Dual vessel arterial spin labeling scheme for regional perfusion imaging.

Regional perfusion imaging (RPI) based on pulsed arterial spin labeling and angulated inversion slabs has been recently proposed. The technique allows mapping of individual brain perfusion territories of the major feeding arteries and could become a valuable clinical tool for evaluation of patients with cerebrovascular diseases. Here we propose a new labeling scheme for RPI where lateral and posterior circulations are labeled simultaneously. Two scans instead of three are sufficient to obtain the same perfusion territories as in the original approach, allowing for a 33% reduction in the total RPI protocol time. Moreover, the position of the inversion slabs with respect to vascular anatomy facilitates the planning and allows potentially better labeling efficiency. The new approach was tested on seven healthy volunteers and compared to the original labeling scheme. The results showed that the same perfusion territories and regional CBF values can be obtained.     

Understanding and optimizing the amplitude modulated control for multiple-slice continuous arterial spin labeling.

Multiple-slice perfusion imaging by continuous arterial spin labeling (CASL) is made possible by amplitude modulation (AM) of the labeling RF pulse, but perfusion sensitivity is reduced relative to the single-slice technique. A computer model of the Bloch equations for velocity driven adiabatic fast passage was developed to elucidate the compromised sensitivity to perfusion of the AM control technique for CASL. Calculations were performed over ranges of RF pulse amplitude, B1; magnetic field gradient, G; phase, phi, and frequency, f, of the modulation function; velocity, v, and relaxation times, T1 and T2, of blood. It was found that unless f>2piB1, phi determines the performance of the AM control; excessively high B1 or v reduces the efficiency of the AM control; and T1 relaxation dominates if f is too great. In vivo, in rat brain (n=5) at 2.35 T, the sensitivity of the AM technique to perfusion was 70% of the sensitivity of single-slice CASL.     

Velocity-driven adiabatic fast passage for arterial spin labeling: results from a computer model.

Velocity-driven adiabatic fast passage (AFP) is commonly employed for perfusion imaging by continuous arterial spin labeling (CASL). The degree of inversion of protons in blood determines the sensitivity of CASL to perfusion. For this study, a computer model of the modified Bloch equations was developed to establish the optimum conditions for velocity-driven AFP. Natural variations in blood velocity over the course of the cardiac cycle were found to result in significant variations in the degree of inversion. However, the mean degree of inversion was similar to that for blood moving at a constant velocity, equal to the time-averaged mean, at peak velocities and heart rates within normal ranges. A train of RF pulses instead of a continuous RF pulse for labeling was found to result in a highly nonlinear dependence of the degree of inversion on RF duty cycle. This may have serious implications for the quantification of perfusion.     

Improving the amplitude-modulated control experiment for multislice continuous arterial spin labeling.

The use of an amplitude-modulated radiofrequency (RF) pulse for a control experiment is a proven method to control for off-resonance effects in multislice continuous arterial spin labeling (CASL) experiments. This method is also known as double adiabatic inversion. The adiabaticity factor of a single half-pulse, beta(1/2), and a new dimensionless parameter alpha, which is obtained from the labeling parameters and the flow velocity, are introduced. This makes it possible to distinguish three distinct cases: 1) With low alpha, a double inversion occurs. 2) With alpha > or = approximately 4, the efficiency with which the longitudinal magnetization is returned to the z-axis depends on the phase of the amplitude modulation at the time the spins cross the center of the labeling plane. 3) In the intermediate region, the efficiency shows undesirable fluctuations. In a Bloch equation simulation, three optimized parameter sets are determined. Near ideal performance should always be achieved by combinations of parameters for which beta(1/2) > or = approximately 2 and alpha approximately pi/beta(1/2). The efficiency increases were realized in a volunteer study, showing the practical application of the suggested optimization.     

