Revisiting the Risk Factors for Multiple Symptoms of Temporomandibular Disorders: A structured Cross-sectional Study

All published articles of this journal are available on ScienceDirect.

RESEARCH ARTICLE

Revisiting the Risk Factors for Multiple Symptoms of Temporomandibular Disorders: A structured Cross-sectional Study

The Open Dentistry Journal 23 Oct 2020 RESEARCH ARTICLE DOI: 10.2174/1874210602014010503

Abstract

Background:

The risk factors for Temporomandibular Disorders (TMD) are extensively studied, but the results showed no consistency. Only a small proportion of patients with TMD are likely to seek help and require treatment. Those individuals tend to present with multiple symptoms. This cohort of patients was not well investigated.

Objective:

The study aimed to examine the association between possible risk factors for presentation with multiple TMD symptoms.

Methods:

A population-based, cross-sectional study was conducted across 2101 individuals with an age range of 19-60 years. The condition was assessed via a detailed questionnaire comprising symptoms, habits, dental history, general health, sleep patterns, along with the completion of the Hospital Anxiety and Depression (HAD) scale, followed by an examination of the hypothesized clinical signs. The obtained data were tabulated and characterized the study population in a descriptive analysis in forms of percentages and frequencies. The significance level was set at P-value less than or equal to 0.005. The chi-squared test was implemented to assess the relationship between the multiple TMD symptoms reported and the potential risk factors.

Results:

Most participants reported a variable amount of stress. Moreover, 1528 (72.7 percent) mentioned abnormalities in sleep. About 80 percent had at least one TMD-related symptom. The multiple symptoms of TMD were identified among the 741 individuals. The following risk factors demonstrated association with a robust statistical significance (P=0.00), 1) occupation, 2) sleeping problems, 3) health concerns, 4) traumatic dental treatment, 5) various somatic symptoms, and 6) elevated HAD scale. When the outcomes of the clinical examination were analyzed, the statistical assessment could link soft tissue changes, namely; the cheek ridging and tongue indentations (P 0.00), with multiple symptoms of the condition.

Conclusion:

Multiple TMD symptoms were prevalent among individuals with elevated stress, abnormal sleep pattern, traumatic dental treatment, elevated HAD scale. The results highlighted the importance of psychological factors in the pathogenesis of TMD.

Keywords: Temporomandibular disorders, Temporomandibular joint, Risk factors, Etiology, Orofacial pain, Hospital anxiety & depression.

1. INTRODUCTION

The Tempro Mandibular Disorders (TMDs) are identified as a major cause of the non-dental pain in the orofacial region [1]. TMDs are not considered as a single syndrome with one common or multifactorial etiology anymore but are a collection of heterogeneous correspondent disorders with underlying pathophysiologic mechanisms. Therefore, enriched clinician knowledge and awareness of TMDs along with the differential diagnosis is of fundamental and upmost importance [2]. The condition affected the jaw musculature, the temporomandibular joints, and associated structures or both and was given several synonyms, which reflect the lack of common understanding of the disease. However, in many patients, the symptoms are not confined to the temporomandibular region but extend to the neck, shoulders and even the upper, middle, and lower back, the upper arms, and the knees [3]. The affected individuals usually present with pain and symptoms of masticatory system dysfunction are a prevalent disorder most commonly observed in individuals between the ages of 20 and 40. Approximately one fifth to one-third of the population has at least one TMD symptom, but 3.6% to 7% of this population may seek medical assistance [4-7].

Table 1.
The elements of the clinical examination.
Elements for Clinical Examination
1. Mandibular retrognathia
2. Limitation in mouth opening
3. The presence of deep Incisor bite  
4. Anterior or posterior tooth wear
5. Tenderness on the temple area, TMJ and back/sides of the neck
6. Marginal tongue indentation    
7. The presence of various dental prosthesis
8. The presence of a cheek ridging 
9. Presence of the jaw Bony exostosis
10. Loss of first molar tooth/teeth

For decades, the risk factors and underlying etiology for TMDs are subject to debate. The etiology is widely regarded as multidimensional, biomechanical in forms of deranged occlusion and displaced meniscus, neuromuscular, psychosocial, and neurobiological factors explained by central somatization [8]. Although the medical library is rich in papers on TMDs, there's a consistent pattern of disagreement on what may cause, initiate, and worsen the morbidity of patients with TMDs. This has resulted in a lack of standardized treatment protocols for treating the condition. This research is aimed at improving understanding of the disease through the analysis of the association between potential risk factors and the presentation of multiple TMD symptoms.

