Cervical spine: MR imaging with a partial flip angle, gradient- refocused pulse sequence. Part II. Spinal cord disease

A magnetic resonance imaging pulse sequence (GRASS) with a short repetition time (TR), short echo time (TE), partial flip angle, and gradient refocused echo was prospectively evaluated for the detection of cervical cord disease that caused minimal or no cord enlargement in eight patients. Sagittal T2-weighted, cerebrospinal fluid (CSF)-gated images and sagittal and axial GRASS images were obtained in all patients. The following GRASS parameters were manipulated to determine their effect on signal-to-noise ratio (S/N) and contrast: flip angle (4 degrees-18 degrees), TR (22-50 msec), and TE (12.5-25 msec). Flip angle had the greatest effect on S/N and contrast. There were no differences between axial and sagittal imaging for the spinal cord or lesion. However, because the signal intensity of CSF did differ on sagittal and axial images and because this influenced the conspicuity of lesions, there was a difference in the useful flip angle range for axial and sagittal imaging. No one set of imaging parameters was clearly superior, and in all patients, the gated image was superior to the sagittal GRASS image in lesion detection. GRASS images should be used in the axial plane primarily to confirm spinal cord disease detected on sagittal CSF-gated images. For this, a balanced approach is suggested (TR = 40 msec, TE = 20 msec, with flip angles of 4 degrees-6 degrees for sagittal and 6 degrees-8 degrees for axial imaging).     

High-resolution MR of the spinal cord in humans and rats

Human and rat cervical spinal cords were imaged with high-resolution spin-echo and inversion-recovery pulse sequences in an experimental 1.9-T MR system. The gross morphology of the cord was easily discernible in fresh and fixed specimens, including the white and gray commissures, dorsal and ventral horns, and lateral and posterior funiculi. The T1, T2, and spin-density values for gray and white matter were determined from these images and were found to be 914 msec, 114 msec, and 71% for white matter other than the dorsal columns, and 946 msec, 87 msec, and 80% for gray matter in human spinal cords. These values are reduced considerably after formalin fixation: T1 to 56% (white matter) and 54% (gray matter) of prefixation values, T2 to 52% (white matter) and 70% (gray matter) of fresh values, and spin density to 90% (white matter) and 96% (gray matter) of prefixation values. Interestingly, the central gray matter demonstrates higher signal intensity than the white matter on both short and long TR/TE images. This intensity difference was observed for both human and rat spinal cords, before and after fixation, and can be explained by the relatively small T1 differences between gray matter and white matter and the gray matter-white matter spin-density ratios: 1.127 for fresh and 1.203 for fixed specimens.     

Measurement of T1 and T2 in the cervical spinal cord at 3 tesla

T(1) and T(2) were measured for white matter (WM) and gray matter (GM) in the human cervical spinal cord at 3T. T(1) values were calculated using an inversion-recovery (IR) and B(1)-corrected double flip angle gradient echo (GRE) and show significant differences (p = 0.002) between WM (IR = 876 +/- 27 ms, GRE = 838 +/- 54 ms) and GM (IR = 973 +/- 33 ms, GRE = 994 +/- 54 ms). IR showed significant difference between lateral and dorsal column WM (863 +/- 23 ms and 899 +/- 18 ms, respectively, p = 0.01) but GRE did not (p = 0.40). There was no significant difference (p = 0.31) in T(2) between WM (73 +/- 6 ms) and GM (76 +/- 3 ms) or between lateral and dorsal columns (lateral: 73 +/- 6 ms, dorsal: 72 +/- 7 ms, p = 0.59). WM relaxation times were similar to brain structures with very dense fiber packing (e.g., corpus callosum), while GM values resembled deep GM in brain. Optimized sequence parameters for maximal contrast between WM and GM, and between WM and cerebrospinal fluid (CSF) were derived. Since the spinal cord has rostral-caudal symmetry, we expect these findings to be applicable to the whole cord.     

