Correlation Between the Masticatory Muscle Dimensions and Internal Derangement of Temporomandibular Joints Based on Magnetic Resonance Imaging

authors:

avatar Niloofar Ghadimi 1 , avatar Sandra Mehralizadeh 1 , * , avatar Elham Rahimian 2 , avatar Ladan Hafezi 1 , avatar Ahmadreza Talaiepour 1

Department of Oral and Maxillofacial Radiology, Dental School, Islamic Azad University of Medical Sciences, Tehran, Iran
European Society of Neuroradiology, Haghighat Medical and Research Center, Tehran, Iran

how to cite: Ghadimi N, Mehralizadeh S, Rahimian E, Hafezi L, Talaiepour A. Correlation Between the Masticatory Muscle Dimensions and Internal Derangement of Temporomandibular Joints Based on Magnetic Resonance Imaging. I J Radiol. 2023;20(1):e131641. https://doi.org/10.5812/iranjradiol-131641.

Abstract

Background:

Temporomandibular joint disorders (TMDs) are the most common cause of non-odontogenic pain in the maxillofacial region. Internal derangement (ID) is one of the most prevalent causes of TMDs, and disc displacement is recognized as the most common ID. The masticatory muscles are among anatomical structures involved in TMDs that may be affected by ID.

Objectives:

This study aimed to evaluate the correlation between the masticatory muscle dimensions and ID of temporomandibular joints using magnetic resonance imaging (MRI).

Patients and Methods:

This cross-sectional study was conducted on the MRI images of 145 patients, retrieved from the archives of the MRI diagnostic and research center during 2020 - 2021. The patients were categorized into three main groups of normal disc position (NP) (n = 42), disc displacement with reduction (DDR) (n = 54), and disc displacement without reduction (DDWR) (n = 49). The maximum width and height of the masseter and medial pterygoid muscles and the maximum height and length of the superior and inferior heads of the lateral pterygoid muscle were measured on MRI images for each of the groups. Data were analyzed using t-test, Pearson’s correlation test, ANOVA test, and Tukey’s test (alpha < 0.05).

Results:

Significant differences were observed between the NP, DDR, and DDWR groups regarding the height (P < 0.001) and length (P < 0.001) of the superior head of the lateral pterygoid muscle; both parameters were significantly higher in the NP group, followed by the DDR and DDWR groups (P < 0.05). The dimensions of masticatory muscles were significantly greater in males than females (P < 0.05), except for the width of the medial pterygoid muscle (P = 0.064). The height of the masseter muscle (r = 0.190, P = 0.022) and the medial pterygoid muscle (r = 0.166, P = 0.046) was significantly correlated with age.

Conclusion:

Significant correlations were found between the height and length of the superior head of the lateral pterygoid muscle and ID of TMJ; the corresponding values were lower in the DDWR group compared to the DDR and NP groups, respectively.

1. Background

Temporomandibular joint disorders (TMDs) are the most common causes of non-odontogenic pain in the maxillofacial region, affecting between 28% and 86% of the adult population. They may involve abnormalities in the masticatory muscles, bones, ligaments, and nerves related to temporomandibular joints (TMJs). The TMJs withstand significant masticatory stress throughout the mastication process and are consequently of great importance (1-4). Internal derangement (ID) is an orthopedic term for a mechanical imperfection, which hinders the normal function of a joint. It is one of the most prevalent causes of TMDs (4-6). Internal derangement may alter the function of the joint and may subsequently cause morphological alterations in the surrounding tissue (7, 8). Disc displacement (DD) is the most common type of ID (9), which is frequently accompanied by symptoms, such as clicking, pain, and constrained mouth opening (10, 11).

Considering the high resolution of magnetic resonance imaging (MRI) in the detection of both hard and soft tissue disorders, as well as the location and morphological shape of the articular disc and adjacent structures, it is currently the modality of choice for the evaluation of TMDs, with approximately 95% accuracy (3, 12-14). Since the masticatory muscles are among anatomical structures involved in TMDs, their size and cross-sectional area often match their functions and may be influenced by TMDs (15). The relationship between joint structures and ID has been investigated in several studies, with contradictory results reported in different populations. Some studies reported a reduction in the dimensions of the masticatory muscles in TMD patients, while some others reported their hypertrophy in patients with ID (14, 16-18).

