Double VEGF/HGF Gene Therapy in Critical Limb Ischemia Complicated by Diabetes Mellitus

J Cardiovasc Transl Res. 2021 Jun;14(3):409-415. doi: 10.1007/s12265-020-10066-9. Epub 2020 Sep 1.

Abstract

Critical leg ischemia (CLI) complicated by diabetes mellitus (DM), which is a very common and dangerous disease, represents the ultimate stage of peripheral arterial disease. Patients are treated with antiplatelet drugs, statins and limb revascularization, but a significant number of patients are not candidate for revascularization. Literature shows that in such cases, gene therapy could be a perfect therapeutic option. The aim of our study was to evaluate efficacy of double vascular endothelial growth factor/hepatocyte growth factor (VEGF/HGF) gene therapy in patients with CLI complicated by DM. We observed that 90 days after administration, serum level of VEGF and ankle-brachial index increased significantly (p < 0.001) and rest pain decreased significantly compared with the control group (p < 0.002). Moreover considerable improvement in vascularization was observed in computed tomography angiography (P = 0.04). Based on the results of this study, we suggest that the therapy with pIRES/VEGF165/HGF bicistronic plasmid administration is a safe and effective method of treatment of patients with both CLI and DM. Graphical abstract.

Keywords: Critical limb ischemia; Diabetes mellitus; Gene therapy; HGF; VEGF.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Biomarkers / blood
  • Blood Glucose / metabolism
  • Critical Illness
  • Diabetes Mellitus, Type 2 / blood
  • Diabetes Mellitus, Type 2 / genetics
  • Diabetes Mellitus, Type 2 / physiopathology
  • Diabetes Mellitus, Type 2 / therapy*
  • Female
  • Functional Status
  • Genetic Therapy*
  • Hepatocyte Growth Factor / genetics*
  • Humans
  • Internal Ribosome Entry Sites / genetics
  • Ischemia / blood
  • Ischemia / genetics
  • Ischemia / physiopathology
  • Ischemia / therapy*
  • Male
  • Middle Aged
  • Neovascularization, Physiologic*
  • Peripheral Arterial Disease / blood
  • Peripheral Arterial Disease / genetics
  • Peripheral Arterial Disease / physiopathology
  • Peripheral Arterial Disease / therapy*
  • Plasmids / genetics
  • Poland
  • Recovery of Function
  • Time Factors
  • Treatment Outcome
  • Vascular Endothelial Growth Factor A / blood
  • Vascular Endothelial Growth Factor A / genetics*

Substances

  • Biomarkers
  • Blood Glucose
  • HGF protein, human
  • Internal Ribosome Entry Sites
  • VEGFA protein, human
  • Vascular Endothelial Growth Factor A
  • Hepatocyte Growth Factor