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Maximum bilateral bite strength and RMS EMG for the diagnosis of myogenic TMD

Abstract

Aim

The study aimed to evaluate the accuracy of the maximum bilateral molar bite force and the Root Mean Square (RMS) Electromyography (EMG) index of the masticatory muscles in the maximum bilateral molar bite (MMBMax) of women with myogenic Temporomandibular Disorder (TMD) and asymptomatic.

Methods

This is a cross-sectional study, composed of 86 women allocated to the TMD Group (n=43) and Control Group (n=43) diagnosis through the Diagnostic Criteria for Temporomandibular Disorders. The maximum bilateral molar bite force was evaluated using a bite dynamometer and the RMS EMG index of the masticatory muscles (anterior temporalis, masseter) during 5 seconds of the MMBMax task. Student t-test was used for data comparison between accuracy of the bite force and RMS EMG of masticatory muscles during the MMBMax.

Results

The maximum bilateral molar bite force showed high accuracy (AUC=0.99) for the diagnosis of women with myogenic TMD and asymptomatic women, and the RMS EMG index evaluated during the MMBMax showed a moderate level of accuracy for all masticatory muscles (AUC=0.70 to 0.75).

Conclusion

The bilateral bite dynamometer with a surface EMG during bilateral bite can be used to diagnose TMD in young women.

Diagnosis; Electromyography; Temporomandibular joint disorders


Introduction

Temporomandibular disorder (TMD), considered the main cause of pain in the orofacial region11. Schiffman E, Ohrbach R, Truelove E, Look J, Anderson G, Goulet JP, et al. Diagnostic Criteria for Temporomandibular Disorders (DC/TMD) for Clinical and Research Applications: recommendations of the International RDC/TMD Consortium Network* and Orofacial Pain Special Interest Group†. J Oral Facial Pain Headache. 2014 Winter;28(1):6-27. doi: 10.11607/jop.1151., is characterized by joint and/or muscular pain, limited or irregular mandibular function, and noises in the temporomandibular joints (TMJ)22. Gonçalves DA, Dal Fabbro AL, Campos JA, Bigal ME, Speciali JG. Symptoms of temporomandibular disorders in the population: an epidemiological study. J Orofac Pain. 2010 Summer;24(3):270-8.,33. Leeuw R, Klasser GD, editors. Orofacial pain: guidelines for assessment, diagnosis, and management. 5. ed. Quintessence Publishing; 2013.. TMD presents a multifactorial etiology44. Gauer RL, Semidey MJ. Diagnosis and treatment of temporomandibular disorders. Am Fam Physician. 2015 Mar;91(6):378-86. making the diagnosis complex55. Al-Khotani A, Naimi-Akbar A, Albadawi E, Ernberg M, Hedenberg-Magnusson B, Christidis N. Prevalence of diagnosed temporomandibular disorders among Saudi Arabian children and adolescents. J Headache Pain. 2016;17:41. doi: 10.1186/s10194-016-0642-9..The Diagnostic Criteria for Temporomandibular Disorders (DC/TMD)11. Schiffman E, Ohrbach R, Truelove E, Look J, Anderson G, Goulet JP, et al. Diagnostic Criteria for Temporomandibular Disorders (DC/TMD) for Clinical and Research Applications: recommendations of the International RDC/TMD Consortium Network* and Orofacial Pain Special Interest Group†. J Oral Facial Pain Headache. 2014 Winter;28(1):6-27. doi: 10.11607/jop.1151. is the gold standard tool for TMD diagnosis.

Individuals with TMD exhibit many changes in the electrical activity of masticatory muscles due to their dysfunction or through a compensatory mechanism associated with symptoms66. Santana-Mora U, Cudeiro J, Mora-Bermúdez MJ, Rilo-Pousa B, Ferreira-Pinho JC, Otero-Cepeda JL, et al. Changes in EMG activity during clenching in chronic pain patients with unilateral temporomandibular disorders. J Electromyogr Kinesiol. 2009 Dec;19(6):e543-9. doi: 10.1016/j.jelekin.2008.10.002.. Therefore, surface electromyography (EMG) emerges as a bioelectric and non-invasive instrument that allows the assessment of muscle electrical activity77. De Luca CJ. The use of surface electromyography in biomechanics. J Appl Biomech. 1997;13(2):135-63. doi: 10.1123/jab.13.2.135., which can be used in the clinical environment to assist in the diagnosis of myogenic TMD88. Manfredini D, Bracci A, Djukic G. BruxApp: the ecological momentary assessment of awake bruxism. Minerva Stomatol. 2016;65(4):252-5.,99. Berni KC, Dibai-Filho AV, Pires PF, Rodrigues-Bigaton D. Accuracy of the surface electromyography RMS processing for the diagnosis of myogenous temporomandibular disorder. J Electromyogr Kinesiol. 2015 Aug;25(4):596-602. doi: 10.1016/j.jelekin.2015.05.004..

