The relationship between spinal pain and temporomandibular joint disorders in Korea: a nationwide propensity score-matched study
BMC Musculoskeletal Disorders volume 20, Article number: 631 (2019)
Patients with temporomandibular joint disorder (TMD) often complain of pain in other areas. Several studies have been conducted on spinal pain in TMD patients, but have contained only limited information. Therefore, this study analyzed the relationship between TMD and spinal pain in greater detail by using nationwide data.
A total of 12,375 TMD patients from the Korean National Health Insurance Review and Assessment database were analyzed. Controls were selected using propensity score-matching. The McNemar test, chi-square test, and paired t-test were used to compare the prevalence and severity of spinal pain between cases and matched controls. Logistic regression and linear regression models were used to analyze factors affecting the prevalence and severity of spinal pain in patients with TMD.
The annual period prevalence of TMD was 1.1%. The prevalence was higher in younger individuals than in individuals of other ages and was higher in women than in men. The medical expenditure for TMD per person was $86. Among TMD patients, 2.5% underwent surgical procedures and 0.3% were hospitalized. The prevalence of spinal pain in patients with TMD was 48%, whereas that in the control group was 34%. Increased severity of TMD was associated with an increased probability of spinal pain. The medical expenditure, mean number of visits, and lengths of treatment for spinal pain were greater for patients with TMD than for controls ($136 vs. $81, 4.8 days vs. 2.7 days, 5.5 days vs. 3.3 days). Higher TMD grade was associated with greater differences in average medical expenditure, number of visits, and lengths of treatment for spinal pain between cases and controls. Additionally, for women, living in a rural area and having an older age and more severe TMD were associated with a greater probability of spinal pain and higher medical expenditure related to spinal pain.
A strong association was observed between the presence of TMD and the presence of spinal pain. The association became stronger as the severity of TMD increased, indicating a positive correlation between the severity of TMD and spinal pain.
Temporomandibular joint disorder (TMD) is a disease in which structural and functional disorders occur in the temporomandibular joints and related structures . Major clinical symptoms include pain, a clicking sound, and limited range of motion in the jaw joint . According to a cohort study of TMD conducted in the 2019 Orofacial Pain: Prospective Evaluation and Risk Assessment (OPPERA) project, approximately 5–12% of the adult US population experiences painful TMD . According to the 2018 Korea National Health Insurance Service analysis of health insurance claim data, the number of patients with TMD increased by more than 62.8% over 9 years, from 244,708 in 2010 to 398,401 in 2018. In the same period, the medical costs increased by 2.6-fold .
TMD is often accompanied by headaches, back pain, joint pain, and abdominal pain [5, 6]. Plesh et al.  reported that only 0.77% of patients with TMD did not complain of other associated pain. The management of associated disease is a very important factor in TMD management, because associated disease is related to a poor prognosis . One explanation of the accompanying pain, especially spinal pain in TMD patients, is whole-body imbalance. Dysfunction in TMD can affect factors such as postural asymmetry, center of foot pressure, and spine curvature, which could induce spinal pain [9,10,11,12].
Spinal pain is a common and socially important musculoskeletal condition. In the United States, the lifetime prevalence of low back pain is 65 to 80% . In addition, spinal pain is associated with productivity loss, increased medical expenditure, and long-term opioid use [14,15,16].
Several studies have investigated the relationship between TMD and spinal pain. Wiesinger reported that the incidence of spinal pain increased with the frequency and intensity of temporomandibular joint pain . In a US study, 54% of TMD patients reported neck pain and 64% reported low back pain . Other studies have shown that chronic spinal pain is associated with TMD [18, 19]. Storm  showed a significant association between TMD treatment with reduction of cervical spine pain and mobility improvement.
However, the evidence of a correlation between TMD and spinal pain has some limitations: first, a number of these previous studies were performed without a control group [7, 19]; second, when control groups were used, the sample sizes were small, homogeneity between cases and controls was not confirmed, or the analysis was simple, such as a frequency analysis suggesting that TMD was related to spinal pain [17, 18, 21, 22]. Thus, in this study, we used nationwide data from the Health Insurance Review and Assessment (HIRA) database, a representative administrative database of Korea, and propensity score matching (PSM) to overcome limitations of previous studies.
Clarifying the correlation between TMD and spinal pain is important, as secondary prevention can be incorporated into the management and treatment guidelines of TMD if the possibility of spinal pain is known . Therefore, this study aimed to generate a more objective rationale to support the hypothesis that TMD induces spinal pain. The purpose of this study was to identify the prevalence and treatment status of TMD, to analyze the relationship between TMD and spinal pain, and to identify factors affecting spinal pain in patients with TMD. The purpose of this study was to identify the prevalence and treatment status of TMD, to analyze the relationship between TMD and spinal pain, and to identify factors affecting spinal pain in patients with TMD.
