MR electrical characteristics tomography
The method normalizes conductivity maps using water content differentiation to accurately distinguish between tissues with high water content and abnormal/malignant tissues, addressing misinterpretation issues in conventional MREPT imaging.
Patent Information
- Application Number
- JP2024547263
- Authority / Receiving Office
- JP · JP
- Patent Type
- Patents
- Current Assignee / Owner
- Priority Date
- 2022-04-21
- Filing Date
- 2023-04-10
- Publication Date
- 2025-12-23
- Estimated Expiration
- 2043-04-10
AI Technical Summary
Conventional MREPT imaging methods often misinterpret high conductivity as abnormal tissue due to its correlation with water content rather than tissue abnormality, leading to potential misdiagnosis.
A method for MR imaging that involves generating MR signals, reconstructing magnitude and phase maps, deriving conductivity maps from both, and normalizing conductivity using a rescaling function based on water content to differentiate between tissues with high water content and abnormal/malignant tissues.
Enables accurate differentiation between tissues with high water content and abnormal/malignant tissues by normalizing conductivity maps, reducing misdiagnosis in MR imaging.
Smart Images

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Abstract
Description
[Technical Field]
[0001] The present invention relates to the field of magnetic resonance (MR) imaging. The present invention relates to a method for MR imaging of an object. The present invention also relates to an MR system and a computer program running on an MR system. [Background technology]
[0002] MR imaging, which utilizes the interaction between magnetic fields and atomic nuclear spins to form two- or three-dimensional images, is widely used today, especially in the field of medical diagnostics, for imaging soft tissues because it is superior in many ways to other imaging methods, does not require ionizing radiation, and is usually non-invasive.
[0003] Electrical properties (EP), also known as dielectric properties, including conductivity, are fundamental properties of materials. Conductivity characterizes the ability to transmit electric current within a medium. In biological tissues, EP is determined by fundamental biophysical properties of the tissue, such as water content, ionic concentration, molecular composition, intracellular space fraction, cell membrane permeability, and cellular structure. Conductivity can potentially be used as a biomarker of tissue health in clinical applications. Previous studies have shown that various diseases cause localized changes in EP compared to healthy neighboring tissue. Among various cancers, breast cancer tissue has been shown to have the most distinct EP compared to normal breast tissue. Benign breast tissue exhibits significantly different conductivity compared to malignant breast cancer.
[0004] Magnetic resonance electrical properties tomography (MREP) is a technique that uses MR images to investigate tissue conductivity (see, e.g., Katscher et al., NMR Biomed., 2017, 30). Conductivity can be obtained from simple and common imaging sequences (e.g., the so-called balanced fast field echo sequence, bFFE). Magnetic resonance excitation is related to the spatial RF (magnetic field) distribution. The RF field distribution can be measured directly using conventional B1 mapping techniques. The unknown conductivity can be calculated by post-processing the RF field distribution in the framework of Maxwell's equations from the acquired phase map, which is related to the spatial RF field distribution induced by the RF pulse in the object.
[0005] For reliable diagnosis, it is important to consider that high conductivity does not necessarily indicate abnormal tissue, and conversely, highly abnormal tissue conditions are not necessarily associated with high conductivity. Conductivity is primarily determined by the water content of the tissue being examined, not the degree of tissue abnormality. Therefore, with conventional MREPT techniques, areas of high conductivity may be intuitively misinterpreted as pathology, while the area actually has only a high water content and is completely healthy. This can result in misdiagnosis. Summary of the Invention [Problem to be solved by the invention]
[0006] From the above, it is readily apparent that there is a need for improved MREPT imaging methods. Accordingly, it is an object of the present invention to enable improved differentiation between tissues with only high water content and abnormal / malignant tissues during MREPT. [Means for solving the problem]
[0007] According to the present invention, a method for MR imaging of an object placed in an examination volume of an MR system is disclosed, the method comprising: generating MR signals by exposing the object to an imaging sequence having RF pulses and switched magnetic field gradients; acquiring the MR signals; reconstructing a magnitude MR image and a phase map from the MR signals for a given field of view within the object, the phase map relating to a spatial RF magnetic field distribution induced by an RF pulse within the field of view; deriving a conductivity map from the phase map, the conductivity map representing a measure of the distribution of conductivity within the field of view; deriving a further conductivity map from the magnitude MR image, the further conductivity map representing an estimate of the conductivity resulting from the distribution of water within the field of view; identifying deviations between the two conductivity maps; It has.
