DIFFERENTIATED TISSUE EXCITATION IN MRI
20170299678 · 2017-10-19
Inventors
Cpc classification
G01R33/543
PHYSICS
G01R33/561
PHYSICS
A61B5/055
HUMAN NECESSITIES
G01R33/485
PHYSICS
G01R33/5607
PHYSICS
International classification
A61B5/055
HUMAN NECESSITIES
Abstract
Selectively exciting bulk protons in certain tissue components, e.g. water, while suppressing the excitation of others, e.g. fat, can lead to images with better contrast for desired features. The invention provides binomial, off-resonance RF excitation pulses for differentiating tissue excitation that yields a larger fat suppression that prior art water excitation methods. Proper balancing of the frequency offset and the pulse duration with a relative phase offset between the pulses leads to large-bandwidth pass- and stopbands for water and fat, respectively. The pulses can be applied with short, or even zero, interpulse delay, leading to substantial time savings in the imaging sequence.
Claims
1. A method for differentiating tissue excitation in magnetic resonance imaging (MRI), comprising applying during an image acquisition sequence of an MRI system first and second radio-frequency (RF) excitation pulses, where the first and second pulses are off-resonance to protons in a tissue component to be excited by having a central frequency, f, offset from a central resonance frequency of protons in the tissue component to be excited, f.sub.e, by a predetermined frequency offset, Δf, in a direction away from a central resonance frequency of protons in a tissue component to be suppressed, f.sub.s, where the first and second pulses have the same RF excitation angle, α, and respective phases, φ.sub.1 and φ.sub.2, characterized in that: a phase shift between the pulses is related to the frequency offset, Δf, and a pulse duration of the first pulse, τ.sub.1, by:
φ.sub.1=φ.sub.0; φ.sub.2=φ.sub.0+r 2π Δf τ.sub.1 with r being a number in the interval [0,9; 1,1] and 2 Δf τ.sub.1≠I, where I is an integer, resulting in a pulse sequence having a passband including f.sub.e in a frequency response profile for protons in the tissue component to be excited and a stopband including f.sub.s in a frequency response profile for protons in the tissue component to be suppressed; and any interpulse delay, t, between the end of the first pulse and the beginning of the second pulse is smaller than a time for 90° phase evolution between protons in the respective tissue components:
t<1/(4 δ B.sub.0 γ), where δ is the chemical shift between protons in tissue to be excited and suppressed, δ=(f.sub.s−f.sub.e)f.sub.e B.sub.0 is the magnetic field strength, and γ is the gyromagnetic ratio of the nucleus.
2. The method according to claim 1, wherein the first and second pulses have the same pulse duration τ.sub.2=τ.sub.1.
3. The method according to claim 1, wherein each of the first and the second pulses has a duration, τ.sub.1,2, in the interval 0.6-0.9 ms.
4. The method according to claim 1, wherein a total pulse duration of the first and second pulses, τ=τ.sub.1+τ.sub.2, is in the interval 1.2-1.8 ms.
5. The method according to claim 1, wherein the first and second RF pulses are rectangular pulses.
6. The method according to claim 1, further comprising selecting a value of at least one of the parameters pulse shape, pulse amplitude, Δf, τ.sub.1, α, φ.sub.0, f.sub.e, f.sub.s, B.sub.0, and t by performing a numerical simulation of the excitation and suppression of bulk protons in the tissue components with at least the parameter to be selected as a variable; and selecting a value of the parameter from the result of the simulation under an objective of the differentiated tissue excitation.
7. The method according to claim 1, wherein the method is directed at water excitation and fat suppression, so that the tissue component to be excited is water and the tissue component to be suppressed is fat.
8. The use of the method according to claim 7 to reduce MR signals originating from fat in an MR image.
9. The use of the method according to claim 1 to generate an image with increased contrast for fatty tissues, wherein the tissue component to be excited is fat and the tissue component to be suppressed is water.
10. The use of the method according to claim 1 to generate an image with increased contrast for silicone gel, wherein the tissue component to be excited is silicone gel and the tissue component to be suppressed is water.