The electrical activity of the masticatory muscles during the sustained submaximal molar bite task has been evaluated using a bite dynamometer or small thickness tension measurement sensors1010. Castroflorio T, Bracco P, Farina D. Surface electromyography in the assessment of jaw elevator muscles. J Oral Rehabil. 2008 Aug;35(8):638-45. doi: 10.1111/j.1365-2842.2008.01864.x.,1111. Xu L, Fan S, Cai B, Fang Z, Jiang X. Influence of sustained submaximal clenching fatigue test on electromyographic activity and maximum voluntary bite forces in healthy subjects and patients with temporomandibular disorders. J Oral Rehabil. 2017 May;44(5):340-6. doi: 10.1111/joor.12497.. Xu, et al.1111. Xu L, Fan S, Cai B, Fang Z, Jiang X. Influence of sustained submaximal clenching fatigue test on electromyographic activity and maximum voluntary bite forces in healthy subjects and patients with temporomandibular disorders. J Oral Rehabil. 2017 May;44(5):340-6. doi: 10.1111/joor.12497. evaluated the submaximal unilateral molar bite sustained at 30% of the maximum bite force (MBF), using a small thickness unilateral bite dynamometer, for the maximum time tolerated by the volunteers, and found significantly higher values of normalized Root Mean Square (RMS) EMG in the TMD group compared to the control group in masticatory muscles.

MBF is one of the indicators of the functional status of the masticatory system1212. Todic J, Martinovic B, Pavlovic J, Tabakovic S, Staletovic M. Assessment of the impact of temporomandibular disorders on maximum bite force. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2019 Sep;163(3):274-8. doi: 10.5507/bp.2019.001. and can be affected by some factors: craniofacial morphology, sex, age, and occlusal status1313. Calderon Pdos S, Kogawa EM, Lauris JR, Conti PC. The influence of gender and bruxism on the human maximum bite force. J Appl Oral Sci. 2006 Dec;14(6):448-53. doi: 10.1590/s1678-77572006000600011.

14. Koc D, Dogan A, Bek B. Bite force and influential factors on bite force measurements: a literature review. Eur J Dent. 2010 Apr;4(2):223-32.
-1515. Castelo PM, Gavião MB, Pereira LJ, Bonjardim LR. Masticatory muscle thickness, bite force, and occlusal contacts in young children with unilateral posterior crossbite. Eur J Orthod. 2007 Apr;29(2):149-56. doi: 10.1093/ejo/cjl089.. Todic et. al.1212. Todic J, Martinovic B, Pavlovic J, Tabakovic S, Staletovic M. Assessment of the impact of temporomandibular disorders on maximum bite force. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2019 Sep;163(3):274-8. doi: 10.5507/bp.2019.001. indicated that the TMD significantly affects the potential of masticatory muscle action which is confirmed by the analysis of MBF with significantly lower values in patients with TMD1616. Tortopidis D, Lyons MF, Baxendale RH. Bite force, endurance and masseter muscle fatigue in healthy edentulous subjects and those with TMD. J Oral Rehabil. 1999 Apr;26(4):321-8. doi: 10.1046/j.1365-2842.1999.00383.x. and with the fact that MBF values decrease with the increase in the severity of TMD. One possibility is that the presence of masticatory muscle pain and/or TMJ inflammation can play a role in the MBF1717. Kogawa EM, Calderon PS, Lauris JR, Araujo CR, Conti PC. Evaluation of maximal bite force in temporomandibular disorders patients. J Oral Rehabil. 2006 Aug;33(8):559-65. doi: 10.1111/j.1365-2842.2006.01619.x.. However, it is currently unclear how TMD affects MBF.

Based on the capacity of EMG to evaluate the electrical activity of the masticatory muscles and the dynamometer to measure force between individuals with TMD and asymptomatic individuals, it becomes important to analyze the instruments in question, by measuring their accuracy, since they present good applicability, easy access, and non-invasive assessments, which could assist health professionals in the diagnosis and treatment of TMD1818. Kordass B, Hugger A, Bernhardt O. Correlation between computer-assisted measurements of mandibular opening and closing movements and clinical symptoms of temporomandibular dysfunction. Int J Comput Dent. 2012;15(2):93-107.,1919. Sforza C, Rosati R, De Menezes M, Musto F, Toma M. EMG analysis of trapezius and masticatory muscles: experimental protocol and data reproducibility. J Oral Rehabil. 2011 Sep;38(9):648-54. doi: 10.1111/j.1365-2842.2011.02208.x..

Accuracy analysis is defined as the amount of agreement between the measurement results of an instrument studied with the measurement results of another instrument already established and used as the gold standard, which can be calculated using the receiver-operating characteristic curve (ROC curve)2020. Akobeng AK. Understanding diagnostic tests 3: Receiver operating characteristic curves. Acta Paediatr. 2007 May;96(5):644-7. doi: 10.1111/j.1651-2227.2006.00178.x.,2121. Hulley SB, Cummings SR, Browner WS, Grady DG, Newman TB. [Outlining clinical research]. 4.ed. Porto Alegre: Artmed; 2015. Portuguese..

