Yukiko Kami1, Toru Chikui1, Osamu Togao2, Masahiro Ooga3, Kazunori Yoshiura1. 1. Department of Oral and Maxillofacial Radiology, Faculty of Dental Science, Kyushu University, Fukuoka, Japan. 2. Department of Clinical Radiology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan. 3. Department of Medical Technology, Kyushu University Hospital, Fukuoka, Japan.
Magnetic resonance imaging (MRI) provides better soft-tissue contrast than computed
tomography (CT), which plays an important role in the evaluation of the location of
the lesion and its relationships with adjacent anatomical structures and also
provides information about the metabolic and physiological features of tissue,
thereby indicating its pathological processes (1–4).A major drawback of MRI is the slow imaging speed. Long acquisition times introduce
motion artifacts, increase costs, and limit the number of patients for whom MRI is
available (5). Although
three-dimensional (3D) scans are preferred for MRI, two-dimensional (2D) scans are
common in clinical practice because 3D scans require much longer scan times and the
gradient (GRE) sequence commonly used for 3D scans is susceptible to inhomogeneity
of magnetic fields. Therefore, achieving a reduction in MRI acquisition time without
causing image degradation has remained a challenge.Parallel imaging (PI) uses an array of receiver coil to collect undersampled k-space
data and reconstructs full field of view (FOV) images by specialized algorithms (6).
The limitation is that the acceleration factor cannot be higher than the number of
coils in the array (7).Compressed sensing (CS), a mathematical framework, provides for reconstruction of
data from highly undersampled measurements, which is exploited effectively under
conditions of sparsity, pseudo-random undersampling, and non-linear reconstruction
(8). CS takes
advantage of the fact that MR images are usually sparse in some transform domains,
such as the wavelet domain, and recovers this sparse representation from
undersampled data (9).
Like PI, CS enables accelerated MRI acquisitions although the two approaches rely on
different ancillary information.CS and PI techniques such as sensitivity encoding (SENSE) can be combined to further
reduce scan time (10).
For example, the compressed SENSE is available on the Philips scanner (11). According to the
report by Sartoretti et al. (12), in individual scans of six different body regions (brain, knee,
lumbar spine, wrist, breast, shoulder) with compressed SENSE, a reduction in
acquisition time of 23%–43% in individual sequences across 2D and 3D scans was
achieved with no image degradation.To our knowledge, there have been no previous studies in which CS has been applied to
head and neck lesions. The aim of the present study was to evaluate the usefulness
of CS for contrast-enhanced oral and maxillofacial MRI by comparing the 3D T1 turbo
field echo with compressed SENSE (CS-3D-T1TFE) sequence with the multi-slice spin
echo (MS-SE) sequence as the reference standard.
Material and Methods
Patients
This retrospective study was approved by the Institutional Review Board of Kyushu
University Hospital (2019-111) and the requirement for informed consent was
waived. The study plan was published on a website and the patients had the right
of refusal to inclusion in this study. For the present study, we included
patients with orofacial lesions who underwent contrast-enhanced MRI including
MS-SE and CS-3D-T1TFE sequences at our hospital between August 2018 and April
2019. We excluded patients with lesions that could not be defined because they
were too small or showed severe metal artifacts.A total of 30/40 patients (18 men, 12 women; mean age = 63.7 ± 17.3 years; age
range = 21–84 years) were identified on the basis of the above criteria. The
lesions were as follows: malignant tumors (squamous cell carcinoma [SCC],
n = 17; malignant lymphoma [ML], n = 2; and osteosarcoma, n = 1); benign tumors
(pleomorphic adenomas, n = 2; lymphangiomas, n = 2; reactive myofibroblastic
lesion, n = 1; and desmoplastic ameloblastoma, n = 1); cysts (ranula, n = 1;
epidermoid cyst, n = 1); and inflammations, n = 2.