11. A magnetic resonance imaging (MRI) system comprising an MRI apparatus having a plurality of gradient coils positioned about a bore of a magnet to impress a polarizing magnetic field, an RF coil assembly, an RF pulse sequence generator and an RF transceiver system to generate and transmit RF excitation pulses to the RF coil assembly; and a computer programmed to construct first and second radio-frequency (RF) excitation pulses and transmitting the constructed first and second pulses to the RF pulse sequence generator, where the first and second pulses are off-resonance to protons in a tissue component to be excited by having a central frequency, f, offset from a central resonance frequency of protons in the tissue component to be excited, f.sub.e, by a predetermined frequency offset, Δf, in a direction away from a central resonance frequency of protons in a tissue component to be suppressed, f.sub.s, where the first and second pulses have the same RF excitation angle, α, and respective phases, φ.sub.1 and φ.sub.2, characterized in that: a phase shift between the pulses is related to the frequency offset, Δf, and a pulse duration of the first pulse, τ.sub.1, by:
φ.sub.1=φ.sub.0; φ.sub.2=φ.sub.0+r 2π Δf τ.sub.1 with r being a number in the interval [0.9; 1.1] and 2 Δf τ.sub.1≠I, where I is an integer, resulting in a pulse sequence having a passband including f.sub.e in a frequency response profile for protons in the tissue component to be excited and a stopband including f.sub.s in a frequency response profile for protons in the tissue component to be suppressed; and any interpulse delay, t, between the end of the first pulse and the beginning of the second pulse is smaller than a time for 90° phase evolution between protons in the respective tissue components:
t<1/(4 δ B.sub.0 γ), where δ is the chemical shift between protons in tissue to be excited and suppressed, δ=(f.sub.s−f.sub.e)/f.sub.e, B.sub.0 is the magnetic field strength, and γ is the gyromagnetic ratio of the nucleus.
12. A computer program product for constructing excitation pulses for a magnetic resonance imaging (MRI) sequence, the product comprising software applications which provides the following when executed by a processor: constructing first and second radio-frequency (RF) excitation pulses, where the first and second pulses are off-resonance to protons in a tissue component to be excited by having a central frequency, f, offset from a central resonance frequency of protons in the tissue component to be excited, f.sub.e, by a predetermined frequency offset, Δf, in a direction away from a central resonance frequency of protons in a tissue component to be suppressed, f.sub.s, where the first and second pulses have the same RF excitation angle, α, and respective phases, φ.sub.1 and φ.sub.2, characterized in that: a phase shift between the pulses is related to the frequency offset, Δf, and a pulse duration of the first pulse, τ.sub.1, by:
φ.sub.1=φ.sub.0; φ.sub.2=φ.sub.0+r 2π Δf τ.sub.1 with r being a number in the interval [0.9; 1.1] and 2 Δf τ.sub.1≠I, where I is an integer, resulting in a pulse sequence having a passband including f.sub.e in a frequency response profile for protons in the tissue component to be excited and a stopband including f.sub.s in a frequency response profile for protons in the tissue component to be suppressed; and any interpulse delay, t, between the end of the first pulse and the beginning of the second pulse is smaller than a time for 90° phase evolution between protons in the respective tissue components:
t<1/(4 δ B.sub.0 γ), where δ is the chemical shift between protons in tissue to be excited and suppressed, δ=(f.sub.s−f.sub.e)/f.sub.e, B.sub.0 is the magnetic field strength, and γ is the gyromagnetic ratio of the nucleus.
Description
BRIEF DESCRIPTION OF THE FIGURES
[0050] The invention will now be described in more detail with regard to the accompanying figures. The figures show one way of implementing the present invention and is not to be construed as being limiting to other possible embodiments falling within the scope of the attached claim set.