2. MATERIALS AND METHODS

This study was a cross-sectional and random population-based that included a pre-validated, self-administered questionnaire, Hospital Anxiety and Depression Scale (HAD Scale), and clinical examination of the signs likely associated with the TMD. The Research Ethics Committee (REC) of the University of Ajman reviewed and approved the study protocol with reference SS2016/17-06 and was conducted according to the Declaration of Helsinki. Informed consent was obtained from all participants.

The questionnaire focused on the demographic data of the participants, in addition to the exploration of the wide range of TMDs symptoms with questions adapted from the anamnesis suggested by the American Academy of Orofacial Pain [9]. The next part investigated the potential risk factors reported in the literature like abnormal oral behaviors, history of traumatic dental visits, orthodontic treatment, general health issues and worries, and sleeping disorders (Table 1). The sleeping problem questions were modified from the scale published by Jenkins and coworkers [10]. The participants were then asked to complete the HAD scale questionnaire form. The degree of anxiety and depression was calculated according to total scores as follows: A) 0-7: normal or absence of anxiety and depression; B) 8-10: cause of concern (borderline); and C) 11-21 and above; a probable clinical case requiring assessment and possible psychiatric interventions. The third component of this work involved a clinical examination for the features linked to patients with TMDs in the available literature and are listed in Table 2.

The data obtained was computerized using the Statistical Package for Social Sciences (SPSS) 64-bit to perform the statistical analysis. To characterize the study population, a descriptive analysis in the form of percentages and frequencies was performed. The P-value was set to below or equal to 0.005. Chi-squared analysis was used for the evaluation of the association between the multiple TMD symptoms and their possible risk factors. These factors were also assessed for their potential contribution to the multiple TMD symptoms via calculation of the Odds ratios (OR). The ratio was measured at 95% confidence interval calculated according to Altman, 1991 [11].

3. RESULTS

3.1. General Characteristics of Participants

Each participant (2101) completed the TMD symptoms and risk factors questionnaire. They also completed the standard HAD scale form. However, only 1456 (69.3%) agreed to undergo the clinical examination component of the study. The population of the study was predominantly females (1741, 82.9%), within the age range of 19 to 60 years. The study targeted people under the age of 50 (2036) with the most abundant age group of the 3rd decade, which made 60.6% (1274) of the study sample. Most of these young participants were university students (896). Only 10.3% of the participants reported a smoking habit. The majority of participants (94.5%) reported a variable amount of life stress. The differential self-report of the stress revealed the following; occasional incidents (1013, 48.2%), frequent episodes (627, 29.8%), and constant stressful life reported by 259 (12.3%) participants while the rest of participants (202, 9.6%) did not recall any significant stresses. When asked to describe their personalities, more than one-third (817) of the participants described themselves as sensitive. On the contrary, another one third were calm individuals, but one-fifth of the respondents (423) believed that they get angry or upset very quickly or have a neurotic personality. Around two-thirds of the participants reported variable degrees of sleeping difficulties (1528). Around one-quarter of participants (552) reported concern about their general health status. The investigation of the history of rough or potentially traumatic past dental treatments revealed that the long dental visits were the most commonly reported incidents reported in 383 cases (18.2%). On the other hand, more than one third (794) of participants reported multiple potentially traumatic dental treatments, including orthodontic treatment and surgical extraction of teeth.