The original data were obtained from the 2016 Korean Health Insurance Review and Assessment Service (HIRA) National Patient Sample. Korea uses a single health insurance system, such that 98% of the population is enrolled in National Health Insurance (NHI) . Claims data in the HIRA are recorded when a claim is made to the corporation for reimbursement of medical services provided by a health care provider. The National Patient Sample data are inclusive of all claims data and randomly stratified according to sex and age, representing the entire Korean population. The National Patient Sample thus comprises cross-sectional data, released yearly, with a sample number of approximately 1.4 million, representing 3% of South Korea’s total population .
Study design and population
This study was a cross-sectional, retrospective study of patients who used medical services at least once in Korea, from January 2016 to December 2016, who were diagnosed with TMD. There have been few studies using International Statistical Classification of Disease (ICD) codes in administrative data. Here, a TMD case was operationally defined as a patient who was diagnosed according to the ICD-10 code K07.6 (temporomandibular joint disorders) or S03.4 (sprain and strain of the jaw), based on internal discussions among research team members.
TMD severity was defined based on the amount of medical services used in relation to the jaw joint. As previous studies have reported that 6 treatments are generally effective [25, 26], we classified the use of fewer than 6 outpatient services as grade 1, 6 or more services but fewer than 12 services as grade 2, and 12 or more outpatient services or inpatient service as grade 3, in terms of TMD severity.
Propensity score matching
In this study, the propensity score-matching method was used to select the control group . The propensity score was calculated according to sex, age, insurance type, region, and Charlson Comorbidity Index (CCI); then, 1:1 matching was performed. Age was classified into 10-year age groups. The regions were classified into Seoul, capital area, metropolitan area, and other areas . Types of insurance were classified as NHI and others (Medicaid); in Korea, Medicaid is a type of health insurance funded by the federal and local governments that provides health coverage for people with low incomes . CCI was initially designed to predict mortality and has been widely used for researchers to measure the burden of disease [30, 31]. CCI was calculated using ICD-10 and the presence of comorbidity was based on whether the code was diagnosed during a 1-year period . Considering the CCI distribution and prior research [33, 34], CCI was classified into 4 grades (0, 1–2, 3–4, and 5 and more). There were 12,375 cases and 1,154,129 controls. After all cases were matched, the final analysis included 12,375 cases and 12,375 controls (Fig. 1).
Outcomes and other variables
The first outcome was the presence of spinal pain. This was operationally defined as when a patient used medical services due to spinal pain more than once, during a 1-year period. Based on the code applied in previous studies of spinal pain using administrative data [35, 36], and in consultation with 3 specialists in the field of musculoskeletal disease, spinal pain was defined as a diagnosis of ICD-10 M40* (kyphosis and lordosis), M41* (scoliosis), M43* (other deforming dorsopathies), M50* (cervical disc disorders), M51* (other intervertebral disc disorders), M53* (other dorsopathies), M54* (dorsalgia), M99* (biomechanical lesions), S335* (sprain and strain of the lumbar spine), or S134 (sprain and strain of the cervical spine). Spinal pain was also classified into 3 grades and the same criteria were applied as for TMD classification, to ensure consistency [25, 26]. Other variables that indicated the severity of spinal pain included the annual total medical expenses, total numbers of visits, and lengths of treatment due to personal spinal pain, as outcome variables.
The variables related to the use of medical care for patients with TMD were surgery, hospitalization, medical institution type, and medical specialty. Surgery and hospitalization were classified into yes (when TMD surgery and hospitalization were utilized once or more) or no. Medical institution type included general hospital, hospital, and clinic. In Korea, according to the Medical Law, secondary medical institutions with more than 100 beds, 7 or 9 medical specialties, and specialists dedicated to each medical field are called general hospitals. Medical institution type and medical specialty were counted according to the most-used institution type and medical specialty for TMD; thus, counts were not duplicated.