MRI acquisition
MRI was performed using a 3.0-T scanner (Ingenia 3.0CX, Philips Healthcare, Best,
The Netherlands) with a 20-channel head-and-neck coil. MS-SE was performed with
the following parameters: repetition time (TR)/echo time (TE) = 431/13 ms; flip
angle = 90°; water fat shift = 1.423 pixels; bandwidth = 305.2 Hz; number of
signal averaged (NSA) = 1; slice thickness = 3 mm; field of view (FOV) = 230 mm;
acquisition voxel = 0.72 × 0.89 × 3.00 mm; reconstruction
voxel = 0.45 × 0.45 × 3.00 mm; and acquisition time = 5 min 56 s. The Dixon
method was used for fat suppression.CS-3D-T1TFE was performed with the following parameters: TR = 5.6 ms;
TE1/TE2 = 1.94/3.4 ms; flip angle = 14°; water fat shift = 0.500 pixels;
bandwidth = 868.1 Hz; NSA = 2; CS-Sense reduction factor = 3.05; FOV = 240 mm;
acquisition voxel = 1.00/1.00/1.00 mm; reconstruction voxel = 0.47/0.47/1.00 mm;
and acquisition time = 1 min 43 s. The Dixon method was used for fat
suppression.Both sequences were performed after administration of 0.1 mmol/kg of
gadolinium-based contrast material. The order of the sequences was
randomized.
Image evaluation
All data were transferred from the hospital’s picture archiving and communication
system (PACS, Fujifilm Medical, Tokyo, Japan) to a personal computer in the
digital imaging and communications in medicine (DICOM) format for further image
analysis. Each patient’s CS-3D-T1TFE imaging dataset (slice thickness = 1 mm)
was resampled to the MS-SE imaging dataset (slice thickness = 3 mm) using the
OsiriX software (Pixmeo SARL, Bernex, Switzerland, version 10.0.3) for both
datasets to be evaluated under the same conditions: the same slice thickness;
the same slice numbers; the same FOV; and the same matrix size.
Quantitative analysis
One radiologist with 10 years of experience in oral and maxillofacial radiology
performed the quantitative analysis. From each dataset of 60 images (30 MS-SE
and CS-3D-T1TFE images each), an axial image that clearly delineated almost
maximum sections of the tongue, masseter muscles, and medial pterygoid muscles
was selected, and 25-pixel circular regions of interes (ROIs) were placed on the
bilateral posterior part of tongue, masseter muscles, and medial pterygoid
muscles using ImageJ software (National Institutes of Health, MD, USA, version
1.51s) (Fig. 1).
Particular attention was paid not to include artifacts, blood vessels, and
muscular fasciae in the ROIs. The signal-to-noise ratio (SNR) was calculated
from each ROI using the following equation:
Fig. 1.
25-pixel circular regions of interest were placed on both sides of the
posterior part of tongue, masseter muscles, and medial pterygoid muscles
to calculate the signal-to-noise ratio.
25-pixel circular regions of interest were placed on both sides of the
posterior part of tongue, masseter muscles, and medial pterygoid muscles
to calculate the signal-to-noise ratio.SNR = SI/SDwhere SI and SD are the average and SD of the signal intensity, respectively.
Qualitative analysis
Two oral and maxillofacial radiologists with 10 and 23 years of experience
(Observer 1 and Observer 2, respectively) independently participated in the
observer test. Both observers were blinded to the sequences analyzed. Image
quality was assessed using seven parameters: degree of lesion conspicuity;
motion artifacts; metal artifacts; pulsation artifacts; quality of fat
suppression; homogeneity of blood vessel signal intensity; and overall image
quality. Each parameter was graded on the following 5-point scale:
5 = excellent; 4 = good; 3 = acceptable; 2 = poor; and 1 = unacceptable.
Statistical analysis
Comparisons of SNR between MS-SE and CS-3D-T1TFE and qualitative scores between
the two sequences were performed using the paired t-test with
Kaleida Graph software (Synergy Software, version 4.1.3). P
values < 0.05 were considered significant. Inter-observer agreement in the
qualitative scoring was assessed by the kappa statistic using SPSS version 21.0
(IBM Corp., Armonk, NY, USA). Agreement was interpreted based on kappa as
follows: ≤0.20 = slight; 0.21–0.40 = fair; 0.41–0.60 = moderate;
0.61–0.80 = substantial; and 0.81–1.00 = almost perfect.