Table 2.
Crosstabulation of the data of some variable against symptoms.
Symptoms HAD Scale Total Sleeping Problems Total Tenderness of muscles and joint Total
Normal Borderline Elevated Occasional Usual on Pills No problem Present Absent
Earache Count 42 24 99 165 71 27 1 56 156 35 83 118
% of patients the symptom 25.5% 14.5% 60.0% 100% 43% 22.5% 0.6% 33.9% 7.9% 29.7% 70.3% 100%
Morning headache Count 22 80 276 378 195 83 5 95 378 132 146 278
% of patients the symptom 5.8% 21.2% 73.0% 100% 51.6 % 21.9% 1.3 % 25.1% 18% 48.5% 52.5% 100%
Jaw/neck fatigue Count 31 26 61 118 71 25 1 21 118 59 29 88
% of patients the symptom 26.3% 22.0% 51.7% 100% 60.2% 21.1% 0.8% 17.8% 5.6% 77% 33% 100%
Difficulty in 
opening the mouth
Count 7 12 38 57 29 5 1 22 57 31 15 46
% of patients the symptom 12.3% 21.1% 66.7% 100% 50.9% 8.8% 1,8% 38.6% 2.7% 67.4% 32.6% 100%
Jaw tires easily when chewing Count 6 5 49 60 38 5 0 17 60 26 15 41
% of patients the symptom 10.0% 8.3% 81.7% 100% 63.3% 8.3% 0% 26.3% 2.9% 63.4% 36.5% 100%
Teeth sore when biting Count 15 16 55 86 47 21 0 18 86 22 32 54
% of patients the symptom 17.4% 18.6% 64.0% 100% 54.7% 24.4% 0% 3.2% 4.1% 40.7% 59.3% 100%
Jaw clicks before opening wide Count 16 13 63 92 43 22 0 27 92 28 17 45
% of patients the symptom 17.4% 14.1% 68.5% 100% 46.7% 23.9% 0% 29.3% 4.4% 62.2% 37.8% 100%
Multiple Count 85 96 560 741 396 172 7 166 741 307 254 561
% of patients the symptom 11.5% 13.0% 75.6% 100% 53.4% 23.3% 0.9% 22.4% 35.3% 54.7% 45.3% 100%
No Symptoms Count 81 47 276 404 197 71 4 132 404 58 167 225
% of patients the symptom 20.0% 11.6% 68.3% 100% 48.8% 17.5% 21.1 32.7% 19.2% 25.8% 74.2% 100%
Total Count 305 319 1477 2101 1087 441 19 554 2101 698 758 1456

3.2. Temporomandibular Disorder Symptoms and their Potential Risk Factors

Around 80% of participants (1697) had experienced at least one symptom related to the TMDs. The most commonly reported single symptom was morning headache, which was reported by 18% (278), followed by a temple headache in 118 cases. On the other hand, the least reported symptoms reported were the joint clicking and pain while chewing regular meals. The control group included 404 individuals without a history of any symptoms related to the TMD (Fig. 1a).

More than one-third (741) of the study population reported more than two symptoms (referred to as multiple) of the TMDs. The symptoms were not limited to jaw muscles and joints in two-thirds of cases (1612). Around one-third of respondents (704) complained of multiple remote somatic symptoms, including neck, shoulders, and other joints and back pain, in addition to various stress-related gastrointestinal disturbances (Fig. 1b). The descriptive analysis and cross-tabulation showed a variable association of study risk factors against symptoms. A representative sample of the data is shown in Table 2.

Fig. (1). The variety of the TMD symptoms reported among the participants (a) and the other associated somatic symptoms (b).

Using the Chi-square test, the following self-reported risk factors were associated to the patient presented with multiple TMDs with high statistical significance (P .000-.002); 1) occupation, 2) sleeping problems, 3) an increased concern about health status, 4) history of potentially traumatic dental treatment, 5) co-existence of multiple somatic associated symptoms, and 6) elevated HAD scale (Table 3). The results also highlighted the probable role of the abnormal oral behaviors like bruxism in the precipitation of the multiple TMD symptoms despite the lack of statistical significance (P 0.107). The cross-tabulation analysis revealed that the most commonly reported pattern of bruxism was that taking place while sleeping and this habit was associated mainly with multiple TMD symptoms (38.5%), with morning discomfort and headache being the most prevalent presentations (19%).

The clinical screening for hard and soft tissue changes could only relate the tongue indentations and cheek ridging to the presence of multiple TMD symptoms (Table 4). The risk assessment was also confirmed by the outcome of the odds ratio calculation. The later statistical assessment showed the association of the same risk factors obtained from the questionnaire, the HAD scale, and the clinical examination, that are shown in Table 5.

