 Volts (p<0.05), but not with 60 Volts (p<0.09) while maintaining a pulse width of 20 milliseconds. The group with gene electro transfer of plasmid encoding vascular endothelial growth factor had increased perfusion in the area at risk compared to control groups. Troponin and creatine kinase increased across all groups, suggesting equivalent ischemia in all groups prior to treatment. Echocardiography was used to assess ejection fraction, cardiac output, stroke volume, left ventricular end diastolic volume, and left ventricular end systolic volume. No statistically significant differences in these parameters were detected during a 2-week time period. However, directional trends of these variables were interesting and offer valuable information about the feasibility of gene electro transfer of vascular endothelial growth factor in the ischemic heart. The results demonstrate that gene electro transfer can be applied safely and can increase perfusion in an ischemic area. Additional study is needed to evaluate potential efficacy.
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Hargrave et al. (2014) studied Myocardial ischemia (n=70). Gene electro transfer (GET) of plasmid encoding vascular endothelial growth factor (pVEGF) vs. No treatment or pVEGF injection only was evaluated on Decrease in fluorescent intensity 2 weeks post-MI compared to pre-MI (perfusion marker) (p=<0.03). Gene electro transfer of a plasmid encoding vascular endothelial growth factor significantly improved perfusion in the ischemic swine heart compared to injection alone or no treatment.
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