[0051]
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[0055]
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[0059]
[0060]
DETAILED DESCRIPTION OF AN EMBODIMENT
[0061] The first aspect of the invention only specifies the settings of certain RF pulse parameters and application of the resulting pulses, and can thus be implemented on any MRI system with pulse sequence generator capable of generating the first and second pulses and an RF transceiver system and an RF coil assembly capable of transmitting the generated pulses. All standard MRI systems have the required hardware for this implementation.
[0062]
[0063] A computer program product used to implement of the seventh aspect of the invention will be described in more detail later. With the computer 8 having a storage medium having such program thereon, the computer 8 can be used to implement the sixth aspect of the invention. Also, the MRI system 1 with such computer can be used to implement the fifth aspect of the invention.
[0064] The individual elements of an embodiment of the invention may be physically, functionally and logically implemented in any suitable way such as in a single unit, in a plurality of units or as part of separate functional units. The invention may be implemented in a single unit, or be both physically and functionally distributed between different units and processors.
[0065] In the following, for practical purposes, the invention, its aspects, embodiments and features will often be exemplified by reference to the water-fat scenario, where water is the tissue component to be excited and fat is the tissue component to be suppressed. The pulses in this scenario are also referred to as lipid-insensitive off-resonance excitation (LIBRE) pulses. In most cases, these aspects, embodiments and features are equivalently applicable to the fat-water and silicone gel-water scenarios also mentioned previously.
[0066]
[0067] Besides the MRI sequence that utilizes a gradient recalled echo (GRE) based signal acquisition, the invention can also be combined with the following MRI techniques: ultra short echo time (UTE) techniques, spin echo (SE) or turbo spin echo (TSE) based acquisitions, (balanced) steady state free precession ((b)SSFP) techniques, as well as different trajectories for sampling the data such as spiral, radial or cartesian based patterns. Also, the technique is not limited to imaging of large 3D volumes, but can also be used in targeted volumes.
[0068] FRPs
[0069]
[0070] Ye et al. uses two pulses of which the second pulse has a fixed 180° (π) phase difference relative to the first pulse, in effective having a RF excitation angles of +α of the first pulse and —α in the second pulse. In the present invention, the phase off-set between the first and the second pulses is not fixed, but a linear function of Δf and τ.
[0071] Numerical simulations were also performed to establish a link between the FRP for the pulses according to an embodiment of the invention and other pulse parameters such as the RF excitation angle, α, and the RF pulse duration, τ.sub.1/2 (here the same for both pulses). Further, the dependence upon local magnetic field inhomogeneities, ΔB.sub.0, was also explored.
[0072]
[0073] Next some general comments to each pulse parameter as well as the excitement objectives is given and thereafter the selection of pulse parameter values based on numerical simulation is demonstrated.
[0074] Frequency Offset, Δf
[0075] The frequency of the excitation pulses, f, are off-resonance to bulk protons in the tissue components to be excited, f.sub.e. The magnetic resonance frequencies of protons generally depend on the magnetic field strength and the chemical configuration of the protons. The following table shows the relative resonance frequencies of bulk protons in some substances for typical magnetic field strengths:
TABLE-US-00003 f.sub.res B.sub.0 = 1.5T B.sub.0 = 3T B.sub.0 = 7T Water 0 Hz 0 Hz 0 Hz Fat/lipids 220 Hz 440 Hz 1030 Hz Silicone gel 320 Hz 640 Hz 1490 Hz
[0076] The frequency off-set, Δf=f−f.sub.e, is selected so that f lies on the opposite side of f.sub.e from a resonance frequency of protons to be suppressed, f.sub.s, in the frequency spectrum, i.e. in a direction away from f.sub.s. For example, to suppress fat and image water, we move away from the fat, i.e. if water is 0 Hz, fat is −440 Hz, and Δf can be at around 200-500 Hz. To suppress water and image fat instead one could change the main frequency to fat and change the frequency offset of pulse to −200-−500 Hz.