Table 3.
The association between multiple TMD symptoms and the potential risk factors obtained from the questionnaire and the completed HAD scale. The * denotes high statistical significance.
- Multiple TMD Symptoms Occupation Reported Amount of Stress Personality Trait Self-Description Sleeping Disorders Health Concerns History of Rough Dental treatment Associated somatic symptoms Reported Bruxism HAD Scale
Multiple TMD Symptoms P value   .010 .061 .381 .002 .000* .000* .000* .107 .000*
Occupation P value .000*   .001* .001* .001 .592 .568 .112 .031 .001*
Reported Amount of Stress P value .061 .001*   .000* .000* .005 .914 .546 .556 .000*
Personality Trait Self-Description P value .381 .001* .000*   .000* .135 .215 .027 .013 .110
Sleeping Disorders P value .002 .001* .000* .000*   .254 .409 .438 .924 .000*
Health Concerns P value .000* .592 .005 .135 .254   .715 .004 .037 .000*
History of Rough Dental treatment P value .000* .568 .914 .215 .409 .715   .000* .000* .505
Associated Symptoms P value .000* .112 .546 .027 .438 .004 .000*   .000* .060
Reported Bruxism P value .107 .031 .556 .013 .924 .037 .000* .000*   .977
HAD Scale P value .000* .001* .000* .110 .000* .000* .505 .060 .977  
Table 4.
Association between multiple TMD symptoms and clinical signs, the * indicate the high significance.
- Multiple TMD Symptoms Mandibular Retrognathia Deep Bite Tooth Wear Tongue Indentation Dental Prosthesi Cheek Ridging Bony Exostosis Loss of Molar teeth
Multiple TMD Symptoms P value   .688 .350 .586 .000* .160 .000* .155 .879
Mandibular Retrognathia P value .688   .000* .297 .573 .007 .000* .007 .792
Deep Bite P value .350 .000*   .000* .009 .015 .000* .156 .486
Tooth Wear P
value
.586 .297 .000*   .590 .013 .629 .454 .521
Tongue Indentation P value .000* .573 .009 .590   .001* .000* .390 .026
Dental Prosthesis P value .160 .007 .015 .013 .001   .331 .000 .000*
Cheek Ridging P value .000* .000* .000* .629 .000* .331   .667 .077
Bony Exostosis P value .155 .007 .156 .454 .390 .000* .667   .000*
Loss of Molar teeth P value .879 .792 .486 .521 .026 .000* .077 .000*  
Table 5.
The Odds ratio of the main potential risk factors for multiple TMD symptoms.
- Sig. odds ratio 95% Confidence Interval
Lower Bound Upper Bound
Occupation .295 .928 .807 1.067
Perception of Stress .758 1.034 .834 1.282
Perception of Personality .842 1.018 .857 1.209
Sleeping problems .036 .843 .720 .989
Elevated HAD scale .000* 1.502 1.202 1.878
General health Concerns .000* 1.234 1.117 1.362
Self-report of Bruxism .818 .991 .917 1.070
Presence of other somatic symptoms .000* 1.148 1.064 1.238
History of multiple rough dental treatment visits .000* 1.240 1.165 1.320
Mandibular Retrognathia .205 1.373 .841 2.241
Anterior deep bite .356 1.244 .782 1.979
Tooth wear .794 .960 .707 1.303
Tongue Indentation .000* .451 .309 .657
Presence of dental prosthesis .014 .992 .863 1.139
Cheek Ridging .000* .414 .262 .652
Jaw bone exostosis .493 1.105 .830 1.472
Loss of first molar teeth .062 .687 .464 1.019

