Vascular endothelial growth factor gene transfer therapy for coronary artery disease: A systematic review and

Rong Yuan1,2, Qiqi Xin2, Weili Shi2

  • 1Graduate School, Beijing University of Chinese Medicine, Beijing, China.

Insights

Vascular endothelial growth factor (VEGF) gene therapy shows promise in reducing serious cardiac events for coronary artery disease (CAD) patients. While safe and effective, particularly with adenoviral vectors, it did not impact mortality or angina scores.

Area of Science:

  • Cardiovascular Medicine
  • Gene Therapy
  • Regenerative Medicine

Background:

  • Coronary artery disease (CAD) poses a significant global health burden.
  • The efficacy of vascular endothelial growth factor (VEGF) gene transfer for improving myocardial ischemia and treating CAD remains unclear.
  • Proangiogenesis mechanisms are central to exploring novel therapeutic strategies for CAD.

Purpose of the Study:

  • To systematically review and meta-analyze randomized controlled trials (RCTs) comparing VEGF gene therapy with standard treatments in CAD patients.
  • To assess the safety and efficacy of VEGF gene therapy in improving cardiac outcomes.
  • To evaluate the impact of VEGF gene therapy on mortality, serious cardiac events, left ventricular ejection fraction (LVEF), and angina.

Main Methods:

  • Systematic literature search of PubMed, Embase, and Cochrane databases up to May 2018.
  • Inclusion of RCTs comparing VEGF gene therapy and standard care for CAD.
  • Meta-analysis using fixed and random effects models with primary outcomes of mortality and serious cardiac events, and secondary outcomes including LVEF and angina.

Main Results:

  • 14 RCTs involving 524 studies were included in the meta-analysis.
  • VEGF gene therapy significantly decreased the risk of serious cardiac events (RR: 0.56; 95% CI: 0.37, 0.84; P=0.005).
  • A slight improvement in follow-up LVEF (WMD: 1.95; 95% CI: 1.28, 2.62) was observed; adenoviral vectors showed enhanced benefits for cardiac events and LVEF, but mortality and angina scores were unchanged.

Conclusions:

  • VEGF gene therapy demonstrates safety and efficacy in reducing serious cardiac events in CAD patients.
  • Adenoviral vector-based VEGF gene therapy offers greater potential benefits.
  • Further research is warranted to fully elucidate the therapeutic potential of VEGF gene therapy in cardiovascular disease.
Abstract

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