Imaging of wall motion coupled with blood flow velocity in the heart and vessels in vivo: a feasibility study.

The mechanical property and geometry changes as a result of cardiovascular disease affect both the wall motion and blood flow in the heart and vessels, whereas the latter two are also coupled and therefore continuously influence one another. Simultaneous and registered imaging of both cardiovascular wall motion and blood velocity may thus contribute to more complete computational models of cardiovascular mechanical and fluid dynamics as well as provide additional diagnostic information. The objective of this paper was to determine the feasibility of imaging cardiovascular wall motion coupled with blood flow in vivo. Normal (n = 6) and infarcted (n = 5) murine left ventricles, and normal (n = 5) and aneurysmal (n = 4) murine abdominal aortas, were imaged in longitudinal views with a 30-MHz ultrasound probe. Using electrocardiogram (ECG) gating, 2-D radio-frequency (RF) data were acquired at a frame rate of 8 kHz. The axial wall velocity and blood velocity were estimated using a speckle-tracking technique. Spatially and temporally registered imaging of both cardiovascular wall motion and blood flow was shown to be feasible. Reduced wall motion was detected in the infarcted region, whereas vortex flow patterns were imaged in diastolic phases of both normal and infarcted left ventricles. The myocardial wall motion and blood flow were found to be more synchronous in the normal heart, where the blood moves toward the anteroseptal wall after the mitral valve opens (i.e., rapid filling phase), and the anteroseptal wall simultaneously undergoes outward motion. In the infarcted heart, however, in the rapid filling phase, the basal anteroseptal wall starts moving about 20 ms before the mitral valve opens and the blood enters the left ventricle. In the normal aorta, the wall motion and blood velocity were uniform and synchronous. In the aneurysmal aorta, reduced and spatially varied wall motion and vortex flow patterns in the aneurysmal sac were found. The wall motion and blood velocity were thus less synchronous in the aneurysmal aorta. Cardiovascular wall motion and blood flow were both imaged in mice in vivo. This dual information may provide important insights for the diagnosis of cardiovascular disease as well as essential parameters for its biomechanical modeling.