Evaluation of three-dimensional fast spoiled gradient recalled acquisition in the steady state (FSPGR) using ultra magnetic field 3-Tesla MRI for optimal pulse sequences of T1-weighted imaging

The advantage of the higher signal-to-noise ratio (SNR) of 3-Tesla magnetic resonance imaging (3TMRI) contributes to the improvement of spatial and temporal resolution. However, T1-weighted images of the brain obtained by the spin-echo (SE) method at 3T MR are not satisfactory for clinical use because of radiofrequency (RF) field inhomogeneity and prolongation of the longitudinal relaxation time (T1) of most tissues. We evaluated optimal pulse sequences to obtain adequate T1 contrast, high gray matter/white matter contrast, and suitable postcontrast T1-weighted images using the three-dimentional (3D) fast spoiled gradient recalled acquisition in the steady state (FSPGR) method instead of the SE method. For the optimization of T1 contrast, the Ernst angle of the optimal flip angle (FA) was obtained from the T1 value of cerebral white matter with the shortest TR and TE. Then the most appropriate FA, showing the maximum contrast-to-noise ratio (CNR) and SNR, was obtained by changing the FA every 5 degrees at about the level of the Ernst angle. Image uniformity was evaluated by a phantom showing similar T1 and T2 values of cerebral white matter. In order to evaluate the effect of the contrast enhancement, signal intensity was compared by the same method using a phantom filled with various dilutions of contrast media. Moreover, clinical studies using full (0.1 mmol/kg) and half (0.05 mmol/kg) doses of Gd-DTPA were carried out with the most appropriate parameters of the 3D-FSPGR method. These studies indicated that the optimal pulse sequences for obtaining an adequate T1-weighted image of the brain using 3D-FSPGR are 9/2 msec (TR/TE) and 13 degrees (FA).     

Volume fast spin-echo imaging of the cervical spine

RATIONALE AND OBJECTIVES: The authors prospectively evaluated a T2-weighted, three-dimensional (3D) volume, fast spin-echo (SE) pulse sequence in assessment of the cervical spine and compared it with standard imaging protocol. MATERIALS AND METHODS: Eighteen patients with neck pain underwent magnetic resonance (MR) imaging at 1.5 T with two-dimensional (2D) fast SE and axial 3D gradient-echo (GRE) protocols and with an additional sagittal T2-weighted volume fast SE protocol. The spinal cord and canal, neural foramina, and intervertebral disks were assessed by two neuroradiologists, and the results were compared with reports from the standard protocol. The quality of the partition (direct sagittal) and reconstructed images were evaluated. RESULTS: No differences existed in the assessment of spinal cord disease or disk herniation with 2D fast SE and volume fast SE imaging. Some mild variation occurred in assessment of the neural foramina. Partition images demonstrated a high level of resolution and contrast, while reconstructed images had consistently lower quality. However, this did not impede detection and grading of disk or spinal abnormalities, which were adequately shown on volume fast SE sagittal images. Neural foramina were well demonstrated on axial reconstructions from volume fast SE imaging. CONCLUSION: Volume fast SE imaging provides information about the spinal cord, canal, disks, and neural foramina that is comparable to the information provided by routine imaging. Its thinner sections and multiplanar reconstruction capability are advantages over 2D imaging. Its greater tissue contrast with better visualization of the cervical cord, greater signal-to-noise ratio, and less susceptibility artifact are advantages over 3D GRE imaging.     

Flip angle dependence of experimentally determined T1sat and apparent magnetization transfer rate constants

The purpose of this work was to develop a method for determining the T1_sat and magnetization transfer (MT) rate constants by analyzing the slice-select flip angle dependent MT behavior of normal white and gray matter. The technique uses a high MT power, three-dimensional (3D) gradient-recalled echo (GRE) sequence, with a well chosen MT pulse frequency offset, such that the experimental conditions closely satisfy requisite assumptions for invoking a first order rate process for MT. Integral to this method is that the T1_sat and MT ratio values are obtained under explicitly identical MT saturation conditions. The T1_sat of white matter was found to be approximately 300 msec, and the MT rate constant was approximately 2.0 sec^?1. The T1_sat of gray matter was approximately 500 msec, and the MT rate constant was 1.1 sec^?1. We also found a strong dependence of the MT rate constant on the slice-select flip angle used for the imaging sequence, independent of the MT saturation parameters. Strongly T1-weighted imaging sequences can result in the underestimation of the MT rate constant by 50%. Practical technical suggestions for quantitative MT experiments are put forth.     