2. Objectives

Despite the existing controversies, MRI is the modality of choice for evaluating the masticatory muscles. The present study aimed to assess the correlation of masticatory muscle dimensions with TMJ ID using MRI.

3. Patients and Methods

This descriptive cross-sectional study was conducted on the TMJ MRI images of 145 patients, retrieved from the archives of an MRI diagnostic and research center during 2020 - 2021. The inclusion criteria were the MRI images of patients with ID of TMJ, including both TMJs, and the availability of MRI images in both open and closed mouth positions. The exclusion criteria were patients under 18 years, history of maxillofacial trauma or fracture, TMJ ankylosis, condylar hyperplasia, TMJ sclerosis, congenital maxillofacial anomalies, coronoid hyperplasia, neoplasm of TMJ or related structures (external ear and parotid gland), stuck disc, rheumatoid arthritis, bone marrow changes, and osteophytes.

3.1. Magnetic Resonance Imaging Acquisition

All examinations were performed on a 1.5 Tesla MRI scanner (MAGNETOM Avanto, Siemens Healthcare GmbH, Germany). In MRI, the sequences and imaging parameters were as follows for T1 coronal spin echo: Repetition time (TR) (msec)/echo time (TE) (msec)/number of excitations (NEX): 460/30/1; acquisition matrix size, 256 × 256; field of view, 160 × 160 mm; and slice thickness, 2.5 mm. Also, the MRI parameters for T1 sagittal spin echo sequences (for both right and left sides) were as follows: TR/TE/NEX: 544/15/2; acquisition matrix size, 256 × 512; field of view, 160 × 200 mm; and slice thickness, 2.0 mm. Additionally, the parameters for images acquired with sagittal T2-weighted spin echo restore sequence (for both right and left sides) were as follows: TR/TE/NEX, 2210/14/2; acquisition matrix size, 336 × 448; field of view, 180 × 180 mm; and slice thickness, 3.0 mm.

3.2. Image Analysis

A radiologist analyzed the MRI images of the patients in the obtained sequences. Initially, 229 participants were included in the study. Out of 229 patients, 23 had neoplasms and lesions in the joints or related structures. Twenty-one patients were only prepared in the open or closed mouth position, 17 patients had a stuck disc, nine cases had ankylosis, nine cases had rheumatoid arthritis, four cases had a history of trauma or fracture of the joints, and one case had a congenital anomaly; they were all excluded from the study according to the exclusion criteria. Finally, 145 samples of ID of TMJ, where the disc had an abnormal relationship with the condyle in the closed and open mouth positions, were included in the study (4). The MRI images were used to classify the patients into three main groups: (1) Normal disc position (NP); (2) disc displacement with reduction (DDR); and (3) disc displacement without reduction (DDWR). According to a study by Koh et al. (19), the disc position was classified as follows:

(1) NP: In the closed mouth position, the posterior band of the disc was located above the condylar head at a 12 o’clock position, and in the one-inch open mouth position, there was a thin intermediate zone between the condyle and the articular eminence.

(2) DDR: In the closed mouth position, the posterior band of the disc was located anteriorly to the 12 o’clock position, but the disc had a normal relationship with the condyle in the one-inch open mouth position.

(3) DDWR: In the closed and open mouth positions, the posterior band of the disc was located anteriorly relative to the condylar head.

The three main muscles evaluated in this study were as follows: Height (superoinferior) and width (anteroposterior) of the masseter muscle; height (superoinferior) and length (anteroposterior) of the superior and inferior heads of the lateral pterygoid muscle; and height (superoinferior) and width (mediolateral) of the medial pterygoid muscle, measured on MRI images (in millimeters), using a Picture Archiving and Communication system (PACS).

The masseter muscle was evaluated in a sagittal open-mouth T1W sequence by measuring its height and width (Figure 1). The medial pterygoid muscle was also evaluated using the coronal T1W sequence by measuring its height and width (Figure 2). Besides, the lateral pterygoid muscle (superior and inferior heads) was evaluated by measuring its height and length in the sagittal T1W closed mouth position (Figure 3) (17). To increase the reliability of measurements, they were repeated twice and reexamined for possible associated anatomical features in the sagittal T2W sequence. Moreover, the maximum diameter of the muscles was selected by considering the anatomical landmarks. All measurements were presented in tables for further evaluation.

