Gradient-echo Echo-planar Imaging Research Articles

Pain fMRI in rat cervical spinal cord: An echo planar imaging evaluation of sensitivity of BOLD and blood volume-weighted fMRI

Objective measure of pain is valuable in drug discovery research and development of analgesics. Spinal cord is an important relay of the pain pathway, and fMRI offers an excellent opportunity to quantify pain using activation in the spinal cord induced by painful stimuli. fMRI literature of cervical spinal cord with regard to the spatial extent, in both longitudinal and cross-sectional directions, of neuronal activation induced by noxious stimulation is ambiguous. This study investigates the feasibility of developing a robust pain assay using fMRI in the cervical spinal cord in α-chloralose anesthetized rats subjected to transcutaneous noxious electrical stimulation of the forepaw. Blood oxygenation level dependent (BOLD) and blood volume (BV)-weighted fMRI data were acquired without and with intravenous injection of ultra small superparamagnetic iron oxide particles (USPIO), respectively. BOLD data were acquired by gradient-echo (GE) and spin-echo (SE) echo planar imaging (EPI), while BV-weighted fMRI data were acquired only by GE EPI. Cervical spinal cord activity was robustly detected by all three fMRI techniques. The sensitivity of the fMRI signal was highest in GE BV-weighted fMRI followed in order by GE BOLD, and SE BOLD, respectively. Spatially, the fMRI signal extended ∼ 9 mm in the longitudinal direction, covering C 4–C 8 segments, coinciding with the synapse location of afferent terminals from the stimulated site. In the cross-sectional direction, the signal change is localized predominantly to the ipsilateral dorsal region. This study demonstrates that cervical spinal cord fMRI can be performed reliably in anesthetized rats offering it as a potential tool for analgesic drug development.

Comparison of Dynamic Susceptibility-weighted Contrast-enhanced MR Methods: Recommendations for Measuring Relative Cerebral Blood Volume in Brain Tumors

To investigate whether estimates of relative cerebral blood volume (rCBV) in brain tumors, obtained by using dynamic susceptibility-weighted contrast material-enhanced magnetic resonance (MR) imaging vary with choice of data acquisition and postprocessing methods. Four acquisition methods were used to collect data in 22 high-grade glioma patients, with informed written consent under HIPAA-compliant guidelines approved by the institutional review board. During bolus administration of a standard single dose of gadolinium-based contrast agent (0.1 mmol per kilogram of body weight), one of three acquisition methods was used: gradient-echo (GRE) echo-planar imaging (echo time [TE], 30 msec; flip angle, 90 degrees ; n = 10), small-flip-angle GRE echo-planar imaging (TE, 54 msec; flip angle, 35 degrees ; n = 7), or dual-echo GRE spiral-out imaging (TE, 3.3 and 30 msec; flip angle, 72 degrees ; n = 5). Next, GRE echo-planar imaging (TE, 30 msec; flip angle, 90 degrees ; n = 22) was used to collect data during administration of a second dose of contrast agent (0.2 mmol/kg). Subsequently, six methods of analysis were used to calculate rCBV. Mean rCBV values from whole tumor, tumor hot spots, and contralateral brain were normalized to mean rCBV in normal-appearing white matter. Friedman two-way analysis of variance and Kruskal-Wallis one-way analysis of variance results indicated that qualitative rCBV values were dependent on acquisition and postprocessing methods for both tumor and contralateral brain. By using the nonparametric Mann-Whitney test, a consistently positive (greater than zero) tumor-contralateral brain rCBV ratio resulted when either the preload-postprocessing correction approach or dual-echo acquisition approach (P < .008 for both methods) was used. The dependence of tumor rCBV on the choice of acquisition and postprocessing methods is caused by their varying sensitivities to T1 and T2 and/or T2* leakage effects. The preload-correction approach and dual-echo acquisition approach are the most robust choices for the evaluation of brain tumors when the possibility of contrast agent extravasation exists.