[0077] The frequency off-set is closely tied to the pulse shape and duration through Fourier Transform analysis. With preferred pulse shapes giving rise to a sinc-like shapes in the frequency domain, in which the positions of peaks and troughs (zero-crossings) depends on both the (carrier) frequency of the pulse (f) and the duration of the pulse. The positions of peaks and troughs in the frequency spectrum again influences the position and bandwidth of the pass- and stopbands in the FRPs of the tissue components.
[0078] Pulse Duration, τ
[0079] The pulse durations of the first and second pulses do generally not differ much from known WE binomial 1-1 pulse, but is not so fixed as the ones from a known WE binomial 1-1 pulse. As the simulations show, the pulse duration in the present invention is more flexible and can be chosen within a range of values.
[0080] As mentioned previously, the pulse duration and frequency off-set is closely related. Generally, a shorter pulse duration can be used if the carrier frequency goes further off-resonance, e.g. from Δf=400 Hz to Δf=800 Hz. This is possible because the pulse becomes less sensitive to fat when applied further off-resonance. In other words, if the pulse becomes shorter, the zero crossings of the sinc-shaped frequency response are more widely spaced, and to align those with the fat resonance frequency the offset moves further off-resonance. The following table shows example values of Δf and total pulse duration τ for different magnetic field strengths as have been applied in some numerical simulations.
TABLE-US-00004 Water - fat B.sub.0 = 1.5T B.sub.0 = 3T B.sub.0 = 7T f.sub.e 0 Hz 0 Hz 0 Hz f.sub.s −220 Hz −440 Hz −1030 Hz Δf 200 Hz 400 Hz 800 Hz τ (max) 4.5 ms 2.3 ms 1.0 ms
[0081] In MRI, it is typically of interest to decrease the measurement to save time and costs. Hence, a shorter excitation pulse duration would be advantageous. Looking at the water-fat FRP for the pulse duration (lower left corner of
[0082] The black regions in the bottom center panel of
[0083] Relative Phase Offset
[0084] It is important to distinguish between prior art pulses with a phase shift of π (as in the Ye et al. papers) and pulses according to the invention where Δφ=2π Δf τ.sub.1=π. It is not sufficient for a prior art excitation pulse pair to accidentally have the same Δφ as a set of LIBRE pulses, if Δf and τ.sub.1 of the first pulse in the pair are not related to this phase shift via Δφ=2π Δf τ.sub.1 (as described previously, the invention still produces applicable results as long as Δφ falls within 10%, 5% or 3% of this expression—this is implicit in the following discussions of Δφ). As stressed previously, the FRPs depends on the relation between several pulse parameters, not just on the value of the phase shift. In
[0085] There are important differences between: [0086] Δφ=π=2π Δf τ.sub.1for pulses in accordance with the present invention, and [0087] Δφ=π≠2π Δf τ.sub.1 for the pulses applied in the Ye et al. papers.
[0088] For pulses in accordance with the invention, as can be seen from the simulations shown in
[0089] It also appears that it is the water signal which is correlated with the Δφ=τ=2π Δf τ.sub.1 line and not that of fat. The fat suppression does not seem to be related to this condition, and depends more on the pulse duration, as described in the previous section—for τ.sub.1=1.1 ms, fat is suppressed irrespective of the frequency. However, the fat suppression of the Ye et al pulses does not show this dependency on the pulse duration, and has no broad passband for τ.sub.1=1.1 ms, see
[0090] In a preferred embodiment of all aspects of the invention, the case Δφ≠π is explicitly disclaimed in that values of Δf and τ.sub.1 are selected so that 2 Δf τ.sub.1≠I, where I is an integer. This serves to avoid accidental disclosures of parameter values in accordance with the invention.
[0091] Another practical advantage of the pulses in accordance with the invention are that their implementation allows the exact same (transmitter) phase offset in the center of each pulse (pulse 1 and pulse 2) as well as the (receiver) phase offset during acquisition. The phase offset of both transmitter and receiver changes in the same fashion with each acquisition (called phase cycling). This feature of the pulse is only possible because in the LIBRE implementation the phase evolution of the transmitter is exactly the same in each pulse, which results in exactly the same phase offset in the center of each pulse, and allows the same phase of the signal receiver. Although this cannot be experimentally verified at present, it might be another beneficial aspect of the LIBRE pulse that contributes to enhanced fat suppression.
