Key result
VEGF therapy fails to demonstrate clinical efficacy for therapeutic vascular growth in ischemic disease.
Despite their profound effects on vascular biology, clinical trials of VEGFs for therapeutic vascular growth have not yet shown convincing efficacy, though anti-VEGF therapies highlight their role in maintaining vascular homeostasis.
Members of the vascular endothelial growth factor (VEGF) family are among the most powerful modulators of vascular biology. They regulate vasculogenesis, angiogenesis, and vascular maintenance during embryogenesis and in adults. Because of their profound effects on blood vessels, VEGFs have received much attention regarding their potential therapeutic use in cardiovascular medicine, especially for therapeutic vascular growth in myocardial and peripheral ischemia. However, completed randomized controlled VEGF trials have not provided convincing evidence of clinical efficacy. On the other hand, recent preclinical proangiogenic VEGF studies have given insight, and anti-VEGF studies have shown that the disturbance of vascular homeostasis by blocking VEGF-A may lead to endothelial dysfunction and adverse vascular effects. Excess VEGF-A may contribute to neovascularization of atherosclerotic lesions but, currently, there is no evidence that transient overexpression by gene transfer could lead to plaque destabilization. Here, we review the biology and effects of VEGFs as well as the current status of clinical applications and future perspectives of the therapeutic use of VEGFs in cardiovascular medicine.
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Ylä‐Herttuala et al. (2007) conducted a review in Myocardial and peripheral ischemia. Vascular Endothelial Growth Factors (VEGFs) was evaluated. Completed randomized controlled trials of VEGFs have not provided convincing evidence of clinical efficacy for therapeutic vascular growth in myocardial and peripheral ischemia.
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