Dynamic contrast-enhanced three-dimensional MR imaging of liver parenchyma: source images and angiographic reconstructions to define hepatic arterial anatomy

PURPOSE: To assess the accuracy of an interpolated breath-hold T1-weighted three-dimensional (3D) gradient-echo (GRE) magnetic resonance (MR) imaging sequence with near-isotropic pixel size (相似文献   

Gray and white matter delineation in the human spinal cord using diffusion tensor imaging and fuzzy logic

RATIONALE AND OBJECTIVES: Diffusion tensor imaging (DTI) has been used extensively in determining morphology and connectivity of the brain; however, similar analysis in the spinal cord has proven difficult. The objective of this study was to improve the delineation of gray and white matter in the spinal cord by applying signal processing techniques to the eigenvalues of the diffusion tensor. Our approach involved creating anisotropy indices based on the difference between eigenvalues and mean diffusivity then using a fuzzy inference system (FIS) to delineate between gray and white matter in the human cervical spinal cord. MATERIALS AND METHODS: DTI was performed on the cervical spinal cord in five neurologically intact subjects. Distributions were extracted for regions of gray and white matter through the use of a digitized histologic template. Fuzzy membership functions were created based on these distributions. Detectability index and receiver operating characteristic (ROC) analysis was performed on traditional DTI indices and FIS classified regions. RESULTS: A significantly higher contrast between gray and white matter was observed using fuzzy classification compared with traditionally used DTI indices based on the detectability index (P < .001) and trends in the ROC analysis. Reconstructed images from the FIS qualitatively showed a better anatomical representation of the spinal cord compared with traditionally used DTI indices. CONCLUSIONS: Diffusion tensor imaging using an FIS for tissue classification provides high contrast between spinal gray and white matter compared with traditional DTI indices and may provide a noninvasive technique to quantify the integrity and morphology of the human spinal cord following injury.     

First-pass contrast-enhanced inversion recovery and driven equilibrium fast gre imaging studies: Detection of acute myocardial ischemia

The purpose of this study was (1) to monitor the dynamic effects Of T1 -enhancing and magnetic SUSCCPtibility contrast material on normal canine myocardium using inversion recovery (IR)- and driven equilibrium @E)-prepared fast gradient-recalled echo (GRE) sequences and (2) to determine the relative value of T1-enhancing and magnetic eusceptibflity contrast material in detecting regions of ischemia in the same animal. Normal dogs (n = 5) and dogs with acute occlusion of the left anterior descending (LAD] coronary artery [n = 11) were studied using a 1.5-T NIR imager. ECG-gated fast IR-prepared GRE images were acquired using TI/TR/TE of 700/7.0/2.9 msec and a flip angle of 7°. Fast DE-prepared GRE images were obtained using a flip angle of 12° and a DE delay /TR/TE of 60/10.2/4.2 msec. Sequential images were acquired to monitor transit of 0.06 mmol/kg gadodiamide injection and 0.2 and 0.4 mmol/kg sprodiamide injection. On slice-nonselective IR fast GRE images. gadodiamide caused signiflcant enhancement of the normal myocardium and the left ventricular (LV) chamber blood. In dogs with LAD occlusion, the ischemic region was defined as an area of low signal intensity (SI). On DE-prepared GRE sequences, administration of sprodiamide resulted in a substantial decrease in signal from normal myocardium and LV chamber blood in normal dogs. In animals subjected to LAD occlusion, this contrast medium produced a transient decrease in SI from normal myocardium [P <.06) and no signiflcant change in SI from ischemic myocardium. IR- and DE-prepared taet GRE imaging can be used to monitor the transit of Tl-enhancing and magnetic susceptibility contrast material in the heart. respectively. Cardiac image quality was much better when slice-nonselective IR-prepared fast GRE sequences were used rather than DE-prepared fast GRE.     

Axial 3D gradient-echo imaging for improved multiple sclerosis lesion detection in the cervical spinal cord at 3T

Introduction

In multiple sclerosis (MS), spinal cord imaging can help in diagnosis and follow-up evaluation. However, spinal cord magnetic resonance imaging (MRI) is technically challenging, and image quality, particularly in the axial plane, is typically poor compared to brain MRI. Because gradient-recalled echo (GRE) images might offer improved contrast resolution within the spinal cord at high magnetic field strength, both without and with a magnetization transfer prepulse, we compared them to T2-weighted fast-spin-echo (T2-FSE) images for the detection of MS lesions in the cervical cord at 3T.

Methods

On a clinical 3T MRI scanner, we studied 62 MS cases and 19 healthy volunteers. Axial 3D GRE sequences were performed without and with off-resonance radiofrequency irradiation. To mimic clinical practice, all images were evaluated in conjunction with linked images from a sagittal short tau inversion recovery scan, which is considered the gold standard for lesion detection in MS. Two experienced observers recorded image quality, location and size of focal lesions, atrophy, swelling, and diffuse signal abnormality independently at first and then in consensus.

