Search PubMed⌕ Search

Biomedical subjects

Masaki Ohkubo

Publications and source records attributed to Masaki Ohkubo.

8 recordsLinked to original sources

An effective method to verify line and point spread functions measured in computed tomography.

This study describes an effective method for verifying line spread function (LSF) and point spread function (PSF) measured in computed tomography (CT). The CT image of an assumed object function is known to be calculable using LSF or PSF based on a model for the spatial resolution in a linear imaging system. Therefore, the validities of LSF and PSF would be confirmed by comparing the computed images with the images obtained by scanning phantoms corresponding to the object function. Differences between computed and measured images will depend on the accuracy of the LSF and PSF used in the calculations. First, we measured LSF in our scanner, and derived the two-dimensional PSF in the scan plane from the LSE Second, we scanned the phantom including uniform cylindrical objects parallel to the long axis of a patient's body (z direction). Measured images of such a phantom were characterized according to the spatial resolution in the scan plane, and did not depend on the spatial resolution in the z direction. Third, images were calculated by two-dimensionally convolving the true object as a function of space with the PSF. As a result of comparing computed images with measured ones, good agreement was found and was demonstrated by image subtraction. As a criterion for evaluating quantitatively the overall differences of images, we defined the normalized standard deviation (SD) in the differences between computed and measured images. These normalized SDs were less than 5.0% (ranging from 1.3% to 4.8%) for three types of image reconstruction kernels and for various diameters of cylindrical objects, indicating the high accuracy of PSF and LSF that resulted in successful measurements. Further, we also obtained another LSF utilizing an inappropriate manner, and calculated the images as above. This time, the computed images did not agree with the measured ones. The normalized SDs were 6.0% or more (ranging from 6.0% to 13.8%), indicating the inaccuracy of the PSF and LSE We could verify LSFs and PSFs for three types of reconstruction kernels, and demonstrated differences between modulation transfer functions (MTFs) derived from validated LSFs and inaccurate LSFs. Our technique requires a simple phantom that is suitable for clinical scanning, and does not require a particular phantom containing some metals or specific fine structures, as required in methods previously used for measurements of spatial resolution. Therefore, the scanned image of the phantom will be reliable and of good quality, and this is used directly as a confident reference image for the verification. When one obtains LSF, PSF or MTF values, verification using our method is recommended. Further, when another method for the measurement of LSF and PSF is developed, it could be validated using our technique, as illustrated in the method proposed by Boone [Med. Phys. 28, 356-360 (2001)] and used in this paper.

Algorithms↗

[Evaluation of the accuracy of line spread function (LSF) and point spread function (PSF) measured in the computed tomography.].

We propose a method to estimate the accuracy of the line spread function (LSF) in computed tomography (CT). When we assume an object for scanning has a shape and CT-value in the x-y scan-plane that are constant in the z-direction perpendicular to the scan-plane, blurring in the image of the object is predicted with calculation by the LSF measured in the scanner. When using the precise LSF, the calculated image must agree well with the scanned image of the phantom corresponding to the object. Then, verification of LSF is performed by comparing the calculated image with the scanned image. We measured the LSF in our scanner, and scanned a cylindrical phantom with constant diameter and CT-value in which the direction of cylinder was parallel to the z-direction, as mentioned above. Images calculated by using the LSF corresponded well to scanned images, indicating the validity of the LSF. We obtained another LSF by an inappropriate manner, and calculated images using it. Those images showed an apparent difference with scanned images, indicating the inaccuracy of the LSF. Our technique is effective to evaluate the accuracy of LSF, PSF, and also modulation transfer function (MTF) derived from the LSF or PSF.

Phantoms, Imaging↗

[Optimization of flip angle for 3D-VIBE technique in liver dynamic MRI].