Measurements of the height and width of the masseter muscles in the open mouth position in the sagittal T1W sequence
Measurements of the height and width of the masseter muscles in the open mouth position in the sagittal T1W sequence
Measurements of the height and width of the medial pterygoid muscle in the coronal T1W sequence
Measurements of the height and width of the medial pterygoid muscle in the coronal T1W sequence
Measurements of the length and height of the superior head (left) and inferior head (right) of the lateral pterygoid muscle in the sagittal T1W sequence
Measurements of the length and height of the superior head (left) and inferior head (right) of the lateral pterygoid muscle in the sagittal T1W sequence

3.3. Statistical Analysis

For statistical analysis, t-test was used to assess significant differences in the dimensional changes of masticatory muscles between males and females. Also, Pearson’s correlation test was performed to examine the correlation of masticatory muscle dimensions with age. Additionally, one-way ANOVA test was performed to compare mean differences in the masticatory muscle dimensions between the three groups. Pairwise comparisons were carried out using Tukey’s post-hoc test. All statistical analyses were performed in SPSS version 26 (IBM Corp., released in 2019., IBM SPSS Statistics for Windows, Version 26.0, Armonk, NY, IBM Corp, USA). The significance level was set at α < 0.05.

4. Results

This study was performed on 145 patients (23.44% male) in the same age range. The male participants were 43.52 ± 20.38 years old, and the females were 39.66 ± 14.05 years old (P > 0.05). Table 1 presents the descriptive data of the masticatory muscle dimensions in terms of sex. All masticatory muscle dimensions were significantly greater in males than females (P < 0.05), except for the width of the medial pterygoid muscle (P = 0.064).

Table 1.

Descriptive Statistics of the Masticatory Muscle Dimensions in Terms of Sex

VariablesMean ± SDP-value
Length of the inferior head of the lateral pterygoid muscle0.0003 a
Females27.509 ± 4.1
Males30.771 ± 4.275
Height of the inferior head of the lateral pterygoid muscle0.0002 a
Females15.833 ± 1.986
Males17.775 ± 2.2
Length of the superior head of the lateral pterygoid muscle0.000 a
Females23.677 ± 3.412
Males27.16 ± 4.091
Height of the superior head of the lateral pterygoid muscle0.001 a
Females5.729 ± 1.357
Males6.602 ± 1.359
Masseter muscle width0.036 a
Females34.933 ± 3.144
Males36.442 ± 4.931
Masseter muscle height0.0003 a
Females63.296 ± 5.308
Males67.937 ± 5.608
Height of the medial pterygoid muscle0.0004 a
Females45.005 ± 6.136
Males50.386 ± 8.984
Width of the medial pterygoid muscle0.064
Females15.717 ± 2.207
Males16.616 ± 3.156

Table 2 presents the central dispersion indices for the masticatory muscle dimensions in the NP, DDR, and DDWR groups. The results of one-way ANOVA showed significant differences between the NP, DDR, and DDWR groups regarding the height (P < 0.001) and length (P < 0.001) of the superior head of the lateral pterygoid muscle (P < 0.05). Pairwise comparisons using Tukey’s post-hoc test showed the highest height and length of the superior head of the lateral pterygoid muscle in the NP group, followed by the DDR and DDWR groups, respectively. According to the Pearson’s correlation coefficient, the height of the masseter muscle (r = 0.190, P = 0.022) and the medial pterygoid muscle (r = 0.166, P = 0.046) had significant positive correlations with age (Table 3).

Table 2.

