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© 2006 by the American Institute of Ultrasound in Medicine
J Ultrasound Med 25:1009-1019 • 0278-4297

Cyclic Variation in Ultrasonic Myocardial Integrated Backscatter Is Due to Phasic Changes in the Number of Patent Myocardial Microvessels

Antonio Micari, MD, Marco Pascotto, MD, Ananda R. Jayaweera, PhD, Jiri Sklenar, PhD, N. Craig Goodman and Sanjiv Kaul, MD

Division of Cardiovascular Medicine, Oregon Health and Science University, Portland, Oregon USA.

Address correspondence to Sanjiv Kaul, MD, Division of Cardiovascular Medicine, Oregon Health and Science University, UHN62, 3181 Sam Jackson Park Rd, Portland, OR 97239 USA. E-mail: kauls{at}ohsu.edu

Objective. We tested the hypothesis that the cyclic variation in ultrasonic myocardial integrated backscatter (IBS) is due to cardiac contraction-induced changes in the number of patent myocardial microvessels. Methods. We performed experiments in open-chest dogs in which we increased the number of patent myocardial microvessels without changing cardiac contraction. We achieved this either by direct intracoronary administration of adenosine (group 1; n = 10) or by producing a noncritical coronary stenosis (group 2; n = 7). Results. At baseline, IBS was lowest in systole and highest in diastole. This cyclic variation in IBS was closely associated with the phasic changes in myocardial blood volume that were measured with myocardial contrast echocardiography. During adenosine administration, the diastolic IBS increased from –18.8 ± 6.5 to –17.5 ± 6.1 dB (P = .002), with an associated increase in the difference between the systolic and diastolic IBS from 3.8 ± 1.1 to 4.6 ± 1.0 dB (P = .009). After a noncritical stenosis was produced, diastolic IBS also increased from –26.6 ± 8.3 to –25.2 ± 7.3 dB (P = .001), with an associated increase in the difference between the systolic and diastolic IBS from 3.7 ± 1.2 to 5.0 ± 1.0 dB (P = .02). No change in IBS was noted in the bed that did not receive adenosine or the bed that had a stenosis. Conclusions. The variation in IBS during the cardiac cycle is closely associated with the phasic changes in myocardial blood volume seen during cardiac contraction. When the number of patent myocardial arterioles is increased via adenosine or placement of a noncritical stenosis, diastolic IBS increases with a concomitant increase in IBS cyclic variation. These results may have important clinical applications for the noninvasive diagnosis of noncritical coronary stenosis at rest.

Key Words: cardiac contraction • cyclic variation • integrated backscatter • myocardial blood volume

Abbreviations: IBS, integrated backscatter • LAD, left anterior descending coronary artery • LCx, left circumflex coronary artery • LV, left ventricular • MBF, myocardial blood flow • MBV, myocardial blood volume • MCE, myocardial contrast echocardiography • WT, wall thickening




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