4. DISCUSSION

TMDs are common disorders and are encountered by a wide range of medical and dental professionals. Because of the diversity of clinical presentation, many cases may not be diagnosed correctly and subsequently subjected to unnecessary investigations and treatments. This study attempted to characterize the patients of TMDs along with their risk factors to help the clinician address such patients more efficiently. This investigation has shown that the TMD symptoms are common in the community, and the major risk factors are related to stress and anxiety with less direct contribution of the pure mechanical factors in the development of the condition. The strength of this study comes from the wide spectrum of aspects of TMD examined together on a relatively large cohort of the population. The inclusion of the TMD symptoms questionnaire, general health worries, self-report of personality trait, sleep disorders, anxiety, and depression scale, along with a clinical examination, was not previously reported in a single study. Furthermore, this study is population-based and, therefore, likely to include an unselected group of mild cases which usually do not report to clinics. The report shows that the TMD symptoms affect a good proportion of the population with around three-quarters of society having at least one symptom that could be linked to the condition. This outcome was in line with many previous reports [12, 13]. However, the prevalence in this study was higher than in other investigations [5, 14-16]. It is doubtful that such inconsistencies are due to disparity in the populations studied. A much more likely justification is to be found in the criteria cited in the studies to define the condition, in addition to the variation in the methodology and sample size in different studies as some were limited to questionnaires, and others included clinical evaluation of participants. The wide disparity of results of TMD population-based previous studies has created confusion regarding the accuracy of prevalence figures, and more importantly, citing individuals who actually require treatment. Based on the demand for treatment, about 3-7% of the population seeks treatment for their TMDs [13, 17, 18]. This proportion of the population likely to require treatment is individual with multiple TMD symptoms. That is why we examined the risk factors among this particular group. Halder et al. [19] concluded that psychological distress, fatigue, health anxiety, and illness behavior are predictors of future onset rather than merely a consequence of somatic symptoms like abdominal pain. The accuracy of using self-reported general health may be questioned. Still, several papers have indicated that it could be a valid measure indicating the magnitude of the individual concern of their well-being, especially as there is a lack of a standard method to classify the overall health in epidemiological researches [20, 21].The results indicate a clear correlation between the general health conditions of the participants in this study and the presence of the TMD symptoms. The individuals who are concerned about their health feel uncertain and anxious and may suffer from sleeping disorders, abnormal oral activities, and other manifestations of central sensitization with an increased risk of developing multiple TMD symptoms. Around one-fourth of the participants of this study have reported the presence of multiple symptoms of TMD, with morning headache being the most reported symptom. On the other hand, the presence of the morning headaches and jaw muscle aches in the TMD patients is likely related to the presence of the nocturnal bruxism since muscles would undergo non-functional activities during the late deep phase of sleep [22]. Moreover, Alvarez et al. [23] also reported a 50% - 90% incidence of headache and tenderness in the temporal region and masseter muscles in individuals with abnormal oral behaviors. However, morning headaches can also be a symptom of the tension-type headache, which is why it should be considered in the differential diagnosis. The TMDs and tension-type headache, in many patients, are characterized by the absence of organic pathologies or degenerative disorders. Both conditions have had debatable etiologies with the psychological factors considered to play a crucial role in the pathogenesis of the three conditions. In connection with this trend, this study shows that more than half of the participants reported an elevated HAD scale, which was closely associated with the presence of multiple TMD symptoms.

CONCLUSION

Hence, these results go together with what is previously reported by various investigators, where psychological factors play an important role in the development and persistence of the TMD symptoms [24, 25]. Furthermore, the improvement of the psychology of the individuals with TMDs has been reported to positively affect the treatment outcome and help the patient to cope better with their long-standing symptoms [26] [27, 28]. Nevertheless, the 701 participants (33.4%) participants who reported an elevated HAD scale also reported the presence of abnormal oral behaviors, especially nocturnal bruxism. This correlated with the previously agreed on in the literature that bruxism can reflect the individual's stresses and trial to escape the fears and the depression or the anxiety that they might be going through. Abnormal oral behaviors have been reported as a means of releasing accumulated tension and stress [29]. However, others have observed no such association between bruxism and TMD [23, 30-34]. Therefore, from the literature, it is deduced that it is bruxism, which is caused by the psychological stresses or depressions that leads to the occurrence of TMD symptoms and not the one present when some mild malocclusions are there [35]. The biopsychosocial theory, first introduced by Schwartz [36], stated that TMDs are a result of the interactions between biological parts (TMJ and muscles), and the psychological and social state. Accordingly this will yield the occurrence of the abnormal oral behaviors. Traumatic dental experience tends to increase anxiety [37]. It was also noted that individuals with a history of rough dental treatment meet most of the criteria for Post-Traumatic Stress Disorder (PTSD). The impact of the adverse dental experience was comparable to that of disasters like road traffic accidents and even terrorist attacks [38, 39]. The correlation noted on a cohort between the history of rough dental treatment and two possible mechanisms may explain the presence of the multiple symptoms. The first is the mechanical trauma that may directly injure the stomatognathic structures. The second is the psychogenic impact of the potential PTSD caused by that experience. The literature attempted to correlate several changes in the hard and soft tissue compartments of the stomatognathic system to the TMD. This investigation, however, could only relate the soft tissue changes seen on the tongue and cheeks but failed to associate any of the dental or bony changes with the presence of multiple TMD symptoms. Both cheek ridging and the tongue indentations appear to be directly linked to the active and aggressive night grinding or clenching. These changes reflect the repetitive contraction and the pressure caused by the swallowing that follows the aggressive bruxism activities. It seems that the hard tissue changes are the wear and adaptive changes of slow chronic abnormal oral behaviors that may not be aggressive enough to contribute to multiple TMD symptoms. In conclusion, it is recommended that all treatment of TMD should primarily focus on improving the psychological state and terminating any abnormal oral behaviors. Secondly, the managing practitioner should consider relieving the muscular and articular symptoms resulting from long-term abnormal oral behavior.

