Key result
Cardiac Micro-computed Tomography with an iodinated contrast agent successfully quantified left ventricular ejection fraction, demonstrating a mean LVEF of 23.1% in infarcted mice versus 60.5% in a sham control.
Absolute Event Rate: 23.1% vs 60.5%
This work provides a practical guide for using high-speed MicroCT and the eXIA160 contrast agent to assess myocardial function, perfusion, and viability in mouse models.
Supports MicroCT for LVEF quantification in murine MI models; leaves open broader preclinical translation.
The use of Micro-Computed Tomography (MicroCT) for in vivo studies of small animals as models of human disease has risen tremendously due to the fact that MicroCT provides quantitative high-resolution three-dimensional (3D) anatomical data non-destructively and longitudinally. Most importantly, with the development of a novel preclinical iodinated contrast agent called eXIA160, functional and metabolic assessment of the heart became possible. However, prior to the advent of commercial MicroCT scanners equipped with X-ray flat-panel detector technology and easy-to-use cardio-respiratory gating, preclinical studies of cardiovascular disease (CVD) in small animals required a MicroCT technologist with advanced skills, and thus were impractical for widespread implementation. The goal of this work is to provide a practical guide to the use of the high-speed Quantum FX MicroCT system for comprehensive determination of myocardial global and regional function along with assessment of myocardial perfusion, metabolism and viability in healthy mice and in a cardiac ischemia mouse model induced by permanent occlusion of the left anterior descending coronary artery (LAD).
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Deel et al. (2016) studied Myocardial Infarction (Mouse Model) (n=4). Cardiac Micro-computed Tomography with iodinated contrast agent vs. Sham operation was evaluated on Left ventricular ejection fraction (LVEF). Cardiac Micro-computed Tomography with an iodinated contrast agent successfully quantified left ventricular ejection fraction, demonstrating a mean LVEF of 23.1% in infarcted mice versus 60.5% in a sham control.
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