Inflow effects on hemodynamic responses characterized by event‐related using gradient‐echo EPI sequences

The purpose of this study is to determine whether blood inflow impacts the temporal behavior of BOLD-contrast fMRI signal changes in a typical event-related paradigm. The inflow contributions in the hemodynamic response to repeated single trials of short visual stimulation were assessed with a gradient-echo EPI sequence by altering the flip angle (FA) from 30 degrees to 90 degrees at a repetition time of 1 s. For each FA condition (30 degrees, 60 degrees, and 90 degrees), 30 trials were performed on 15 healthy volunteers on a 3T MRI scanner. Comparing the percent BOLD contrast, prominent inflow effects were found with statistical significance between the 90 degrees- and 30 degrees-FA conditions (0.73 +/- 0.15 versus 0.67 +/- 0.12%, p=0.028). BOLD responses with FA=30 degrees exhibited latencies significantly slower than those with FA=90 degrees (3.69 +/- 0.39 s versus 3.37 +/- 0.28 s, p=0.001). The falling time of the 30 degrees-FA responses was earlier but not statistically different from that of the 90 degrees-FA (8.17 +/- 1.04 s versus 8.03 +/- 1.15 s, p=0.3). Using a voxelwise analysis, the latency variations of the activated visual areas were determined at several contrast-to-noise ratio (CNR) levels (controlled by averaging different numbers of randomly selected trials). The latency variations from the 90 degrees-FA responses were greater at lower CNR but similar at higher CNR levels when comparing to the 30 degrees-FA ones. This study suggests that inflow effects contribute to the BOLD signal, resulting in hemodynamic response with shorter latency.

Validation of fast MR thermometry at 1.5 T with gradient‐echo echo planar imaging sequences: phantom and clinical feasibility studies

The purpose of this work was to validate in phantom studies and demonstrate the clinical feasibility of MR proton resonance frequency thermometry at 1.5 T with segmented gradient-echo echo planar imaging (GRE-EPI) sequences during liver tumour radiofrequency (RF) ablation. Classical GRE acquisitions and segmented GRE-EPI acquisitions were performed at 1.5 T during simultaneous RF heating with an MR-compatible RF electrode placed in an agar gel phantom. Temperature increments were calculated and compared with four optical temperature probe measurements using Bland- Altman analysis. In a preliminary clinical feasibility study, the rapid GRE-EPI sequence (echo train length = 13) was used for MR temperature monitoring of RF ablation of liver tumours in three patient procedures. For phantom experiments, the Bland-Altman mean of differences between MR and optical probe temperature measurements was <0.4 degrees C, and the 95% limits of agreement value was <1.4 degrees C. For the in vivo studies, respiratory-triggered GRE-EPI acquisitions yielded a temperature accuracy of 1.3 +/- 0.4 degrees C (acquisition time = 0.6 s/image, spatial coverage of three slices/respiratory cycle). MR proton resonance frequency thermometry at 1.5 T yields precise and accurate measurements of temperature increment with both classical GRE and rapid GRE-EPI sequences. Rapid GRE-EPI sequences minimize intra-scan motion effects and can be used for MR thermometry during RF ablation in moving organs.

Spinal cord functional MRI at 3 T: Gradient echo echo-planar imaging versus turbo spin echo

The purpose of this study was to evaluate and compare turbo spin echo (TSE) with gradient echo echo-planar imaging (GE-EPI) pulse sequences for functional magnetic resonance imaging (fMRI) of spinal cord activation at 3 T field strength. Healthy volunteers underwent TSE and GE-EPI spinal fMRI. The activation paradigm comprised the temporal alternation of finger motion and rest. Pulse sequences were optimized to obtain sufficient image quality and optimal sensitivity to small T 2 or T 2⁎ relaxation time changes. Spinal cord activation measured by the two pulse sequences was evaluated with respect to spatial distribution of activation, signal sensitivity, and reproducibility. For the GE-EPI sequence, fMRI activation was maximal in the spinal cord segments at the levels of the fifth cervical down to the first thoracic vertebra. For the TSE sequence, fMRI measurements showed no distinct location with maximal activation. Percentage signal change and number of activated voxels were approximately twice as high for GE-EPI compared to TSE fMRI. Reproducibility of the signal changes was much better for GE-EPI than for TSE imaging. To conclude, multi-subjects averaged GE-EPI is more location specific for blood-oxygen-level-dependent (BOLD) activation, more sensitive, and is suggested to be more reproducible than TSE fMRI.