Results
MRI
The examples of MS-SE and CS-3D-T1TFE images are shown in Fig. 2.
Fig. 2.
A 60-year-old man with right tongue squamous cell carcinoma. Imaging was
performed with the MS-SE sequence (a) and the CS-3D-T1TFE sequence (b).
Both images delineate the tongue lesions clearly. Blood vessels are more
clearly on the CS-3D-T1TFE image than the MS-SE. CS-3D-T1TFE,
three-dimensional T1 turbo field echo with compressed SENSE; MS-SE,
multi-slice spin echo.
A 60-year-old man with right tongue squamous cell carcinoma. Imaging was
performed with the MS-SE sequence (a) and the CS-3D-T1TFE sequence (b).
Both images delineate the tongue lesions clearly. Blood vessels are more
clearly on the CS-3D-T1TFE image than the MS-SE. CS-3D-T1TFE,
three-dimensional T1 turbo field echo with compressed SENSE; MS-SE,
multi-slice spin echo.The mean and SD of the SNR and P values for MS-SE and
CS-3D-T1TFE sequences are shown in Table 1. SNR of CS-3D-T1TFE was
significantly higher than that of MS-SE in the right masseter muscle
(P = 0.0003), the left masseter muscle
(P < 0.0001), the right medial pterygoid muscle
(P = 0.0002), and the left medial pterygoid muscle
(P < 0.0001). There were no significant differences
between the two sequences in the right posterior part of tongue
(P = 0.8945) and the left posterior part of tongue
(P = 0.2734).
Table 1.
SNR of MS-SE and CS-3D T1TFE.
SNR
P*
MS-SE
CS-3D-T1TFE
Right tongue root
20.92 ± 7.14
20.67 ± 8.11
0.8945
Left tongue root
20.26 ± 5.69
18.75 ± 7.00
0.2734
Right masseter muscle
15.36 ± 5.99
21.99 ± 9.10
0.0003
Left masseter muscle
15.67 ± 5.37
20.85 ± 6.79
<0.0001
Right medial pterygoid muscle
13.32 ± 4.76
18.46 ± 6.39
0.0002
Left medial pterygoid muscle
12.15 ± 5.32
19.23 ± 6.81
<0.0001
Values are given as mean ± SD.
*Paired t-test.
CS-3D T1TFE, three-dimensional T1 turbo field echo with Compressed
SENSE; MS-SE, multi slice spin echo; SD, standard deviation; SNR,
signal-to-noise ratio.
SNR of MS-SE and CS-3D T1TFE.Values are given as mean ± SD.*Paired t-test.CS-3D T1TFE, three-dimensional T1 turbo field echo with Compressed
SENSE; MS-SE, multi slice spin echo; SD, standard deviation; SNR,
signal-to-noise ratio.The individual observer grades for each parameter are listed in Table 2. For Observers
1 and 2, the scores recorded with CS-3D-T1TFE were higher than those with MS-SE
for motion artifacts (P = 0.0009613 and
P < 0.0001, respectively) (Fig. 3), pulsation artifacts
(P < 0.0001 and P < 0.0001,
respectively) (Fig. 4),
and homogeneity of blood vessel signal intensity (P < 0.0001
and P < 0.0001, respectively) (Fig. 5). The scores for quality of fat
suppression were significantly higher with MS-SE than with CS-3D-T1TFE for
Observer 2 (P = 0.001426), whereas they did not significantly
differ between the methods for Observer 1 (P = 0.08307). No
significant differences were observed in the scores for lesion conspicuity
(P = 0.4888 and P = 0.5725), metal
artifacts (P = 0.1683 and P = 1), and overall
image quality (P = 0.3256 and P = 0.6015) for
both observers. Table
3 summarizes the kappa statistics for the inter-rater agreement
between the two observers. The agreements on lesion conspicuity, quality of fat
suppression, and overall image quality were fair. The agreement on motion
artifacts was moderate. The agreements on pulsation artifacts and homogeneity of
blood vessel signal intensity were substantial, while the agreement on metal
artifacts was almost perfect.
