IP Library Granted Patent US 9,791,529
Granted Patent B2
US 9,791,529 · App. 14/587,085 · Granted Oct 17, 2017

Method and device for indicating differentiation between tissues

Inventor: Bin Kuang (Shenzhen, CN)
Assignee: Siemens Aktiengesellschaft
G01R33/50A61B5/055A61B5/7246G06F17/10G06F17/11G06F19/12G06F19/18A61B5/7264G01R33/5608
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Quick Facts
Patent No.
US 9,791,529
App. No.
14/587,085
Granted
Oct 17, 2017
Kind
B2
Abstract

The present invention provides a method for indicating differentiation between tissues. For each tissue amongst multiple tissues, a magnetization vector corresponding to each tissue is generated on the basis of a random scan sequence; on the basis of the magnetization vector corresponding to each of the multiple tissues, a differentiation-indicating value between each pair of the multiple tissues is calculated. Thus, a physician can select a suitable random scan sequence, according to the method provided in the present invention, and generate a magnetic resonance image comprising multiple brightness curves corresponding to multiple tissues, such that the trends of the brightness curves corresponding to the multiple tissues in the magnetic resonance image differ significantly. The present invention also provides a device for indicating differentiation between tissues.

Claims (57)

1. A method for indicating differentiation between tissues of a subject, comprising:

in a computer, identifying multiple tissues in a subject and, for each tissue among said multiple tissues, executing a simulation comprising a random scan sequence, wherein a magnetic resonance scan of each tissue is simulated with a selected parameter of the scan being randomly varied so as to have different parameter values and in which, as a result of the different parameter values, the respective tissue is given a magnetization vector in the simulation;

in said computer, dependent on the respective magnetization vectors for each of the multiple tissue, calculating a differentiation-indicating value between each pair of tissues among said multiple tissues;

in said computer, simulating a pair of brightness curves for each said pair of tissues among said multiple tissues and using the respective differentiation-indicating values to differentiate between each pair of brightness curves, and thereby obtaining a differentiation for each pair of brightness curves; and

in said computer, based on said differentiation, selecting a magnetic resonance fingerprinting (MRF) protocol for scanning the multiple tissues, and making said MRF protocol available from the computer in electronic form with a format configured to operate a magnetic resonance imaging apparatus in order to execute the selected MRF protocol.

2. The method as claimed in claim 1 , comprising, in said simulation, generating, for each tissue among said multiple tissues, said magnetization vector corresponding to the tissue based on said random scan sequence, by:

generating a radio frequency (RF) pulse rotation matrix R RF of each tissue on the basis of the random scan sequence;

generating a relaxation matrix R relax of each tissue on the basis of the random scan sequence;

determining whether the multiple tissues include a tissue having an off-resonance property df (Hz);

if so, then generating an off-resonance rotation matrix R off of each tissue having an off-resonance property on the basis of the random scan sequence, applying the RF pulse rotation matrix R RF , the relaxation matrix R relax and the off-resonance rotation matrix R off to an initial magnetization vector, and generating a magnetization vector of each tissue by iterative calculation; and

otherwise, applying the RF pulse rotation matrix R RF and the relaxation matrix R relax to an initial magnetization vector, and generating the magnetization vector of each tissue by iterative calculation.

3. The method as claimed in claim 2 , comprising selecting the random scan sequence as at least one random scan sequence from the group consisting of a flip angle random scan sequence, and a repetition time random scan sequence.

4. The method as claimed in claim 3 , comprising generating said RF pulse rotation matrix R RF of the tissue on the basis of the random scan sequence by:

determining whether the random scan sequence comprises the flip angle random scan sequence;

if the random scan sequence comprises the flip angle random scan sequence, generating the RF pulse rotation matrix R RF of each tissue on the basis of the flip angle random scan sequence; and

if the random scan sequence does not comprise a flip angle random scan sequence, generating the RF pulse rotation matrix R RF of each tissue on the basis of a preset flip angle non-random scan sequence.

5. The method as claimed in claim 3 comprising generating a relaxation matrix R relax of the tissue based on the random scan sequence by:

determining whether the random scan sequence comprises a repetition time random scan sequence;

if the random scan sequence comprises a repetition time random scan sequence, generating a relaxation matrix R relax of each tissue on the basis of the repetition time random scan sequence; and

if the random scan sequence does not comprise a repetition time random scan sequence, generating a relaxation matrix R relax of each tissue on the basis of a preset repetition time non-random scan sequence.

