Literature DB >> 11352080

Myocardial Doppler tissue velocity improves following myocardial gene therapy with VEGF-A165 plasmid in patients with inoperable angina pectoris.

C Sylvén1, N Sarkar, A Rück, V Drvota, S Y Hassan, B Lind, A Nygren, Q Källner, P Blomberg, J van der Linden, D Lindblom, L A Brodin, K B Islam.   

Abstract

BACKGROUND: Myocardial tissue velocity and perfusion were studied in patients with severe angina pectoris following gene therapy by intramyocardial injection of phVEGF-A165 via thoracotomy. Plasma concentrations of VEGF-A increased postoperatively. Two months after treatment anginal status and myocardial tissue velocity improved and perfusion showed a tendency to improve. Tissue velocity imaging appears to be a sensitive, objective method for detecting changes in myocardial function following gene therapy.
OBJECTIVE: To study effects on myocardial tissue velocity and perfusion in patients with angina pectoris following intramyocardial injection of phVEGF-A165 via thoracotomy.
DESIGN: Open label, phase I/II.
METHODS: Six patients with Canadian Cardiovascular Society (CCS) angina pectoris functional class III - IV and with major defects at adenosine stress single-photon emission computerized tomography (SPECT) were studied. In addition to SPECT, coronary angiography and dobutamine stress echocardiography with tissue Doppler velocity imaging were performed before and two months after gene transfer.
RESULTS: Plasma concentrations of VEGF-A increased 2 to 3 times (P < 0.04) over baseline from 2 to 14 days after injection with normalization after 4 weeks. The CCS class improved about 40%, from 3.3 +/- 0.2 to 2.0 +/- 0.3 (P < 0.02) and nitroglycerine consumption decreased 30 - 40%, from 44 +/- 17 to 15 +/- 5 tablets per week (P < 0.05). The maximal systolic myocardial tissue velocity increased in all patients about 25% (P < 0.02) but did not reach the reference range. Myocardial perfusion at SPECT improved in four of the six patients.
CONCLUSIONS: Anginal status, myocardial tissue velocity and perfusion can be improved by phVEGF-A165 intramyocardial injection. Tissue velocity imaging appears to be a sensitive, objective method for detecting changes in myocardial function following gene therapy.

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Year:  2001        PMID: 11352080     DOI: 10.1097/00019501-200105000-00010

Source DB:  PubMed          Journal:  Coron Artery Dis        ISSN: 0954-6928            Impact factor:   1.439


  6 in total

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Review 2.  Gene targeting in ischemic heart disease and failure: translational and clinical studies.

Authors:  Shaina R Eckhouse; Jeffrey A Jones; Francis G Spinale
Journal:  Biochem Pharmacol       Date:  2012-08-28       Impact factor: 5.858

3.  Protein and angiogenic dose-response expression of phVEGF-A(165) gene in rat myocardium.

Authors:  C Sylvén; N Sarkar; E Wärdell; A Jämsä; V Drvota; P Blomberg; K Bin Islam
Journal:  J Thromb Thrombolysis       Date:  2001-10       Impact factor: 2.300

4.  Sp1-dependent regulation of the RTP801 promoter and its application to hypoxia-inducible VEGF plasmid for ischemic disease.

Authors:  Minhyung Lee; Malavosklish Bikram; Seungjoon Oh; David A Bull; Sung Wan Kim
Journal:  Pharm Res       Date:  2004-05       Impact factor: 4.200

5.  Exercise training does not improve myocardial diastolic tissue velocities in Type 2 diabetes.

Authors:  Antti Loimaala; Kaj Groundstroem; Marjo Rinne; Arja Nenonen; Heini Huhtala; Ilkka Vuori
Journal:  Cardiovasc Ultrasound       Date:  2007-09-26       Impact factor: 2.062

6.  Non-viral VEGF(165) gene therapy--magnetofection of acoustically active magnetic lipospheres ('magnetobubbles') increases tissue survival in an oversized skin flap model.

Authors:  Thomas Holzbach; Dialekti Vlaskou; Iva Neshkova; Moritz A Konerding; Klaus Wörtler; Olga Mykhaylyk; Bernd Gänsbacher; H-G Machens; Christian Plank; Riccardo E Giunta
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  6 in total

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