Selective multivessel labeling approach for perfusion territory imaging in pseudo-continuous arterial spin labeling

Recently, a new method for perfusion territory imaging named superselective pseudo-continuous arterial spin labeling was introduced. The method uses additional time-varying gradients to create a circular labeling spot that can be adjusted in size and thus adapted to individual arteries. In this study, the additional gradients are adjusted in such a way that an elliptical labeling spot is formed, which can be applied to label the blood in multiple vessels simultaneously in conjunction with an increased labeling efficiency compared with the original superselective approach. When compared with other selective multivessel strategies, the proposed technique allows for an improved and flexible adaption of the labeling focus to different anatomical variations of the arteries in the neck so that a total of five perfusion territories from the data acquired in three measurements can be recalculated in a reduced scan time. These include not only the perfusion territories of the cerebrum but also the perfusion territories in the cerebellum fed by individual vertebral arteries.     

Superselective arterial spin labeling applied for flow territory mapping in various cerebrovascular diseases

In three example patients suffering from internal carotid artery occlusion, intracranial steno‐occlusive disease, and symptomatic arteriovenous malformation (AVM), a new method named superselective pseudo‐continuous arterial spin labeling (pCASL) was used in addition to clinical routine measurements. The capabilities of this method are demonstrated to gain important information in diagnosis, risk analysis, and treatment monitoring that are neither accessible by digital subtraction angiography nor by existing selective arterial spin labeling methods and thus to propose future applications in clinical routine. In all cases superselective pCASL enabled the assessment of tissue viability and of territorial brain perfusion at different levels starting from major brain feeding vessels to collateral circulation at the level of the Circle of Willis to even distal branching arteries. This made it possible to estimate the contribution of an extracranial‐intracranial bypass to the brain perfusion; to depict individual arteries to important functional brain areas; to identify en‐passant feeding vessels of an AVM and to track possible changes in their perfusion territories after intervention. J. Magn. Reson. Imaging 2013;38:496–503. © 2013 Wiley Periodicals, Inc.     

Continuous arterial spin labeling using a local magnetic field gradient coil.

Continuous arterial spin labeling (ASL) using a locally induced magnetic field gradient for adiabatic inversion of spins in the common carotid artery of human volunteers is demonstrated. The experimental setup consisted of a helmet resonator for imaging, a circular RF surface coil for labeling, and gradient loops to produce a magnetic field gradient. A spin-echo (SE) echo-planar imaging (EPI) sequence was used for imaging. The approach is independent of the gradients of the MR scanner. This technology may be used if the imaging gradient system does not produce an appropriate magnetic field gradient at the location of the carotid artery-for example, in a head-only scanner-and is a prerequisite for the development of a system that allows continuous labeling during the imaging experiment.     

Multislice imaging of quantitative cerebral perfusion with pulsed arterial spin labeling

A method is presented for multislice measurements of quantitative cerebral perfusion based on magnetic labeling of arterial spins. The method combines a pulsed arterial inversion, known as the FAIR (Flow-sensitive Alternating Inversion Recovery) experiment, with a fast spiral scan image acquisition. The short duration (22 ms) of the spiral data collection allows simultaneous measurement of up to 10 slices per labeling period, thus dramatically increasing efficiency compared to current single slice acquisition protocols. Investigation of labeling efficiency, suppression of unwanted signals from stationary as well as intraarterial spins, and the FAIR signal change as a function of inversion delay are presented. The assessment of quantitative cerebral blood flow (CBF) with the new technique is demonstrated and shown to require measurement of arterial transit time as well as suppression of intraarterial spin signals. CBF values measured on normal volunteers are consistent with results obtained from H₂O¹⁵ positron emission tomography (PET) studies and other radioactive tracer approaches. In addition, the new method allows detection of activation-related perfusion changes in a finger-tapping experiment, with locations of activation corresponding well to those observed with blood oxygen level dependent (BOLD) fMRI.     

Functional perfusion imaging using continuous arterial spin labeling with separate labeling and imaging coils at 3 T.