Distributions of categorical sociodemographic variables (sex, age, insurance type, region, CCI, and region) between cases and controls before matching were compared using standardized differences. In this study, because the control group was matched by using a propensity score, the sample were paired. There is no consensus method for comparing variables after propensity score matching, but as the standardized difference is an accepted method according to some previous studies [27, 37] we used it to analyze samples after matching. Standardized difference was also used to analyze samples before matching to compare analysis results between before and after matching groups. The odds ratio for TMD was also calculated to identify risk factors (sex, age, insurance type, region, CCI) for TMD. Distributions of categorical sociodemographic variables between cases and controls after matching were compared using the standardized differences [37, 38]. All categorical variables were summarized as counts and percentages. The prevalence of spinal pain was compared between cases and matched controls for each grade of TMD with the McNemar test because paired categorical samples were used in this study. The difference among TMD grades was also examined using the chi-square test. The prevalence of each grade of spinal pain was compared between cases and matched controls for each grade of TMD with the McNemar–Bowker test, which is used when outcomes are classified into more than 2 categories . Differences among TMD grades and spinal pain grades were also examined using the chi-square test. Medical expenditures, numbers of visits, and lengths of treatment caused by spinal pain were compared between cases and matched controls for each grade of TMD with the paired t-test because paired continuous samples were used in this study. A Kolmogorov–Smirnov test revealed the data were not normally distributed, and thus the differences in medical expenditures, numbers of visits, and lengths of treatment among TMD grades were examined using the Kruskal–Wallis test. For post-hoc analysis, Dunnett’s test was performed because the assumption of equal variance was rejected in Levene’s test .
For the logistic regression and linear regression analyses, 3 models were constructed by classifying the factors that affect medical use according to characteristics based on previous studies [41, 42]. The model used in the analysis is shown in Eq. (1-1 to 3-2 below.
Model 1: sex, age.
Model 2: Model 1 + (insurance type, region, medical institution type).
Model 3: Model 2 + (CCI, TMD grade, surgery, hospitalization).
Y1i:dummy variable with 1 for spinal pain and 0 for without spinal pain in ‘i’th TMD patients.
Y2i: medical expenditure for spinal pain in ‘i’th TMD patients.
X1: sex, X2: age, X3: insurance type, X4: region, X5: medical institution type, X6: CCI, X7: TMD grade, X8: surgery, X10: hospitalization.
Logistic regression analyses were performed for each model to determine the odds ratio of covariates that influence the prevalence of spinal pain in patients with TMD. Linear regression analyses were performed for each model to examine how covariates influence medical expenditure for spinal pain in patients with TMD. Medical expenditure was log-transformed because its distribution was non-normal and shifted to the left . In the logistic regression and linear regression models, sociodemographic variables of the study population and the TMD grade were also included. All analyses were performed with SAS statistical software (version 9.4 for Windows; SAS Institute, Inc., Cary, NC, USA). The significance level was set to 0.05.
Sociodemographic characteristics of the study population
Table 1 shows the sociodemographic characteristics of the study population. In 2016, 12,375 patients used medical services more than once due to TMD, which constituted 1.07% of the total study population over 20 years of age. Women were more likely to be affected than men (OR 1.51). Regarding age, most TMD patients were aged 20–29 years and the incidence tended to decrease with age. In addition, possession of NHI, residence in Seoul, and high CCI were risk factors for TMD. After 1:1 propensity score matching, the distributions of all sociodemographic covariates were similar between the two groups (Table 2). While standardized differences were 0.078 to 0.388 before matching, all of them were 0 after matching.
Prevalence of spinal pain in cases and controls, according to TMD grade
Table 3 shows the prevalence of spinal pain in cases and controls, according to TMD grade. The prevalence of spinal pain was significantly higher in the case group than in the control group for all TMD grades. In addition, when compared by grade, higher TMD grade was associated with an increased prevalence of spinal pain. Changes in prevalence of spinal pain according to TMD grade are shown visually in Additional file 1: Figure S1.
Prevalence of each grade of spinal pain in cases and controls, according to TMD grade
Table 4 shows the prevalence of spinal pain for each grade in the cases and controls, according to TMD grade. The prevalence of spinal pain was higher in cases than in controls for all grades of spinal pain. A higher grade of spinal pain was associated with a greater difference in the prevalence of spinal pain between case and control groups. This suggests that the severity of spinal pain increased with the severity of TMD. There was no trend for the control group in terms of spinal pain level. In all cases, the prevalence of spinal pain was higher in the case group than in the control group. Changes in the prevalence of spinal pain for each level according to TMD grade are shown visually in Additional file 2: Figure S2.
Medical expenditure, number of visits, and length of treatment for spinal pain in cases and controls, according to TMD grade
Table 5 shows the medical expenditures, numbers of visits, and lengths of treatment for spinal pain in cases and controls, according to TMD grade. For all TMD patients, the medical expenditure for spinal pain in the case group was significantly higher than the expenditure in the control group. Increased TMD grade was associated with increased medical expenditure for spinal pain in both cases and controls; moreover, the difference between the two groups in medical expenses for spinal pain increased with increasing TMD grade. The same tendency was observed for the mean numbers of visits and lengths of treatment. ANOVA showed significant differences between controls and cases by TMD grade with respect to all outcomes (medical expenditures, numbers of visits, and numbers of treatments). In post- hoc analysis with the Dunnett test, differences were significant among all grade groups for all outcomes, except for the difference in numbers of treatment between grades 2 and 3 (Additional file 3: Table S1).