Berni et al.99. Berni KC, Dibai-Filho AV, Pires PF, Rodrigues-Bigaton D. Accuracy of the surface electromyography RMS processing for the diagnosis of myogenous temporomandibular disorder. J Electromyogr Kinesiol. 2015 Aug;25(4):596-602. doi: 10.1016/j.jelekin.2015.05.004. demonstrated that the RMS EMG index of the masticatory muscles has a moderate level of accuracy for discrimination between individuals with myogenic TMD and asymptomatic individuals during the TMJ rest task and inadequate levels of accuracy during the maximum isometric bilateral molar bite task. In contrast, Manfredini et al.88. Manfredini D, Bracci A, Djukic G. BruxApp: the ecological momentary assessment of awake bruxism. Minerva Stomatol. 2016;65(4):252-5. demonstrated that the RMS EMG index of the masticatory muscles shows moderate to high accuracy for the diagnosis of myogenic TMD during the maximal isometric bilateral molar bite task, but low accuracy levels in the TMJ resting task.

Based on the cited literature, data on the accuracy of the RMS EMG index of masticatory muscles during specific tasks are still conflicting. Furthermore, no information was found on the electrical activity of the anterior masseter and temporal muscles considering the use of a bilateral molar bite dynamometer. We hypothesized that there is a significant difference between women with TMD and asymptomatic women for values of maximum force of bilateral molar bite using the bite dynamometer, in the RMS EMG index of the masticatory muscles during the maximum bilateral molar bite and that these are accurate for the diagnosis of women with muscular TMD and asymptomatic women.

The present study aimed to evaluate the accuracy of the maximum bilateral molar bite force and the RMS EMG index of the masticatory muscles during the maximum bilateral molar bite in women with myogenic and asymptomatic TMD.

Methods

Study design

This is a cross-sectional study, approved by the Research Ethics Committee of the University, protocol no. 25/2015. The volunteers who agreed to participate in this research signed a Consent Form.

Subjects

A sample size calculation was performed based on a pilot study. The outcome used was the surface EMG (masticatory pattern). The mean and standard deviation normalized RMS values of the anterior temporal muscle during the biting phase of the Control (n=10) and the TMD group (n=10) were, respectively, 89.06±8.21% and 83.44±6.64%, and, an effect size of 0.34 was found. For a power of 95% and a 5% alpha, n was determined as 43 volunteers per group. The calculation was performed using GPower® software, version 3.1.9.2. (Uiversität Kiel Kiel, Schleswig-Holstein, Germany).

The volunteers were recruited, from May 2016 to April 2017, from the Surgery Sector of a School of Dentistry (Sao Paulo State, Brazil).

Inclusion and Exclusion Criteria

Women aged between 18 and 45 years and Body Mass Index (BMI)<25 kg/m2727. Greiner M, Pfeiffer D, Smith RD. Principles and practical application of the receiver-operating characteristic analysis for diagnostic tests. Prev Vet Med. 2000 May;45(1-2):23-41. doi: 10.1016/s0167-5877(00)00115-x.,2222. Chowdhury RH, Reaz MB, Ali MA, Bakar AA, Chellappan K, Chang TG. Surface electromyography signal processing and classification techniques. Sensors (Basel). 2013 Sep;13(9):12431-66. doi: 10.3390/s130912431. were selected. For the TMD group, the volunteers were required to be diagnosed with myogenic TMD (DC/TMD)11. Schiffman E, Ohrbach R, Truelove E, Look J, Anderson G, Goulet JP, et al. Diagnostic Criteria for Temporomandibular Disorders (DC/TMD) for Clinical and Research Applications: recommendations of the International RDC/TMD Consortium Network* and Orofacial Pain Special Interest Group†. J Oral Facial Pain Headache. 2014 Winter;28(1):6-27. doi: 10.11607/jop.1151. with the presence of present pain and/or fatigue in the masticatory muscles for at least 6 months.

Women who received physical or pharmacological treatment (eg. analgesic), with dental losses, who used total or partial dentures, with a history of facial and TMJ trauma, a history of subluxation or dislocation of the TMJ, and who were diagnosed with degenerative joint diseases through the DC/TMD were excluded from the study. For the control group, the volunteers were required not to present pain and any diagnosis of TMD (DC/TMD).

It is important to highlight that both groups contain only women for convenience, according to epidemiological studies, TMD is more prevalent in women than in men2323. Lora VR, Canales GL, Gonçalves LM, Meloto CB, Barbosa CM. Prevalence of temporomandibular disorders in postmenopausal women and relationship with pain and HRT. Braz Oral Res. 2016 Aug;30(1):e100. doi: 10.1590/1807-3107BOR-2016.vol30.0100..

Materials

Diagnostic Criteria of Temporomandibular Disorder (DC/TMD)

The DC/TMD is a validated questionnaire to diagnose TMD. Axis I of the DC/TMD contains a physical evaluation and considers recurrent factors of the patient’s daily life; Axis II considers the previous history, beginning, and perpetuating factors of the dysfunction11. Schiffman E, Ohrbach R, Truelove E, Look J, Anderson G, Goulet JP, et al. Diagnostic Criteria for Temporomandibular Disorders (DC/TMD) for Clinical and Research Applications: recommendations of the International RDC/TMD Consortium Network* and Orofacial Pain Special Interest Group†. J Oral Facial Pain Headache. 2014 Winter;28(1):6-27. doi: 10.11607/jop.1151..