[0008] In other words, the present invention proposes using an estimated conductivity map related to water content to "normalize" the conductivity map actually measured by MREPT. The resulting normalized tissue conductivity can be directly interpreted as the degree of tissue abnormality indicated by the deviation between the two conductivity maps. Implementation of the present invention involves reconstructing the "measured" conductivity from the phase image and estimating the conductivity related to tissue water content from the magnitude MR image (i.e., showing proton density and therefore water content). This allows for direct voxel-by-voxel calculation of normalized conductivity from a single MR scan, for example, by subtracting the two conductivity maps. Tissue abnormalities can be identified by non-zero (positive or negative) voxel values in this normalized conductivity map.
[0009] In one embodiment, the imaging sequence is a steady-state gradient echo sequence, preferably a balanced fast field echo (bFFE) sequence. Steady-state imaging sequences are typically based on gradient echo imaging sequences with a short repetition time TR. Steady-state sequences involve transverse coherence tomography from overlapping multi-order spin echoes and stimulated echoes. This is typically achieved by refocusing the phase encoding gradients at each repetition interval to keep the phase integral (or gradient moment) constant. A fully balanced steady-state imaging sequence achieves zero phase by refocusing all imaging gradients. Phase maps are suitable for MREPT when they relate only to B1 and are not affected by inhomogeneities in the main magnetic field B0. Conventionally, spin-echo-based imaging sequences avoid any undesirable effects of B0 inhomogeneities. However, the effect of B0 inhomogeneities on the phase map is negligible in steady-state acquisition because the phase barely changes for off-resonance within the passband (frequency region corresponding to 1 / TR) of the imaging sequence. The B1-related phase map can be derived directly from the real and imaginary parts of each voxel value for each location in the reconstructed complex MR image.
[0010] In another embodiment, the derivation of the further conductivity map includes rescaling the magnitude image. Thus, the present invention takes advantage of the fact that the relationship between the voxel values of the magnitude MR image and the conductivity at each location can be parameterized using a simple empirical rescaling function. The rescaling can then be based on a calibration that involves fitting the empirical rescaling function to measured conductivity maps of different fields of view, i.e., healthy tissue, where deviations between the conductivity measured by MREPT and the conductivity resulting from water distribution are not expected.
[0011] In yet another embodiment, the method further includes acquiring a B1 magnitude map representing the distribution of the magnitude of the RF field induced by the RF pulse within the field of view, wherein the conductivity map is derived from the phase map and the B1 magnitude map. To rigorously calculate the conductivity according to Maxwell's equations, both the magnitude and phase of B1 are required. Therefore, it may be advantageous to not only rely on the phase map but also perform an additional B1 mapping step to obtain the distribution of the B1 magnitude. However, a sufficiently good approximation of the conductivity is often obtained by using only the phase map and considering the B1 magnitude to be constant. This approximation can be used in practice because it saves the time-consuming measurement of the B1 magnitude map.
[0012] The method of the present invention does not necessarily have to be performed in direct combination with the acquisition of MR signals: it can also be performed independently outside the MR system, as a purely post-processing step of the acquired and reconstructed image data. In this respect, the present invention provides, in a further aspect, providing a magnitude MR image and a phase map for a given field of view; deriving a conductivity map from the phase map, the conductivity map representing a measure of the distribution of conductivity within the field of view; deriving a further conductivity map from the magnitude image, the further conductivity map representing an estimate of conductivity resulting from the distribution of water within the field of view; identifying deviations between the two conductivity maps; The present invention relates to a computer-implemented method comprising:
[0013] The inventive method described above can be performed by an MR system comprising at least one main magnet coil for generating a homogeneous static magnetic field in an examination volume, a plurality of gradient coils for generating switched magnetic field gradients in different spatial directions in the examination volume, at least one RF coil for generating RF pulses in the examination volume and / or for receiving MR signals from an object placed in the examination volume, a control unit for controlling the time sequence of the RF pulses and the switched magnetic field gradients, and a reconstruction unit. The inventive method can, for example, be implemented by a corresponding program in the reconstruction unit and / or the control unit of the MR system.
