Wei-Yin Liu1, Hung-Ta Wu2, Chien-Yuan Eddy Lin3, Hsiao-Ling Lee3, and Wan-You Guo2
1Institute of Biomedical Engineering, National Yang-Ming University, Taipei, Taiwan, 2Department of Radiology, Taipei Veterans General Hospital, Taipei, Taiwan, 3GE Healthcare, Taipei, Taiwan
Synopsis
The first clinical application with zero echo time (ZTE) based MR bone
depiction and segmentation in the temporomandibular
joint (TMJ) was presented in
this study. Our result revealed that ZTE showed computed tomography (CT)-like
bone contrast and more detailed demonstration of bony structures, which contributed
more reliable structure images and volume measurements. A potential alternative radiation-free diagnostic approach, especially for
patients who receive initial workups or serial follow-ups, can be adopted to
assess the staging of temporomandibular disorder (TMD) by segmenting cortical
bone of the condyle into normal bone, erosion, and sclerosis.
Purpose:
The condyloid process (also
named condyle) plays a critical role in mandibular movements of gliding and
hinge of the temporomandibular joint (TMJ). The previous studies suggested that
the volume and shape of the condyle in patients with temporomandibular disorder
(TMD) have been continuously altered and remodeled in a process of flattening,
sclerosis, erosion, osteophytes, and absorption. Many imaging modalities, such
as cone-beam computed tomography (CT) and MRI1 have
been applied to facilitate the assessment of TMD, including the condyle-disc
position, condylar cortical thickness, volume, and so on. The correlation of
the signs (e.g., the positions of condyle, articular disc and fossa) and symptoms
(e.g., pain) has been reported but with controversial results.2 With zero-echo
time (ZTE) MR imaging, the bone-tissue discrepancy in the bilateral condyles can
be more distinguishable than conventional MR images due to efficient sampling
short T2* signals in cortical
bone. The aim of this study is to quantify each subgroup volume of the bilateral condyles via
three-dimensional (3D) reconstructed ZTE images and evaluate its value in
clinical TMD.Methods:
Six patients with clinically proved TMD were enrolled in this study. All
six patients were assessed based on the clinical Wilkes stage (staging of
internal derangement of TMJ by dentist: Stage I: early, II: early/intermediate,
III: Intermediate, IV: Intermediate/late, V: late) . All MRI acquisitions were
performed on a 1.5 T clinical scanner (Optima MR450w, GE Healthcare, Milwaukee,
USA) using a head and-neck array coil as the signal detection and whole-body
coil for radio-frequency excitation. ZTE data were carried out in a supine
position and acquired using a non-selective hard pulse excitation followed by
3D center-out radial sampling. The scanning parameters were as follows: TR=548 ms,
flip angle=1 degree, receiver bandwidth= 31.2 kHz, field-of-view= 20 cm, in-plane resolution=
0.39 mm, slice thickness=0.8 mm, scan time ≈ 3 mins.
2D sagittal and 3D view of the bilateral condyles were obtained and post-processed
with ImageJ and a semi-automatic segmentation tool, ITK-SNAP.
The condylar position in bilateral sides was calculated according to the
formula3: CP= (posterior-anterior)/(posterior+anterior)×100%.
Three subgroups in the cortex of corresponding condyle
were classified as normal bone (normal cortex osseous component), erosion (including
flattening) and sclerosis. The classified cortical volumes of condyles in
bilateral sides of each patient were assessed and correlated with Wilkes stages.
Statistics was performed with SPSS 17.0.Results and Discussions:
The bilateral condyle with ZTE MRI of a representative patient was shown in Fig. 1. The descriptive and inferential statistics were shown
in Table 1 and Table 2, respectively. The consistency of the bilateral CP4 and the total volumes
was found (p > 0.05). Sperman’s
rank correlation coefficient was calculated for the correlation between the
Wilkes stage and the volume of each group. The correlations
between the subgroup volumes (normal and erosion) of the corresponding
condyle and the Wilks stage were found (p < 0.05). In order to exclude the effect of the total volume
(the sum of the normal bone and erosion) on the correlation between the Wilkes stage and the volume of each subgroup, the partial correlation was performed. It showed correlation between the volume of the sclerosis in the right condyle and Wilkes stage (p < 0.05),
which may explain the pain dysfunction syndrome orally described by patients, even
with the signs of condyle displacement (the recommended value of the centric
position ranged within ±12)3. Even if there is no
significant correlation between clinical staging and each volume (except the
volume of the right-condyle sclerosis) while controlling for the total volume, accurate
description of the temporomandibular size and shape is critical for clinical
diagnosis and surgical planning.Conclusion:
We reported the first clinical application of ZTE MRI to segment TM condyles into three
subgroups (normal, erosion, and sclerosis) and measure the
condylar position and volume of each subgroup. A potential alternative
radiation-free diagnostic option can be provided, especially for young patients
who will receive the initial checkup or serial follow-ups and even surgeries. Further
assessment of more TMJ with different stages is mandatory.Acknowledgements
No acknowledgement found.References
1. Bag
AK, Gaddikeri S, Singhal A, et al. Imaging of the temporomandibular joint: An
update. World J Radiol. 2014;6(8):567-582.
2. Liu
Q, Wei X, Guan J, Wang R, Zou D, Yu L. Assessment of condylar morphology and
position using MSCT in an Asian population. Clin
Oral Investig. 2018;22(7):2653-2661.
3. Colonna
AD, Manfredini D Dds PM, Lombardo LD, et al. Comparative analysis of jaw morphology
and temporomandibular disorders: A three-dimension imaging study. Cranio. 2018:1-10.
4. Ren YF, Isberg A, Westesson PL. Condyle position in the
temporomandibular joint. Comparison between asymptomatic volunteers with normal
disk position and patients with disk displacement. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1995;80(1):101-107.