Systems and methods for magnetic resonance imaging
US-2024264257-A1 · Aug 8, 2024 · US
US2016187445A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016187445-A1 |
| Application number | US-201514973897-A |
| Country | US |
| Kind code | A1 |
| Filing date | Dec 18, 2015 |
| Priority date | Dec 18, 2014 |
| Publication date | Jun 30, 2016 |
| Grant date | — |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present invention provides a novel approach for CEST MR imaging, called Multi-echo Parametric VARiation Saturation (Me-PaVARS) CEST. This method places multiple image readouts in between a series of saturation pulses. The saturation pulse parameters are varied in a designated systematic pattern, which allows the generation of CEST contrast maps by encoding the patterns of signal loss into the images for better discrimination between various CEST imaging agents. The saturation parameter changes include, but are not limited to, saturation amplitude (B 1 ), saturation length (t sat ), number of pulses, shape of saturation pulses, amplitude of saturation pulses, saturation offset frequency, or a combination of these variations.
Opening claim text (preview).
1 . A method for magnetic resonance imaging of a subject comprising: using a magnetic resonance imaging machine to generate a series of saturation pulses, wherein the saturation pulses or the series of saturation pulses have varied parameters to generate CEST contrast, and wherein there are two or more series of saturation pulses; obtaining multiple signal readouts between the series of saturation pulses; and processing the multiple signal readouts into an image of the subject. 2 . The method for magnetic resonance imaging of the subject of claim 1 further comprising varying parameters chosen from a group consisting of saturation amplitude (B 1 ), saturation length (t sat ), number of pulses, shape of saturation pulses, amplitude of saturation pulses, offset frequency of saturation pulses, or a combination of these parameters. 3 . The method for magnetic resonance imaging of the subject of claim 1 further comprising using a low flip-angle gradient-echo readout. 4 . The method for magnetic resonance imaging of the subject of claim 1 further comprising using a flip back pulse in between the series of saturation pulses. 5 . The method for magnetic resonance imaging of the subject of claim 1 further comprising varying the parameters between series of saturation pulses, such that subsequent series do not have identical parameters. 6 . The method for magnetic resonance imaging of the subject of claim 1 further comprising creating saturation-transfer contrast patterns that depend on the chemical exchange properties of exchanging protons. 7 . The method for magnetic resonance imaging of the subject of claim 6 further comprising detecting saturation-contrast patterns in the resultant signal readouts. 8 . The method for magnetic resonance imaging of the subject of claim 1 further comprising processing the multiple signal readouts with at least one selected from a group consisting of fast fourier transform (FFT), the general linear model (GLM) or other signal conditioning methods. 9 . The method for magnetic resonance imaging of the subject of claim 1 further comprising delivering a CEST contrast agent to the subject or monitoring the tissue endogenous contrast without a CEST contrast agent. 10 . The method for magnetic resonance imaging of the subject of claim 1 further comprising using a non-transitory computer readable medium. 11 . A system for magnetic resonance imaging of a subject comprising: a magnetic resonance imaging machine configured to generate a series of saturation pulses, wherein the saturation pulses or the series of saturation pulses have varied parameters to generate CEST contrast, and wherein there are two or more series of saturation pulses; a non-transitory computer readable medium programmed for: obtaining multiple signal readouts between the series of saturation pulses; and processing the multiple signal readouts into an image of the subject. 12 . The system for magnetic resonance imaging of the subject of claim 11 further comprising the varied parameters being chosen from a group consisting of saturation amplitude (B 1 ), saturation length (t sat ), number of pulses, shape of saturation pulses, amplitude of saturation pulses, offset frequency of saturation pulses, or a combination of these parameters. 13 . The system for magnetic resonance imaging of the subject of claim 11 further comprising a low flip-angle gradient-echo readout. 14 . The system for magnetic resonance imaging of the subject of claim 11 further comprising the magnetic resonance imaging machine being configured for a flip back pulse in between the series of saturation pulses. 15 . The system for magnetic resonance imaging of the subject of claim 11 further comprising the varied parameters being varied between series of saturation pulses, such that subsequent series do not have identical parameters. 16 . The system for magnetic resonance imaging of the subject of claim 11 further comprising saturation-transfer contrast patterns that depend on the chemical exchange properties of exchanging protons. 17 . The system for magnetic resonance imaging of the subject of claim 16 further comprising the non-transitory computer readable medium being programmed for detecting saturation-contrast patterns in the resultant signal readouts. 18 . The system for magnetic resonance imaging of the subject of claim 11 further comprising the non-transitory computer readable medium being programmed for processing the multiple signal readouts with at least one selected from a group consisting of fast fourier transform (FFT), the general linear model (GLM) or other signal conditioning methods. 19 . The system for magnetic resonance imaging of the subject of claim 11 further comprising a CEST contrast agent delivered to the subject or monitoring the tissue endogenous contrast without a CEST contrast agent. 20 . The system for magnetic resonance imaging of the subject of claim 11 further comprising the non-transitory computer readable medium being loaded onto a computing device in communication with the magnetic resonance imaging machine.
using gradient refocusing, e.g. EPI · CPC title
involving use of a contrast agent for contrast manipulation, e.g. a paramagnetic, super-paramagnetic, ferromagnetic or hyperpolarised contrast agent · CPC title
using Fourier transforms · CPC title
involving electronic [EMR] or nuclear [NMR] magnetic resonance, e.g. magnetic resonance imaging · 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
Related publications grouped by family.
Answers are generated from the same data shown on this page.