ETHICS APPROVAL AND CONSENT TO PARTICIPATE

The study was approved by the Research Ethics Committee (REC) of the University of Ajman, UAE, with reference SS2016/17-06.

HUMAN AND ANIMAL RIGHTS

No animals were used in this research. All human research procedures followed were in accordance with the ethical standards of the committee responsible for human experimentation (institutional and national), and with the Helsinki Declaration of 1975, as revised in 2013.

CONSENT FOR PUBLICATION

Written informed consent was obtained from participants prior to inclusion.

AVAILABILITY OF DATA AND MATERIALS

Not applicable.

FUNDING

No fund or financial support was received for this work.

CONFLICTS OF INTEREST

The author declares no conflict of interest, financial or otherwise.

ACKNOWLEDGEMENTS

Declared none.

REFERENCES

1
Korszun A, Papadopoulos E, Demitrack M, Engleberg C, Crofford L. The relationship between temporomandibular disorders and stress-associated syndromes. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1998; 86(4): 416-20.
2
Tegelberg A, Wenneberg B, List T. General practice dentists’ knowledge of temporomandibular disorders in children and adolescents. Eur J Dent Educ 2007; 11(4): 216-21.
3
Prasad SR1, Kumar NR1, Shruthi HR1, Kalavathi SD1.. Temporomandibular pain. J Oral Maxillofac Pathol 2016; 20: 272-5.
4
Al-Jundi MA, John MT, Setz JM, Szentpétery A, Kuss O. Meta-analysis of treatment need for temporomandibular disorders in adult nonpatients. J Orofac Pain 2008; 22(2): 97-107.
5
Bonjardim LR, Lopes-Filho RJ, Amado G, Albuquerque RL Jr, Goncalves SR. Association between symptoms of temporomandibular disorders and gender, morphological occlusion, and psychological factors in a group of university students. Indian J Dent Res 2009; 20(2): 190-4.
6
Aggarwal VR, Macfarlane GJ, Farragher TM, McBeth J. Risk factors for onset of chronic oro-facial pain--results of the North Cheshire oro-facial pain prospective population study. Pain 2010; 149(2): 354-9.
7
Al-Moraissi EA, Wolford LM, Perez D, Laskin DM, Ellis E III. Does orthognathic surgery cause or cure temporomandibular disorders? A systematic review and meta-analysis. J Oral Maxillofac Surg 2017; 75(9): 1835-47.
8
Gaballah KY, Elerbi MS. Factors associated with temporomandiblular disorders in eastern LIBYA. Pak Oral Dent J 2002; 22: 111-6.
9
de Leeuw R, Ed. American Academy of Orofacial Pain.Orofacial Pain: Guidelines for Assessment, Diagnosis and Management 4th ed. 2008.
10
Jenkins CD, Stanton BA, Niemcryk SJ, Rose RM. A scale for the estimation of sleep problems in clinical research. J Clin Epidemiol 1988; 41(4): 313-21.
11
Altman DG. Practical statistics for medical research 1991.
12
Conti A, Freitas M, Conti P, Henriques J, Janson G. Relationship between signs and symptoms of temporomandibular disorders and orthodontic treatment: A cross-sectional study. Angle Orthod 2003; 73(4): 411-7.
13
Nassif NJ, Talic YF. Classic symptoms in temporomandibular disorder patients: A comparative study. Cranio 2001; 19(1): 33-41.
14
Fabian FM, Mumghamba EG. Risk factors for signs and symptoms of TMD in a rural adult southeast Tanzanian population. Cranio 2008; 26(1): 44-9.
15
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; 24(3): 270-8.
16
Magalhães BG, de-Sousa ST, de Mello VV, et al. Risk factors for temporomandibular disorder: Binary logistic regression analysis. Med Oral Patol Oral Cir Bucal 2014; 19(3): e232-6.
17
Schiffman EL, Fricton JR, Haley DP, Shapiro BL. The prevalence and treatment needs of subjects with temporomandibular disorders. J Am Dent Assoc 1990; 120(3): 295-303.
18
Carlsson GE. Epidemiology and treatment need for temporomandibular disorders. J Orofac Pain 1999; 13(4): 232-7.
