Sultan Zaman Mahmud1, Bruce Gladden2, Andreas Kavazis2, Robert Motl3, Thomas Denney1, and Adil Bashir1
1Department of Electrical and Computer Engineering, Auburn University, Auburn, AL, United States, 2School of Kinesiology, Auburn University, Auburn, AL, United States, 3Department of Physical Therapy, University of Alabama at Birmingham, Birmingham, AL, United States
Synopsis
Impairments in oxygen delivery and consumption can lead to reduced
muscle endurance and physical disability. Perfusion, a measure of microvascular
blood flow, provides information on nutrient delivery. T2* provides information about
relative tissue oxygenation. Changes in these parameters following stress, such
as exercise, can yield important information about imbalance between delivery
and consumption. In this study we implemented golden angle radial MRI
acquisition technique to simultaneously quantify muscle perfusion and T2* at 7T, and demonstrate assessment
of spatial and temporal changes in these parameters within calf muscles during recovery
from plantar flexion exercise.
Introduction
Reduced muscle endurance is a leading cause of disability in
a host of conditions such as neuromuscular disease, heart failure, aging, etc.
Reduced blood flow,
delivery
to, and consumption by the working muscle are likely to cause decline in muscle
ability to sustain workloads 1. Thus, understanding of spatial and
temporal aspects of muscle perfusion is important for our understanding of sustained
muscle performance. Muscle perfusion can be measured using arterial spin
labeling and provides information about microvascular blood flow. T2* is related to the total amount
of deoxyhemoglobin in the tissue and, by extension, is an estimate of blood
oxygen saturation, an indirect measurement of oxygen extraction by the tissue.
The methods for measurement of perfusion and T2* have been previously reported 2. However these methods have not been demonstrated with
dynamic exercise at 7T. Herein, we implemented novel interleaved golden angle
radial MRI acquisition technique to simultaneously quantify muscle perfusion
and T2* We further demonstrated the assessment
of spatial and temporal changes in perfusion and T2* in calf muscle during recovery
from plantar flexion exercise. Methods
Pulse sequence was developed to acquire data simultaneously from
two different slices. Arterial spin labeling sequence SATIR 3 was
implemented using hyperbolic secant inversion pulse for spin tagging and golden
angle radial readout (Fig 1 - slice 1). Time delay between perfusion tagging
and acquisition was used for interleaved acquisition of T2* data for a slice located 3 cm
distally from the perfusion slice (Fig 1 – slice 2). A multi-echo radial GRE sequence with radial
acquisition was used for T2* mapping. Temporal resolution for
perfusion and T2* was approximately 1.3 seconds.
MR imaging was performed on a Siemens 7T system (Erlangen, Germany) using a surface
coil. Six subjects participated in the study.
Quantitative perfusion and T2* maps were acquired at rest.
Common acquisition parameters: FOV = 192 mm, slice = 5 mm, TR = 1.28 s, Flip
angle = 15⁰ and 64 radial acquisition. Resting perfusion
measurements were acquired with a slice selective and nonselective tagging
pulse, tagging time = 1 sec. T2* was acquired with TEs = 2.2,
5.0, 7.8, 10.6 and 13.4 ms. The subjects
then performed 2 minutes of plantar flexion at 0.5 Hz against a resistance of 40%
of MVC. Data was acquired for 3 minutes in recovery. Quantitative perfusion
maps were determined as described before3. T2* was calculated by fitting a mono-exponential function to magnitude signal
intensity. Results
A representative slice selective perfusion weighted image
and T2* map at rest are shown in Figure
2. Blood vessels on perfusion images show high signal due to flow. At rest the
perfusion in calf muscle was 5 ± 2 mL/min/100g. Figure 3 shows changes
in perfusion and T2* immediately after exercise
indicating regions of muscle activation. These overlay maps are changes from
the resting state. A region of interest (ROI) corresponding to the activated muscle
regions identified on the perfusion maps was manually traced on the images. ROI
analysis showed that perfusion was significantly increased reaching 70 ±
10 mL/min/100g immediately after exercise. Perfusion recovered slowly during post-exercise
rest period and average time to return to baseline was approximately 100 s. Shim
difference between experiments affects baseline (resting) T2* therefore post exercise T2* normalized to the resting
map from each individual. T2* in the selected ROI decreased by
15 % immediately after exercise from the resting value. T2* recovery showed exponential
behavior; i.e., a fast recovery followed by much slower recovery to resting
values.Discussions
This study demonstrates the ability to simultaneously quantify
skeletal muscle perfusion and T2*, both at rest and dynamically, for post
exercise recovery in calf muscle at 7T. An interleaved golden angle radial
acquisition pulse sequence was implemented for the study which helps reduce
bulk motion artifacts. The temporal and spatial resolution of the protocol was
sufficient to measure changes in metabolism-related parameters post exercise. Dynamic
plantar flexion exercise isolates the calf muscles and might provide valuable
insight into pathophysiological processes independent of impaired heart
function. Accordingly, the information provided by this technique may prove to
be very valuable in understanding muscle metabolism in healthy subjects as well
as patient populations who experience mobility disability.Acknowledgements
No acknowledgement found.References
- Jacobi B, et al. Skeletal muscle bold MRI: from
underlying physiological concepts to its usefulness in clinical conditions. J
Magn Reson Imaging. 2012; 35(6):1253-65.
- Englund EK, et al. Combined measurement of perfusion,
venous oxygen saturation and skeletal muscle T2* during reactive hyperemia in the
leg. J Cardiovasc Magn Reson. 2013; 15(1):70.
- Raynaud JS, et al. Determination of skeletal muscle
perfusion using arterial spin labeling NMRI: validation by comparison with venous
occlusion plethysmography. Magn Reson Med. 2001; 46(2):305-11.