False‐positive analysis of functional MRI during simulated deep brain stimulation: A phantom study

To investigate the false-positive activations/deactivations in functional MRI (fMRI) of deep brain stimulation (DBS) using a phantom. fMRI experiments were performed on a 1.5T scanner using a single-shot gradient-echo echo-planar imaging (GE-EPI) sequence (TR/TE/FA = 6000 msec/60 msec/90 degrees ) on an agar-gel phantom inserted with DBS electrodes. During the experimental blocks, two-second stimuli were delivered during the interscan waiting time (ISWT), which was adjusted by changing the number of slices acquired within the TR (3500 msec with 30 slices and 5160 msec with 10 slices). Data were analyzed using SPM2 software, and the false-positive voxels were detected with five different P-value thresholds. The number of false-positive voxels in experimental conditions had no significant differences from those in control conditions with either long or short ISWT, which increased with the P-value threshold from zero at P < 0.0001 to approximately 40 at P < 0.05. The pattern of increasing number of false-positive reactions along with P-value was similar between all conditions. False-positive findings from fMRI with similar experimental design can be well controlled with a statistical threshold of P < 0.001 or tighter. The short ISWT of 3500 msec did not increase false-positive reactions compared to the long ISWT of 5160 msec.

Non-invasive characterization of β-amyloid 1-40 vasoactivity by functional magnetic resonance imaging in mice

Neurovascular regulation, which is critical to the efficient functioning of the brain, is impaired in Alzheimer's disease and in transgenic mice overexpressing Aβ. Although senile plaques and neurofibrillary tangles represent neuropathological hallmarks of Alzheimer's disease, deposition of Aβ in cerebral blood vessels also likely plays a significant role in this debilitating and fatal disease. Further, soluble Aβ, which shows greater correlation with disease progression and severity than deposited plaques or tangles, displays strong vasoactive properties. The aim of this study was to develop a non-invasive model of cerebral vasoactivity that would ultimately be translatable to Alzheimer's disease as a marker for disease-modifying efficacy of novel small molecule and biologics drugs. Relative changes in cerebral blood volume following relevant doses of soluble Aβ 1-40 (0.01 or 0.1 mg/mouse), PBS, or the reverse peptide, Aβ 40-1 (0.01 or 0.1 mg/mouse), were monitored non-invasively by contrast-enhanced functional magnetic resonance imaging in anesthetized C57BL/6 mice. Experiments were performed on a 7T horizontal bore scanner using gradient echo echo-planar imaging. As expected, PBS and Aβ 40-1 did not induce any significant change in vascular response. In contrast, Aβ 1-40 significantly decreased CBV in a quantifiable, dose-related and region-specific manner. These data demonstrate for the first time the feasibility of characterizing pathogenic Aβ 1-40-induced vascular dysfunction in vivo using a non-invasive approach. Further, this technique can be readily applied to preclinical screening in a longitudinal manner for novel drugs or antibodies targeting disease modification.

Improved image reconstruction for partial fourier gradient‐echo echo‐planar imaging (EPI)

The partial Fourier gradient-echo echo planar imaging (EPI) technique makes it possible to acquire high-resolution functional MRI (fMRI) data at an optimal echo time. This technique is especially important for fMRI studies at high magnetic fields, where the optimal echo time is short and may not be achieved with a full Fourier acquisition scheme. In addition, it has been shown that partial Fourier EPI provides better anatomic resolvability than full Fourier EPI. However, the partial Fourier gradient-echo EPI may be degraded by artifacts that are not usually seen in other types of imaging. Those unique artifacts in partial Fourier gradient-echo EPI, to our knowledge, have not yet been systematically evaluated. Here we use the k-space energy spectrum analysis method to understand and characterize two types of partial Fourier EPI artifacts. Our studies show that Type 1 artifact, originating from k-space energy loss, cannot be corrected with pure postprocessing, and Type 2 artifact can be eliminated with an improved reconstruction method. We propose a novel algorithm, that combines images obtained from two or more reconstruction schemes guided by k-space energy spectrum analysis, to generate partial Fourier EPI with greatly reduced Type 2 artifact. Quality control procedures for avoiding Type 1 artifact in partial Fourier EPI are also discussed.