Measures of Central Dispersion for the Masticatory Muscle Dimensions in the Normal Disc Position, Disc Displacement with Reduction, and Disc Displacement Without Reduction Groups

VariablesMean ± SDANOVA P-valueTukey’s SD P-value
Length of the inferior head of the lateral pterygoid muscle0.753
NP28.7 ± 4.29
DDR28.07 ± 3.81
DDWR28.13 ± 4.99
Height of the inferior head of the lateral pterygoid muscle0.093
NP16.59 ± 2.26
DDR16.56 ± 2.04
DDWR15.73 ± 2.24
Length of the superior head of the lateral pterygoid muscle0.001 a
NP26.95 ± 3.57
DDR25.4 ± 3.26NPDDR0.045 a
DDWR21.39 ± 2.47DDWR0.001 a
Height of the superior head of the lateral pterygoid muscle0.0025 a
NP6.55 ± 1.04DDRDDWR0.0001 a
DDR6.51 ± 1.37NPDDR0.043 a
DDWR4.78 ± 0.92DDWR0.001 a
Masseter muscle width0.846
NP35.56 ± 3.52DDRDDWR0.0023 a
DDR35.22 ± 3.89
DDWR35.12 ± 3.64
Masseter muscle height0.50
NP64.04 ± 6.68
DDR65.11 ± 5.75
DDWR63.88 ± 4.73
Height of the medial pterygoid muscle0.073
NP48.36 ± 7.35
DDR45.75 ± 7.69
DDWR45.04 ± 6.35
Width of the medial pterygoid muscle0.365
NP15.9 ± 2.76
DDR16.27 ± 2.58
DDWR15.58 ± 2.08
Table 3.

Pearson’s Correlation Coefficients for the Central Dispersion of Masticatory Muscle Dimensions and Age

VariablesPearson’s correlation coefficient aP-value
Length of the inferior head of the lateral pterygoid muscle-0.0520.534
Height of the inferior head of the lateral pterygoid muscle0.0840.317
Length of the superior head of the lateral pterygoid muscle0.0240.770
Width of the superior head of the lateral pterygoid muscle0.0550.510
Masseter muscle height0.1900.022 b
Masseter muscle width-0.1520.069
Height of the medial pterygoid muscle0.1660.046 b
Width of the medial pterygoid muscle-0.1180.159

5. Discussion

This study assessed the correlation of masticatory muscle dimensions and TMJ ID using MRI. To the best of our knowledge, this is the first study to address the correlation of masticatory muscle dimensions with ID of TMJ using MRI. The results showed a significant difference between the NP, DDR, and DDWR groups regarding the height (P = 0.000) and length (P = 0.000) of the superior head of the lateral pterygoid muscle; both variables were significantly greater in the NP group, followed by the DDR and DDWR groups (P < 0.05). All masticatory muscle dimensions were significantly greater in males than females (P < 0.05), except for the width of the medial pterygoid muscle (P = 0.064), which suggested no sex differences. According to Pearson’s correlation coefficient, the height of the masseter (r = 0.190, P = 0.022) and medial pterygoid (r = 0.166, P = 0.046) muscles showed significant positive correlations with age.

In this regard, Duman et al. (17) reported that the length and width of the masticatory muscles reduced dramatically in TMD patients, resulting in muscular atrophy, which might cause limited jaw mobility. Due to restricted jaw mobility, the masticatory muscles may no longer operate within their normal range, leading to their long-term atrophy. Also, the length of the masseter muscle, the superior head of the lateral pterygoid muscle, and the medial pterygoid muscle on both sides, along with the width of the masseter and medial pterygoid muscles on the left side, were significantly shorter in TMD patients compared to the control group. In the present study, the height and length of the superior head of the lateral pterygoid muscle were significantly larger in the NP group compared to the DDR and DDWR groups, which is contrary to the findings of the study by Duman et al. (17). This discrepancy may be attributed to the fact that the inclusion criteria for TMDs in the study by Duman et al. did not include cases of ID and DD, and only patients with mouth opening restrictions were included (17). On the other hand, in the current study, TMD patients were classified into three main groups: NP, DDR, and DDWR. Besides, the sample size of the study by Duman et al. was smaller than that of our study (17).

Additionally, in a study by Melke et al., a total of 24 patients with anterior DD, TMJ effusion, and abnormal discs were evaluated (20). They found that the superior head of the lateral pterygoid muscle was smaller than its inferior head on both sides in both open and closed mouth positions (20). Moreover, in the open mouth position, the total volume of the lateral pterygoid muscle and its inferior head on both sides was substantially lower than that of the closed mouth position. Sex had a significant effect on the muscle volume, namely, the superior head of the lateral pterygoid muscle.

