Yiming Wang1, Limin Zhou1, Joshua S. Greer1,2, Edward Pan3,4,5, Marco C. Pinho1,6, Joseph A. Maldjian1,6, and Ananth J. Madhuranthakam1,6
1Radiology, UT Southwestern Medical Center, Dallas, TX, United States, 2Pediatrics, UT Southwestern Medical Center, Dallas, TX, United States, 3Neurology and Neurotherapeutics, UT Southwestern Medical Center, Dallas, TX, United States, 4Neurological Surgery, UT Southwestern Medical Center, Dallas, TX, United States, 5Harold C. Simmons Cancer Center, UT Southwestern Medical Center, Dallas, TX, United States, 6Advanced Imaging Research Center, UT Southwestern Medical Center, Dallas, TX, United States
Synopsis
3D arterial spin
labeled (ASL) MRI using turbo spin echo (TSE) acquisition suffers from image
blurring, due to T2 decay along the echo train. In this study, a k-space
filtering method proposed earlier was optimized to compensate T2
blurring, incorporating ASL T2 measurements in healthy volunteers
for T2 decay estimation. This method was then applied to 3D ASL
images acquired in healthy volunteers and patients with glioblastoma (GBM) from
an ongoing clinical trial. Results showed reduced image blurring in both
volunteers and patients.
Introduction
3D TSE and GRASE
acquisitions are recommended for brain ASL because of their high SNR and
compatibility with optimal background suppression [1]. While 3D TSE acquisitions
are more robust to B0 inhomogeneities, they suffer from image blurring due to T2
decay along the long echo trains. k-space filtering based on accurate
estimation of signal decay can reduce image blurring [2] and is
well-suited for ASL images with optimized background suppression, since the
majority of the signal is from a single tissue component. In this study, the
k-space filtering was optimized by accurately simulating the signal decay along
the 3D TSE echo train using the measured T2 of the brain ASL signals
in healthy volunteers. The performance of the optimized k-space filtering was evaluated
on 3D ASL images in healthy volunteers and glioblastoma (GBM) patients.Methods
EPG
Signal: This study used pseudo-continuous ASL (pCASL)
with optimized background suppression and a 3D TSE Cartesian acquisition with
Spiral Profile Reordering (CASPR) (Fig. 1a) [3] on a 3T scanner
(Ingenia, Philips Healthcare). The signal decay along the echo train was calculated
using the extended phase graph (EPG) algorithm [4]. Since the EPG
signal is a function of T1 and T2, the sensitivity of signal
difference at different T1 and T2 values compared to a
constant value (e.g. gray matter with T1 = 1600 ms and T2 =
100 ms) [5] was calculated as \[\sqrt{\sum^{ETL}_{i=1}{{\left[S_i\left(T_1,T_2\right)-S_i\left(T_{1g},T_{2g}\right)\right]}^2}}(1),\] where ETL is the echo train length, s is the EPG signal, T1g and T2g are the gray matter T1
and T2.
MR Acquisition: 3D ASL was
performed in 9 healthy volunteers and 5 GBM patients with IRB approval. The
imaging parameters were: TR/TE = 6000/14 ms, FOV = 220x220x110 mm3,
matrix = 64x64 with 36 slices, acquired resolution = 3.5x3.5x6 mm3,
reconstructed resolution = 3x3x3 mm3, label duration = 1.8 s,
post-label delay = 1.8 s, 1 repetition, 4 background suppression pulses and
acquisition time = 3 minutes. A M0 image was acquired using same
acquisition parameters in 1:30 minutes. Other parameters were echo spacing =
2.8 ms and ETL = 80. In 5 healthy volunteers, the T2 values of
background suppressed ASL signal was also measured using 3D TSE-CASPR with 5
TEs (14, 42, 70, 98, and 126 ms). For comparison, ASL images were also acquired
using the vendor supplied 3D GRASE acquisition in all volunteers matching the
same imaging parameters as 3D TSE-CASPR except: TR/TE = 3900/14 ms, signal
averages = 3, and total acquisition time = 4:30 mins, included a M0
acquisition, matching the total acquisition time of 3D TSE-CASPR.
Image
Analysis: T2 values were calculated using mono-exponential
regression of image intensities in multiple ROIs . A truncated k-space filter was
designed, such that,\begin{equation} I(n) = \begin{cases}\frac{1}{s\left(n\right)},\ n<n_c \\ F\left(n\right),\ otherwise \end{cases} (2) ,\end{equation}where I
is the filter intensity, n is the
echo index, s is the EPG signal using
the measured T2 and the gray matter T1, F is a Fermi window with optimized width
and radius, nc is a
‘cut-off’ echo where the truncation of the filter begins. The filters with different
cut-off echoes were designed and applied to 3D ASL images on the scanner
reconstruction platform (Philips Recon 2.0), and their performance was evaluated
by a blur metric [6], for which a higher value reflects a more
blurred image. Paired t-test was used for blur metric comparison. The SNRs were
quantified using the differences of two pairs of ASL images [7],
acquired in 2 healthy volunteers. Cerebral blood flow (CBF) maps were calculated
and compared between the original and the filtered images using Bland-Altman
analysis.Results
The
EPG signal difference shows minimal variation for different T1 values but
increased variation to T2 values (Fig. 1b), indicating that accurate measurement
of T2 is important for true signal estimation. Across 5 subjects, the measured T2 value of
background suppressed ASL signal was 106 ± 8 ms (Fig. 2). Fig. 3a shows the
filter intensity as a function of echo index at 3 cut-off echoes (nc) and the 3D rendering of
the filter at 50% nc using
T1 = 1600 ms and T2 = 106 ms. The k-space filtering improved image sharpness
with increasing nc but at
the expense of SNR (Fig. 4a). A 50% nc
was chosen to be the optimal ratio that provided improved sharpness without
significant SNR loss, compared to 3D GRASE images in healthy volunteers (Fig. 4b)
as well as in GBM patients (Fig. 4c). With filtering at 50% nc, images showed significantly
reduced (p<0.01) blurring in healthy volunteers (Fig. 5a) and GBM patients
(Fig. 5b). On average, 50% nc
filtering reduced SNR by 27% across different brain regions (Fig. 5c), but
without affecting the CBF values (Fig. 5d). Discussion and Conclusion
The k-space
filtering method can be used to improve image sharpness of 3D TSE-CASPR pCASL
images, without significant SNR loss. This would allow robust ASL images using
3D TSE acquisition in regions with increased B0 inhomogeneities, such as brain
stem and GBM patients that often have craniotomy. Acknowledgements
This work was partly
supported by the NIH/NCI grant U01CA207091.References
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