Left Ventricular Electromechanical Mapping to Assess Efficacy of phVEGF 165 Gene Transfer for Therapeutic Angiogenesis in Chronic Myocardial Ischemia

Author:

Vale Peter R.1,Losordo Douglas W.1,Milliken Charles E.1,Maysky Michael1,Esakof Darryl D.1,Symes James F.1,Isner Jeffrey M.1

Affiliation:

1. From the Divisions of Cardiology and Vascular Medicine (P.R.V., D.W.L., M.M., D.D.E., J.M.I.), Cardiovascular Research (C.E.M.), and Cardiothoracic Surgery (J.F.S.), St. Elizabeth’s Medical Center and Tufts University School of Medicine, Boston, Mass.

Abstract

Background —NOGA left ventricular (LV) electromechanical mapping (EMM) can be used to distinguish among infarcted, ischemic, and normal myocardium. We investigated the use of percutaneous LV EMM to assess the efficacy of myocardial gene transfer (GTx) of naked plasmid DNA encoding for vascular endothelial growth factor (phVEGF 165 ), administered during surgery by direct myocardial injection in patients with chronic myocardial ischemia. Methods and Results —A total of 13 consecutive patients (8 men, mean age 60.1±2.3 years) with chronic stable angina due to angiographically documented coronary artery disease, all of whom had failed conventional therapy (drugs, PTCA, and/or CABG), were treated with direct myocardial injection of phVEGF 165 via a minithoracotomy. Foci of ischemic myocardium were identified on LV EMM by preserved viability associated with an impairment in linear local shortening. Myocardial viability, defined by mean unipolar and bipolar voltage recordings ≥5 and ≥2 mV, respectively, did not change significantly after GTx. Analysis of linear local shortening in areas of myocardial ischemia, however, disclosed significant improvement after (15.26±0.98%) versus before (9.94±1.53%, P =0.004) phVEGF 165 GTx. The area of ischemic myocardium was consequently reduced from 6.45±1.37 cm 2 before GTx to 0.95±0.41 cm 2 after GTx ( P =0.001). These findings corresponded to improved perfusion scores calculated from single-photon emission CT–sestamibi myocardial perfusion scans recorded at rest (7.4±2.1 before GTx versus 4.5±1.4 after GTx, P =0.009) and after pharmacological stress (12.8±2.7 before GTx versus 8.5±1.7 after GTx, P =0.047). Conclusions —The results of EMM constitute objective evidence that phVEGF 165 GTx augments perfusion of ischemic myocardium. These findings, together with reduction in the size of the defects documented at rest by serial single-photon emission CT–sestamibi imaging, suggest that phVEGF 165 GTx may successfully rescue foci of hibernating myocardium.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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