Visual Analogue Scale (VAS)

The VAS was used to measure orofacial pain. It is a linear scale, 10 cm in length, labeled at the two extremes with the boundaries of pain sensation: “no pain” at one end, and “worst pain imaginable” at the other end2424. Collins SL, Moore RA, McQuay HJ. The visual analogue pain intensity scale: what is moderate pain in millimetres? Pain. 1997 Aug;72(1-2):95-7. doi: 10.1016/s0304-3959(97)00005-5.,2525. Lundeberg T, Lund I, Dahlin L, Borg E, Gustafsson C, Sandin L, et al. Reliability and responsiveness of three different pain assessments. J Rehabil Med. 2001 Nov;33(6):279-83. doi: 10.1080/165019701753236473..

Maximum bilateral molar bite force (MMBMax)

The MMBMax force was assessed using a bite dynamometer DFM021115/200 (EMG System do Brasil, São José dos Campos, Brazil) with iron rods designed for the oral bite, protected by silicone material 15 mm thick. The device has a Kgf scale with a reading capacity from 0 to 200 Kgf and was connected directly to one of the channels of the electromyographic acquisition module. The bite dynamometer was used to assess strength during MMBMax, maintaining a sampling frequency of 2000 Hz.

Before the tasks, all volunteers were trained on the day of collection to use the instrument and were asked to bite the instrument stem with upper and lower molar teeth bilaterally. Verbal encouragement was given during the bite tasks.

Electromyography

The EMG 830C signal acquisition module (EMG System do Brasil, São José dos Campos, Brazil) was used for reading the sEMG signals, with an impedance of >10 MΩ, analog/digital converter, 16-bit resolution, a sampling frequency of 2000 Hz, and fourth-order Butterworth filter.

Four differential surface electrodes (self-adhesive, Ag/AgCl, conductive gel) were used, and the distance inter-electrode was 10 mm. A reference electrode (30×40 mm) was positioned on the manubrium of the sternum. The electrodes were positioned following the criteria proposed by Cram2626. Cram JR. Electrode Placement. In: Cram’s introduction to surface electromyography. Boston: Jones & Bartlett Publishers; 2005. Chapter 14, p.237-389.. The gain was 20×, a common mode rejection >130 dB, an input impedance of 10 GΩ, and signal-to-noise ratio <3 μV RMS.

Procedures

On the same day, after recruiting volunteers according to screening via the DC/TMD, anthropometric data, pain, EMG assessment of masticatory muscles, and MMBMax were collected in each volunteer for 5 seconds.

For the EMG evaluation procedure and MBF, the volunteers stayed seated in a chair respecting the Frankfurt parallel plan. For the MMBMax task, the volunteers were asked to perform the bilateral molar bite on the dynamometer with the maximum strength possible, even if they felt pain in the TMJ, to obtain the maximum bite force value and evaluation of the electrical activity of the masticatory muscles.

EMG signal processing and maximum bite force

The Matlab® Software 8.5.0.1976.13 (R2015a, MathWorks Inc., Natick, Massachusetts, USA) was used to process the EMG, and bite force data. A 4th order digital Butterworth filter was applied to the EMG signal, with zero phase delay (high pass of 10 Hz, low pass of 400 Hz). The first and second EMG signals were always eliminated to avoid interferences that occurred at the beginning and end of each collection.

The EMG indices were processed in the amplitude domain to determine the RMS values, through the evaluation of the magnitude of the electrical activity of the masticatory muscles during the MMBMax task.

Statistical Analysis

Data were submitted to the normality test (Kolmogorov-Smirnov) and described as mean, standard deviation, and 95% confidence interval.

The student t-test was used for intergroup comparisons of the RMS EMG index in the MMBMax task, as well as for anthropometric data, TMJ ROM movement, and maximum bilateral bite force.

The ROC curve was analyzed to determine the diagnostic accuracy (area under the curve - AUC), cut-off point, sensitivity and specificity of the maximum bilateral molar bite force, and RMS EMG index of the masticatory muscles referring to the MMBMax task. The values used for the AUC classification followed the recommendations of Greiner et al.2727. Greiner M, Pfeiffer D, Smith RD. Principles and practical application of the receiver-operating characteristic analysis for diagnostic tests. Prev Vet Med. 2000 May;45(1-2):23-41. doi: 10.1016/s0167-5877(00)00115-x. and Akobeng et al.2020. Akobeng AK. Understanding diagnostic tests 3: Receiver operating characteristic curves. Acta Paediatr. 2007 May;96(5):644-7. doi: 10.1111/j.1651-2227.2006.00178.x.: excellent discrimination (0.90 to 1.0); good discrimination (0.80 to 0.90); moderate discrimination (0.70 to 0.80); poor discrimination (0.60 to 0.70); and discrimination no better than chance (≤0.50). The Youden index (YI) was also calculated by the formula: YI = ([sensitivity + specificity]–1)2828. Yin J, Mutiso F, Tian L. Joint hypothesis testing of the area under the receiver operating characteristic curve and the Youden index. Pharm Stat. 2021 May;20(3):657-74. doi: 10.1002/pst.2099..

Based on the study by Akobeng, et al.2020. Akobeng AK. Understanding diagnostic tests 3: Receiver operating characteristic curves. Acta Paediatr. 2007 May;96(5):644-7. doi: 10.1111/j.1651-2227.2006.00178.x., to identify the best cut-off point, the point with the lowest resultant value for the expression was selected: (1-sensitivity)2 + (1-specificity)2.

