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Journal ArticleDOI

Psychological Factors Associated With Development of TMD: The OPPERA Prospective Cohort Study

TL;DR: Evidence is provided that measures of psychological functioning can predict first onset of TMD, and several premorbid psychological variables predict first-onset TMD in the OPPERA study, a large prospective cohort study designed to discover causal determinants of T MD pain.
About: This article is published in The Journal of Pain.The article was published on 2013-12-01 and is currently open access. It has received 312 citations till now. The article focuses on the topics: Chronic pain.

Summary (2 min read)

Introduction

  • Author manuscript; available in PMC 2014 December 01.
  • The authors recently reported psychological findings from the OPPERA baseline case-control study, in which a cohort of participants meeting diagnostic criteria for chronic TMD were compared to a control cohort comprised of individuals who did not have TMD.30,78 Chronic TMD cases reported higher levels of psychological symptoms, affective distress, somatic symptoms, and pain catastrophizing compared to TMD-free controls.
  • Through self-selection, slightly more than one-third of participants (ranged from 36.2% to 39.5% depending on the questionnaire) completed the instruments via paper and just under two-thirds completed them electronically, and mode of J Pain.
  • This questionnaire assesses both positive and negative affective dimensions.

The Lifetime Stressor List/PTSD Checklist-Civilian Version (LSL/PCL-C)—The

  • LSL presents a checklist of 15 different traumatic events, and participants indicate which (if any) of these events they have experienced.
  • Author manuscript; available in PMC 2014 December 01.
  • This measure has been reported to have adequate internal consistency, ranging from alpha of 0.73 to 0.83 in previous studies47 and 0.81 in their sample.
  • Additional details regarding follow-up rates are provided in Bair, et al.5 Statistical Analysis A multi-stage analytic approach was developed to identify psychological characteristics that predicted TMD onset and to determine which psychological variables interacted with demographic factors and with other psychological variables in predicting risk for TMD onset.
  • 1,35 Thus, a random forest model was used to address these shortcomings.

Measures of Global Psychological and Somatic Function, Stress and Mood

  • (see Table 1)—Among the psychological characteristics reported in Table 1, the highest hazard ratio (HR) for predicting TMD onset emerged for the PILL (imputed HR=1.55), a measure of somatic symptoms.
  • The effect was statistically significant, as demonstrated by the associated 95% confidence interval (1.33 to 1.66) that excluded the null of one.
  • Also, greater scores on all SCL90R subscales were associated with increased incidence of TMD, with hazard ratios ranging from 1.22 (for the Phobia and Paranoid scales) to 1.44 for the Somatization scale.
  • Both trait and state anxiety were associated with increased incidence of TMD, with hazard ratios of 1.4 and 1.22, respectively.
  • Author manuscript; available in PMC 2014 December 01.

Measures of Active and Passive Coping and Reactivity (see Table 1)—None of

  • The subscales of the Pain Catastrophizing Scale (Rumination, Magnification, Helplessness) predicted TMD onset to a statistically significant degree, although the Helplessness scale was weakly significant when using imputed data (HR=1.12).
  • Likewise, no subscales from the Coping Strategies Questionnaire were statistically significant predictors of TMD incidence.
  • As in their original PCA 30, a four-component solution emerged based on the scree plot and parallel analysis .
  • The loadings for the PCA model are shown in Table 2.
  • These four components were used in further univariate and multivariable analyses presented below.

Univariate Analyses of PCA Components as Predictors of First-Onset TMD—

  • In univariate analyses of single PCA scores, high levels of Global Psychological and Somatic Symptoms (imputed HR=1.37) and Stress and Negative Affectivity (imputed HR=1.31) predicted increased TMD incidence in both the unimputed and imputed analyses while Passive Pain Coping was a weaker, though statistically significant, predictor of TMD incidence (imputed HR=1.16, see Supplementary e-Table 1 for detailed information).
  • Table 3 presents the outcomes of analyses examining PCA components as predictors of TMD onset, stratified separately by age, gender, and race/ethnicity.
  • In general, PCA components did not interact with demographic factors in predicting TMD onset, such that hazard ratios were similar across age groups, gender and race/ethnicity.
  • Global Psychological and Somatic Symptoms was the exception, showing a modest interaction with age group (p=0.03), such that this component was a stronger predictor of TMD incidence in the two younger age groups compared to the 35–44 year old group.