The effect of the stimulus frequency, stimulus amplitude and blood pressure on the signal response in functional MRT: studies on an animal model

To examine the influence of frequency and amplitude of a stimulus and the effect of blood pressure on signal intensity changes in functional MRI. Somatosensory stimulation of five (normotonic/hypotonic) anesthetized rats was performed with different stimulus frequencies and amplitudes. Measurements were performed with a 2.4 Tesla experimental scanner using a gradient-echo (GE) echo-planar imaging (EPI) sequence. The highest signal change was found at a frequency of 3 Hz and a stimulation amplitude of ten times the threshold value. A decrease of blood pressure to half the normotonic value gave rise to a decrease of the neuronal response of about 17%. Optimization of the stimulation frequency and stimulation amplitude maximizes signal changes in functional MRI of the somatosensory cortex. Even with a standardized paradigm, variations in measured neuronal activity may occur when blood pressure changes cannot be compensated by autoregulation.

ORIGINAL RESEARCH—PHYSIOLOGY: Assessment of Cerebrocortical Areas Associated with Sexual Arousal in Depressive Women Using Functional MR Imaging

ABSTRACT Introduction Mental illness is closely related with sexual dysfunction. A number of investigators have reported that depressive women have difficulties in sexual arousal. Aim The purpose of this study was to compare the cerebrocortical regions associated with sexual arousal between the healthy and depressive women using functional magnetic resonance imaging (fMRI) based on the blood-oxygenation-level-dependent (BOLD) technique. Methods Together with nine healthy women (mean age: 40.3), seven depressive women (mean age: 41.7 years, mean Beck Depression Inventory: 35.6, mean Hamilton Rating Scale Depression-17: 34.9) underwent fMRI examinations using a 1.5T MR scanner (Signa Horizon; GE Medical Systems, Milwaukee, WI, USA). The fMRI data were obtained from seven oblique planes using gradient-echo EPI. Sexual stimulation paradigm began with a 1-minute rest and then 4-minute stimulation using an erotic video film. The brain activation maps and their resulting quantification were analyzed by the statistical parametric mapping (SPM99) program. The number of pixels activated by each task was used as brain activity, where the significance of the differences was evaluated by using independent t-test. Main Outcome Measures We measured brain activation areas using BOLD-based fMRI with visual sexual stimulation in healthy volunteers and depressive patients. Results Healthy women were significantly (P &amp;lt;0.05) activated in the regions of middle occipital gyrus, middle temporal gyrus, inferior frontal gyrus, insula, hypothalamus, septal area, anterior cingulate gyrus, parahippocampal gyrus, thalamus, and amygdala by erotic visual stimulation. In comparison with the healthy women, the depressive women gave lower activity, especially in the brain regions of hypothalamus (55.5:3.0), septal area (49.6:8.6), anterior cingulate gyrus (23.5:11.0), and parahippocampal gyrus (18.2:5.8). Conclusions This preliminary study performed by fMRI gives valuable information on differentiation of the activated cerebral regions associated with visually evoked sexual arousal between healthy and depressive women. In addition, these findings might be useful to understand neural mechanisms for female sexual dysfunction in depressive women.

Different Dynamics of Performance and Brain Activation in the Time Course of Perceptual Learning

Perceptual learning is regarded as a manifestation of experience-dependent plasticity in the sensory systems, yet the underlying neural mechanisms remain unclear. We measured the dynamics of performance on a visual task and brain activation in the human primary visual cortex (V1) across the time course of perceptual learning. Within the first few weeks of training, brain activation in a V1 subregion corresponding to the trained visual field quadrant and task performance both increased. However, while performance levels then saturated and were maintained at a constant level, brain activation in the corresponding areas decreased to the level observed before training. These findings indicate that there are distinct temporal phases in the time course of perceptual learning, related to differential dynamics of BOLD activity in visual cortex.

