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(Circulation. 2004;110:1946-1952.)
© 2004 American Heart Association, Inc.
Coronary Heart Disease |
From the Department of Physiology and Biomedical Engineering (N.M.M., M.G., P.E.B., E.L.R.) and the Department of Internal Medicine, Division of Nephrology and Hypertension (L.O.L.), Mayo Clinic College of Medicine, Rochester, Minn.
Correspondence to Erik L. Ritman, MD, PhD, Department of Physiology and Biomedical Engineering, Alfred 2-409, Mayo Clinic, 200 First St SW, Rochester, MN 55905. E-mail elran{at}mayo.edu
Received June 21, 2004; revision received June 21, 2004; accepted July 23, 2004.
Background After occlusion of an epicardial artery, left ventricular (LV) dysfunction is closely related to the volume of nonperfused myocardium (NPM). The impact of coronary microembolization (ME) on LV function, however, is larger relative to the total volume of NPM. We hypothesized that the total surface area (SA), rather than the total volume, of NPM is the major determinant of ME-induced LV dysfunction.
Methods and Results We injected microspheres of 10-, 30-, or 100-µm diameter at each of 3 doses selectively into the left anterior descending coronary artery of 48 anesthetized pigs. Electron beam computed tomography (CT) was used to measure regional myocardial perfusion and changes in LV wall thickening (
WT) and stroke volume (
SV) after ME. At postmortem, a transmural "biopsy" of 1 to 2 cm3 of embolized myocardium was imaged by micro-CT, resulting in 3D images that provided volumes and SAs of the individual nonperfused foci. Additionally, in 9 pigs, creatine phosphokinase (CK) activity in embolized myocardium was measured as an index of washout of substances from the NPM. After ME,
WT,
SV, and CK washout were correlated more closely with the total SA (r=0.95, P<0.001; r=0.68, P<0.01; and r=0.88, P=0.01, respectively) than with the total NPM volume (r=0.59, P>0.05; 0.46, P>0.05; and r=0.69, P=0.04, respectively).
Conclusion After coronary ME, LV dysfunction is more closely related to the total SA than to the total volume of nonperfused microregions in the myocardium.
Key Words: microcirculation embolism infarction ventricles tomography
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