Multivariable Analyses of PCA Components as Predictors of First-Onset TMD

  • —In fully-adjusted models (i.e., including study site and demographic factors) that examined main effects of multiple PCA components predicting TMD incidence after controlling for the other components, Global Psychological and Somatic Symptoms remained the only strong predictor (imputed HR=1.33 , Table 4).
  • The findings indicated that Global Psychological and Somatic Symptoms interacted with each of the other components in predicting TMD onset (all p’s < 0.01).
  • Author manuscript; available in PMC 2014 December 01.
  • Sullivan MJ, Bishop S, Pivik J. The Pain Catastrophizing Scale: development and validation.

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Citations
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Journal ArticleDOI
TL;DR: The newly recommended evidence-based new DC/TMD protocol is appropriate for use in both clinical and research settings and includes both a valid screener for detecting any pain-related TMD as well as valid diagnostic criteria for differentiating the most common pain- related TMD.
Abstract: Temporomandibular disorders (TMD) are a significant public health problem affecting approximately 5% to 12% of the population.1 TMD is the second most common musculoskeletal condition (after chronic low back pain) resulting in pain and disability.1 Pain-related TMD can impact the individual's daily activities, psychosocial functioning, and quality of life. Overall, the annual TMD management cost in the USA, not including imaging, has doubled in the last decade to $4 billion.1 Patients often seek consultation with dentists for their TMD, especially for pain-related TMD. Diagnostic criteria for TMD with simple, clear, reliable, and valid operational definitions for the history, examination, and imaging procedures are needed to render physical diagnoses in both clinical and research settings. In addition, biobehavioral assessment of pain-related behavior and psychosocial functioning—an essential part of the diagnostic process—is required and provides the minimal information whereby one can determine whether the patient's pain disorder, especially when chronic, warrants further multidisciplinary assessment. Taken together, a new dual-axis Diagnostic Criteria for TMD (DC/TMD) will provide evidence-based criteria for the clinician to use when assessing patients, and will facilitate communication regarding consultations, referrals, and prognosis.2 The research community benefits from the ability to use well-defined and clinically relevant characteristics associated with the phenotype in order to facilitate more generalizable research. When clinicians and researchers use the same criteria, taxonomy, and nomenclature, then clinical questions and experience can be more easily transferred into relevant research questions, and research findings are more accessible to clinicians to better diagnose and manage their patients. The Research Diagnostic Criteria for Temporomandibular Disorders (RDC/TMD) have been the most widely employed diagnostic protocol for TMD research since its publication in 1992.3 This classification system was based on the biopsychosocial model of pain4 that included an Axis I physical assessment, using reliable and well-operationalized diagnostic criteria, and an Axis II assessment of psychosocial status and pain-related disability. The intent was to simultaneously provide a physical diagnosis and identify other relevant characteristics of the patient that could influence the expression and thus management of their TMD. Indeed, the longer the pain persists, the greater the potential for emergence and amplification of cognitive, psychosocial, and behavioral risk factors, with resultant enhanced pain sensitivity, greater likelihood of additional pain persistence, and reduced probability of success from standard treatments.5 The RDC/TMD (1992) was intended to be only a first step toward improved TMD classification, and the authors stated the need for future investigation of the accuracy of the Axis I diagnostic algorithms in terms of reliability and criterion validity—the latter involving the use of credible reference standard diagnoses. Also recommended was further assessment of the clinical utility of the Axis II instruments. The original RDC/TMD Axis I physical diagnoses have content validity based on the critical review by experts of the published diagnostic approach in use at that time and were tested using population-based epidemiologic data.6 Subsequently, a multicenter study showed that, for the most common TMD, the original RDC/TMD diagnoses exhibited sufficient reliability for clinical use.7 While the validity of the individual RDC/TMD diagnoses has been extensively investigated, assessment of the criterion validity for the complete spectrum of RDC/TMD diagnoses had been absent until recently.8 For the original RDC/TMD Axis II instruments, good evidence for their reliability and validity for measuring psychosocial status and pain-related disability already existed when the classification system was published.9–13 Subsequently, a variety of studies have demonstrated the significance and utility of the original RDC/TMD biobehavioral measures in such areas as predicting outcomes of clinical trials, escalation from acute to chronic pain, and experimental laboratory settings.14–20 Other studies have shown that the original RDC/TMD biobehavioral measures are incomplete in terms of prediction of disease course.21–23 The overall utility of the biobehavioral measures in routine clinical settings has, however, yet to be demonstrated, in part because most studies have to date focused on Axis I diagnoses rather than Axis II biobehavioral factors.24 The aims of this article are to present the evidence-based new Axis I and Axis II DC/TMD to be used in both clinical and research settings, as well as present the processes related to their development.