Quantitative myocardial distribution volume from dynamic contrast-enhanced MRI

The objective of this study was to investigate if dynamic contrast-enhanced magnetic resonance imaging (MRI) can be used to quantitate the distribution volume (v(e)) in regions of normal and infarcted myocardium. v(e) reflects the volume of the extracellular, extravascular space within the myocardial tissue. In regions of the heart where an infarct has occurred, the loss of viable cardiac cells results in an elevated v(e) compared to normal regions. A quantitative estimate of the magnitude and spatial distribution of v(e) is significant because it may provide information complementary to delayed enhancement MRI alone. Using a hybrid gradient echo-echoplanar imaging pulse sequence on a 1.5T MRI scanner, 12 normal subjects and four infarct patients were imaged dynamically, during the injection of a contrast agent, to measure the regional blood and tissue enhancement in the left ventricular (LV) myocardium. Seven of the normal subjects and all of the infarct patients were also imaged at steady-state contrast enhancement to estimate the steady-state ratio of contrast agent in the tissue and blood (Ct/Cb) - a validated measure of v(e). Normal and infarct regions of the LV were manually selected, and the blood and tissue enhancement curves were fit to a compartment model to estimate v(e). Also, the effect of the vascular blood signal on estimates of v(e) was evaluated using simulations and in the dynamic and steady-state studies. Aggregate estimates of v(e) were 23.6+/-6.3% in normal myocardium and 45.7+/-3.4% in regions of infarct. These results were not significantly different from the reference standards of Ct/Cb (22.9+/-6.8% and 42.6+/-6.3%, P=.073). From the dynamic contrast-enhanced studies, approximately 1 min of scan time was necessary to estimate v(e) in the normal myocardium to within 10% of the steady-state estimate. In regions of infarct, up to 3 min of dynamic data were required to estimate v(e) to within 10% of the steady-state v(e) value. By measuring the kinetics of blood and tissue enhancement in the myocardium during an extended dynamic contrast enhanced MRI study, v(e) may be estimated using compartment modeling.

Spatiotemporal nonlinearity in resting-state fMRI of the human brain

In this work, the spatiotemporal nonlinearity in resting-state fMRI data of the human brain was detected by nonlinear dynamics methods. Nine human subjects during resting state were imaged using single-shot gradient echo planar imaging on a 1.5T scanner. Eigenvalue spectra for the covariance matrix, correlation dimensions and Spatiotemporal Lyapunov Exponents were calculated to detect the spatiotemporal nonlinearity in resting-state fMRI data. By simulating, adjusting, and comparing the eigenvalue spectra of pure correlated noise with the corresponding real fMRI data, the intrinsic dimensionality was estimated. The intrinsic dimensionality was used to extract the first few principal components from the real fMRI data using Principal Component Analysis, which will preserve the correct phase dynamics, while reducing both computational load and noise level of the data. Then the phase-space was reconstructed using the time-delay embedding method for their principal components and the correlation dimension was estimated by the Grassberger-Procaccia algorithm of multiple variable series. The Spatiotemporal Lyapunov Exponents were calculated by using the method based on coupled map lattices. Through nonlinearity testing, there are significant differences of correlation dimensions and Spatiotemporal Lyapunov Exponents between fMRI data and their surrogate data. The fractal dimension and the positive Spatiotemporal Lyapunov Exponents characterize the spatiotemporal nonlinear dynamics property of resting-state fMRI data. Therefore, the results suggest that fluctuations presented in resting state may be an inherent model of basal neural activation of human brain, cannot be fully attributed to noise.

&lt;b&gt;Cerebral substrates of experimental low back pain explored by functional magnetic resonance imaging &lt;/b&gt;