Results

The number and volume of lesions detected with high confidence was more than three times as high on both GRE sequences compared to T2-FSE (p?<?0.0001). Approximately 5 % of GRE scans were affected by artifacts that interfered with image interpretation, not significantly different from T2W-FSE.

Conclusions

Axial 3D GRE sequences are useful for MS lesion detection when compared to 2D T2-FSE sequences in the cervical spinal cord at 3T and should be considered when examining intramedullary spinal cord lesions.     

Diffusion-weighted MR imaging of the normal human spinal cord in vivo

BACKGROUND AND PURPOSE: Diffusion-weighted imaging is a robust technique for evaluation of a variety of neurologic diseases affecting the brain, and might also have applications in the spinal cord. The purpose of this study was to determine the feasibility of obtaining in vivo diffusion-weighted images of the human spinal cord, to calculate normal apparent diffusion coefficient (ADC) values, and to assess cord anisotropy. METHODS: Fifteen healthy volunteers were imaged using a multi-shot, navigator-corrected, spin-echo, echo-planar pulse sequence. Axial images of the cervical spinal cord were obtained with diffusion gradients applied along three orthogonal axes (6 b values each), and ADC values were calculated for white and gray matter. RESULTS: With the diffusion gradients perpendicular to the orientation of the white matter tracts, spinal cord white matter was hyperintense to central gray matter at all b values. This was also the case at low b values with the diffusion gradients parallel to the white matter tracts; however, at higher b values, the relative signal intensity of gray and white matter reversed. With the diffusion gradients perpendicular to spinal cord, mean ADC values ranged from 0.40 to 0.57 x 10(-3) mm2/s for white and gray matter. With the diffusion gradients parallel to the white matter tracts, calculated ADC values were significantly higher. There was a statistically significant difference between the ADCs of white versus gray matter with all three gradient directions. Strong diffusional anisotropy was observed in spinal cord white matter. CONCLUSION: Small field-of-view diffusion-weighted images of the human spinal cord can be acquired in vivo with reasonable scan times. Diffusion within spinal cord white matter is highly anisotropic.     

Comparison of two-dimensional gradient echo, turbo spin echo and two-dimensional turbo gradient spin echo sequences in MRI of the cervical spinal cord anatomy

The aim of this study was to assess the detectability and distinguishability of the cervical spinal cord, the anterior and posterior spinal roots and of the internal anatomy of the cord (distinction of grey and white matter). For this purpose 20 healthy volunteers were examined using a 1.5 T MR unit with 20 mT/m gradient strength and a dedicated circular polarized neck array coil. Three T2* weighted (w). 2D gradient echo sequences, two T2 w. 2D turbo spin echo (TSE) sequences and one T2 w. 2D turbo gradient spin echo (TGSE) sequence were compared. The multiecho 2D fast low angle shot (FLASH) sequence with magnetization transfer saturation pulse (me FLASH+MTS) yielded the best results for liquor/compact bone, liquor/spinal cord and grey/white matter contrast, as found with regions of interest (ROI) analysis. The single echo 2D FLASH sequence was significantly poorer than the two me FLASH+/-MTS sequences. Two-dimensional TGSE as well as 2D TSE with a 256 matrix and with a 512 matrix yielded the poorest results. In the visual analysis the contrast between liquor and compact bone, liquor and cord as well as liquor and roots was best with me FLASH+MTS, whereas grey/white matter distinction was best using me FLASH-MTS. In conclusion, we would therefore recommend the inclusion of an axial T2* w. multiecho 2D spoiled gradient echo sequence with magnetization transfer saturation pulse and gradient motion rephasing in a MR imaging protocol of the cervical spine.     

Magnetic resonance imaging of mouse spinal cord.

The feasibility of performing high-resolution in vivo MRI on mouse spinal cord (SC) at 9.4 T magnetic field strength is demonstrated. The MR properties of the cord tissue were measured and the characteristics of water diffusion in the SC were quantified. The data indicate that the differences in the proton density (PD) and transverse relaxation time between gray matter (GM) and white matter (WM) dominate the contrast seen on the mouse SC images at 9.4 T. However, on heavily T(2)-weighted images these differences result in a reversal of contrast. The diffusion of water in the cord is anisotropic, but the WM exhibits greater anisotropy and principal diffusivity than the GM. The quantitative data presented here should establish a standard for comparing similar measurements obtained from the SCs of genetically engineered mouse or mouse models of SC injury (SCI).     