2,283 citations

01 Jan 2014
TL;DR: In this article, the authors proposed a new RDC/TMD Axis I and Axis II diagnostic algorithms for temporomandibular joint (TMJ) intra-articular disorder.
Abstract: Aims: The original Research Diagnostic Criteria for Temporomandibular Disorders (RDC/TMD) Axis I diagnostic algorithms have been demonstrated to be reliable. However, the Validation Project determined that the RDC/TMD Axis I validity was below the target sensitivity of ≥ 0.70 and specificity of ≥ 0.95. Consequently, these empirical results supported the development of revised RDC/TMD Axis I diagnostic algorithms that were subsequently demonstrated to be valid for the most common pain-related TMD and for one temporomandibular joint (TMJ) intra-articular disorder. The original RDC/TMD Axis II instruments were shown to be both reliable and valid. Working from these findings and revisions, two international consensus workshops were convened, from which recommendations were obtained for the finalization of new Axis I diagnostic algorithms and new Axis II instruments. Methods: Through a series of workshops and symposia, a panel of clinical and basic science pain experts modified the revised RDC/TMD Axis I algorithms by using comprehensive searches of published TMD diagnostic literature followed by review and consensus via a formal structured process. The panel’s recommendations for further revision of the Axis I diagnostic algorithms were assessed for validity by using the Validation Project’s data set, and for reliability by using newly collected data from the ongoing TMJ Impact Project—the follow-up study to the Validation Project. New Axis II instruments were identified through a comprehensive search of the literature providing valid instruments that, relative to the RDC/TMD, are shorter in length, are available in the public domain, and currently are being used in medical settings. Results: The newly recommended Diagnostic Criteria for TMD (DC/TMD) Axis I protocol includes both a valid screener for detecting any pain-related TMD as well as valid diagnostic criteria for differentiating the most common pain-related TMD (sensitivity ≥ 0.86, specificity ≥ 0.98) and for one intra-articular disorder (sensitivity of 0.80 and specificity of 0.97). Diagnostic criteria for other common intra-articular disorders lack adequate validity for clinical diagnoses but can be used for screening purposes. Inter-examiner reliability for the clinical assessment associated with the validated DC/TMD criteria for pain-related TMD is excellent (kappa ≥ 0.85). Finally, a comprehensive classification system that includes both the common and less common TMD is also presented. The Axis II protocol retains selected original RDC/TMD screening instruments augmented with new instruments to assess jaw function as well as behavioral and additional psychosocial factors. The Axis II protocol is divided into screening and comprehensive selfreport instrument sets. The screening instruments' 41 questions assess pain intensity, pain-related disability, psychological distress, jaw functional limitations, and parafunctional behaviors, and a pain drawing is used to assess locations of pain. The comprehensive instruments, composed of 81 questions, assess in further detail jaw functional limitations and psychological distress as well as additional constructs of anxiety and presence of comorbid pain conditions. Conclusion: The recommended evidence-based new DC/TMD protocol is appropriate for use in both clinical and research settings. More comprehensive instruments augment short and simple screening instruments for Axis I and Axis II. These validated instruments allow for identification of patients with a range of simple to complex TMD presentations. J Oral Facial Pain Headache 2014;28:6–27. doi: 10.11607/jop.1151

1,356 citations

Journal ArticleDOI
TL;DR: Evidence that psychosocial variables play key roles in conferring risk for the development of pain, in shaping long-term pain-related adjustment, and in modulating pain treatment outcomes is described.

504 citations


Cites background from "Psychological Factors Associated Wi..."

  • ...Although psychological symptomatology is often interpreted as a consequence of chronic pain, prospective studies suggest that premorbid psychological dysfunction represents a risk factor for the future development of numerous chronic pain conditions.(54,66,139) Moreover, similar psychosocial constructs and processes predict the likelihood of transition from acute to chronic musculoskeletal pain (ie, higher distress levels are prospectively related to an increased probability of transitioning to chronic pain)....

    [...]

  • ...awareness assess important psychosocial characteristics as well, particularly in the setting of chronic widespread pain conditions such as FM or its comorbid conditions.(54,66,67) These measures have rarely been studied as targets of change in interventional studies, but a good deal of evidence exists for their role as key risk factors predicting the development and course (including the transition from acute to chronic pain) of numerous pain conditions such as temporomandibular joint disorders,(66) and neuropathic pain conditions like postherpetic neuralgia(57,110) or burning mouth syndrome....

