Combined Arterial Spin Labeling Research Articles

Repeatability assessment for simultaneous measurement of arterial blood flow, venous oxygen saturation, and muscle perfusion following dynamic exercise.

The purpose of the present study was to demonstrate a new sequence and determine the repeatability of simultaneous dynamic measurements of blood flow, venous oxygen saturation (SvO2 ), and relative perfusion (change from resting perfusion) in calf muscle during recovery from plantar flexion exercise. The feasibility of near simultaneous measurement of bio-energetic parameters was also demonstrated. A sequence was developed to simultaneously measure arterial blood flow using flow-encoded projection, SvO2 using susceptibility-based oximetry, and relative perfusion using arterial spin labeling in combination with dynamic plantar flexion exercise. The parameters were determined at rest and during recovery from single leg plantar flexion exercise. Test-retest repeatability was analyzed using Bland-Altman analysis and intraclass correlation coefficients (ICC). The mitochondrial capacity of skeletal muscle was also measured immediately afterwards with dynamic phosphorus magnetic resonance spectroscopy. Eight healthy subjects participated in the study for test-retest repeatability. Popliteal artery blood flow at rest was 1.79 ± 0.58 ml/s and increased to 11.18 ± 3.02 ml/s immediately after exercise. Popliteal vein SvO2 decreased to 45.93% ± 6.5% from a resting value of 70.46% ± 4.76% following exercise. Relative perfusion (change from rest value) was 51.83 ± 15.00 ml/100 g/min at the cessation of exercise. The recovery of blood flow and SvO2 was modeled as a single exponential with time constants of 38.03 ± 6.91 and 71.19 ± 14.53 s, respectively. All the measured parameters exhibited good repeatability with ICC ranging from 0.8 to 0.95. Bioenergetics measurements were within normal range, demonstrating the feasibility of near simultaneous measurement of hemodynamic and energetic parameters. Clinical feasibility was assessed with Barth syndrome patients, demonstrating reduced oxygen extraction from the blood and reduced mitochondrial oxidative capacity compared with healthy controls. The proposed protocol allows rapid imaging of multiple parameters in skeletal muscle that might be affected in disease.

Acceleration of vessel-selective dynamic MR Angiography by pseudocontinuous arterial spin labeling in combination with Acquisition of ConTRol and labEled images in the Same Shot (ACTRESS).

PurposeThe recently introduced “Acquisition of ConTRol and labEled imaging in the Same Shot” (ACTRESS) approach was designed to halve the scan time of arterial spin labeling (ASL) ‐based 4D‐MRA by obtaining both labeled and control images in a single Look‐Locker readout. However, application for vessel‐selective labeling remains difficult. The aim of this study was to achieve a combination of ACTRESS and vessel‐selective labeling to halve the scan time of vessel‐selective 4D‐MRA.MethodsBy Bloch equation simulations, Look‐Locker pseudocontinuous‐ASL (pCASL) was optimized to achieve constant static tissue signal across the multidelay readout, which is essential for the ACTRESS approach. Additionally, a new subtraction scheme was proposed to achieve visualization of the inflow phase even when labeled blood will have already arrived in the distal arteries during the first phase acquisition due to the long duration of the pCASL labeling module. In vivo studies were performed to investigate the signal variation of the static tissue, as well as to assess image quality of vessel‐selective 4D‐MRA with ACTRESS.ResultsIn in vivo studies, the mean signal variation of the static tissue was 8.98% over the Look‐Locker phases, thereby minimizing the elevation of background signal. This allowed visualization of peripheral arteries and slowly arriving arterial blood with image quality as good as conventional pCASL within half the acquisition time. Vessel‐selective pCASL‐ACTRESS enabled the separated visualization of vessels arising from internal and external carotid arteries within this shortened acquisition time.ConclusionBy combining vessel‐selective pCASL and ACTRESS approach, 4D‐MRA of a single targeted arterial tree was achieved in a few minutes.

In vivo quantification of hyperoxic arterial blood water T1.

