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Shankha S. Biswas
G. Chad Hughes
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J Thorac Cardiovasc Surg 2004;127:34-43
© 2004 The American Association for Thoracic Surgery


Cardiopulmonary support and physiology

Intramyocardial and intracoronary basic fibroblast growth factor in porcine hibernating myocardium: A comparative study

Shankha S. Biswas, MDa, G. Chad Hughes, MDa, John E. Scarborough, MDa, Patrick W. Domkowski, MD, PhDa, Luis Diodato, MDa, Monica L. Smith, BSa, Carolyn Landolfo, MDb, James E. Lowe, MDa, Brian H. Annex, MDa, Kevin P. Landolfo, MDa,*

a Division of Cardiothoracic Surgery, Duke University Medical Center, Durham, NC, USA
b Division of Cardiology, Cardiology, Duke University Medical Center, Durham, NC, USA

Read at the Eighty-first Annual Meeting of The American Association for Thoracic Surgery, San Diego, Calif, May 6-9, 2001.

Received for publication February 7, 2002; revisions received June 30, 2003; accepted for publication July 10, 2003.

* Address for reprints: James E. Lowe, MD, Duke University Medical Center, Box 3954, Durham, NC 27710, USA
lowe0004{at}mc.duke.edu

OBJECTIVE: Therapeutic angiogenesis is an alternative method of revascularization for end-stage coronary artery disease. We determined the effects of intramyocardial and intracoronary basic fibroblast growth factor 2 on myocardial blood flow and function in a porcine model of hibernating myocardium.

METHODS: Twenty-four mini-swine with 90% left circumflex artery stenosis and documented hibernating myocardium by positron emission tomography and dobutamine stress echocardiography were randomized to intramyocardial basic fibroblast growth factor 2 at 0.6 µg/kg (mid-dose, n = 6, 30 injections/animal), 6 µg/kg (high-dose, n = 6, 30 injections/animal), or intramyocardial vehicle control (n = 6). The intracoronary group received 6 µg/kg basic fibroblast growth factor 2 (n = 6) into the right and left circumflex artery coronary arteries. Positron emission tomography and dobutamine stress echocardiography were repeated at 1 and 3 months.

RESULTS: In the vehicle group, normalized left circumflex artery myocardial blood flow was 0.74 ± 0.04 at 1 month and 0.75 ± 0.07 at 3 months compared with 0.68 ± 0.03 at baseline. In the intracoronary group, myocardial blood flow was 0.71 ± 0.03 at 1 month and 0.72 ± 0.04 at 3 months compared with 0.67 ± 0.04 at baseline. In the mid group, myocardial blood flow was 0.73 ± 0.06 at 1 month and 0.85 ± 0.05 at 3 months (P < .001) compared with 0.67 ± 0.04 at baseline. In the high group, myocardial blood flow was 0.81 ± 0.06 at 1 month and 0.83 ± .04 at 3 months (P = .03) compared with 0.71 ± 0.02 at baseline. No significant improvements in ischemia were demonstrated in any of the groups by dobutamine stress echocardiography at 1 or 3 months.

CONCLUSIONS: In porcine hibernating myocardium, intramyocardial basic fibroblast growth factor 2 significantly improved regional myocardial blood flow 3 months after treatment. There was no significant change in function in any of the 4 groups. These data suggest that intramyocardial dosing of basic fibroblast growth factor 2 (0.6 µg/kg) may be an optimal dose for improving perfusion in the treatment of end-stage coronary artery disease.





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