[0014] The method of the present invention can be advantageously implemented in most MR systems currently in clinical use. To this end, it is only necessary to utilize a computer program that controls the MR system to execute the above-described method steps of the present invention. The computer program may reside on a data carrier or within a data network so that it can be downloaded for installation into the control unit of the MR system. The computer program may also be executable independently of the MR system, for example, on a commercially available personal computer.
[0015] The accompanying drawings disclose preferred embodiments of the present invention, however, it is to be understood that the drawings are designed for illustrative purposes only and are not intended as a definition of the limits of the invention. [Brief explanation of the drawings]
[0016] [Figure 1] 1 shows an MR system for carrying out the method of the present invention. [Figure 2] The method of the present invention is illustrated as a flow chart. [Figure 3] 1 shows a diagram illustrating the calibration for rescaling of magnitude MR images according to the present invention. [Figure 4]1 shows a conductivity map illustrating the normalization approach of the present invention. DETAILED DESCRIPTION OF THE INVENTION
[0017] Referring to Figure 1, there is shown an MR system 1. The apparatus comprises superconducting or resistive main magnet coils 2, 2' such that a substantially uniform, temporally constant main magnetic field is generated along the z-axis throughout the examination volume.
[0018] The magnetic resonance generation and manipulation system applies a series of RF pulses and switched magnetic field gradients to invert or excite nuclear magnetic spins, induce magnetic resonance, refocus magnetic resonance, manipulate magnetic resonance, spatially and otherwise encode magnetic resonance, saturate spins, etc. to perform MR imaging.
[0019] More specifically, gradient pulse amplifiers 3 apply current pulses to selected ones of whole-body gradient coils 4, 5, and 6 along the x-, y-, and z-axes of the examination volume. Digital RF transmitter 7 transmits RF pulses or pulse packets to body-volume RF coil 9 via transmit / receive switch 8, which transmits RF pulses into the examination volume. A typical MR imaging sequence consists of packets of short-duration RF pulse segments taken together with optional applied magnetic field gradients to achieve selected manipulation of nuclear magnetic resonance. The RF pulses are used to saturate resonance, excite resonance, invert magnetization, refocus resonance, or manipulate resonance to select a portion of a body 10 located within the examination volume. MR signals are also picked up by body-volume RF coil 9.
[0020] To generate MR images of limited regions of the body 10, a set of local array RF coils 11, 12, 13 are positioned adjacent to the region selected for imaging. The array coils 11, 12, 13 can be used to receive MR signals induced by body coil RF transmissions.
[0021] The resulting MR signals are picked up by a whole-body volume RF coil 9 and / or array RF coils 11, 12, 13 and demodulated by a receiver 14, which preferably includes a preamplifier (not shown). The receiver 14 is connected to the RF coils 9, 11, 12, 13 via a transmit / receive switch 8.
[0022] A host computer 15 controls the gradient pulse amplifiers 3 and transmitter 7 to generate any of several MR imaging sequences, such as a balanced fast field echo (bFFE) imaging sequence. For the selected sequence, the receiver 14 receives single or multiple MR data lines in rapid succession following each RF excitation pulse. A data acquisition system 16 performs analog-to-digital conversion of the received signals and converts each MR data line into a digital format suitable for further processing. In most modern MR systems, the data acquisition system 16 is a separate computer dedicated to collecting raw image data.
[0023] Ultimately, the digital raw image data is reconstructed into an image representation by a reconstruction processor 17, which applies a Fourier transform or other suitable reconstruction algorithm, such as SENSE, SMASH, or GRAPPA. The MR image may represent a planar slice through the patient, an array of parallel planar slices, a three-dimensional volume, etc. The image is then stored in an image memory, where it can be accessed to convert the slices, projections, or other portions of the image representation into an appropriate format for visualization, for example, via a video monitor 18, which provides a human-readable display of the resulting MR image.
[0024] With continued reference to FIG. 1 and further reference to FIGS. 2-4, an embodiment of the method of the present invention will now be described.