Functional perfusion imaging with a separate labeling coil located above the common carotid artery was demonstrated in human volunteers at 3 T. A helmet resonator and a spin-echo echo-planar imaging (EPI) sequence were used for imaging, and a circular surface coil of 6 cm i.d. was employed for labeling. The subjects performed a finger-tapping task. Signal differences between the condition of finger tapping and the resting state were between -0.5% and -1.1 % among the subjects. The imaging protocol included a long post-label delay (PLD) to reduce transit time effects. Labeling was applied for all repetitions of the functional run to reduce the sampling interval.     

MR perfusion imaging using the arterial spin labeling technique for breast cancer

Purpose:

To investigate the feasibility of perfusion imaging using an arterial spin labeling (ASL) technique for breast cancer.

Materials and Methods:

Thirteen female patients with primary breast cancers were included in this study. All examinations were performed on 1.5 Tesla MRI systems. Visual evaluations of the colored perfusion map and MRI perfusion values were assessed. MRI and computed tomography (CT) perfusion values were compared.

Results:

Thirteen of 14 tumor lesions could be visualized on the colored perfusion map. CT perfusion examinations were performed in eight breasts, and the relationship between the blood flow values of CT perfusion and of MR perfusion showed a significant correlation.

Conclusion:

Nonenhanced MR imaging by an ASL technique is valid for depicting breast cancer, and the MR perfusion value is thought to be helpful for quantitative diagnosis of breast cancer. J. Magn. Reson. Imaging 2012;436‐440. © 2011 Wiley Periodicals, Inc.     

Continuous artery-selective spin labeling (CASSL).

A new technique for selective spin labeling of individual arteries is presented. It is based on continuous arterial spin labeling (CASL) with an amplitude-modulated control experiment. Precessionary motion of the labeling gradient about the axis of the artery, combined with an appropriate frequency modulation of the labeling RF pulse, restricts the adiabatic inversion to the desired artery. In phantom studies, it was found that the level of selectivity could be controlled by the sequence parameters, and that the achievable labeling efficiency was at a level of approximately 80% compared to a regular, nonselective CASL experiment. In a volunteer study we acquired high-quality images of the perfusion territories of the internal carotid artery (ICA), the basilar artery (BA), the middle cerebral artery (MCA), and both anterior cerebral arteries (ACAs). The results show the method's flexibility for different geometries and flow velocities. Potential applications include perfusion territory imaging of smaller cerebral arteries, and selective angiography techniques.     

Efficiency of inversion pulses for background suppressed arterial spin labeling.

Background suppression strategies for arterial spin labeling (ASL) MRI offer reduced noise from motion and other system instabilities. However, the inversion pulses used for suppression can also attenuate the ASL signal, which may offset the advantages of background suppression. Numerical simulations were used to optimize the inversion efficiency of four candidate pulses over a range of radiofrequency (RF) and static magnetic field variations typical of in vivo imaging. Optimized pulses were then used within a pulsed ASL sequence to assess the pulses' in vivo inversion efficiencies for ASL. The measured in vivo inversion efficiency was significantly lower than theoretical predictions (e.g., 93% experimental compared to 99% theoretical) for the tangent hyperbolic pulse applied in a background suppression scheme. This inefficiency was supported by an in vitro study of human blood. These results suggest that slow magnetization transfer (MT) in blood, either with bound water or macromolecular protons, dominates the inversion inefficiency in blood. Despite the attenuated signal relative to unsuppressed ASL, the signal-to-noise ratio (SNR) with suppression was improved by 23-110% depending on the size of the region measured. Knowledge of efficiency will aid optimization of the number of suppression pulses and provide more accurate quantification of blood flow.     