To guarantee the methodological quality of this study, intra-rater reliability was also analyzed for each muscle on the RMS EMG index and the maximum bilateral bite force considering the two repetitions collected in the MMBMax. For this purpose, the intraclass correlation coefficients (ICC), model: two-way mixed; type: absolute agreement; calculated reliability: single measurement. The ICC values were classified according to Weir2929. Weir JP. Quantifying test-retest reliability using the intraclass correlation coefficient and the SEM. J Strength Cond Res. 2005 Feb;19(1):231-40. doi: 10.1519/15184.1.: ICC<0.40 (low reliability), ICC≥0.40to≤0.75 (good reliability), and ICC>0.75 (excellent reliability). The following formula was used to calculate the SEM: SEM=Standard Deviationx√(1-ICC).

Data processing was performed using SPSS® software, version 17.0 (Chicago, IL, USA). Significance was set at 5% (p<0.05).

Results

The final sample was composed of 86 women, divided into two groups: TMD Group (n=43) and Control Group (n=43).

Concerning the level of overall intra-rater reliability of the data, between the 2 repetitions in the MMBMax, excellent reliability was observed for the maximum bite force assessed through the dynamometer (ICC=0.97; EPM=6.67 Kgf). For the RMS EMG index, excellent levels of reliability were found for the right anterior temporal muscle (ICC=0.94; EPM:51.38 µV), left anterior temporal muscle (ICC=0.95; EPM:42.27 µV), right masseter (ICC=0.85; EPM:100.7 µV), and left masseter (ICC=0.86; EPM:101.39 µV).

Table 1 shows the TMD classifications of all volunteers, diagnosed using the DC/TMD.

Table 1
Diagnosis of volunteers according to the DC/TMD (n=86).

Table 2 shows that the groups were homogeneous in terms of age and BMI and presented a significant difference in ROM of mouth opening without pain. The groups also demonstrated homogeneity regarding the preference of the chewing side (X2=2.90; p=.14), since in the TMD group 15 volunteers had a preference for chewing on the left side and 28 on the right side and, in the Control Group, 8 volunteers had a preference for chewing on the left side and 35 on the right side.

Table 2
Intergroup comparison of anthropometric data and ROM of the TMJ.

Table 3 expresses the values of bite force and RMS EMG in the MMBMax task, in which a significant intergroup difference was found in the MMBMax and the electrical activity of the temporal and masseter muscles, with greater strength and activity in the control group.

Table 3
Comparison of maximum bite force (Kgf), orofacial pain (cm), and RMS EMG index (µV) in the MMBMax task.

Figure 1. ROC curve A of the maximum bilateral molar bite force; B EMG RMS of masticatory muscles in the MMBMax.

Figure 1
shows the ROC curves, respectively, of the MMBMax and the RMS EMG values of the masticatory muscles in the MMBMax.

Table 4 shows the levels of accuracy, sensitivity, specificity, and best cut-off point of the data illustrated in figure 2. It was observed that the maximum force of the bilateral molar bite showed a high level of accuracy and the values of RMS EMG during the MMBMax showed a moderate level of accuracy for the masseter and temporal muscles.

Table 4
Accuracy level of maximum bite force (Kgf) and RMS EMG values (µV) of masticatory muscles in MMBMax.

Discussion

Force

The results demonstrated a high level of accuracy in the maximum bilateral molar bite strength assessed using a bite dynamometer for the diagnosis of women with myogenic TMD. It is important to emphasize that this research is pioneering since it defines the best cut-off point in the use of the instrument in question for the diagnosis of myogenic dysfunction. These findings need to be interpreted with caution, since they should be used in line with the criteria employed in this study, that is, in young women, using a 15 mm thick bilateral molar bite dynamometer.

Considering the methodology used in this research, the value of 52.41 Kgf was established as the best cut-off point for the diagnosis of myogenic TMD; positive cases should be diagnosed when the MMBMax is less than the cut-off point, and negative cases when the maximum force is equal to or greater than the cut-off point.

This research also found a significantly greater difference in MBF for the control group compared to the TMD group. This fact is in agreement with previous research, such as the study by Kroon and Naeije3030. Kroon GW, Naeije M. Electromyographic evidence of local muscle fatigue in a subgroup of patients with myogenous craniomandibular disorders. Arch Oral Biol. 1992 Mar;37(3):215-8. doi: 10.1016/0003-9969(92)90091-l., who evaluated maximum strength with a force transducer for an incisive bite; Castroflorio et al.1010. Castroflorio T, Bracco P, Farina D. Surface electromyography in the assessment of jaw elevator muscles. J Oral Rehabil. 2008 Aug;35(8):638-45. doi: 10.1111/j.1365-2842.2008.01864.x. who portrayed the maximum force of the bilateral molar bite with an intraoral force transducer; and Xu et al.1111. Xu L, Fan S, Cai B, Fang Z, Jiang X. Influence of sustained submaximal clenching fatigue test on electromyographic activity and maximum voluntary bite forces in healthy subjects and patients with temporomandibular disorders. J Oral Rehabil. 2017 May;44(5):340-6. doi: 10.1111/joor.12497. who observed maximum strength with a unilateral molar bite dynamometer. On the other hand, Koyano, Kim and Clark3131. Koyano K, Kim YJ, Clark GT. Electromyographic signal changes during exercise in human chronic jaw-muscle pain. Arch Oral Biol. 1995 Mar;40(3):221-7. doi: 10.1016/0003-9969(95)98811-c., analyzed maximum strength with a bilateral molar bite dynamometer and found no significant difference between the group with dysfunction of the masticatory muscles and the control group.

