Evaluation of Plaque Characteristics and Inflammation Using Magnetic Resonance Imaging

Figures

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  Figure 1. Four-dimensional (4D) flow and wall shear stress (WSS) measurements in the murine aortic arch. (A) Wall shear stress map of the aortic arch of an ApoE−/− mouse fed a Western diet, assessed with a self-gated radial 4D phase-contrast magnetic resonance imaging (PC-MRI) sequence [79]. Especially in the ascending aortic arch, a large region of low WSS can be observed in the inner curvature. This area is known to be prone to plaque development. (B) Streamline presentation of the measured flow and through plane flow for 6 exemplary analysis planes, obtained from the same 4D flow measurement [79,80].

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  Figure 2. Global and local measurements of pulse wave velocity in murine vessels. (A) Assessment of global pulse wave velocity (PWV) for exemplary measurements in the aortic arch of a wild-type and an ApoE−/− mouse. For determination of the global PWV values, the time points of the early systolic upstrokes were measured for multiple planes along the aortic arch (see Figure 1B) and plotted against the locations of the planes. The PWV is derived from the slope of a line fitted to the data points [80]. (B) Exemplary measurement of the local PWV in the abdominal aorta of a wild-type mouse using a retrospectively navigated PC-Cine MRI technique [121]. The through-plane flow (Q) and the cross-sectional areas (A) were determined. The local PWV is derived from the Q-A curve by fitting a line to the early systolic data points.

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  Figure 3. Morphology and inflammation imaging in murine atherosclerotic vessels. (A) Multispin multi echo (MSME) imaging of the ascending aorta (A) and the carotid artery (B) of an ApoE−/− mouse fed a western diet. FG: Fibrotic tissue. L: Lipid rich core. C: Calcified tissue. (C,D) 3D VCAM-1 (vascular cell adhesion molecule-1) Measurement [141]. (C) Sagittal, transverse, and coronal orientation of the aorta extracted from the radial 3D-Cine measurement (TE1 = 1.5 ms) before administration of the contrast agent (pre) and after administration of the contrast agent (post). The lines mark the slice orientations. Areas of signal cancellation due to iron particles are marked with red arrows. (D) Measurement of the aortic arch at one exemplary position (see purple line in Figure 3C). Measurement with TE1 = 1.5 ms, TE2 = 2.3 ms and map of the phase differences Φ = TE2 − TE1. No significant phase jumps can be found in the aortic vessel wall in the pre-contrast agent measurement (red arrow, pre), whereas in the phase difference map of the post-contrast agent (CA) measurement (see red arrow in bottom right image (post)), significant phase jumps are observable.