19
Halder SL, McBeth J, Silman AJ, Thompson DG, Macfarlane GJ. Psychosocial risk factors for the onset of abdominal pain. Results from a large prospective population-based study. Int J Epidemiol 2002; 31(6): 1219-25.
20
Berg S. Aging, behavior and terminal decline.Handbook of the psychology of aging 4th ed. 1996.
21
Johansson A, Unell L, Carlsson G, Söderfeldt B, Halling A, Widar F. Associations between social and general health factors and symptoms related to temporomandibular disorders and bruxism in a population of 50-year-old subjects. Acta Odontol Scand 2004; 62(4): 231-7.
22
Lobbezoo F, Ahlberg J, Glaros AG, et al. Bruxism defined and graded: An international consensus. J Oral Rehabil 2013; 40(1): 2-4.
23
Alvarez-Arenal A, Junquera LM, Fernandez JP, Gonzalez I, Olay S. Effect of occlusal splint and transcutaneous electric nerve stimulation on the signs and symptoms of temporomandibular disorders in patients with bruxism. J Oral Rehabil 2002; 29(9): 858-63.
24
Wright EF. Manual of TemSciffmanporomandibular Disorders 2005.
25
Molin C. From bite to mind: TMD--a personal and literature review. Int J Prosthodont 1999; 12(3): 279-88.
26
Keefe FJ, Rumble ME, Scipio CD, Giordano LA, Perri LM. Psychological aspects of persistent pain: Current state of the science. J Pain 2004; 5(4): 195-211.
27
Sonnesen L, Svensson P. Temporomandibular disorders and psychological status in adult patients with a deep bite. Eur J Orthod 2008; 30(6): 621-9.
28
Cascos-Romero J, Vázquez-Delgado E, Vázquez-Rodríguez E, Gay-Escoda C. The use of tricyclic antidepressants in the treatment of temporomandibular joint disorders: Systematic review of the literature of the last 20 years. Med Oral Patol Oral Cir Bucal 2009; 14(1): E3-7.
29
Moulton RE. Emotional factors in non-organic temporomandibular joint pain. Dent Clin North Am 1966; 609-20.
30
Marbach JJ, Raphael KG, Dohrenwend BP, Lennon MC. The validity of tooth grinding measures: Etiology of pain dysfunction syndrome revisited. J Am Dent Assoc 1990; 120(3): 327-33.
31
Abraham J, Pierce C, Rinchuse D, Zullo T. Assessment of buccal separators in the relief of bruxist activity associated with myofascial pain-dysfunction. Angle Orthod 1992; 62(3): 177-84.
32
Yustin D, Neff P, Rieger MR, Hurst T. Characterization of 86 bruxing patients with long-term study of their management with occlusal devices and other forms of therapy. J Orofac Pain 1993; 7(1): 54-60.
33
Bader GG, Kampe T, Tagdae T, Karlsson S, Blomqvist M. Descriptive physiological data on a sleep bruxism population. Sleep 1997; 20(11): 982-90.
34
Kieser JA, Groeneveld HT. Relationship between juvenile bruxing and craniomandibular dysfunction. J Oral Rehabil 1998; 25(9): 662-5.
35
Turner JA, Dworkin SF, Mancl L, Huggins KH, Truelove EL. The roles of beliefs, catastrophizing, and coping in the functioning of patients with temporomandibular disorders. Pain 2001; 92(1-2): 41-51.
36
Schwartz RA, Greene CS, Laskin DM. Personality characteristics of patients with myofascial pain-dysfunction (MPD) syndrome unresponsive to conventional therapy. J Dent Res 1979; 58(5): 1435-9.
37
De Jongh A, van der Burg J, van Overmeir M, Aartman I, van Zuuren FJ. Trauma-related sequelae in individuals with a high level of dental anxiety. Does this interfere with treatment outcome? Behav Res Ther 2002; 40(9): 1017-29.
38
Vaiva G, Ducrocq F, Jezequel K, et al. Immediate treatment with propranolol decreases posttraumatic stress disorder two months after trauma. Biol Psychiatry 2003; 54(9): 947-9. [published correction appears in Biol Psychiatry. 2003 Dec 15;54(12):1471].
39
Pitman RK, Delahanty DL. Conceptually driven pharmacologic approaches to acute trauma. CNS Spectr 2005; 10(2): 99-106.