[0025] In step 21 (FIG. 2), the body 10 undergoes a steady-state bFFE imaging sequence. The generated echo signals are acquired and reconstructed into a complex MR image of a given field of view (2D or 3D). From the complex MR image, a magnitude MR image is derived, and each complex image value Sc From the real and imaginary parts of
[0026] Φ(r)=atan2(Im (S c ), Re(S c )) is derived directly from
[0027] This phase information is used in step 22 of the conventional phase-based EPT method to calculate the conductivity σ meas The resulting conductivity map is used to calculate a conductivity map representing a measure of the distribution of water in the field of view. In step 23, different fields of view are identified, i.e., "healthy" regions within the imaged anatomy where no conductivity abnormalities are expected. The different fields of view may, for example, be different image slices or subregions within a given field of view for which magnitude images and conductivity maps have already been derived in steps 21 and 22. A rescaling function is determined in step 24 to estimate the conductivity resulting from the distribution of water within the field of view. Empirically, the bFFE magnitude MR image, the estimated conductivity of healthy tissue at each location, σ, est For example, the relationship between It can be parameterized by TIFF0007790587000001.tif10130.
[0028] σ est and S m Both are related to water content. An example of this relationship is shown in the diagram in Figure 3 (scatter plot of the conductivity reconstructed from the bFFE phase versus the bFFE magnitude). The parameters a, b, and c depend on the system settings and must be adjusted individually for each MR imaging scan (a: adjust the conductivity scaling, b: adjust the curvature of the function, c: adjust the range of the bFFE magnitude MR image). For calibration of the rescaling function, a least-squares fit is performed to find the best match between the magnitude MR image and the measured conductivity in the identified healthy regions. The solid line in Figure 3 represents the S m and σ measThe fit based on the above equation is shown with a visualization of the relationship between a and b. For the in vivo example shown, the adjusted optimal parameters were a = 1.14, b = 40.0, and c = 211. Once the optimal parameters a, b, and c are found in this way, the magnitude MR image for the entire given field of view (including the suspect, potentially abnormal tissue region) is rescaled using the rescaling function in step 25 to obtain the estimated conductivity σ resulting from the distribution of water within the given field of view. est Finally, in step 26, Estimated conductivity σ as in TIFF0007790587000002.tif16133 est is the conductivity σ measured over a given field of view. meas The normalized conductivity σ is subtracted from norm σ norm can be negative or positive, and the estimated conductivity σ est The measured conductivity σ from meas and therefore indicates abnormal regions. In the (assumed healthy) regions used to adjust the constants a, b, c in step 24, the resulting σ norm should therefore be approximately 0.
[0029] This is shown diagrammatically in Figure 4, which shows the example of a brain tumor. A given field of view is called a "slice through the tumor," while a different field of view, i.e., a healthy region used to calibrate the rescaling function, is called a "calibration slice." The top row shows the EPT-reconstructed conductivity maps σ for two slices (left: containing only healthy tissue; right: containing the tumor). meas The cerebrospinal fluid (CSF) exhibits the highest conductivity in the center of a given field of view, which is not a pathological region within the field of view. The bottom row shows the normalized conductivity σ for the same two slices. norm Since the normalization is based on the "healthy" calibration slice (left), the normalized conductivity of this slice σ normis 0. Normalization in the tumor slice shows zero in healthy areas where conductivity is lower than normal, non-zero in the tumor core, and zero in the edema surrounding the tumor where conductivity is higher than normal. The following describes embodiments of the present invention. (Appendix 1) 1. A method for MR imaging of an object placed in an examination volume of an MR system, the method comprising: generating MR signals by exposing the object to an imaging sequence having RF pulses and switched magnetic field gradients; acquiring the MR signals; reconstructing a magnitude MR image and a phase map from the MR signals for a given field of view within the object, the phase map relating to a spatial RF magnetic field distribution induced by an RF pulse within the field of view; deriving a conductivity map from the phase map, the conductivity map representing a measure of the distribution of conductivity within the field of view; deriving a further conductivity map from the magnitude MR image, the further conductivity map representing an estimate of the conductivity resulting from the distribution of water within the field of view; identifying deviations between the two conductivity maps; A method comprising: (Appendix 2) 2. The method of claim 1, wherein the imaging sequence is a steady-state gradient echo sequence, preferably a balanced fast field echo sequence. (Appendix 3) 3. The method of claim 1 or 2, wherein the deriving of the further conductivity map comprises rescaling the magnitude image. (Appendix 4) 4. The method of claim 3, wherein the rescaling is based on a calibration that includes fitting an empirical rescaling function to measured conductivity maps for different fields of view, and wherein deviations between the measured conductivity and conductivity resulting from water distribution are not estimated. (Appendix 5) 5. The method of any one of claims 1 to 4, wherein