Covariates that influence the prevalence of spinal pain in patients with TMD
Covariates that influenced the prevalence of spinal pain in TMD patients are shown in Table 6; the results of Model 1, Model 2, Model 3 are presented. Among the 3 models, Model 3 had the highest explanatory power. According to Model 3, the probability of spinal pain in patients with TMD was higher in women than in men; it was also higher in older individuals, in those without NHI, and in those living in rural areas (rather than in urban areas) (Table 6). In addition, increased CCI (i.e., increased severity), increased TMD grade, and hospitalization were associated with an increased probability of spinal pain.
Medical expenditure for spinal pain in patients with TMD
Analysis of factors influencing medical expenses resulting from spinal pain in patients with TMD are show in Table 7. Among the 3 models, Model 3 had the highest R square value. The results showed that medical expenses related to spinal pain were higher in women than in men, and were higher in patients with older age than in those with younger age. If the type of insurance was not NHI, the medical expenditure was high; moreover, by region, Seoul (capital city) had the lowest medical expenditure, while rural areas had the highest expenditure. Increased CCI and increased TMD grade were associated with increased expenditure related to spinal pain. The expenditure for TMD was high when the patient was hospitalized for TMD, as well as for patients who used mainly medical clinics rather than general hospitals.
The annual period prevalence of TMD in this study was 1.1%, which was relatively low compared to the findings of previous studies (5–40%) [3, 44,45,46]. This is potentially because TMD was defined only when medical service use occurred due to TMD symptoms, which differed from the approach used in previous studies [25, 44,45,46]. Assuming a TMD prevalence of 5–40% [3, 44,45,46] according to studies, 2.8% (1.1/40) to 22% (1.1/5) of TMD patients may use medical services for treatment.
In addition, in the present study, the prevalence of TMD was higher in women and in younger age groups, as in previous studies [6, 45,46,47]. Some studies have suggested that hormones play a role in the onset of TMD [45, 46]. However, further research is needed regarding the high prevalence of TMD in women. In addition to sex and age, health insurance types and areas of residence were risk factors for TMD. The prevalence of TMD was higher in patients with NHI. There is a medical care system in Korea that guarantees medical assistance for low-income groups , and beneficiaries receive assistance without the requirement to enroll in a NHI scheme. Thus, it is implied that patients without NHI may be part of the low-income group. No previous study has investigated the relationship between income and prevalence of TMD, but the results of this study suggest that TMD prevalence is low when income is low. Further study is needed to reveal correlation.
In this study, we found that there was a positive correlation between TMD and spinal pain. Patients with TMD were more likely to have spinal pain than non-TMD patients; moreover, they were more likely to have greater medical expenditure and an increased number of treatments for spinal pain. In addition, a higher degree of TMD was associated with a greater probability of spinal pain; greater severity of spinal pain was associated with increased cost of medical care and increased length of treatment. The medical service use of TMD patients in 2016 Korea (Additional file 4: Table S2) showed that medical expenditure was $1,058,841 per year, which is considerably high. According to this study, although the expenditure due to TMD alone is large, TMD patients with spinal pain have greater expenditure. The high prevalence of spinal pain in patients with TMD may be a result of TMD affecting whole-body posture. Ries and Berzin  found that patients with TMD showed greater postural asymmetry than a control group; they concluded that TMD was associated with cervical pain.
A previous study also reported that TMD can affect overall body function; for example, it can influence the location of the center of foot pressure, body sway, and spine curvature [11, 12]. Additionally, the origin of spinal pain in TMD patients may be related to dysregulation of the autonomic nervous system and dysfunction of the hypothalamic–pituitary–adrenal axis . From this perspective, temporomandibular joint pain is a referred pain [49, 50]. Furthermore, patients with TMD tend to have many accompanying diseases . Although TMD is a musculoskeletal disorder, psychosocial factors such as life satisfaction and job satisfaction, mood or emotion, acute trauma, rheumatic diseases, and poor health habits are involved in TMD [46, 51, 52]. Taken together, it can be inferred that there are many factors influencing the accompanying pain of patients with TMD. However, such factors have been poorly studied, with the exception of the twin studies of Visscher et al. , who concluded that accompanying pain in TMD was more common in women; they also reported that age, education level, and birth state were not related to accompanying pain.