[0092] Interpulse Delay, t
[0093] Typical WE binomial 1-1 pulses consist of two short pulses with a interpulse delay corresponding to 180° phase evolution between water and fat protons, this is 1.1 ms at 3 T. This is important in order to turn the fat magnetization back to alignment with B.sub.0 while keeping the water magnetization excited.
[0094] The present invention allows for a smaller or even zero interpulse delay, which can significantly reduce imaging sequence durations.
[0095] RF Excitation Angle
[0096] The Excitation pulses according to the invention can have higher RF excitation angles than prior art excitation pulses. Firstly, the relatively long pulse duration allows for the use of lower RF power for identical RF excitation angles as it is defined by the pulse duration times its amplitude. The RF energy (˜Amplitude.sup.2) deposit in the tissue is thus significantly lower in pulses of similar angle but are of longer duration with less amplitude. Since the RF energy deposit is often limited and fixed on MRI systems for safety reasons, using lower power pulses might contribute to less RF energy deposit, and shortens scan time. Secondly,the simulations show that there is a larger range of optimal RF excitation angles. Even if the RF energy deposit in tissues is not everywhere equal, this range of optimal RF excitation angles indicates that the method according to the invention is less sensitive to B1 inhomogeneities.
[0097] Magnetic Field Inhomogeneities
[0098] In practice in MRI there are small magnetic field inhomogeneities that vary across different spatial locations and which cause the Larmor frequency and all values related to vary across the body. It is therefore important that methods to be implemented are insensitive to such inhomogeneities in order to give consistent results.
[0099] Depending on the type of imaging and the volume to be imaged, the sensitivity towards magnetic field inhomogeneities can go from essential to of less importance. Low sensitivity to inhomogeneities is therefore a relevant objective when designing (i.e. selecting parameters for) pulses in MRI sequences.
[0100] As can be seen from the upper row of
[0101] Pass- and Stopband Bandwidth
[0102] Due to the local changes in magnetic field strength there are changes in the resonance frequency of tissues. It could thus be that a certain tissue type resonates at a small range of frequencies and therefore it is desirable to have a certain level of pass band and stopband so that it is effectively targeting a range of frequencies.
[0103] Selection of Pulse Parameters
[0104] Designing pulses for differentiating tissue excitation in accordance with the invention involves selecting values for a number of pulse and inter-pulse parameters. According to an embodiment of the invention, such parameter values can be selected by performing a numerical simulation of the excitation and suppression of bulk protons in the tissue components with the parameter to be selected as a variable. The results could look like the FRPs presented in
[0105] Since, the effective excitation and suppression depends on many parameters and since the parameters are interrelated, it is typically not possible to simply choose the values with maximum effect for all parameters. Therefore, the choice of parameter values often depends on the purpose of the imaging, which can be reduced to the objective with applying the differentiated tissue excitation. As an example, for some parameters, values are chosen that may not give the largest fat suppression, but instead gives a suppression that is less sensitive to magnetic field inhomogeneities. Therefore, after the simulation, values for the parameters can be selected from the result of the simulation under one or more objectives of the differentiated tissue excitation.
[0106] Several such objectives are described in the previous sections, and more can be found and developed.
[0107] Silicone Gel-Water
[0108] The invention can be applied to enhance and/or suppress excitation in different systems than water and fat.
[0109] Fat-Water
[0110] Similarly, it may be of interest to enhance the excitation of fat and suppress water. This can be used to generate an image with increased contrast for fat, which may be helpful when assessing body fat indices or quantizing obesity.
[0111] Experimental Results (Phantoms)
[0112] This section describes some experimental tests using phantoms.
[0113]
[0114] It is shown that the LIBRE pulses results in a visibly better fat suppression that the other methods.
[0115]
[0116] Experimental Results (In Vivo)
[0117]