The aim of this study was to determine a moderate flip angle (FA) for dynamic liver MR imaging (MRI) with the three-dimensional volumetric interpolated breath-hold examination (3D-VIBE) technique. Images of phantoms with various T(1) values (44-560 msec) were acquired with the 3D-VIBE sequence (TR/TE=5.2/2.6 msec) using different FA (5-50 degree). We estimated signal-to-noise ratio (SNR) and contrast-to-noise ratio (CNR), considered to indicate tumor-to-liver contrast, as a function of FA. In phantoms, in which T(1) values (44-191 msec) were assumed to be shortened by the effect of Gd-DTPA in hepatocellular carcinoma (HCC), the highest SNR in each phantom was observed at FA ranging from 15 to 30 degrees. SNRs in other phantoms, in which T(1) values (298-560 msec) were assumed to be normal liver-tissue pre- or post-enhancement, were high with FA of 10-12 degrees, and were remarkably decreased with FA of more than 30 degrees. CNR increased as FA increased in every phantom, especially in the phantom with shortened T(1) values (44-191 msec), suggesting that enlarging FA improved the tumor-to-liver contrast. Taking both results of SNR and CNR into account, we concluded that a moderate FA was approximately 25 degrees. The advantage with an FA of 25 degrees was confirmed in a clinical study of a patient with hypervascular HCC, in which we could observe coronal enhancement surrounding the lesion in the late phase of the double arterial phase by dynamic MRI using the 3D-VIBE technique.

Carcinoma, Hepatocellular↗

[Relationship between line spread function (LSF), or slice sensitivity profile (SSP), and point spread function (PSF) in CT image system.].

In the CT image system, we revealed the relationship between line spread function (LSF), or slice sensitivity profile (SSP), and point spread function (PSF). In the system, the following equation has been reported; I(x,y) = O(x,y) ** PSF(x,y), in which I(x,y) and O(x,y) are CT image and object function, respectively, and ** is 2-dimensional convolution. In the same way, the following 3-dimensional expression applies; I'(x,y,z) = O'(x,y,z) *** PSF'(x,y,z), in which z-axis is the direction perpendicular to the x/y-scan plane. We defined that the CT image system was separable, when the above two equations could be transformed into following equations; I(x,y) = [O(x,y) * LSF(x)(x) ] * LSF(y)(y) and I' (x,y,z) = [ O'(x,y,z) * SSP(z) ] ** PSF(x,y), respectively, in which LSF(x)(x) and LSF(y)(y) are LSFs in x- and y-direction, respectively. Previous reports for the LSF and SSP are considered to assume the separable-system. Under the condition of separable-system, we derived following equations; PSF(x,y)=LSF(x)(x) LSF(y)(y) and PSF' (x,y,z) = PSF(x,y) SSP(z). They were validated by the computer-simulations. When the study based on 1-dimensional functions of LSF and SSP are expanded to that based on 2- or 3-dimensional functions of PSF, derived equations must be required.

Computer Simulation↗

[Duration of enhancement and scan timing in three-dimensional contrast-enhanced MR angiography using the elliptical centric phase-encoding technique].

In the present study, we quantitatively investigated the relationship between the signal intensity in a vessel and the duration of contrast enhancement as well as scan timing in 3D contrast-enhanced MR angiography using an elliptical centric phase-encoding technique. A tube phantom filled with Gd-DTPA, acting as a vessel, was taken out from the field of view during data acquisition, by using the "pause" function of our MR scanner (GE Signa, 1.5 Tesla), thereby simulating the presence and absence of a vessel. The shortening of the duration of enhancement corresponds to the delay of scan timing from the optimal point in the phase-encoding of the centric-ordering system. The signal intensity in a vessel (1-5 mm in diameter) decreased as the duration of enhancement became shorter and the diameter of the vessel decreased. When the number of partitions was 16 or 32 in a 128-mm-thick slab, the signal intensity obtained by the elliptical centric phase-encoding technique was almost the same as that obtained by the conventional centric phase-encoding technique. However, when the number of partitions was increased (64-124), and if the duration of enhancement was short, the signal intensity obtained by the elliptical centric phase-encoding technique was higher than that obtained by the conventional centric phase-encoding technique. In conclusion, in terms of the duration of enhancement and the delay of scan timing, the elliptical centric phase-encoding technique is superior to the conventional centric phase-encoding technique when the number of partitions in a slab for 3D MR angiography is increased.

