Reducing imaging-scan times for MRI systems
View Patent ↗Provided are methods and systems for rapid MRI imaging-scanning that provides 2D or 3D coverage, high precision, and high-temporal efficiency, without exceeding SAR limits. In one embodiment, a pulse sequence process is performed that includes a T 1ρ preparation period, followed by a very rapid image acquisition process, which acquires multiple lines of k-space data. The combination of T 1ρ preparation and acquisition of multiple lines of k-space, allows scan times to be shortened by as much as 3- or 4-fold or more, over conventional MRI scanning methods.
1. A method for magnetic resonance imaging, the method comprising:
1) generating a pulse sequence that includes a T 1ρ preparation period, including generating a series of radio frequency (RF) pulses to obtain T 1ρ contrast, comprising first preparing a spinlock pulse cluster by:
applying a first RF pulse for flipping magnetization,
applying a one or more RF pulses, with different phase combinations, to spin lock and provide the T 1ρ contrast; and
applying another RF pulse to flip the magnetization storage; then
2) applying at least one additional gradient pulse;
3) acquiring multiple lines of k-space, and restoring at least part of the T 1ρ -weighted magnetization created by the spin lock pulse cluster; and then following whole segment acquisition of the k-space,
4) allowing magnetization to relax toward thermal equilibrium for a time to restore at least partial equilibrium magnetization.
2. A method of using a T 1ρ weighted pulse sequence for magnetic resonance imaging as provided according to claim 1 , the method of use further comprising:
generating T 1ρ contrast by applying three or more RF pulses, wherein the pulses comprise a first RF pulse, followed by the application of RF spin-locking pulses of any phase, and another final RF pulse (angle α/2) prior to applying the at least one excitation pulse and acquiring the multiple lines of k-space data after application of the at least one excitation pulse.
3. The method of claim 2 , further comprising applying pre-preparation pulses, gradients and delays before preparing the T 1ρ the spinlock pulse cluster.
4. The method of claim 2 , further comprising applying post-preparation pulses, gradients and delays after the application of the T 1ρ preparation, but prior to image acquisition.
5. The method of claim 4 , wherein said spin-locking pulse may range from ±pi from the phase of the first RF pulse.
6. The method of claim 2 , further comprising applying post-image acquisition pulses, gradients, and delays.
7. The method of claim 2 , wherein the spin locking pulse may be varied in duration and amplitude.
8. A parametric map, calculated from the T 1ρ weighted pulse sequence provided by the method of claim 2 .
9. A T 1ρ dispersion map, calculated from the T 1ρ maps obtained with varying spin lock pulse amplitude pulse sequence of claim 2 .
10. The method of claim 2 , further comprising a time delay inserted after the final (α/2) pulse.
11. The method of claim 3 , further comprising a time delay inserted before a pre-preparation pulse, wherein the pre-preparation pulse is a pre-preparation saturation pulse.
12. The method of claim 11 , further comprising a time delay to reduce specific absorption rate (SAR) of a steady-state free precession pulse sequence.
13. The method of claim 2 , wherein the use of the T 1ρ -weighted pulse sequence comprises an evaluation of pathologies selected from the group consisting of cartilage pathology, arthritis, intervertebral disk pathologies, lower back pain, tumors, Alzheimer's disease, neuro-degeneration, myocardial abnormality, heart disease, and functional imaging.
14. The method of claim 1 , further comprising a time delay inserted before the pulse cluster.