Table 2.
Individual observer grades for MS-SE and CS-3D T1TFE
Observer 1
Observer 2
MS-SE
CS-3D-T1TFE
P*
MS-SE
CS-3D-T1TFE
P*
Degree of lesion conspicuity
4.90 ± 0.31
4.83 ± 0.46
0.4888
4.83 ± 0.38
4.80 ± 0.48
0.5725
Motion artifact
4.30 ± 0.88
4.90 ± 0.40
0.0009613
3.83 ± 1.02
4.53 ± 0.73
<0.0001
Metal artifact
4.20 ± 0.76
4.13 ± 0.78
0.1608
4.33 ± 0.71
4.33 ± 0.66
1
Pulsation artifact
3.43 ± 1.07
5
<0.0001
3.17 ± 1.23
4.97 ± 0.18
<0.0001
Quality of fat suppression
5
4.90 ± 0.31
0.08307
4.97 ± 0.18
4.67 ± 0.48
0.001426
Homogeneity of blood vessel signal intensity
1.80 ± 0.66
4.93 ± 0.25
<0.0001
1.60 ± 0.50
4.87 ± 0.35
<0.0001
Overall image quality
4.10 ± 0.76
4.20 ±0.61
0.3256
4.10 ± 0.96
4.17 ± 0.70
0.6015
Values are given as mean ± SD.
*Paired t-test.
CS-3D T1TFE, three-dimensional T1 turbo field echo with Compressed
SENSE; MS-SE, multi slice spin echo; SD, standard deviation.
Fig. 3.
Motion artifact: An 83-year-old woman with left tongue squamous cell
carcinoma. Imaging was performed with the MS-SE sequence (a) and the
CS-3D-T1TFE sequence (b). The tongue lesion is difficult to be
identified on the MS-SE image because of the heavy motion artifact,
while the CS-3D-T1TFE image delineates the lesion clearly. CS-3D-T1TFE,
three-dimensional T1 turbo field echo with compressed SENSE; MS-SE,
multi-slice spin echo.
Fig. 4.
Pulsation artifact: A 39-year-old woman with left maxillary desmoplastic
ameloblastoma. Imaging was performed with the MS-SE sequence (a) and the
CS-3D-T1TFE sequence (b). The MS-SE image shows the flow-related
artifact in the posterior cranial fossa. CS-3D-T1TFE, three-dimensional
T1 turbo field echo with compressed SENSE; MS-SE, multi-slice spin
echo.
Fig. 5.
Homogeneity of blood vessel signal intensity: An 81-year-old man with
right tongue squamous cell carcinoma. Imaging was performed with the
MS-SE sequence (a) and the CS-3D-T1TFE sequence (b). The MS-SE image
shows inhomogeneity of blood vessel signal intensity, while the
CS-3D-T1TFE image shows homogeneity. CS-3D-T1TFE, three-dimensional T1
turbo field echo with compressed SENSE; MS-SE, multi-slice spin
echo.
Table 3.
Kappa statistics between two observers.
Kappa statistics
Degree of lesion conspicuity
0.339
Motion artifact
0.416
Metal artifact
0.83
Pulsation artifact
0.759
Quality of fat suppression
0.38
Homogeneity of blood vessel signal intensity
0.796
Overall image quality
0.321
Individual observer grades for MS-SE and CS-3D T1TFEValues are given as mean ± SD.*Paired t-test.CS-3D T1TFE, three-dimensional T1 turbo field echo with Compressed
SENSE; MS-SE, multi slice spin echo; SD, standard deviation.Motion artifact: An 83-year-old woman with left tongue squamous cell
carcinoma. Imaging was performed with the MS-SE sequence (a) and the
CS-3D-T1TFE sequence (b). The tongue lesion is difficult to be
identified on the MS-SE image because of the heavy motion artifact,
while the CS-3D-T1TFE image delineates the lesion clearly. CS-3D-T1TFE,
three-dimensional T1 turbo field echo with compressed SENSE; MS-SE,
multi-slice spin echo.Pulsation artifact: A 39-year-old woman with left maxillary desmoplastic
ameloblastoma. Imaging was performed with the MS-SE sequence (a) and the
CS-3D-T1TFE sequence (b). The MS-SE image shows the flow-related
artifact in the posterior cranial fossa. CS-3D-T1TFE, three-dimensional
T1 turbo field echo with compressed SENSE; MS-SE, multi-slice spin
echo.Homogeneity of blood vessel signal intensity: An 81-year-old man with
right tongue squamous cell carcinoma. Imaging was performed with the
MS-SE sequence (a) and the CS-3D-T1TFE sequence (b). The MS-SE image
shows inhomogeneity of blood vessel signal intensity, while the
CS-3D-T1TFE image shows homogeneity. CS-3D-T1TFE, three-dimensional T1
turbo field echo with compressed SENSE; MS-SE, multi-slice spin
echo.Kappa statistics between two observers.