Introduction: Low back pain (LBP) is often reported as dull pain in the deep, musculoskeletal system around the lumbar spine. Although the chronic LBP could potentially involve the supraspinal pathology, its cerebral substrates have not been defined. We have developed a human model of LBP to identify such substrates by functional magnetic resonance imaging (fMRI) and further to investigate the plastic changes that may underlie the chronic progression of LBP. Methods: Six healthy volunteers, laid in the prone position in a 3-Tesla MRI scanner, were stimulated with a tail of an occluded disposable 20-ml syringe, filled with 25-ml air, orthogonally placed at 5 cm lateral to the L4/5. Calibrated, manual pressure was applied on the syringe so that each subject reported pain intensity at either 3 or 5 out of 10-cm visual analogue scale (VAS). Three blocks of 30-s pain stimulus, at either 3 or 5 of VAS, were given with 30-s intervening rest conditions, while the whole-brain gradient-echo echo-planar imaging, optimized for blood oxygenation level-dependent (BOLD) contrast, was performed. Functional data were aligned with each subject's 3-dimentional high-resolution image obtained during the same session, and analyzed with general linear model using BrainVoyager QX (BrainInnovation, Maastricht, Netherlands). After being averaged across subjects, the cerebral activation map was obtained with the false discovery rate at q<0.05. Results: The average force required to induce pain at the VAS of 3 and 5 was 376 ± 72 kPa and 538 ± 66 kPa, respectively. Pain at the VAS of 3 and 5 commonly activated the prefrontal cortex and the supplementary motor area at nearly the same BOLD amplitude, but spared the primary and secondary somatosensory cortices. Discussion: The present model of LBP induced cerebral activation in the medial nociceptive system and the motor-related areas, but did not show any activation in the lateral nociceptive system. Such lack of somatotopic representation might indicate that the present model of LBP involves the deep, heterogeneous structures around the lumbar spine.

Accounting for Signal Loss Due to Dephasing in the Correction of Distortions in Gradient-Echo EPI Via Nonrigid Registration

Gradient-echo (GE) echo planar imaging (EPI) is susceptible to both geometric distortions and signal loss. This paper presents a retrospective correction approach based on nonrigid image registration. A new physics-based intensity correction factor derived to compensate for intravoxel dephasing in GE EPI images is incorporated into a previously reported nonrigid registration algorithm. Intravoxel dephasing causes signal loss and thus intensity attenuation in the images. The new rephasing factor we introduce, which changes the intensity of a voxel in images during the registration, is used to improve the accuracy of the intensity-based nonrigid registration method and mitigate the intensity attenuation effect. Simulation-based experiments are first used to evaluate the method. A magnetic resonance (MR) simulator and a real field map are used to generate a realistic GE EPI image. The geometric distortion computed from the field map is used as the ground truth to which the estimated nonrigid deformation is compared. We then apply the algorithm to a set of real human brain images. The results show that, after registration, alignment between EPI and multi-shot, spin-echo images, which have relatively long acquisition times but negligible distortion, is improved and that signal loss caused by dephasing can be recovered.

Automatic correction of echo‐planar imaging (EPI) ghosting artifacts in real‐time interactive cardiac MRI using sensitivity encoding

To develop a method that automatically corrects ghosting artifacts due to echo-misalignment in interleaved gradient-echo echo-planar imaging (EPI) in arbitrary oblique or double-oblique scan planes. An automatic ghosting correction technique was developed based on an alternating EPI acquisition and the phased-array ghost elimination (PAGE) reconstruction method. The direction of k-space traversal is alternated at every temporal frame, enabling lower temporal-resolution ghost-free coil sensitivity maps to be dynamically estimated. The proposed method was compared with conventional one-dimensional (1D) phase correction in axial, oblique, and double-oblique scan planes in phantom and cardiac in vivo studies. The proposed method was also used in conjunction with two-fold acceleration. The proposed method with nonaccelerated acquisition provided excellent suppression of ghosting artifacts in all scan planes, and was substantially more effective than conventional 1D phase correction in oblique and double-oblique scan planes. The feasibility of real-time reconstruction using the proposed technique was demonstrated in a scan protocol with 3.1-mm spatial and 60-msec temporal resolution. The proposed technique with nonaccelerated acquisition provides excellent ghost suppression in arbitrary scan orientations without a calibration scan, and can be useful for real-time interactive imaging, in which scan planes are frequently changed with arbitrary oblique orientations.