Normocapnic hyperoxic and hypercapnic hyperoxic gas challenges are increasingly being used in cerebrovascular reactivity (CVR) and calibrated functional MRI experiments. The longitudinal arterial blood water relaxation time (T1a) change with hyperoxia will influence signal quantification through mechanisms relating to elevated partial pressure of plasma-dissolved O2 (pO2) and increased oxygen bound to hemoglobin in arteries (Ya) and veins (Yv). The dependence of T1a on Ya and Yv has been elegantly characterized ex vivo; however, the combined influence of pO2, Ya and Yv on T1a in vivo under normal ventilation has not been reported. Here, T1a is calculated during hyperoxia in vivo by a heuristic approach that evaluates T1 -dependent arterial spin labeling (ASL) signal changes to varying gas stimuli. Healthy volunteers (n = 14; age, 31.5 ± 7.2 years) were scanned using pseudo-continuous ASL in combination with room air (RA; 21% O2/79% N2), hypercapnic normoxic (HN; 5% CO2/21% O2/74% N2) and hypercapnic hyperoxic (HH; 5% CO2/95% O2) gas administration. HH T1a was calculated by requiring that the HN and HH cerebral blood flow (CBF) change be identical. The HH protocol was then repeated in patients (n = 10; age, 61.4 ± 13.3 years) with intracranial stenosis to assess whether an HH T1a decrease prohibited ASL from being performed in subjects with known delayed blood arrival times. Arterial blood T1a decreased from 1.65 s at baseline to 1.49 ± 0.07 s during HH. In patients, CBF values in the affected flow territory for the HH condition were increased relative to baseline CBF values and were within the physiological range (RA CBF = 36.6 ± 8.2 mL/100 g/min; HH CBF = 45.2 ± 13.9 mL/100 g/min). It can be concluded that hyperoxic (95% O2) 3-T arterial blood T1aHH = 1.49 ± 0.07 s relative to a normoxic T1a of 1.65 s.

Abstract WP35: An ASL Collateral Score Can Identify Improved Quantitative Cerebral Blood Flow in Acute Stroke Patients

Objective: To measure quantitative hemodynamic parameters in acute stroke patients using a tomographic collateral assessment based on arterial spin labeling (ASL) [1]. Methods: Patients were retrospectively identified who met these criteria: symptom onset <27 hrs, DWI volume >=10 ml, and ASL and bolus contrast PWI, 1.5T. Pseudocontinuous 3D fast spin echo ASL was performed with the parameters: TR/TE/label time/post-label delay 5500/9.5/1500/2000 ms. PWI was performed using 0.1 mmol Gd and single-shot EPI with the parameters: TR/TE 1800/40 ms. Automated software (RAPID) was used to measure relative CBF, CBV, and time to peak of the residue function (Tmax) [2]. The combined ASL and DSC method was used to determine quantitative CBF and CBV [3]. A four point collateral score (CS) (0=poor, 1=intermediate, 2=good, 3=antegrade perfusion) [4] was determined based on ASL arterial transit artifact (ATA) in 20 ASPECTS ROI’s in each patient [1]. Tests for significant relationships between CS and each parameter was performed. Findings: 13 patients were identified (4 M, 63±13 yrs, 17±7 hrs from symptom onset, DWI size 61±52 ml, PWI Tmax>6 sec size 84±65 ml). CBF increased with increasing CS, with the highest CBF in the antegrade perfused regions. CBV also increased with CS, but there was no difference between good collateral and antegrade regions. Tmax decreased significantly as CS increased. Acute stroke patients with good and poor collaterals are shown in the Figure (yellow arrows = collaterals). Conclusions: Collaterals are important because they supply CBF. ASL is able to predict the quality of collaterals in acute stroke, as was shown previously in Moyamoya disease [1]. This non-contrast assessment of collaterals on MRI may improve patient selection for stroke therapy.