Discussion
CS-3D-T1TFE imaging required shorter acquisition time than MS-SE (1 min 43 s and
5 min 56 s, respectively) and showed no image degradation while maintaining equal or
higher SNR and image quality. In the qualitative analysis, CS-3D-T1TFE imaging was
better than MS-SE in assessments of motion artifacts, pulsation artifacts, and
homogeneity of blood vessel signal intensity. The short acquisition time for
CS-3D-T1TFE, which was only less than 30% of scan time for MS-SE, might have been
effective in reducing motion artifacts. GRE sequences might have suppressed the
artifacts created by pulsation or blood flow: in routine SE imaging, at least part
of the reason for flow-related signal loss is that spins move out of the section
between the two pulses. In GRE imaging, refocusing is performed by means of a
gradient reversal, and short TE minimizes flow-related signal losses (13). In the head and neck
region, since flow-related signal losses sometimes make it difficult to distinguish
cervical lymph node from adjacent vessels, homogeneous blood vessel signal intensity
might be helpful for detection of metastatic lymph nodes. The quality of fat
suppression was significantly higher with MS-SE than with CS-3D-T1TFE in assessments
by Observer 2, whereas they were not significantly different between the methods in
assessments by Observer 1. This difference between observers could be attributed to
the fact that Observer 2 gave low scores for the deficient fat suppression by
aliasing in the bottom near the supraclavicular slice in CS-3D-T1TFE imaging (Fig. 6). Except for those
slices, fat suppression in CS-3D-T1TFE was entirely good: scores for all images were
4 (good) or 5 (excellent), with mean scores of 4.90 ± 0.31 and 4.67 ± 0.48 for
Observers 1 and 2, respectively. The fat suppression was also good around the skull
base and the intraorbital regions that are susceptible to artifacts. We employed the
two-point Dixon method for fat suppression (14). Dixon sequences can compensate the
inhomogeneity of static magnetic field (B0), thereby providing accurate separation
between water and fat. The Dixon method provides us with water, fat, in phase, out
of phase, and B0 images; however, the water image that represents the
fat-suppression image, is helpful for lesion conspicuity in contrast-enhanced MRI.
Therefore, we used only the water images in this study.
Fig. 6.
A 77-year-old woman with right tongue squamous cell carcinoma. The image
obtained by the CS-3D-T1TFE sequence shows deficient fat suppression caused
by aliasing in a near supraclavicular slice (arrow). CS-3D-T1TFE,
three-dimensional T1 turbo field echo with compressed SENSE.