These disagreements are due to the influence of anatomical and physiological factors of each individual evaluated, which directly influences the measurement of the bite force. It is also known that the MBF varies according to the location of the force transducer or bite dynamometer in the oral cavity; the more posterior, the greater the maximum bite force record1414. Koc D, Dogan A, Bek B. Bite force and influential factors on bite force measurements: a literature review. Eur J Dent. 2010 Apr;4(2):223-32.. For the most adequate record of maximum bite force, an interocclusal distance of 9 to 20 mm should be used, with a load applied on several teeth for larger support area3232. Ahlberg JP, Kovero OA, Hurmerinta KA, Zepa I, Nissinen MJ, Könönen MH. Maximal bite force and its association with signs and symptoms of TMD, occlusion, and body mass index in a cohort of young adults. Cranio. 2003 Oct;21(4):248-52. doi: 10.1080/08869634.2003.11746258..

In the present study, the greater magnitude of maximum bite force found in the control group may be justified by the 15 mm thickness of the bite dynamometer, which in turn may have favored the optimization of the length-tension relationship of masseter muscles during the evaluation in the masticatory muscles or TMJ in this group. The myogenic TMD group, due to the chronic installed dysfunction and pain during the bite task, may have presented inhibitory mechanisms of the maximum bite force1717. Kogawa EM, Calderon PS, Lauris JR, Araujo CR, Conti PC. Evaluation of maximal bite force in temporomandibular disorders patients. J Oral Rehabil. 2006 Aug;33(8):559-65. doi: 10.1111/j.1365-2842.2006.01619.x.,3333. Bezerra BPN, Ribeiro AIAM, Farias ABL, Farias AB, Fontes LBC, Nascimento SR, et al. Prevalence of temporomandibular joint dysfunction and different levels of anxiety among college students. Rev Dor. 2012;13(3):235-42. doi: 10.1590/S1806-00132012000300008..

Electromyography

This study showed a moderate level of accuracy in the RMS EMG values of the masticatory muscles during the MMBMax for the diagnosis of women with myogenic TMD.

Considering the masticatory muscles, the following values are established as the best cut-off points for the diagnosis of myogenic TMD, in which positive cases should be diagnosed when the RMS EMG value is less than the cut-off point, and negative cases when the maximum force is equal to or greater than the cut-off point: left anterior temporal muscle (107.4 µV), right anterior temporal muscle (136.9 µV), left masseter (173.3 µV), and right masseter (208.59 µV).

Manfredini et al.88. Manfredini D, Bracci A, Djukic G. BruxApp: the ecological momentary assessment of awake bruxism. Minerva Stomatol. 2016;65(4):252-5. and Berni et al.99. Berni KC, Dibai-Filho AV, Pires PF, Rodrigues-Bigaton D. Accuracy of the surface electromyography RMS processing for the diagnosis of myogenous temporomandibular disorder. J Electromyogr Kinesiol. 2015 Aug;25(4):596-602. doi: 10.1016/j.jelekin.2015.05.004. assessed the accuracy levels of the RMS EMG parameter in a bite task and reported inconsistent findings. In general Berni, et al.99. Berni KC, Dibai-Filho AV, Pires PF, Rodrigues-Bigaton D. Accuracy of the surface electromyography RMS processing for the diagnosis of myogenous temporomandibular disorder. J Electromyogr Kinesiol. 2015 Aug;25(4):596-602. doi: 10.1016/j.jelekin.2015.05.004. demonstrated that the RMS EMG parameter of the masticatory muscles showed a moderate level of accuracy for the discrimination between individuals with myogenic TMD and asymptomatic individuals during the TMJ rest task and inadequate levels of accuracy during the maximum isometric bilateral molar bite. Conversely, Manfredini, et al.88. Manfredini D, Bracci A, Djukic G. BruxApp: the ecological momentary assessment of awake bruxism. Minerva Stomatol. 2016;65(4):252-5. demonstrated that the RMS EMG parameter of the masticatory muscles demonstrated a high level of accuracy for the diagnosis of myogenic TMD during the maximal isometric bilateral molar bite task, but low levels of accuracy in the TMJ rest task.

Strengths and Limitations

This study presents as strengths a large sample size, robust statistical analysis, the cut-off of MMBMax and the RMS EMG index of the masticatory muscles during the maximum bilateral molar bite, and a new perspective of tools already used in research and clinical practice.

The limitations were: absence of an evaluation of the facial pattern of the volunteers; the need for caution when interpreting and using the accuracy cut-off point for MMBMax for discrimination of women with myogenic and asymptomatic TMD, as these values should be used only for young women and with the use of a 15 mm thick bilateral molar dynamometer; the presence of some cases with other joint symptoms, such as disk displacement and arthralgia, in the sample.