identifying a deviation between the two conductivity maps comprises subtracting the two conductivity maps. (Appendix 6) B of the RF pulse, which represents the distribution of the magnitude of the RF magnetic field induced by the RF pulse within the field of view. 1 The method further comprises acquiring an RF magnetic field induced by a magnitude map, the conductivity map being a function of the phase map and the B 1 6. The method of any one of claims 1 to 5, derived from a magnitude map. (Appendix 7) 1. A computer-implemented method comprising: providing a magnitude MR image and a phase map for a given field of view from MR signals generated by exposing the object to an imaging sequence having RF pulses and switched magnetic field gradients; deriving a conductivity map from the phase map, the conductivity map representing a measure of the distribution of conductivity within the field of view; deriving a further conductivity map from the magnitude image, the further conductivity map representing an estimate of conductivity resulting from the distribution of water within the field of view; identifying deviations between the two conductivity maps; A method comprising: (Appendix 8) 8. An MR system comprising: at least one main magnet coil for generating a homogeneous static magnetic field in an examination volume; a plurality of gradient coils for generating switched magnetic field gradients in different spatial directions in the examination volume; at least one RF coil for generating RF pulses in the examination volume and / or for receiving MR signals from an object disposed in the examination volume; a control unit for controlling the time sequence of the RF pulses and the switched magnetic field gradients; and a reconstruction unit, wherein the MR system is configured to perform a method according to any one of claims 1 to 7. (Appendix 9) 8. A computer program comprising instructions which, when the program is executed by a computer, preferably by a reconstruction unit of an MR system, cause the computer to carry out the method according to any one of claims 1 to 7.
Claims
1. 1. A method for MR imaging of an object placed in an examination volume of an MR system, the method comprising: generating MR signals by exposing the object to an imaging sequence having RF pulses and switched magnetic field gradients; acquiring the MR signals; reconstructing a magnitude MR image and a phase map from the MR signals for a given field of view within the object, the phase map relating to a spatial RF magnetic field distribution induced by an RF pulse within the field of view; deriving a conductivity map from the phase map, the conductivity map representing a measure of the distribution of conductivity within the field of view; deriving a further conductivity map from the magnitude MR image, the further conductivity map representing an estimate of the conductivity resulting from the distribution of water within the field of view; identifying deviations between the two conductivity maps; A method comprising:
2. The method of claim 1 , wherein the imaging sequence is a steady-state gradient echo sequence.
3. The method of claim 2 , wherein the steady-state gradient echo sequence is a balanced fast field echo sequence.
4. 4. The method of claim 1, wherein the derivation of the further conductivity map comprises rescaling the magnitude MR image.
5. 5. The method of claim 4, wherein the rescaling is based on a calibration that includes fitting an empirical rescaling function to measured conductivity maps for different fields of view, and wherein deviations between the measured conductivity and conductivity resulting from water distribution are not estimated.
6. The method of claim 1 or 2, wherein identifying the deviation between the two conductivity maps comprises subtracting the two conductivity maps.
7. B of the RF pulse, which represents the distribution of the magnitude of the RF magnetic field induced by the RF pulse within the field of view. 1 The method further comprises acquiring an RF magnetic field induced by a magnitude map, the conductivity map being a function of the phase map and the B 1 The method of claim 1 or 2, derived from a magnitude map.
8. 1. A computer-implemented method comprising: providing a magnitude MR image and a phase map for a given field of view from MR signals generated by exposing the object to an imaging sequence having RF pulses and switched magnetic field gradients; deriving a conductivity map from the phase map, the conductivity map representing a measure of the distribution of conductivity within the field of view; deriving a further conductivity map from the magnitude MR image, the further conductivity map representing an estimate of the conductivity resulting from the distribution of water within the field of view; identifying deviations between the two conductivity maps; A method comprising:
9. 10. An MR system comprising: at least one main magnet coil for generating a homogeneous static magnetic field in an examination volume; a plurality of gradient coils for generating switched magnetic field gradients in different spatial directions in the examination volume; at least one RF coil for generating RF pulses in the examination volume and / or for receiving MR signals from an object disposed in the examination volume; a control unit for controlling the time sequence of the RF pulses and the switched magnetic field gradients; and a reconstruction unit, wherein the MR system is configured to perform the method according to claim 1, 2 or 8.
10. A computer program comprising instructions which, when executed by a computer, cause said computer to carry out the method according to claim 1, 2 or 8.
Citation Information
Patent Citations
Measurement of intra-cellular conductivity using magnetic resonance imaging
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