A 77-year-old woman with right tongue squamous cell carcinoma. The image
obtained by the CS-3D-T1TFE sequence shows deficient fat suppression caused
by aliasing in a near supraclavicular slice (arrow). CS-3D-T1TFE,
three-dimensional T1 turbo field echo with compressed SENSE.There were no significant differences in metal artifacts, lesion conspicuity, and
overall image quality. While the GRE sequence is more sensitive to field
heterogeneity or metal-induced susceptibility artifacts than SE (15), there were no
significant differences between the two sequences in the present study. This could
have occurred because the aforementioned improved B0 correction compensated the
field heterogeneity and the use of a higher bandwidth in CS-3D-T1TFE reduced the
distortion by the artifact (16,17). The
increased bandwidth might cause decreased SNR, but the SNR of CS-3D-T1TFE was kept
equal or higher than MS-SE in our settings. Dental prostheses induce metal artifact,
which often interferes with lesion conspicuity; the result showed that CS-3D-T1TFE
did not induce any worse effects in terms of forming metal artifact. The kappa
statistics were fair or moderate in four out of seven parameters (degree of lesion
conspicuity, motion artifact, quality of fat suppression, and overall image
quality), even though the actual scores (Table 2) appeared to be similar. Since,
both the observers provided quite high grades for these four parameters, the skewed
distribution of the data eventually resulted in fair or moderate kappa values.We employed 3D scans with CS because there is more room for aggressive undersampling
compared to 2D scans (12), and 3D imaging is particularly attractive as it is often time-consuming
and reduction of scan time is a higher priority than 2D imaging. 3D imaging enables
us to reconstruct the sagittal and coronal plane images from the original axial
plane images. Fig. 7 shows
the reconstructed sagittal and coronal plane images. We can see the positional
relationship between the inflamed region and the mandibular canal clearly; however,
more precise assessment of reconstructed images will be needed with more cases.
Fig. 7.
A 35-year-old woman with inflammation after extraction of a right mandibular
wisdom tooth. Reconstructed sagittal (a) and coronal (b) plane images from
axial images of the CS-3D-T1TFE sequence shows the relationship between the
inflamed region (arrow heads) and the mandibular canal (arrows) clearly.
CS-3D-T1TFE, three-dimensional T1 turbo field echo with compressed
SENSE.
A 35-year-old woman with inflammation after extraction of a right mandibular
wisdom tooth. Reconstructed sagittal (a) and coronal (b) plane images from
axial images of the CS-3D-T1TFE sequence shows the relationship between the
inflamed region (arrow heads) and the mandibular canal (arrows) clearly.
CS-3D-T1TFE, three-dimensional T1 turbo field echo with compressed
SENSE.The present study has some limitations. First, the optimal CS-Sense reduction factor
has not been examined. Moreover, the advantages of CS-Sense over the conventional
SENSE were not examined. We chose the CS-Sense reduction factor to set an
acquisition time that was lower than 2 min 47 s of the existing 2D non-enhanced
T1-SE sequence without fat suppression that seemed to be a clinically important
standard. Higher CS-Sense reduction factor could be used; however, it is associated
with a greater risk of image degradation. To the best of our knowledge, CS-Sense
reduction factor in the head and neck area that has many artifacts like oral
prosthesis and air has not been studied previously. We had to be careful because the
images were taken after the administration of contrast material. Thus, we chose the
clinically acceptable setting rather than the fastest setting. Second, the numbers
of cases in which each of the two sequences was performed first after administration
of contrast material were not the same, since MS-SE imaging was performed first in
20 cases while CS-3D-T1TFE imaging was performed first in 10 cases. This suggests
that the condition was worse for CS-3D-T1TFE, but this study showed that CS-3D-T1TFE
imaging was better or equal to MS-SE. Third, we did not evaluate the conspicuity of
perineural growth and lymph nodes that may be subtle but can greatly impact the
choice of therapy. This is an important aspect that requires further evaluation.In conclusion, the CS-3D-T1TFE sequence was useful for oral and maxillofacial MRI:
the acquisition time decreased to less than 30% of that for MS-SE without image
degradation, maintaining equal or higher SNR and image quality, which led to
throughput enhancement. There would be no need for additive sagittal and coronal
plane image acquisition, which will lead to a further reduction in examination
time.
Authors: T Chikui; E Kitamoto; Y Kami; S Kawano; K Kobayashi; T Kamitani; M Obara; K Yoshiura Journal: Br J Radiol Date: 2015-04-23 Impact factor: 3.039
Authors: Elisabeth Sartoretti; Thomas Sartoretti; Christoph Binkert; Arash Najafi; Árpád Schwenk; Martin Hinnen; Luuk van Smoorenburg; Barbara Eichenberger; Sabine Sartoretti-Schefer Journal: PLoS One Date: 2019-04-12 Impact factor: 3.240