T2 contrast in magnetic resonance imaging with gradient echoes

Surgery – Diagnostic testing – Detecting nuclear – electromagnetic – or ultrasonic radiation

Reexamination Certificate

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Reexamination Certificate

active

06603989

ABSTRACT:

BACKGROUND OF THE INVENTION
The present invention relates generally to the field of Magnetic Resonance Imaging (MRI) and Magnetic Resonance Spectroscopy (MRS), and more particularly, to a method and apparatus for gradient echo MR imaging to measure a T
2
relaxation rate constant and/or to create T
2
contrast images together with T
1
or spin density and T
2
* weighted images, all from the same MR data set.
When a substance such as human tissue is subjected to a uniform magnetic field (polarizing field B
0
), the individual magnetic moments of the spins in the tissue attempt to align with this polarizing field, but precess about it in random order at their characteristic Larmor frequency. If the substance, or tissue, is subjected to a magnetic field (excitation field B
1
) which is in the x-y plane and which is near the Larmor frequency, the net aligned moment, or “longitudinal magnetization”, M
z
, may be rotated, or “tipped”, into the x-y plane to produce a net transverse magnetic moment M
t
. A signal is emitted by the excited spins after the excitation signal B
1
is terminated and this signal may be received and processed to form an image.
When utilizing these signals to produce images, magnetic field gradients (G
x
G
y
and G
z
) are employed. Typically, the region to be imaged is scanned by a sequence of measurement cycles in which these gradients vary according to the particular localization method being used. The resulting set of received NMR signals are digitized and processed to reconstruct the image using one of many well-known reconstruction techniques.
One of the problems with acquiring T
2
weighted images is that conventional techniques require a relatively long repetition time (TR) in order to achieve a pure T
2
(proton density) image contrast. In other words, T
2
weighted imaging is generally associated with long imaging times, as compared to T
1
weighted imaging. T
1
imaging is much faster since such imaging is achieved by shortening the repetition time.
Measuring T
2
relaxation time in MRI or MRS, as well as creating T
2
contrast in MRI typically requires use of a version of spin echo (SE) pulse sequences. These sequences can differ in how signal excitation, phase encoding, and acquisition are combined together to form a pulse sequence. Different pulse sequences result in different image acquisition times, signal-to-noise (SNR) ratios and image contrasts. The most frequently used sequences for clinical diagnostic applications are traditional multi-slice two-dimensional Fourier Transform SE sequences and single-slice fast spin echo sequence techniques such as the Rapid Acquisition Relaxation Enhanced (RARE) sequence which is described by J. Hennig et al. in an article in
Magnetic Resonance in Medicine
3,823-833 (1986) entitled “RARE Imaging: A Fast Imaging Method for Clinical MR.” The former usually requires long acquisition times, on the order of minutes, and the latter represents a fast imaging approach where only a single slice can be acquired in a subsecond time scale. The common attribute of all SE techniques is the presence of refocusing RF pulses. Most often, 180° RF pulses are used. The major reason to use SE techniques stems from the refocusing nature of the 180° RF pulses, which substantially reduces the influence of unwanted magnetic field inhomogeneities on MRI signals. These approaches can suffer from motion artifacts and imperfections in slice profiles resulting from the presence of the 180° refocusing pulses. More importantly, however, SE techniques suffer from restrictions on RF power deposition. This factor substantially limits the clinical application of these techniques for high-field MR imaging.
It would therefore be desirable to have a method and apparatus capable of creating T
2
contrast images using gradient echo imaging to acquire T
2
contrast images in a time that approximates T
1
imaging. It would also be advantageous to be able to use the same MR data that is used to construct the T
2
weighted images to construct T
1
or spin density images, and T
2
* weighted images.
SUMMARY OF THE INVENTION
The present invention provides a method of measuring T
2
relaxation time constant in MRS and MRI, and creates T
2
image contrast in MRI using gradient echo imaging that solves the aforementioned problems. In accordance with the present invention, the influence of magnetic field inhomogeneities on MRI signals can be removed by making use of a unique signal post-processing procedure in combination with a specially designed MRI pulse sequence without the use of refocusing RF pulses.
This technique is based on multi-gradient-echo approach and allows obtaining a T
2
contrast images in MRI without using any type of SE techniques. Through use of the present invention, both T
2
and T
1
or spin density contrast images can be obtained in a single scan by adjusting flip angle and repetition time (TR). Further, images corresponding to long gradient echo times in a multi-gradient-echo train can be used to form T
2
* contrast. Therefore, this technique allows obtaining T
2
, T
1
or spin density, and T
2
* weighted images in a single scan. All such images will also be naturally co-registered which is particularly advantageous for certain clinical applications.
The present invention can be implemented using either two dimensional or three dimensional pulse sequencing and since relatively low flip angles are used, the present invention requires substantially less RF power than SE acquisition techniques. The low flip angles also provide improved slice profiles as compared to traditional SE acquisition techniques. The present technique allows for fast imaging with repetition times (TR) on the order of 25 msec. on a typical clinical scanner, which promotes breath-held scanning to reduce motion artifacts. A half-Fourier approach can also be applied to increase the speed of the acquisition further.
Application of the present invention provides images that are largely insensitive to RF field inhomogeneities and also allows separation of water and lipid contributions in an image. A magnetization preparation block can also be used to suppress lipid or CSF signals, or to enhance T
1
contrast.
A method of acquiring MR images, according to the present invention, includes determining a nonlinear function of gradient echo time to offset magnetic field inhomogeneities. Multiple sets of MR data are acquired from a series of read-out gradients in a pulse sequence. The invention also includes fitting the MR data to an equation that includes the nonlinear function, and then creating T
1
or spin density images, and T
2
images using the results of the fitting step. The invention can also be used to create T
2
* images using the same data set.
In accordance with another aspect of the invention, an MRI apparatus is disclosed to rapidly acquire T
2
weighted images that includes a magnetic resonance imaging (MRI) system having a plurality of gradient coils positioned about a bore of a magnet to impress a polarizing magnetic field. An RF transceiver system and an RF switch are controlled by a pulse module to transmit and receive RF signals to and from an RF coil assembly to acquire the MR images. The MRI apparatus also has a computer programmed to acquire multiple sets of MR data from a series of read-out gradient pulses in a pulse sequence and determine signal intensity for each MR data. The computer then fits the MR data to a signal magnitude equation that includes a nonlinear function, and then reconstructs T
2
weighted MR images that are substantially free of magnetic field inhomogeneities.
In order to reconstruct the T
2
weighted images, the method includes a computer program for use with an MRI apparatus that includes instructions which, when executed by a computer, cause the computer to apply a pulse sequence with a train of gradient read-out pulses and acquire MR data during the train of gradient read-out pulses. The program determines a nonlinear function of gradient echo time based on the object scanned and the physical characteristics of the MR ap

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