PURPOSE: To visualize the hemodynamics of the intracranial arteries using time-resolved three-dimensional phase-contrast (PC)-MRI (4D-Flow). MATERIALS AND METHODS: MR examinations were performed with a 1.5T MR unit on six healthy volunteers (22-50 years old, average = 30 years). 4D-Flow was based on a radiofrequency (RF)-spoiled gradient-echo sequence, and velocity encoding (VENC) was performed along all three spatial directions. Measurements were retrospectively gated to the electrocardiogram (ECG), and cine series of three-dimensional (3D) data sets were generated. The voxel size was 1 x 1 x 1 mm, and acquisition time was 30-40 minutes. 4D data sets were calculated into time-resolved images of 3D streamlines, 3D particle traces, and 2D velocity vector fields by means of flow visualization software. RESULTS: We were able to see the 3D streamlines from the circle of Willis to the bilateral M2 segment of the middle cerebral arteries (MCAs). Time-resolved images of 3D particle traces also clearly demonstrated intracranial arterial flow dynamics. 2D velocity vector fields on the planes traversing the carotid siphon or the basilar tip were clearly visualized. These results were obtained in all six volunteers. CONCLUSION: 4D-Flow helped to elucidate the in vivo 3D hemodynamics of human intracranial arteries. This method may be a useful noninvasive means of analyzing the hemodynamics of intracranial arteries in vivo.
PURPOSE: To visualize the hemodynamics of the intracranial arteries using time-resolved three-dimensional phase-contrast (PC)-MRI (4D-Flow). MATERIALS AND METHODS: MR examinations were performed with a 1.5T MR unit on six healthy volunteers (22-50 years old, average = 30 years). 4D-Flow was based on a radiofrequency (RF)-spoiled gradient-echo sequence, and velocity encoding (VENC) was performed along all three spatial directions. Measurements were retrospectively gated to the electrocardiogram (ECG), and cine series of three-dimensional (3D) data sets were generated. The voxel size was 1 x 1 x 1 mm, and acquisition time was 30-40 minutes. 4D data sets were calculated into time-resolved images of 3D streamlines, 3D particle traces, and 2D velocity vector fields by means of flow visualization software. RESULTS: We were able to see the 3D streamlines from the circle of Willis to the bilateral M2 segment of the middle cerebral arteries (MCAs). Time-resolved images of 3D particle traces also clearly demonstrated intracranial arterial flow dynamics. 2D velocity vector fields on the planes traversing the carotid siphon or the basilar tip were clearly visualized. These results were obtained in all six volunteers. CONCLUSION: 4D-Flow helped to elucidate the in vivo 3D hemodynamics of human intracranial arteries. This method may be a useful noninvasive means of analyzing the hemodynamics of intracranial arteries in vivo.
Authors: Stephan Meckel; Lorenz Leitner; Leo H Bonati; Francesco Santini; Tilman Schubert; Aurelien F Stalder; Philippe Lyrer; Michael Markl; Stephan G Wetzel Journal: Neuroradiology Date: 2012-11-10 Impact factor: 2.804
Authors: Stephan Meckel; Aurelien F Stalder; Francesco Santini; Ernst-Wilhelm Radü; Daniel A Rüfenacht; Michael Markl; Stephan G Wetzel Journal: Neuroradiology Date: 2008-03-19 Impact factor: 2.804