    [...]

Journal ArticleDOI
TL;DR: In 2006, the OPPERA project (Orofacial pain: Prospective Evaluation and Risk Assessment) set out to identify risk factors for development of painful temporomandibular disorder (TMD) as discussed by the authors.
Abstract: In 2006, the OPPERA project (Orofacial Pain: Prospective Evaluation and Risk Assessment) set out to identify risk factors for development of painful temporomandibular disorder (TMD). A decade later, this review summarizes its key findings. At 4 US study sites, OPPERA recruited and examined 3,258 community-based TMD-free adults assessing genetic and phenotypic measures of biological, psychosocial, clinical, and health status characteristics. During follow-up, 4% of participants per annum developed clinically verified TMD, although that was a "symptom iceberg" when compared with the 19% annual rate of facial pain symptoms. The most influential predictors of clinical TMD were simple checklists of comorbid health conditions and nonpainful orofacial symptoms. Self-reports of jaw parafunction were markedly stronger predictors than corresponding examiner assessments. The strongest psychosocial predictor was frequency of somatic symptoms, although not somatic reactivity. Pressure pain thresholds measured at cranial sites only weakly predicted incident TMD yet were strongly associated with chronic TMD, cross-sectionally, in OPPERA's separate case-control study. The puzzle was resolved in OPPERA's nested case-control study where repeated measures of pressure pain thresholds revealed fluctuation that coincided with TMD's onset, persistence, and recovery but did not predict its incidence. The nested case-control study likewise furnished novel evidence that deteriorating sleep quality predicted TMD incidence. Three hundred genes were investigated, implicating 6 single-nucleotide polymorphisms (SNPs) as risk factors for chronic TMD, while another 6 SNPs were associated with intermediate phenotypes for TMD. One study identified a serotonergic pathway in which multiple SNPs influenced risk of chronic TMD. Two other studies investigating gene-environment interactions found that effects of stress on pain were modified by variation in the gene encoding catechol O-methyltransferase. Lessons learned from OPPERA have verified some implicated risk factors for TMD and refuted others, redirecting our thinking. Now it is time to apply those lessons to studies investigating treatment and prevention of TMD.

347 citations


Cites background from "Psychological Factors Associated Wi..."

  • ...Much smaller contributions were made from measures of psychological stress, anxiety, obsessive-compulsive feelings, and pain-coping strategies (Fillingim et al. 2013)....

    [...]

  • ...Frequency of somatic symptoms was the strongest psychosocial predictor of TMD incidence (Fillingim et al. 2013)....

    [...]

Journal ArticleDOI
01 Apr 2017-Pain
TL;DR: The individual and combined influences of these biological and psychosocial variables results in a unique mosaic of factors that contributes pain in each individual, which is critically important in order to provide optimal pain treatment.
Abstract: The experience of pain is characterized by tremendous inter-individual variability. Multiple biological and psychosocial variables contribute to these individual differences in pain, including demographic variables, genetic factors, and psychosocial processes. For example, sex, age and ethnic group differences in the prevalence of chronic pain conditions have been widely reported. Moreover, these demographic factors have been associated with responses to experimentally-induced pain. Similarly, both genetic and psychosocial factors contribute to clinical and experimental pain responses. Importantly, these different biopsychosocial influences interact with each other in complex ways to sculpt the experience of pain. Some genetic associations with pain have been found to vary across sex and ethnic group. Moreover, genetic factors also interact with psychosocial factors, including stress and pain catastrophizing, to influence pain. The individual and combined influences of these biological and psychosocial variables results in a unique mosaic of factors that contributes pain in each individual. Understanding these mosaics is critically important in order to provide optimal pain treatment, and future research to further elucidate the nature of these biopsychosocial interactions is needed in order to provide more informed and personalized pain care.

292 citations


Cites background from "Psychological Factors Associated Wi..."

  • ...We found that poorer psychological functioning across 2 broad domains, global psychological symptoms (eg, somatic symptoms, general psychological distress) and stress and negative affectivity (eg, perceived stress, trait negative affect), predicted significantly increased risk for future development of TMD.(29) Importantly, psychological processes can interact with other individual difference variables, including demographic and genetic factors, to influence pain responses....

    [...]