6. The method as claimed in claim 5 , comprising generating an off-resonance rotation matrix R off of each tissue having an off-resonance property based on the random scan sequence by:

if the random scan sequence comprises the repetition time random scan sequence, then obtaining an off-resonance rotation matrix R off each tissue having an off-resonance property on the basis of the off-resonance property df (Hz) of each tissue having an off-resonance property and the repetition time random scan sequence; and

if the random scan sequence does not comprise the repetition time random scan sequence, then obtaining an off-resonance rotation matrix R off of each tissue having an off-resonance property on the basis of the off-resonance property df (Hz) of each tissue having an off-resonance property and the preset repetition time non-random scan sequence.

7. The method as claimed in claim 1 , comprising, in said simulation, calculating said differentiation-indicating values of the multiple tissues based on the magnetization vector corresponding to each of the multiple tissues by:

based on the magnetization vector corresponding to each tissue, obtaining a tissue magnetic resonance fingerprinting (MRF) evolution vector of the tissue, each tissue MRF evolution vector comprising the modulus of a vector of projection on the XOY plane of each element in the magnetization vector corresponding to each tissue; and

subjecting the tissue MRF evolution vectors of any two of the multiple tissues to cross-correlation calculation, to obtain a differentiation-indicating value of any two tissues.

8. The method as claimed in claim 7 , further comprising determining, based on the differentiation-indicating values, the differentiation between each pair of brightness curves corresponding to the multiple tissues in a magnetic resonance image generated using the random scan sequence.

9. The method as claimed in claim 8 , comprising determining, based on the differentiation-indicating values, the differentiation between each pair of brightness curves corresponding to the multiple tissues in a magnetic resonance image generated using the random scan sequence, by:

determining whether the differentiation-indicating value of any two of the multiple tissues is less than a set threshold; and

if the differentiation-indicating value of the any two tissues is less than the set threshold, then determining that in one image, the differentiation of the two brightness curves corresponding to the any two tissues is high.

10. The method as claimed in claim 1 , further comprising:

based on the differentiation-indicating values of the multiple tissues, generating a differentiation-indicating matrix of multiple tissues, the element in row i and column j of the differentiation-indicating matrix of multiple tissues being the differentiation-indicating value of the i th tissue and the j th tissue.

11. A device for indicating differentiation between tissues of a subject, comprising:

a computer configured to identify multiple tissues in a subject and, for each tissue among said multiple tissues, executing a simulation comprising a random scan sequence, wherein a magnetic resonance scan of each tissue is simulated with a selected parameter of the scan being randomly varied so as to have different parameter values and in which, as a result of the different parameter values, the respective tissue is given a magnetization vector in the simulation;

said computer being configured to calculate dependent on the respective magnetization vectors for each of the multiple tissue, a differentiation-indicating value between each pair of tissues among said multiple tissues;

said computer being configured to simulate a pair of brightness curves for each said pair of tissues among said multiple tissues and to use the respective differentiation-indicating values to differentiate between each pair of brightness curves, and thereby obtaining a differentiation for each pair of brightness curves; and

said computer being configured to select, based on said differentiation, a magnetic resonance fingerprinting (MRF) protocol for scanning the multiple tissues, and to make said MRF protocol available from the computer in electronic form with a format configured to operate a magnetic resonance imaging apparatus in order to execute the selected MRF protocol.

12. The device as claimed in claim 11 , wherein the computer is configured to:

generate an RF pulse rotation matrix R RF of each tissue on the basis of the random scan sequence; \

generate a relaxation matrix R relax of each tissue on the basis of the random scan sequence;

determine whether the multiple tissues include a tissue having an off-resonance property df (Hz);

generate an off-resonance rotation matrix R off of each tissue having an off-resonance property on the basis of the random scan sequence; and

apply the RF pulse rotation matrix R RF , the relaxation matrix R relax and the off-resonance rotation matrix R off to an initial magnetization vector, and generate a magnetization vector of each tissue by iterative calculation, if the multiple tissues include a tissue having an off-resonance property df (Hz); otherwise, to apply the RF pulse rotation matrix R RF and the relaxation matrix R relax to an initial magnetization vector, and generate the magnetization vector of each tissue by iterative calculation.