Future studies

The evaluation of the volunteers’ menstrual cycle phase is suggested. The literature portrays a greater capacity for modulating pain in the ovulatory phase of the cycle, which may complement the findings of this research.

Considering the ability of surface EMG to assess myogenic TMD, non-invasively and painlessly, providing quantitative and reliable information both in the clinical and research environment1010. Castroflorio T, Bracco P, Farina D. Surface electromyography in the assessment of jaw elevator muscles. J Oral Rehabil. 2008 Aug;35(8):638-45. doi: 10.1111/j.1365-2842.2008.01864.x., its use is suggested for monitoring and directing the treatment of myogenic TMD, as already used in research over the years.

In conclusion, the research hypothesis was confirmed, the maximum bilateral bite force demonstrated high precision for myogenic TMD diagnosis women, and the RMS EMG index of the masticatory muscles in the MMBMax was able to discriminate between groups. The bilateral bite dynamometer with a surface EMG during bilateral bite can be used to diagnose TMD in young women.

Data availability

Datasets related to this article will be available upon request to the corresponding author.

Acknowledgments

This study was financed by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior – Brazil (CAPES). Finance Code 001.

References

  • 1
    Schiffman E, Ohrbach R, Truelove E, Look J, Anderson G, Goulet JP, et al. Diagnostic Criteria for Temporomandibular Disorders (DC/TMD) for Clinical and Research Applications: recommendations of the International RDC/TMD Consortium Network* and Orofacial Pain Special Interest Group†. J Oral Facial Pain Headache. 2014 Winter;28(1):6-27. doi: 10.11607/jop.1151.
  • 2
    Gonçalves DA, Dal Fabbro AL, Campos JA, Bigal ME, Speciali JG. Symptoms of temporomandibular disorders in the population: an epidemiological study. J Orofac Pain. 2010 Summer;24(3):270-8.
  • 3
    Leeuw R, Klasser GD, editors. Orofacial pain: guidelines for assessment, diagnosis, and management. 5. ed. Quintessence Publishing; 2013.
  • 4
    Gauer RL, Semidey MJ. Diagnosis and treatment of temporomandibular disorders. Am Fam Physician. 2015 Mar;91(6):378-86.
  • 5
    Al-Khotani A, Naimi-Akbar A, Albadawi E, Ernberg M, Hedenberg-Magnusson B, Christidis N. Prevalence of diagnosed temporomandibular disorders among Saudi Arabian children and adolescents. J Headache Pain. 2016;17:41. doi: 10.1186/s10194-016-0642-9.
  • 6
    Santana-Mora U, Cudeiro J, Mora-Bermúdez MJ, Rilo-Pousa B, Ferreira-Pinho JC, Otero-Cepeda JL, et al. Changes in EMG activity during clenching in chronic pain patients with unilateral temporomandibular disorders. J Electromyogr Kinesiol. 2009 Dec;19(6):e543-9. doi: 10.1016/j.jelekin.2008.10.002.
  • 7
    De Luca CJ. The use of surface electromyography in biomechanics. J Appl Biomech. 1997;13(2):135-63. doi: 10.1123/jab.13.2.135.
  • 8
    Manfredini D, Bracci A, Djukic G. BruxApp: the ecological momentary assessment of awake bruxism. Minerva Stomatol. 2016;65(4):252-5.
  • 9
    Berni KC, Dibai-Filho AV, Pires PF, Rodrigues-Bigaton D. Accuracy of the surface electromyography RMS processing for the diagnosis of myogenous temporomandibular disorder. J Electromyogr Kinesiol. 2015 Aug;25(4):596-602. doi: 10.1016/j.jelekin.2015.05.004.
  • 10
    Castroflorio T, Bracco P, Farina D. Surface electromyography in the assessment of jaw elevator muscles. J Oral Rehabil. 2008 Aug;35(8):638-45. doi: 10.1111/j.1365-2842.2008.01864.x.
  • 11
    Xu L, Fan S, Cai B, Fang Z, Jiang X. Influence of sustained submaximal clenching fatigue test on electromyographic activity and maximum voluntary bite forces in healthy subjects and patients with temporomandibular disorders. J Oral Rehabil. 2017 May;44(5):340-6. doi: 10.1111/joor.12497.
  • 12
    Todic J, Martinovic B, Pavlovic J, Tabakovic S, Staletovic M. Assessment of the impact of temporomandibular disorders on maximum bite force. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub. 2019 Sep;163(3):274-8. doi: 10.5507/bp.2019.001.
  • 13
    Calderon Pdos S, Kogawa EM, Lauris JR, Conti PC. The influence of gender and bruxism on the human maximum bite force. J Appl Oral Sci. 2006 Dec;14(6):448-53. doi: 10.1590/s1678-77572006000600011.
  • 14
    Koc D, Dogan A, Bek B. Bite force and influential factors on bite force measurements: a literature review. Eur J Dent. 2010 Apr;4(2):223-32.
  • 15