Improving MRI differentiation of gray and white matter in epileptogenic lesions based on nonlinear feedback.

A new method for enhancing MRI contrast between gray matter (GM) and white matter (WM) in epilepsy surgery patients with symptomatic lesions is presented. This method uses the radiation damping feedback interaction in high-field MRI to amplify contrast due to small differences in resonance frequency in GM and WM corresponding to variations in tissue susceptibility. High-resolution radiation damping-enhanced (RD) images of in vitro brain tissue from five patients were acquired at 14 T and compared with corresponding conventional T(1)-, T(2) (*)-, and proton density (PD)-weighted images. The RD images yielded a six times better contrast-to-noise ratio (CNR = 44.8) on average than the best optimized T(1)-weighted (CNR = 7.92), T(2) (*)-weighted (CNR = 4.20), and PD-weighted images (CNR = 2.52). Regional analysis of the signal as a function of evolution time and initial pulse flip angle, and comparison with numerical simulations confirmed that radiation damping was responsible for the observed signal growth. The time evolution of the signal in different tissue regions was also used to identify subtle changes in tissue composition that were not revealed in conventional MR images. RD contrast is compared with conventional MR methods for separating different tissue types, and its value and limitations are discussed.     

MR image contrast at high field strength.

The T1 of soft tissues increases with magnetic field strength. Some tissue contrast may be diminished on high-field-strength magnetic resonance (MR) images when conventional TRs are used, because of altered T1 effects on the MR signals. This necessitates longer TRs in techniques that use long TRs, which prolongs the examination excessively. Behavior of macroscopic magnetization is governed by the Bloch equations. Therefore, T1 contributions to the MR signal can be modulated by means of both timing intervals and radio-frequency pulses. The analytic solution to the Block equations allowed calculation of white matter/gray matter and gray matter/cerebrospinal fluid contrast in both spin-echo and inversion-recovery (IR) imaging. Rabbit brains (normal and tumor-containing) were then imaged in vivo at 1.5 and 4.7 T. In addition, MR images of a human head were obtained at 4.0 T. Experimental results supported the theoretical predictions that brain contrast on long TR spin-echo or IR images increases with field strength. However, varying the excitation flip angle allowed optimization of the T1 contribution to the MR signals, improving image contrast and/or reducing examination time. Thus, the dependence of T1 on field strength determines the optimum choice of imaging techniques and parameters in a predictable fashion.     

The MR appearance of gray and white matter in the cervical spinal cord

Artifacts that can distort the appearance of the cervical spinal cord are caused by data truncation during MR image reconstruction. We used a phantom and then correlated anatomic sections with MR images in cadavers and normal volunteers to evaluate the effect of truncation artifacts on the MR appearance of the spinal cord. When truncation artifacts are minimized, the gray matter and major white-matter columns in the cervical cord can be recognized. T2-weighted gradient-echo MR techniques can best differentiate gray from white matter.     

Experimental autoimmune encephalomyelitis in the rat spinal cord: lesion detection with high-resolution MR microscopy at 17.6 T

BACKGROUND AND PURPOSE: Experimental autoimmune encephalomyelitis (EAE) is an inflammatory demyelinating disorder of the CNS and an animal model of multiple sclerosis. We used high-field MR microscopy at 17.6 T to image spinal cord inflammatory lesions in the acute stage of chronic relapsing rat EAE. We sought to compare lesions detected on MR imaging with histopathologic findings and to quantify the inflammatory lesion load. METHODS: Imaging of fixed spinal cord specimens was performed by using a 3D gradient-echo sequence with a spatial resolution of 35 x 35 x 58 microm3 and a total imaging time of 5.5 hours. Histopathologic analysis was performed by staining axial sections with hematoxylin-eosin or Luxol fast blue to identify cellular infiltration and demyelination. RESULTS: Clinical signs of EAE occurred on days 10-14 after immunization. On day 22, healthy white matter and gray matter were differentiated by high contrast on T2*-weighted images, with white matter lesions appearing as hyperintense areas in the normal-appearing white matter. Inflammatory lesions identified on histopathologic evaluation were readily detected with MR imaging and vice versa. MR imaging and histopathologic analysis had excellent correlation regarding the extent of white matter lesions. Inflammatory infiltrates of gray matter were not detectable with MR imaging. Using a semiautomatic segmentation of the acquired MR data, we could quantify white matter lesion load. CONCLUSION: Ex vivo high-resolution MR microscopy of the spinal cord at 17.6 T allows rapid and highly accurate determination of CNS inflammation by demonstrating virtually all histologically detectable white matter inflammatory lesions.     