In line with the results of a study by Melke et al., the current study revealed that males had larger muscle dimensions than females, except for the width of the medial pterygoid muscle (20). Moreover, in our study, the height and length of the superior head of the lateral pterygoid muscle were significantly greater in the NP group compared to the DDR and DDWR groups. However, Melke et al. did not include a control group and did not differentiate patients with DD, TMJ effusion, and abnormal disc (20). They neither disclosed the type of anterior DD and only compared open and closed mouth positions (20).

Additionally, Hasan and Abdelrahman reported that the probability of effusion and degenerative modifications of the joint increased dramatically by increasing the anterior DD (18). They reported that the degree of anterior DD was strongly associated with the thickening of the lateral pterygoid muscle attachments and retrodiscal tissue abnormalities. It may be assumed that both atrophy and hypertrophy of the masticatory muscles result in muscular dysfunction. In the current study, there was a possible correlation between the ID of TMJs and masticatory muscle measurements. However, future longitudinal studies are suggested to investigate the effects of various treatments for ID on the structure and function of masticatory muscles.

In conclusion, significant correlations were found between the height and length measurements of the superior head of the lateral pterygoid muscle and ID of TMJs.

Acknowledgements

References

  • 1.

    Cisewski SE, Zhang L, Kuo J, Wright GJ, Wu Y, Kern MJ, et al. The effects of oxygen level and glucose concentration on the metabolism of porcine TMJ disc cells. Osteoarthritis Cartilage. 2015;23(10):1790-6. [PubMed ID: 26033165]. [PubMed Central ID: PMC4577453]. https://doi.org/10.1016/j.joca.2015.05.021.

  • 2.

    Embree MC, Iwaoka GM, Kong D, Martin BN, Patel RK, Lee AH, et al. Soft tissue ossification and condylar cartilage degeneration following TMJ disc perforation in a rabbit pilot study. Osteoarthritis Cartilage. 2015;23(4):629-39. [PubMed ID: 25573797]. [PubMed Central ID: PMC4368469]. https://doi.org/10.1016/j.joca.2014.12.015.

  • 3.

    Hupp JR, Tucker MR, Ellis E. Contemporary Oral and maxillofacial surgery-E-book. Amsterdam, The Netherlands: Elsevier Health Sciences; 2013.

  • 4.

    de Farias JF, Melo SL, Bento PM, Oliveira LS, Campos PS, de Melo DP. Correlation between temporomandibular joint morphology and disc displacement by MRI. Dentomaxillofac Radiol. 2015;44(7):20150023. [PubMed ID: 25806865]. [PubMed Central ID: PMC4628409]. https://doi.org/10.1259/dmfr.20150023.

  • 5.

    Hirata FH, Guimaraes AS, Oliveira JX, Moreira CR, Ferreira ET, Cavalcanti MG. Evaluation of TMJ articular eminence morphology and disc patterns in patients with disc displacement in MRI. Braz Oral Res. 2007;21(3):265-71. [PubMed ID: 17710294]. https://doi.org/10.1590/s1806-83242007000300013.

  • 6.

    Kakimoto N, Shimamoto H, Kitisubkanchana J, Tsujimoto T, Senda Y, Iwamoto Y, et al. T2 relaxation times of the retrodiscal tissue in patients with temporomandibular joint disorders and in healthy volunteers: a comparative study. Oral Surg Oral Med Oral Pathol Oral Radiol. 2019;128(3):311-8. [PubMed ID: 31076328]. https://doi.org/10.1016/j.oooo.2019.02.005.

  • 7.

    Luder HU. Articular degeneration and remodeling in human temporomandibular joints with normal and abnormal disc position. J Orofac Pain. 1993;7(4):391-402. [PubMed ID: 8118443].

  • 8.

    Stegenga B, de Bont LG, Boering G, van Willigen JD. Tissue responses to degenerative changes in the temporomandibular joint: a review. J Oral Maxillofac Surg. 1991;49(10):1079-88. [PubMed ID: 1890521]. https://doi.org/10.1016/0278-2391(91)90143-a.

  • 9.

    Murakami S, Takahashi A, Nishiyama H, Fujishita M, Fuchihata H. Magnetic resonance evaluation of the temporomandibular joint disc position and configuration. Dentomaxillofac Radiol. 1993;22(4):205-7. [PubMed ID: 8181648]. https://doi.org/10.1259/dmfr.22.4.8181648.