Combined arterial spin label and dynamic susceptibility contrast measurement of cerebral blood flow

Dynamic susceptibility contrast (DSC) and arterial spin labeling (ASL) are both used to measure cerebral blood flow (CBF), but neither technique is ideal. Absolute DSC-CBF quantitation is challenging due to many uncertainties, including partial- volume errors and nonlinear contrast relaxivity. ASL can measure quantitative CBF in regions with rapidly arriving flow, but CBF is underestimated in regions with delayed arrival. To address both problems, we have derived a patient-specific correction factor, the ratio of ASL- and DSC-CBF, calculated only in short-arrival-time regions (as determined by the DSC-based normalized bolus arrival time [Tmax]). We have compared the combined CBF method to gold-standard xenon CT in 20 patients with cerebrovascular disease, using a range of Tmax threshold levels. Combined ASL and DSC CBF demonstrated quantitative accuracy as good as the ASL technique but with improved correlation in voxels with long Tmax. The ratio of MRI-based CBF to xenon CT CBF (coefficient of variation) was 90 +/- 30% (33%) for combined ASL and DSC CBF, 43 +/- 21% (47%) for DSC, and 91 +/- 31% (34%) for ASL (Tmax threshold 3 sec). These findings suggest that combining ASL and DSC perfusion measurements improves quantitative CBF measurements in patients with cerebrovascular disease.

Single‐shot 3D imaging techniques improve arterial spin labeling perfusion measurements

Arterial spin labeling (ASL) can be used to measure perfusion without the use of contrast agents. Due to the small volume fraction of blood vessels compared to tissue in the human brain (typ. 3-5%) ASL techniques have an intrinsically low signal-to-noise ratio (SNR). In this publication, evidence is presented that the SNR can be improved by using arterial spin labeling in combination with single-shot 3D readout techniques. Specifically, a single-shot 3D-GRASE sequence is presented, which yields a 2.8-fold increase in SNR compared to 2D EPI at the same nominal resolution. Up to 18 slices can be acquired in 2 min with an SNR of 10 or more for gray matter perfusion. A method is proposed to increase the reliability of perfusion quantification using QUIPSS II derivates by acquiring low-resolution maps of the bolus arrival time, which allows differentiation between lack of perfusion and delayed arrival of the labeled blood. For arterial spin labeling, single-shot 3D imaging techniques are optimal in terms of efficiency and might prove beneficial to improve reliability of perfusion quantitation in a clinical setup.

Arterial spin labeling in combination with a look‐locker sampling strategy: Inflow turbo‐sampling EPI‐FAIR (ITS‐FAIR)

Arterial spin labeling in combination with a look‐locker sampling strategy: Inflow turbo‐sampling EPI‐FAIR (ITS‐FAIR)

Arterial spin labeling in combination with a look‐locker sampling strategy: Inflow turbo‐sampling EPI‐FAIR (ITS‐FAIR)

Arterial spin labeling (ASL) permits quantification of tissue perfusion without the use of MR contrast agents. With standard ASL techniques such as flow-sensitive alternating inversion recovery (FAIR) the signal from arterial blood is measured at a fixed inversion delay after magnetic labeling. As no image information is sampled during this delay, FAIR measurements are inefficient and time-consuming. In this work the FAIR preparation was combined with a Look-Locker acquisition to sample not one but a series of images after each labeling pulse. This new method allows monitoring of the temporal dynamics of blood inflow. To quantify perfusion, a theoretical model for the signal dynamics during the Look-Locker readout was developed and applied. Also, the imaging parameters of the new ITS-FAIR technique were optimized using an expression for the variance of the calculated perfusion. For the given scanner hardware the parameters were: temporal resolution 100 ms, 23 images, flip-angle 25.4 degrees. In a normal volunteer experiment with these parameters an average perfusion value of 48.2 +/- 12.1 ml/100 g/min was measured in the brain. With the ability to obtain ITS-FAIR time series with high temporal resolution arterial transit times in the range of -138 - 1054 ms were measured, where nonphysical negative values were found in voxels containing large vessels.