CEST phase and magnitude imaging using a multi-parametric varied saturation scheme
US-9121917-B2 · Sep 1, 2015 · US
US10175332B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10175332-B2 |
| Application number | US-201214009551-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 2, 2012 |
| Priority date | Apr 19, 2011 |
| Publication date | Jan 8, 2019 |
| Grant date | Jan 8, 2019 |
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A method of MR imaging a moving portion of a body includes detecting a motion signal from the body while continuously subjecting the moving portion of the body to one or more preparation RF pulses; subjecting the moving portion of the body to an imaging sequence including an excitation RF pulse and switched magnetic field gradients, wherein the imaging sequence is triggered by the detected motion signal; acquiring MR signals from the moving portion of the body; and reconstructing an MR image from the acquired MR signals.
Opening claim text (preview).
The invention claimed is: 1. A method of magnetic resonance (MR) imaging a moving portion of a body, the method comprising: detecting a motion signal from the body while continuously subjecting the portion of the body to one or more preparation radio-frequency (RF) pulses; detecting a desired respiratory motion state of the moving portion of the body from the detected motion signal; subjecting the moving portion of the body to an imaging sequence comprising an excitation RF pulse and switched magnetic field gradients, wherein the imaging sequence is triggered by the detection of the desired respiratory motion state; acquiring MR signals from the moving portion of the body, wherein the MR signals are affected by one or more of the preparation RF pulses and the imaging sequence, and reconstructing an MR image from the acquired MR signals, wherein the radiation of the one or more preparation RF pulses is interrupted when the duration between two consecutive imaging sequences exceeds a pre-defined limit. 2. The method of claim 1 , wherein the desired respiratory motion state is a pre-defined motion state. 3. The method of claim 1 , wherein the motion signal is detected via a motion sensor. 4. The method of claim 1 , wherein the preparation RF pulses are: saturation RF pulses for saturating nuclear magnetization, spin locking RF pulses, polarization transfer RF pulses for transferring magnetization between different nuclear spins, or proton decoupling RF pulses. 5. The method of claim 4 , wherein the preparation RF pulses are frequency-selective saturation RF pulses for saturating nuclear magnetization of protons of an exchangeable endogenous proton pool or of a chemical-exchange saturation transfer (CEST) contrast agent. 6. The method of claim 1 , wherein: the number (N) of the repeatedly radiated preparation RF pulses are monitored, and the radiation of the preparation RF pulses is interrupted as soon as the monitored number (N) of the repeatedly radiated preparation RF pulses exceeds a pre-defined limit (N max ). 7. The method of claim 1 , wherein the preparation RF pulses are spin locking RF pulses. 8. The method of claim 1 , wherein the preparation RF pulses are polarization transfer RF pulses for transferring magnetization between different nuclear spins. 9. The method of claim 1 , wherein the preparation RF pulses are proton decoupling RF pulses. 10. The method of claim 1 , wherein the acquiring of the MR data is performed at every N th occurrence of detecting the desired respiratory motion state of the moving portion of the body for a period of time. 11. A magnetic resonance (MR) device comprising: a main magnet coil for generating a uniform, steady magnetic field within an examination volume; gradient coils for generating switched magnetic field gradients in different spatial directions within the examination volume; a radio-frequency (RF) coil for generating an excitation RF pulse within the examination volume and/or for receiving MR signals from the body of a patient positioned in the examination volume; a motion sensor which is sensitive to motion of a moving portion of the body; a controller configured to control the temporal succession of the excitation RF pulse and the switched magnetic field gradients; and a processor configured to reconstruct an MR image from the received MR signals, wherein: the controller is further configured to perform the operations of: detecting a motion signal from the body via the motion sensor while continuously subjecting the moving portion of the body to one or more preparation RF pulses; subjecting the moving portion of the body to an imaging sequence comprising the excitation RF pulse and the switched magnetic field gradients, wherein the imaging sequence is triggered by the detection of the motion signal; and interrupting the radiation of the one or more preparation RF pulses when the duration between two consecutive imaging sequences exceeds a pre-defined limit, and the processor is further configured to perform the operations of: acquiring MR signals from the moving portion of the body; and reconstructing an MR image from the acquired MR signals. 12. A non-transitory computer-readable medium comprising instructions that, when executed by a computer processor, execute a method of magnetic resonance (MR) imaging a moving portion of a body, the method comprising: detecting a motion signal from the body while continuously subjecting the moving portion of the body to one or more preparation radio-frequency (RF) pulses; detecting a desired respiratory motion state of the moving portion of the body from the detected motion signal; subjecting the moving portion of the body to an imaging sequence comprising an excitation RF pulse and switched magnetic field gradients, wherein the imaging sequence is triggered by the detection of the desired respiratory motion state; acquiring MR signals from the moving portion of the body, wherein the MR signals are affected by one or more of the preparation RF pulses and the imaging sequence, and reconstructing an MR image from the acquired MR signals, wherein the radiation of the one or more preparation RF pulses is interrupted when the duration between two consecutive imaging sequences exceeds a pre-defined limit.
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 · CPC title
by transferring coherence or polarization from a spin species to another, e.g. creating magnetization transfer contrast [MTC], polarization transfer using nuclear Overhauser enhancement [NOE] · CPC title
gated by physiological signals {, i.e. synchronization of acquired MR data with periodical motion of an object of interest, e.g. monitoring or triggering system for cardiac or respiratory gating} · CPC title
involving electronic [EMR] or nuclear [NMR] magnetic resonance, e.g. magnetic resonance imaging · CPC title
involving use of a contrast agent for contrast manipulation, e.g. a paramagnetic, super-paramagnetic, ferromagnetic or hyperpolarised contrast agent · CPC title
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