    Castelo PM, Gavião MB, Pereira LJ, Bonjardim LR. Masticatory muscle thickness, bite force, and occlusal contacts in young children with unilateral posterior crossbite. Eur J Orthod. 2007 Apr;29(2):149-56. doi: 10.1093/ejo/cjl089.
  • 16
    Tortopidis D, Lyons MF, Baxendale RH. Bite force, endurance and masseter muscle fatigue in healthy edentulous subjects and those with TMD. J Oral Rehabil. 1999 Apr;26(4):321-8. doi: 10.1046/j.1365-2842.1999.00383.x.
  • 17
    Kogawa EM, Calderon PS, Lauris JR, Araujo CR, Conti PC. Evaluation of maximal bite force in temporomandibular disorders patients. J Oral Rehabil. 2006 Aug;33(8):559-65. doi: 10.1111/j.1365-2842.2006.01619.x.
  • 18
    Kordass B, Hugger A, Bernhardt O. Correlation between computer-assisted measurements of mandibular opening and closing movements and clinical symptoms of temporomandibular dysfunction. Int J Comput Dent. 2012;15(2):93-107.
  • 19
    Sforza C, Rosati R, De Menezes M, Musto F, Toma M. EMG analysis of trapezius and masticatory muscles: experimental protocol and data reproducibility. J Oral Rehabil. 2011 Sep;38(9):648-54. doi: 10.1111/j.1365-2842.2011.02208.x.
  • 20
    Akobeng AK. Understanding diagnostic tests 3: Receiver operating characteristic curves. Acta Paediatr. 2007 May;96(5):644-7. doi: 10.1111/j.1651-2227.2006.00178.x.
  • 21
    Hulley SB, Cummings SR, Browner WS, Grady DG, Newman TB. [Outlining clinical research]. 4.ed. Porto Alegre: Artmed; 2015. Portuguese.
  • 22
    Chowdhury RH, Reaz MB, Ali MA, Bakar AA, Chellappan K, Chang TG. Surface electromyography signal processing and classification techniques. Sensors (Basel). 2013 Sep;13(9):12431-66. doi: 10.3390/s130912431.
  • 23
    Lora VR, Canales GL, Gonçalves LM, Meloto CB, Barbosa CM. Prevalence of temporomandibular disorders in postmenopausal women and relationship with pain and HRT. Braz Oral Res. 2016 Aug;30(1):e100. doi: 10.1590/1807-3107BOR-2016.vol30.0100.
  • 24
    Collins SL, Moore RA, McQuay HJ. The visual analogue pain intensity scale: what is moderate pain in millimetres? Pain. 1997 Aug;72(1-2):95-7. doi: 10.1016/s0304-3959(97)00005-5.
  • 25
    Lundeberg T, Lund I, Dahlin L, Borg E, Gustafsson C, Sandin L, et al. Reliability and responsiveness of three different pain assessments. J Rehabil Med. 2001 Nov;33(6):279-83. doi: 10.1080/165019701753236473.
  • 26
    Cram JR. Electrode Placement. In: Cram’s introduction to surface electromyography. Boston: Jones & Bartlett Publishers; 2005. Chapter 14, p.237-389.
  • 27
    Greiner M, Pfeiffer D, Smith RD. Principles and practical application of the receiver-operating characteristic analysis for diagnostic tests. Prev Vet Med. 2000 May;45(1-2):23-41. doi: 10.1016/s0167-5877(00)00115-x.
  • 28
    Yin J, Mutiso F, Tian L. Joint hypothesis testing of the area under the receiver operating characteristic curve and the Youden index. Pharm Stat. 2021 May;20(3):657-74. doi: 10.1002/pst.2099.
  • 29
    Weir JP. Quantifying test-retest reliability using the intraclass correlation coefficient and the SEM. J Strength Cond Res. 2005 Feb;19(1):231-40. doi: 10.1519/15184.1.
  • 30
    Kroon GW, Naeije M. Electromyographic evidence of local muscle fatigue in a subgroup of patients with myogenous craniomandibular disorders. Arch Oral Biol. 1992 Mar;37(3):215-8. doi: 10.1016/0003-9969(92)90091-l.
  • 31
    Koyano K, Kim YJ, Clark GT. Electromyographic signal changes during exercise in human chronic jaw-muscle pain. Arch Oral Biol. 1995 Mar;40(3):221-7. doi: 10.1016/0003-9969(95)98811-c.
  • 32
    Ahlberg JP, Kovero OA, Hurmerinta KA, Zepa I, Nissinen MJ, Könönen MH. Maximal bite force and its association with signs and symptoms of TMD, occlusion, and body mass index in a cohort of young adults. Cranio. 2003 Oct;21(4):248-52. doi: 10.1080/08869634.2003.11746258.
  • 33
    Bezerra BPN, Ribeiro AIAM, Farias ABL, Farias AB, Fontes LBC, Nascimento SR, et al. Prevalence of temporomandibular joint dysfunction and different levels of anxiety among college students. Rev Dor. 2012;13(3):235-42. doi: 10.1590/S1806-00132012000300008.

Edited by

Editor: Dr. Altair A. Del Bel Cury

Publication Dates

  • Publication in this collection
    20 Mar 2023
  • Date of issue
    2023

History

  • Received
    3 July 2022
  • Accepted
    8 Feb 2022
Faculdade de Odontologia de Piracicaba - UNICAMP Avenida Limeira, 901, cep: 13414-903, Piracicaba - São Paulo / Brasil, Tel: +55 (19) 2106-5200 - Piracicaba - SP - Brazil
E-mail: brjorals@unicamp.br