13. The device as claimed in claim 12 , wherein the random scan sequence is at least one random scan sequence selected from the group consisting of a flip angle random scan sequence and a repetition time random scan sequence.

14. The device as claimed in claim 13 , wherein the computer is configured to:

determine whether the random scan sequence is a flip angle random scan sequence; and

generate, if the random scan sequence comprises a flip angle random scan sequence, the RF pulse rotation matrix R RF of each tissue on the basis of the flip angle random scan sequence; and if the random scan sequence does not comprise a flip angle random scan sequence, generate the RF pulse rotation matrix R RF of each tissue on the basis of a preset flip angle non-random scan sequence.

15. The device as claimed in claim 13 , wherein the computer is configured to:

determine whether the random scan sequence comprises a repetition time random scan sequence; and

generate, if the random scan sequence comprises the repetition time random scan sequence, a relaxation matrix R relax of each tissue on the basis of the repetition time random scan sequence; and if the random scan sequence does not comprise a repetition time random scan sequence, generate a relaxation matrix R relax of each tissue on the basis of a preset repetition time non-random scan sequence.

16. The device as claimed in claim 15 , wherein the computer is configured to obtain an off-resonance rotation matrix R off of each tissue having an off-resonance property on the basis of the off-resonance property df (Hz) of each tissue having an off-resonance property and the repetition time random scan sequence, if the random scan sequence comprises the repetition time random scan sequence; and if the random scan sequence does not comprise the repetition time random scan sequence, obtain an off-resonance rotation matrix R off of each tissue having an off-resonance property based on the off-resonance property df (Hz) of each tissue having an off-resonance property and the preset repetition time non-random scan sequence.

17. The device as claimed in claim 11 , wherein the computer is configured to:

obtain, based on the magnetization vector corresponding to each tissue, a tissue MRF evolution vector of each tissue, the tissue MRF evolution vector comprising the modulus of a vector of projection on the XOY plane of each element in the magnetization vector corresponding to the tissue; and

subject the tissue MRF evolution vectors of any two of the multiple tissues to cross-correlation calculation, to obtain a differentiation-indicating value of any two tissues.

18. The device as claimed in claim 17 , wherein the computer is further configured to determine, based on the differentiation-indicating values, the differentiation between each pair of brightness curves corresponding to the multiple tissues in a magnetic resonance image generated using the random scan sequence.

19. The device as claimed in claim 18 , wherein the computer is configured to determine whether the differentiation-indicating value between any two of the multiple tissues is less than a set threshold; and if the differentiation-indicating value of the any two tissues is less than the set threshold, to determine that in one image, the differentiation of the two brightness curves corresponding to the any two tissues is high.

20. The device as claimed in claim 11 , wherein the computer is further configured to generate, based on the differentiation-indicating values of the multiple tissues, a differentiation-indicating matrix of multiple tissues, the element in row i and column j of the differentiation-indicating matrix of multiple tissues being the differentiation-indicating value of the i th tissue and the j th tissue.

Assignments (5)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE PREVIOUSLY RECORDED AT REEL: 066088 FRAME: 0256. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jan 17, 2024
From: SIEMENS HEALTHCARE GMBH
To: SIEMENS HEALTHINEERS AG
Reel/Frame 071178/0246 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 20, 2023
From: SIEMENS HEALTHCARE GMBH
To: SIEMENS HEALTHINEERS AG
Reel/Frame 066088/0256 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 27, 2018
From: SIEMENS AKTIENGESELLSCHAFT
To: SIEMENS HEALTHCARE GMBH
Reel/Frame 047022/0164 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 14, 2015
From: KUANG, BIN
To: SIEMENS SHENZHEN MAGNETIC RESONANCE LTD
Reel/Frame 035405/0858 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 14, 2015
From: SIEMENS SHENZHEN MAGNETIC RESONANCE LTD
To: SIEMENS AKTIENGESELLSCHAFT
Reel/Frame 035405/0985 →
Priority Claims (1)
CN 2013 1 0753430 · Dec 31, 2013 · national
Continuity (1)
Related Publication 20150186606A1 · Jul 2, 2015