  • 10.

    Tanaka E, Detamore MS, Mercuri LG. Degenerative disorders of the temporomandibular joint: etiology, diagnosis, and treatment. J Dent Res. 2008;87(4):296-307. [PubMed ID: 18362309]. https://doi.org/10.1177/154405910808700406.

  • 11.

    Cai XY, Jin JM, Yang C. Changes in disc position, disc length, and condylar height in the temporomandibular joint with anterior disc displacement: a longitudinal retrospective magnetic resonance imaging study. J Oral Maxillofac Surg. 2011;69(11):e340-6. [PubMed ID: 21723023]. https://doi.org/10.1016/j.joms.2011.02.038.

  • 12.

    Ahmad M, Hollender L, Anderson Q, Kartha K, Ohrbach R, Truelove EL, et al. Research diagnostic criteria for temporomandibular disorders (RDC/TMD): development of image analysis criteria and examiner reliability for image analysis. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009;107(6):844-60. [PubMed ID: 19464658]. [PubMed Central ID: PMC3139469]. https://doi.org/10.1016/j.tripleo.2009.02.023.

  • 13.

    Ahn SJ, Baek SH, Kim TW, Nahm DS. Discrimination of internal derangement of temporomandibular joint by lateral cephalometric analysis. Am J Orthod Dentofacial Orthop. 2006;130(3):331-9. [PubMed ID: 16979491]. https://doi.org/10.1016/j.ajodo.2005.02.019.

  • 14.

    Kretapirom K, Okochi K, Nakamura S, Tetsumura A, Ohbayashi N, Yoshino N, et al. MRI characteristics of rheumatoid arthritis in the temporomandibular joint. Dentomaxillofac Radiol. 2013;42(4):31627230. [PubMed ID: 22842633]. [PubMed Central ID: PMC3667508]. https://doi.org/10.1259/dmfr/31627230.

  • 15.

    Goto TK, Yahagi M, Nakamura Y, Tokumori K, Langenbach GE, Yoshiura K. In vivo cross-sectional area of human jaw muscles varies with section location and jaw position. J Dent Res. 2005;84(6):570-5. [PubMed ID: 15914597]. https://doi.org/10.1177/154405910508400616.

  • 16.

    Wang S, Chen Y, She D, Xing Z, Guo W, Wang F, et al. Evaluation of lateral pterygoid muscle in patients with temporomandibular joint anterior disk displacement using T1-weighted Dixon sequence: a retrospective study. BMC Musculoskelet Disord. 2022;23(1):125. [PubMed ID: 35135518]. [PubMed Central ID: PMC8826701]. https://doi.org/10.1186/s12891-022-05079-1.

  • 17.

    Duman F, Çiçekçibaşı AE, Atçı N, Öztürk F, Yücekaya B, Doğru Hüzmeli E, et al. Morphological changes in temporomandibular joint dysfunction and effectiveness of different treatment methods. Anatomy. 2020;14(2):102-10. https://doi.org/10.2399/ana.20.037.

  • 18.

    Hasan NMA, Abdelrahman TEF. MRI evaluation of TMJ internal derangement: Degree of anterior disc displacement correlated with other TMJ soft tissue and osseous abnormalities. Egypt J Radiol Nucl Med. 2014;45(3):735-44. https://doi.org/10.1016/j.ejrnm.2014.03.013.

  • 19.

    Koh KJ, Park HN, Kim KA. Relationship between anterior disc displacement with/without reduction and effusion in temporomandibular disorder patients using magnetic resonance imaging. Imaging Sci Dent. 2013;43(4):245-51. [PubMed ID: 24380063]. [PubMed Central ID: PMC3873312]. https://doi.org/10.5624/isd.2013.43.4.245.

  • 20.

    Melke GSF, Costa ALF, Lopes S, Fuziy A, Ferreira-Santos RI. Three-dimensional lateral pterygoid muscle volume: MRI analyses with insertion patterns correlation. Ann Anat. 2016;208:9-18. [PubMed ID: 27287742]. https://doi.org/10.1016/j.aanat.2016.05.007.