Tetsuya Tokushima1, Satoshi Yatsushiro2, Saeko Sunohara1, Mitsunori Matsumae3, Hideki Atsumi3, and Kagayaki Kuroda1,2
1Cource of Electrical and Electric Engineering, Guraduate School of Engineering, Tokai University, Hiratsuka, Kanagawa, Japan, 2Guraduate School of Information Science and Technology, Tokai University, Hiratsuka, Kanagawa, Japan, 3Department of Neurosurgery, Tokai University, Isehara, Kanagawa, Japan
Synopsis
To separate the respiratory- and cardiac-driven motions
of cerebrospinal fluid (CSF) under free breathing, CSF velocity in 7 healthy
volunteers and 3 hydrocephalus patients were observed by asynchronous phase
contrast (PC) technique with monitoring respiratory and ECG signals. Spectrograms of CSF velocity and respiratory signal obtained
by short-term Fourier transform (STFT) with 8-sec length Hamming window revealed
that the peak respiratory motion appeared in 0-0.5 Hz band, while the cardiac motion
appeared around 1-1.5 Hz. These results suggest that the separation of the two
motion components is possible by sliding the frequency bands temporarily
according to the spectrogram.
Introduction
Separation of respiratory- and cardiac- driven Cerebrospinal Fluid (CSF) pulsation is important for categorizing the pathological status of hydrocephalus. When breathing is controlled by an audio guidance for healthy volunteers, separation of the respiratory and cardiac components is possible in the frequency domain(1). Under free breathing, however the separation became problematic since the breathing frequency or period varies. In order to separate the two types motions under free breathing, frequency-temporal properties of the motions were analyzed by spectrogram approach.
Method
Our institution’s review board approved this study. All volunteers were examined after we obtained appropriate informed consent. Asynchronous PC-MR images of the following conditions were acquired: TR, 6.0 msec; TE, 3.9 msec; flip angle, 10 degrees; slice thickness, 7 mm; matrix, 256×256; encode direction, FH; time resolution, 217 msec, SENSE factor; 4, and velocity encoding (VENC), 10 cm/sec. All volunteers and patients imaged by synchronous PC-MR images of 3 healthy volunteers under controlled of breathing (2 males (21yo, 22yo, 25yo), 1 female (25yo)), 3 healthy volunteers under free breathing (2 males (54yo, 48yo), 1 female (51yo)), and 3 patients of hydrocephalus (1 male (74yo), 2 females (30yo, 70yo)) were examined with a 3T-MRI (Ingenia, Philips). Respiratory signals obtained from MR correspondence pressure sensor. The CSF velocity plotted against both Cardiac- and Respiratory- signals to seize the overall behavior of the motion. STFT with hamming window function applied to the CSF velocity waveforms and respiratory signals of all volunteers and patients. A hamming window with 3 to 10sec with 1 sec steps and 10 to 16 sec with 2sec steps were used to the CSF velocity. The window was then shifted for 1 % of its length with 99% overlap with the adjacent window position. Furthermore, STFT with 8sec window width applied to CSF velocity waveforms and respiratory signals of all volunteers and patients. More 0.7 Hz was set to 0 and a low pass filter was applied to the respiratory signals.
Results
Figure
1 shows the
overall behavior of the CSF motion relating to the cardiac pulsation and
respiration. Spectrogram of the CSF velocity waveform with 3sec
to 6sec (upper row), 7sec to 10sec (middle row) and 12sec to 16sec (bottom row)
window functions are shown in Figure 2 for 1 volunteer. Spectrogram of CSF
velocity waveform with 8sec window function width obtained for 3 healthy
volunteers under controlled breathing (upper row), under free breathing (middle
row), and patients (bottom row) are shown in Figure 3. Spectrogram of the
respiratory waveform with 8sec window function width are shown in Figure 4 for
controlled and free breathing volunteers and patients. The frequency plotting
maximum value are shown in Figure 5.
Discussion
Figure 1 (a) demonstrates that the CSF motion
changes complicatedly even in the case of controlled respiration. In the case
of free breathing the behavior look like small variation of the CSF velocity by the respiration. In Figure 2, the peaks from 1
Hz to 1.5Hz are cardiac signals. The more window function width extends, the
more cardiac frequency bands narrow, because cardiac cycle usually steady. Most
signals in (i-k) were averaged and there were no major changes. The other
volunteers were similar results. Respiratory signal
doesn’t appear in all spectrogram in Figure 3, because respiratory signal is
weaker than cardiac and respiratory cycle is unstable. The reason why window
function width set 8sec, because it covers from instantaneous breathing like
cough to long breathing like deep breathing. In Figure 3 (f), it is not
detected cardiac signals because CSF lumen is narrow and contains components of
other tissues. Referring to the Figure 4 and Figure 5, respiratory peaks are
present from 0.23 to 0.33 Hz in (d, e), and (i), and others exist from 0 to 0.5 Hz.
Difference in respiratory band caused by several factors such as disturbed
breathing and displacement of the bellows sensor due to body movement. In
Figure 5 (g). this patient respiratory waveform has partial turbulence.Conclusion
To separate respiratory- and cardiac-driven CSF
motion under free breathing, spectrogram analysis based on STFT seemed to be
one of the possible techniques. In the future, the time domain window length has to be optimized for
detecting both cardiac- and respiratory-driven components. Dynamic adjustment
of the frequency band for detecting respiratory-driven component has to be
examined. Acknowledgements
The authors thank Dr. Koichi Oshio, Prof, Kazuhiko
Hamamoto, Prof. Osamu Uchida and Dr. Ken
Takizawa for valuable discussions. The authors also thank Mr.
Tomoaki Horie and Mr. Nao Kajihara for their great help in the volunteer experiments.
References
1. Yatsushiro S. et al., Characterization
of cardiac- and respiratory-driven cerebrospinal fluid motion based on
asynchronous phase-contrast magnetic resonance imaging in volunteers. IEEE EMBC
2016;3867-3870.
2.
Yildiz S. et al., Quantifying the Influence of
Respiration and Cardiac Pulsations on Cerebrospinal Fluid Dynamics Using
Real-Time Phase-Contrast MRI. J Magn Reson Imag 2017;46(2):431-439.