A theoretical and experimental comparison of continuous and pulsed arterial spin labeling techniques for quantitative perfusion imaging

Under ideal conditions, continuous arterial spin labeling (ASL) techniques are higher in SNR than pulsed ASL techniques by a factor of e. Presented here is a direct theoretical and experimental comparison of continuous ASL and pulsed ASL, using versions of both that are amenable to multislice imaging and insensitive to variations in transit times (continuous ASL with a delay before imaging, and QUIPSS II (Quantitative Imaging of Perfusion Using a Single Subtraction–second version)). Perfusion image quality for comparable imaging time was nearly identical for both single-slice and multislice imaging. The measured raw signal was approximately 25% higher with continuous ASL, but the SNR per unit time was identical.     

Modified pulsed continuous arterial spin labeling for labeling of a single artery

Imaging the contribution of different arterial vessels to the blood supply of the brain can potentially guide the treatment of vascular disease and other disorders. Previously available only with catheter angiography, vessel‐selective labeling of arteries has now been demonstrated with pulsed and continuous arterial spin labeling methods. Pulsed continuous labeling, which permits continuous labeling on standard scanner radiofrequency hardware, has been used to encode the contribution of different vessels to the blood supply of the brain. Vessel encoding requires a longer scan and a more complex reconstruction algorithm and may be more sensitive to fluctuations in flow, however. Here a method is presented for single‐artery selective labeling, in which a disk around the targeted vessel is labeled. Based on pulsed continuous labeling, this method is achieved by rotating the directions of added in‐plane gradients. Numerical simulations of the simplest strategy show good efficiency but poor suppression of labeling at large distances from the target vessel. Amplitude modulation of the rotating in‐plane gradients results in better suppression of distant vessels. In vivo results demonstrate highly selective labeling of individual vessels and a rapid falloff of the labeling with distance from the center of the labeling disk, in agreement with the simulations. Magn Reson Med, 2010. © 2010 Wiley‐Liss, Inc.     

Reduced resolution transit delay prescan for quantitative continuous arterial spin labeling perfusion imaging

Arterial spin labeling perfusion MRI can suffer from artifacts and quantification errors when the time delay between labeling and arrival of labeled blood in the tissue is uncertain. This transit delay is particularly uncertain in broad clinical populations, where reduced or collateral flow may occur. Measurement of transit delay by acquisition of the arterial spin labeling signal at many different time delays typically extends the imaging time and degrades the sensitivity of the resulting perfusion images. Acquisition of transit delay maps at the same spatial resolution as perfusion images may not be necessary, however, because transit delay maps tend to contain little high spatial resolution information. Here, we propose the use of a reduced spatial resolution arterial spin labeling prescan for the rapid measurement of transit delay. Approaches to using the derived transit delay information to optimize and quantify higher resolution continuous arterial spin labeling perfusion images are described. Results in normal volunteers demonstrate heterogeneity of transit delay across different brain regions that lead to quantification errors without the transit maps and demonstrate the feasibility of this approach to perfusion and transit delay quantification.     

Model-free arterial spin labeling quantification approach for perfusion MRI.

In this work a model-free arterial spin labeling (ASL) quantification approach for measuring cerebral blood flow (CBF) and arterial blood volume (aBV) is proposed. The method is based on the acquisition of a train of multiple images following the labeling scheme. Perfusion is obtained using deconvolution in a manner similar to that of dynamic susceptibility contrast (DSC) MRI. Local arterial input functions (AIFs) can be estimated by subtracting two perfusion-weighted images acquired with and without crusher gradients, respectively. Furthermore, by knowing the duration of the bolus of tagged arterial blood, one can estimate the aBV on a voxel-by-voxel basis. The maximum of the residue function obtained from the deconvolution of the tissue curve by the AIF is a measure of CBF after scaling by the locally estimated aBV. This method provides averaged gray matter (GM) perfusion values of 38 +/- 2 ml/min/100 g and aBV of 0.93% +/- 0.06%. The average CBF value is 10% smaller than that obtained on the same data set using the standard general kinetic model (42 +/- 2 ml/min/100 g). Monte Carlo simulations were performed to compare this new methodology with parametric fitting by the conventional model.