High resolution single-shot EPI at 7T

Single-shot echo planar imaging (EPI) acquisitions at 7T are challenging due to increased distortions, signal dropouts, RF-power requirements, and reduced T2*. This study developed and tested pulse sequence and protocol modifications required to allow high resolution EPI for whole brain functional neuroimaging. Using geometric distortion correction methods, modified fat saturation, and parallel imaging, we acquired high resolution single-shot gradient-echo EPI data at 7T with different spatial resolution. The BOLD sensitivity was evaluated and quantified in a breath hold experiment. Single-shot EPI data with isotropic resolution from 3 to 1.1 mm were acquired in human subjects. The RF-power deposition has been reduced to allow up to 22 slices per second. In addition, acoustic noise and helium boil-off have been reduced. A reduction of the fat saturation flip angle resulted in up to 20% signal gain without compromising the fat suppression quality. For the coil used, the BOLD sensitivity is highest for 2 or 1.4 mm isotropic resolution. High resolution single-shot EPI in the whole brain can be performed at 7T with high efficiency, low signal dropout, and without major geometric distortions.

Spatial resolution enhancement using sensitivity-encoded echo-planar imaging at 3 T in a typical motor paradigm

We employ a single-shot sensitivity-encoded (SENSE) gradient-echo EPI acquisition in order to enhance spatial resolution in a typical motor fMRI experiment at 3 T. Functional time series were acquired with an acquisition matrix size of 56 × 192 within a readout time of 82 ms, yielding an effective in-plane resolution of 0.94 mm × 0.94 mm and compared to a conventional acquisition. Our data suggest that fMRI can readily be performed with a spatial resolution adapted to detailed cortical functional topography. However, in all potential applications the specific behavior of spatial specificity and statistical sensitivity needs to be taken into account.

Measurement of cerebral blood volume in humans using hyperoxic MRI contrast

To develop a new method of measuring quantitative regional cerebral blood volume (CBV) using epochs of hyperoxia as an intravenous contrast agent with T2*-weighted MRI. Images were acquired from six subjects (four male, two female, mean age 29 +/- 3.7 years) using a sequence combining pulsed arterial spin labeling interleaved with a gradient echo echo-planar imaging (EPI) blood oxygenation level-dependent (BOLD) sequence at 3T. The hyperoxia paradigm lasted 28 minutes consisting of 4 minutes of normoxia, two 6-minute blocks of hyperoxia separated by 6 minutes of normoxia. During the hyperoxic blocks the subjects were delivered a fractional oxygen concentration of 0.5. The mean CBV was calculated to be 3.77 +/- 1.05 mL/100 g globally, 3.93 +/- 0.90 mL/100 g in gray matter (GM), and 2.52 +/- 0.78 mL/100 g in white matter (WM). The mean GM/WM ratio was thus found to be 1.56. These values are comparable to those obtained in other studies. The hyperoxia technique for measuring CBV may be particularly useful for patient groups where an injected bolus of contrast agent is contraindicated. As more functional studies are employing epochs of inspired gases for calibration purposes, this method is easily incorporated into existing paradigms to produce a noninvasive, repeatable, easily tolerated, and quantitative measurement of regional CBV.

Absolute quantification of cerebral blood flow in normal volunteers: Correlation between Xe‐133 SPECT and dynamic susceptibility contrast MRI

To compare absolute cerebral blood flow (CBF) estimates obtained by dynamic susceptibility contrast MRI (DSC-MRI) and Xe-133 SPECT. CBF was measured in 20 healthy volunteers using DSC-MRI at 3T and Xe-133 SPECT. DSC-MRI was accomplished by gradient-echo EPI and CBF was calculated using a time-shift-insensitive deconvolution algorithm and regional arterial input functions (AIFs). To improve the reproducibility of AIF registration the time integral was rescaled by use of a venous output function. In the Xe-133 SPECT experiment, Xe-133 gas was inhaled over 8 minutes and CBF was calculated using a biexponential analysis. The average whole-brain CBF estimates obtained by DSC-MRI and Xe-133 SPECT were 85 +/- 23 mL/(min 100 g) and 40 +/- 8 mL/(min 100 g), respectively (mean +/- SD, n = 20). The linear CBF relationship between the two modalities showed a correlation coefficient of r = 0.76 and was described by the equation CBF(MRI) = 2.4 . CBF(Xe)-7.9 (CBF in units of mL/(min 100 g)). A reasonable positive linear correlation between MRI-based and SPECT-based CBF estimates was observed after AIF time-integral correction. The use of DSC-MRI typically results in overestimated absolute perfusion estimates and the present study indicates that this trend is further enhanced by the use of high magnetic field strength (3T).