Martin Schwartz1,2, Günter Steidle1, Petros Martirosian1, Ander Ramos-Murguialday3, Bin Yang2, and Fritz Schick1
1Section on Experimental Radiology, Department of Radiology, University of Tuebingen, Tuebingen, Germany, 2Institute of Signal Processing and System Theory, University of Stuttgart, Stuttgart, Germany, 3Institute for Medical Psychology and Behavioural Neurobiology, University of Tuebingen, Tuebingen, Germany
Synopsis
Diffusion-weighted
images of the lower leg have shown to be impaired by signal voids in different
muscle groups with unknown underlying physiological processes. For more
detailed insight into this topic, simultaneous surface electromyography
measurements of the electrical activity of muscles during the MR scan were
recorded. A classification of the appeared signal voids in the diffusion-weighted
images based on initial findings in the EMG measurements is demonstrated.Purpose
Repetitive
single-shot diffusion weighted (DW) imaging
of the lower leg was reported to reveal spontaneous signal voids in different
muscle groups with a random pattern in temporal and spatial domain
1.
Most probably incoherent mechanical activities of muscle fibers are causing
this phenomenon, but the underlying physiological processes are still unknown.
This study is dedicated to analyze whether the signal voids are related to electrical
neuromuscular activity. Surface electromyography (EMG) recorded the electrical
activity of muscles during the MR examinations in order to assess potential
relations of signal voids in DW
images of the right calf with coincident EMG signals.
Methods
MR acquisition: Three healthy volunteers (age: 35 ± 14,
BMI: 25.4 kg/m² ± 3.4 kg/m²) were examined with at least
5 min rest before the measurement was starting. The DW images were
acquired with a stimulated echo DW EPI with: matrix size: 64 x 64, FoV = 200 x 200 mm²,
TE = 31 ms, TR = 500 ms,
BW = 2004 Hz/px, TM = 145 ms, 500 repetitions and
SPAIR (Spectral Attenuated Inversion Recovery). All measurements were performed
on a 3 T MR Scanner (Magnetom Skyra, Siemens Healtcare, Erlangen, Germany).
Transverse DW images were acquired at the position with the maximum diameter of
the calf. The signal voids were detected and segmented by an automatic
evaluation framework
2.
EMG
acquisition: The EMG signal was acquired with an eight channel BrainAmp ExG
MR (Brain Products GmbH, Gilching, Germany) with a sampling rate of f
sampling = 5 kHz
and the BrainVision Recoder software (Brain Products GmbH, Gilching, Germany).
Due to the expected high induction current from MR gradient switching,
electrodes with a current limiting resistor with R = 15 kΩ were
utilized to ensure patient safety during the MR measurement protocol. An
inter-electrode distance of 2 cm was utilized
3. The schematic
electrode placement is illustrated in Fig. 1. The EMG sampling clock was
synchronized with the MR scanner gradient clock with the Brain Vision SyncBox
utilities. The artifact correction was performed with the BrainVision Analyzer
2.0 software (Brain Products GmbH, Gilching, Germany), while the MR gradient
induced artifacts were corrected with a sliding average window (size: 21) and
the cardioballistic artifact template related to blood flow pulsation were
estimated from the first 20 seconds of the measurement without active MR measurement
protocol
4,5. Additionally, a notch filter with rejection-band from
45-55 Hz and a pass-band filter with a lower cut-off frequency f
low = 0.5 Hz
and an upper cut-off frequency f
upper = 250 Hz were
applied to reduce environmental and high frequency distortions. An exemplary
result of the EMG artifact correction is illustrated in Fig. 2. The EMG
signal was measured at electrode #4. The maximum allowed signal amplitude of
the measured EMG signal (±16.384 mV) was not exceeded and thus the front-end
of the amplifier was not in saturation.
Results & Discussion
Three different kinds
of signal voids can be identified: 1) spontaneous often perceptible motion of
the volunteer, 2) fasciculation related motion of muscle regions, and 3) signal
voids without measureable electrical activity. In Fig. 3, the m. tibialis
posterior shows an extended signal void. Due to the fact that the whole muscle
area is affected and a measureable EMG event is recognizable, a reflectory and
nervally coordinated motion of the volunteer is assumed. In Fig. 4, a signal
void in the diffusion-weighted image of the m. soleus is
illustrated. The EMG event shows a fasciculation activity measured only by
electrode #2 just before the MR acquisition starts. Fig. 5 illustrates one
exemplary signal void without measureable EMG event.
Conclusion
Based on the results
from simultaneous MRI and EMG measurements the signal voids can be classified in
several groups: It is shown that only a part of the signal voids are related to
neuromuscular electrical activity. Other spontaneous muscular activities seem
to be not associated with electrically measurable events.
Acknowledgements
We thank Hubert Preißl, Nerea Irastorza-Landa, Andrea Sarasola-Sanz and Boris Kotchoubey from the Institute for Medical Psychology and Behavioural Neurobiology, University of Tuebingen, for their valuable technical support on this project.
References
[1]: Steidle et al., NMR in Biomedicine 2015:28(7);
[2]: Schwartz et al., Proc. ESMRMB 2015;
[3]: Hermens et al., Journal of Electromyography and Kinesiology 2000:10(5);
[4]: Allen et al., Neuroimage 2000:12(2);
[5]: Allen et al., Neuroimage 1998:8(3)