Contrast Media↗

[Evaluation of the increase in signal intensity from applying the fast recovery technique to fast spin echo images].

The aim of the present study was to evaluate the increase in signal intensity caused by applying the fast recovery (FR) technique to fast spin echo (FSE) images, that is, the fast recovery fast spin echo (FR-FSE) method. All images of phantoms, whose T(2) values were different, were acquired with a Signa 1.5 Tesla system (GE Medical Systems) using the three-dimensional (3D) FSE and 3D FR-FSE sequences. We assessed the increased signal intensity as follows: (signal intensity on the FR-FSE image - FSE image) / FSE image (%). Our results showed that the increased signal intensity became high when 1) T(2) of the phantom was prolonged, 2) TR was shortened, and 3) echo train length (ETL) was decreased. By utilizing the results of this study, the increased signal caused by the FR technique could be estimated quantitatively when the TR, ETL, and T(2) of investigated substances were determined. For example, when TR, ETL, and T(2) were 1500 msec, 16-64, and 1500 msec, respectively, the increase in signal intensity was estimated to be approximately 70%. In addition, when T(2) was less than approximately 250 msec, signal intensity was not significantly increased by the FR pulses, that is, the FR-FSE image was the same as the FSE image. Accordingly, the FR-FSE method was confirmed to enhance the signal in substances with longer T(2), while maintaining the same contrast of the image as that obtained by the conventional FSE method. Our results are useful for evaluating the increased signal intensity caused by employing the FR technique.

Image Enhancement↗

Evaluation of efficacy of an automated single-voxel proton MRS algorithm on a 3T system.

PURPOSE: To evaluate the efficacy of a fully automatic, single-voxel, proton MR spectroscopy algorithm on a 3.0T MR system. METHODS: The PROBE/SVQ algorithm (GE Medical Systems) was evaluated on a General Electric (GE) Signa LX-3T system. Ten normal volunteers (female, 21.1+/-2.0 years old) participated in the study. Nine representative regions of interest were examined, namely, right and left frontal white matter; right and left parietal white matter; right and left basal ganglia; right and left dentate nucleus; and pons. RESULTS: The mean coefficients of variation in all regions for the N-acetyl-aspartate to creatine ratio (NAA/Cr), choline to creatine ratio (Cho/Cr), and choline to N-acetyl-aspartate ratio (Cho/NAA) were 10.2+/-2.4%, 11.4+/-3.2% and 12.6+/-1.4%, respectively. CONCLUSION: A fully automated spectroscopic examination under clinical setting utilizing the PROBE/SVQ algorithm appears to be a reliable method, extending the window of routine clinical assessment of brain metabolism.

Adult↗

[Simulation study of scan timing in three-dimensional contrast-enhanced MR angiography].

In our study of three-dimensional contrast-enhanced MR angiography, we performed a computer simulation to quantitatively investigate vessel visibility according to scan timing. To construct the simulated MR images, we varied the position (scan timing) and range (enhancement-duration) of k-space data assumed to be acquired during contrast enhancement. In the present study, either the sequential or centric phase-encoding order in k(y) and k(z) on k-space was assumed to be used. When scan timing was shifted from the optimal timing, the visibility of thick vessels decreased, and the signal intensity in thin vessels was higher than that in thick vessels. We found that the appropriate setting of scan timing was an important factor in the visibility of thick vessels. Meanwhile, we also noted that extending the enhancement-duration (or shortening the scan time) could increase the visibility of thin vessels. Our results and the simple technique used for simulation are considered to be useful for the study of three-dimensional contrast-enhanced MR angiography.

Computer Simulation↗