  • ...As noted above, perceived stress at the time of enrollment was a premorbid risk factor for development of new onset TMD....

    [...]

  • ...We found that poorer psychological functioning across 2 broad domains, global psychological symptoms (eg, somatic symptoms, general psychological distress) and stress and negative affectivity (eg, perceived stress, trait negative affect), predicted significantly increased risk for future development of TMD.29 Importantly, psychological processes can interact with other individual difference variables, including demographic and genetic factors, to influence pain responses....

    [...]

  • ...COMT has been associated with pain-related mu-opioid receptor binding in the brain.87 In addition, Diatchenko et al.19 identified 3 COMT haplotypes that were related to global pain sensitivity and to risk of developing TMD....

    [...]

References
More filters
Journal ArticleDOI
01 Oct 2001
TL;DR: Internal estimates monitor error, strength, and correlation and these are used to show the response to increasing the number of features used in the forest, and are also applicable to regression.
Abstract: Random forests are a combination of tree predictors such that each tree depends on the values of a random vector sampled independently and with the same distribution for all trees in the forest. The generalization error for forests converges a.s. to a limit as the number of trees in the forest becomes large. The generalization error of a forest of tree classifiers depends on the strength of the individual trees in the forest and the correlation between them. Using a random selection of features to split each node yields error rates that compare favorably to Adaboost (Y. Freund & R. Schapire, Machine Learning: Proceedings of the Thirteenth International conference, aaa, 148–156), but are more robust with respect to noise. Internal estimates monitor error, strength, and correlation and these are used to show the response to increasing the number of features used in the splitting. Internal estimates are also used to measure variable importance. These ideas are also applicable to regression.

79,257 citations

01 Jan 1970
TL;DR: The STAI as mentioned in this paper is an indicator of two types of anxiety, the state and trait anxiety, and measure the severity of the overall anxiety level, which is appropriate for those who have at least a sixth grade reading level.
Abstract: The STAI serves as an indicator of two types of anxiety, the state and trait anxiety, and measure the severity of the overall anxiety level.The STAI, which is appropriate for those who have at least a sixth grade reading level, contains four-point Likert items. The instrument is divided into two sections, each having twenty questions. Approximately 15 minutes are required for adults to complete the both STAI. The number on the scale is positively correlated to the anxiety related to in the question.

24,997 citations

Journal ArticleDOI
TL;DR: The Perceived Stress Scale showed adequate reliability and, as predicted, was correlated with life-event scores, depressive and physical symptomatology, utilization of health services, social anxiety, and smoking-reduction maintenance and was a better predictor of the outcome in question than were life- event scores.
Abstract: This paper presents evidence from three samples, two of college students and one of participants in a community smoking-cessation program, for the reliability and validity of a 14-item instrument, the Perceived Stress Scale (PSS), designed to measure the degree to which situations in one's life are appraised as stressful. The PSS showed adequate reliability and, as predicted, was correlated with life-event scores, depressive and physical symptomatology, utilization of health services, social anxiety, and smoking-reduction maintenance. In all comparisons, the PSS was a better predictor of the outcome in question than were life-event scores. When compared to a depressive symptomatology scale, the PSS was found to measure a different and independently predictive construct. Additional data indicate adequate reliability and validity of a four-item version of the PSS for telephone interviews. The PSS is suggested for examining the role of nonspecific appraised stress in the etiology of disease and behavioral disorders and as an outcome measure of experienced levels of stress.

23,500 citations

Book
28 Jul 2013
TL;DR: In this paper, the authors describe the important ideas in these areas in a common conceptual framework, and the emphasis is on concepts rather than mathematics, with a liberal use of color graphics.
Abstract: During the past decade there has been an explosion in computation and information technology. With it have come vast amounts of data in a variety of fields such as medicine, biology, finance, and marketing. The challenge of understanding these data has led to the development of new tools in the field of statistics, and spawned new areas such as data mining, machine learning, and bioinformatics. Many of these tools have common underpinnings but are often expressed with different terminology. This book describes the important ideas in these areas in a common conceptual framework. While the approach is statistical, the emphasis is on concepts rather than mathematics. Many examples are given, with a liberal use of color graphics. It is a valuable resource for statisticians and anyone interested in data mining in science or industry. The book's coverage is broad, from supervised learning (prediction) to unsupervised learning. The many topics include neural networks, support vector machines, classification trees and boosting---the first comprehensive treatment of this topic in any book. This major new edition features many topics not covered in the original, including graphical models, random forests, ensemble methods, least angle regression and path algorithms for the lasso, non-negative matrix factorization, and spectral clustering. There is also a chapter on methods for ``wide'' data (p bigger than n), including multiple testing and false discovery rates. Trevor Hastie, Robert Tibshirani, and Jerome Friedman are professors of statistics at Stanford University. They are prominent researchers in this area: Hastie and Tibshirani developed generalized additive models and wrote a popular book of that title. Hastie co-developed much of the statistical modeling software and environment in R/S-PLUS and invented principal curves and surfaces. Tibshirani proposed the lasso and is co-author of the very successful An Introduction to the Bootstrap. Friedman is the co-inventor of many data-mining tools including CART, MARS, projection pursuit and gradient boosting.