Quantitation of structural distortion of the cervical neural foramina in gradient-echo MR imaging

Quantitative errors (due to magnetic susceptibility artifacts) in the measurement of the cervical spinal neural foramina with fast gradient-echo (GRE) magnetic resonance imaging were assessed. Cylindric phantoms of different materials were used to demonstrate the nature of magnetic susceptibility artifacts, emphasizing the dependence of the artifact on tissue geometry. Neural foramina diameters measured on thin, sagittal GRE and spin-echo (SE) images through the neural foramina of a fresh human cervical spine specimen were then compared with direct measurements with calipers. The GRE images showed more apparent narrowing than did the SE images. The absolute distortion of seven neural foramina was rather constant (less than two pixels) on the GRE images; therefore, the relative distortion was inversely proportional to the size of the neural foramen, ranging up to 10% in the upper cervical region at a short TE. The absolute and relative distortion increased as TE increased. At a constant TE, the structural distortion did not change with different TRs or flip angles. The shortest possible TE is recommended in evaluation of the cervical spine.     

Quantitative T2 in the occipital lobe: the role of the CPMG refocusing rate

PURPOSE: To investigate the dependence of occipital gray and white matter T(2) on the Carr-Purcell-Meiboom-Gill (CPMG) refocusing interval, thereby testing the basis of a novel functional magnetic resonance imaging (fMRI) method for blood volume quantification, and addressing recent questions surrounding T(2) contrast in the occipital lobe. MATERIALS AND METHODS: A CPMG sequence with 1 x 1 x 5 mm(3) resolution was used to quantify T(2) in a single axial slice at the midlevel of the occipital lobe in 23 healthy adult volunteers. Refocusing intervals of 8, 11, and 22 msec were compared. A Bayesian classifier was used to classify a 1 x 1 x 1 mm(3) T(1)-weighted three-dimensional data set into gray matter, white matter, and cerebrospinal fluid, with an average 95% a posteriori probability used as the threshold for inclusion into a tissue-specific region of interest (ROI). RESULTS: The usual T(2) contrast between the gray and white matter (i.e., T(2GM) > T(2WM)) was observed, with a highly significant effect of tissue type on the estimated T(2) (P < 10(-5)). The observed T(2) gradually decreased with increasing refocusing interval, for a decrease of 3.3 +/- 1.5 msec in gray matter and 3.0 +/- 1.5 msec in white matter between the 8 and 22 msec refocusing interval acquisitions. CONCLUSION: The observed T(2) shortening is consistent with the effect of the dramatic decrease in T(2) of partly deoxygenated blood on this range of refocusing rates.     

MR imaging of the liver with Gd-BOPTA: quantitative analysis of T1-weighted images at two different doses.

This study evaluates the efficacy of gadobentate-dimeglumine (Gd-BOPTA) for enhancement of liver signal-to-noise ratio (SNR) and lesion-liver contrast-to-noise ratio (CNR) on T1-weighted spin-echo (SE) and gradient-recalled-echo (GRE) images at two different doses. Fifty patients with known or suspected liver lesions were examined at 1.5 T. T1-weighted SE (TR/TE 300/12 msec) and GRE images (TR/TE80/4.2 msec/flip angle 80 degrees) were obtained before and at 40-80 minutes and 90-120 minutes after administration of 0.05 or 0.1 mmol/kg Gd-BOPTA. Quantitative measurements of tissue signal intensity were performed at each dose. Liver showed significant enhancement after Gd-BOPTA on T1-weighted SE and GRE images (0.05 mmol: P < 0.05; 0.1 mmol: P < 0.001). The dose of 0.1 mmol/kg provided higher liver SNR than 0.05 mmol/kg. Mean liver SNR was higher on GRE than SE images (P < 0.0001). Lesion-liver CNR significantly increased on GRE images after 0.1 mmol (P < 0.05). There was a trend toward superiority of 0.1 mmol over 0.05 mmol/kg. GRE images were superior to SE images for pre- and post Gd-BOPTA lesion-liver CNR (P < 0.05). Our study suggests that Gd-BOPTA provides prolonged enhancement of liver SNR and CNR, that a dose of 0.1 mmol/Kg appears to be superior than 0.05 mmol/Kg, and that GRE techniques should be used in preference over SE techniques.