Time Resolved Spin Labeled MRI Cineangiography

• US 20110260725A1
• Filed: 04/27/2010
• Published: 10/27/2011
• Est. Priority Date: 04/27/2010
• Status: Active Grant

• Current Assignee: Northshore University Healthsystem (Advocate Aurora Health, Inc.)
• Original Assignee: Northshore University Healthsystem (Advocate Aurora Health, Inc.)
• Inventors: Koktzoglou, Ioannis, Mordini, Federico E, Edelman, Robert R.
• Granted Patent: US 8,441,257 B2
• Time in Patent Office: Days
• US Class Current: 324/309
• CPC Class Codes: G01R 33/4818 MR characterised by data acquisition along a specific k-space trajectory or by the temporal order of k-space coverage, e.g. centric or segmented coverage of k-space
• CPC Class Codes: G01R 33/5602 by filtering or weighting based on different relaxation times within the sample, e.g. T1 weighting using an inversion pulse
• CPC Class Codes: G01R 33/56325 Cine imaging
• CPC Class Codes: G01R 33/56366 Perfusion imaging
• CPC Class Codes: G01R 33/5673 Gating or triggering based on a physiological signal other than an MR signal, e.g. ECG gating or motion monitoring using optical systems for monitoring the motion of a fiducial marker

Abstract

A sequence of magnetic resonance images of the beating heart depicts the flow of blood through the heart chambers. Blood appears bright and background tissues are darkened by acquiring MR data following a preparatory pulse sequence in which spin magnetization throughout the field of view is inverted using a non-selective RF inversion pulse and spin magnetization in a selected pool of blood moving into the heart is re-inverted by a selective RF inversion pulse.

Claims

1. A method for producing a series of image frames of a moving subject using a magnetic resonance imaging (MRI) system, the steps comprising:

a) acquiring MR signals to form an image data set for each image frame by performing a pulse sequence with the MRI system, the pulse sequence including;

a)i) a preparatory pulse sequence comprised of a non-selective RF inversion pulse that inverts spin magnetization throughout the field of view of the image frames and a selective RF inversion pulse that re-inverts spin magnetization in a pool of moving spins flowing into a region of interest within a field of view of each image frame; and

a)ii) a plurality of image data acquisition pulse sequences performed in sequence after the preparatory pulse sequence to acquire the MR signals for the image data set for each image frame as the inverted spin magnetization in the field of view of each image frame recovers;

b) reconstructing the image frames from the acquired image frame data sets; and

c) displaying in sequence the reconstructed image frames to depict the flowing spins having re-inverted spin magnetization as they flow throughout the region of interest.

2. The method as recited in claim 1 in which the moving subject is a beating heart and the pool of moving spins is blood flowing into the heart.

3. The method as recited in claim 2 in which the performance of step a) is initiated by a cardiac gating signal such that each acquired image frame depicts the beating heart at a selected cardiac phase.

4. The method as recited in claim 3 in which the data acquisition in step a) is segmented such that only a portion of each image frame data set is acquired in step a)ii) and step a)i) and a)ii) are repeated to acquire the remaining portion of each image frame data set.

5. The method as recited in claim 2 in which the image frame data sets are acquired over substantially two cardiac cycles.

6. The method as recited in claim 1 in which the image data acquisition pulse sequence is a balanced, steady-state free precession pulse sequence.

7. The method as recited in claim 1 in which each image frame data set substantially under samples k-space.

8. The method as recited in claim 1 in which steps a) through c) are repeated to produce image frames in near real time.

9. The method as recited in claim 1 in which the image frame reconstruction in step b) includes:

b)i) calculating the magnitude of the MR signal at each image frame pixel; and

b)ii) controlling the brightness of each image frame pixel using the magnitude calculated in step b)i).

10. The method as recited in claim 9 in which step b) further includes:

b)iii) calculating the phase of the MR signal at each image frame pixel; and

b)iv) altering the brightness of image frame pixels produced in step b)ii) using the phase calculated in step b)iii).

11. The method as recited in claim 10 in which step b) further includes:

b)v) producing a separate phase image for each image frame using the phase information produced in step b)iii).