19,261 citations

Journal ArticleDOI
TL;DR: In this paper, the Pain Catastrophizing Scale (PCS) was administered to 425 undergraduates and a three component solution comprising (a) rumination, (b) magnification, and (c) helplessness.
Abstract: In Study 1, the Pain Catastrophizing Scale (PCS) was administered to 425 undergraduates. Analyses yielded a three component solution comprising (a) rumination, (b) magnification, and (c) helplessness. In Study 2, 30 undergraduate participants were classified as catastrophizers (n = 15) or noncatastrophizers (n = 15) on the basis of their PCS scores and participated in an cold pressor procedure. Catastrophizers reported significantly more negative pain-related thoughts, greater emotional distress, and greater pain intensity than noncatastrophizers. Study 3 examined the relation between PCS scores, negative pain-related thoughts, and distress in 28 individuals undergoing an aversive electrodiagnostic medical procedure. Catastrophizers reported more negative pain-related thoughts, more emotional distress, and more pain than noncatastrophizers. Study 4 examined the relation between the PCS and measures of depression, trait anxiety, negative affectivity, and fear of pain. Analyses revealed moderate correlations among these measures, but only the PCS contributed significant unique variance t o the prediction of pain intensity.

6,173 citations

Related Papers (5)
Frequently Asked Questions (12)
Q1. What are the contributions in "Psychological factors associated with development of tmd: the oppera prospective cohort study" ?

For this study, 3,263 TMD-free participants completed a battery of psychological instruments assessing general psychological adjustment and personality, affective distress, psychosocial stress, somatic symptoms, and pain coping and catastrophizing. This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to their customers the authors are providing this early version of the manuscript. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain. 

The second stage of the analysis involved a series of multivariable Cox regression models in which the entered psychological variables were derived from a principal component analysis (PCA), which was performed in order to reduce the number of psychological variables by identifying putative latent constructs. 

in univariate analyses as well as both multivariable approaches the somatic symptom construct represented the strongest predictor of TMD onset, suggesting convergence of findings regarding somatic symptoms across analytic methods. 

The Stress and Negative Affectivity component was a weakly significant predictor in the unimputed analysis, but did not significantly predict TMD onset in the analysis using imputed data (HR=1.12). 

Of the 3,263 participants enrolled into the inception cohort, 2,737 (84%) completed one or more quarterly follow-up questionnaires, with a median of 10 follow-up questionnaires over a median 2.8 follow-up year period. 

While multiple psychological measures predicted TMD onset in univariate analyses, results of multivariable models provide strong evidence that reported somatic symptoms represents the strongest predictor of incident TMD in this analysis. 

When the average eigenvalue from these randomly generated data sets is larger than the corresponding eigenvalue of the original data, then the principal component associated with that eigenvalue is likely to be random noise (see Supplementary e-Figure 1). 

This suggests that Stress and Negative Affectivity does not additively contribute to TMD risk over and above Global Psychological and Somatic Symptoms, rather in the absence of global symptomatology, stress/negative affect emerges as a potentially important risk factor. 

For the CSQ Ignoring Pain Sensations scale, TMD incidence was greatest at a score of 0 and decreased in linear fashion until a score of approximately two, beyond which incidence increased slightly. 

Parallel analysis estimates the number of components to include in a PCA model by generating random data sets with the same numbers of observations and predictor variables as the original data. 

In univariate analyses, Stress and Negative Affectivity also predicted incident TMD; however, this association became weak or non-significant in multivariable analyses that adjusted for the other principal components. 

the subscales of the Pain Catastrophizing Scale (Rumination, Magnification, Helplessness) predicted TMD onset to a statistically significant degree, although the Helplessness scale was weakly significant when using imputed data (HR=1.12).