The risk factors for spinal pain in TMD patients analyzed in this study tended to overlap with the risk factors for spinal pain in the general population. Female sex and older age are well-known risk factors for spinal pain [53, 54]. There have been few studies regarding the relationships between region or income and spinal pain; however, some studies have shown that the prevalence of spinal pain is high in rural areas and among individuals at low-income levels [55, 56]. Thus, factors that cause spinal pain in general also comprise risk factors for spinal pain in TMD patients.
This study had the following limitations. First, the data analyzed in this study were cross-sectional data; therefore, the findings of this study do not confirm causality between TMD and spinal pain; notably, they suggest a positive correlation. The findings support the theory that TMD can affect the whole body by deforming body sway or spine curvature [11, 12]. Further studies using cohort data are needed to determine causality.
Second, this study included limited information regarding clinical data because we analyzed the administrative research data. In particular, the degree of TMD severity is not specified in the administrative data; thus, this study attempted to correct those missing data by including the number of medical services used and CCI. In addition, the presence of pain was not specified in the data; thus, diagnosis was used to define spinal pain and select subjects. Although, diagnosis may not accurately reflect spinal pain, the diagnosis in this study was established as close to spinal pain as possible by referring to previous studies [35, 36] and consultations of specialists. Further studies using hospital data to analyze clinical values such as Range Of Motion (ROM) or Numeric Rating Scale (NRS) and analyzing relationship between TMD and other pain like headache or joint pain is needed.
Nonetheless, this study also had the following advantages. First, this study revealed the effects of various factors (i.e., sex, age, type of health insurance, area, CCI, TMD severity, TMD medical service, and type of medical institution) on the prevalence of spinal pain in TMD patients and the medical expenditure related to spinal pain. Second, we have overcome the limitations of previous studies by using large-scale data that can represent Korea and provide a variety of objective parameters, such as medical expenses and treatment details, as well as by using propensity score-matching methodology. The results of this study provide useful information for the management of TMD and treatment of patients with both TMD and spinal pain. In addition, when spine problems do not continue to improve in general spine treatment, TMD could be considered. In practice, this suggests that consultations with several specialists such as a dentist and neurologist are necessary. The availability of a consultation system can help patients receive quality care and reduce the costs associated with TMD. Further studies to quantify the degree of the correlation between TMD and spinal pain, and to confirm causality, are needed.
A strong association was observed between TMD and spinal pain. The association became stronger as severity of TMD increased, indicating a positive correlation between severity of TMD and spinal pain. This information can aid in the management of TMD and treatment of patients with both TMD and spinal pain.
Availability of data and materials
The datasets generated and analyzed in the current study are available in the HIRA-NPS repository. The study utilized HIRA data, which are third-party data and thus not owned by the authors. The HIRA data are available upon direct request, via email or fax, and submission of the request form and declaration of data use, which are downloadable from the HIRA website [http://opendata.hira.or.kr/op/opc/selectPatDataAplInfoView.do], and upon payment of a data request fee (300,000 KRW per dataset).
Area Under the Curve
Charlson Comorbidity Index
National Health Insurance
Stechman-Neto J, Porporatti AL, Porto de Toledo I, Costa YM, Conti PC, De Luca Canto G, Mezzomo LA. Effect of temporomandibular disorder therapy on otologic signs and symptoms: a systematic review. J Oral Rehabil. 2016;43:468–79. https://doi.org/10.1111/joor.12380 published Online First: 2016/01/11.
Manfredini D, Guarda-Nardini L, Winocur E, Piccotti F, Ahlberg J, Lobbezoo F. Research diagnostic criteria for temporomandibular disorders: a systematic review of axis I epidemiologic findings. Oral Surg Oral Med Oral Ppathol Oral Radiol Endod. 2011;112:453–62. https://doi.org/10.1016/j.tripleo.2011.04.021 published Online First: 2011/08/13.
Sharma S, Wactawski-Wende J, LaMonte MJ, Zhao J, Slade GD, Bair E, Greenspan JD, Fillingim RB, Maixner W, Ohrbach R. Incident injury is strongly associated with subsequent incident temporomandibular disorder: results from the OPPERA study. Pain. 2019;160:1551–61. https://doi.org/10.1097/j.pain.0000000000001554 published Online First: 2019/03/19.
National health insurance service. Available online: [Available from: https://nhiss.nhis.or.kr/bd/ab/bdaba000eng.do Accessed 2 Sept 2019.
Visscher CM, Ligthart L, Schuller AA, Lobbezoo F, de Jongh A, van Houtem CM, Boomsma DI. Comorbid disorders and sociodemographic variables in temporomandibular pain in the general Dutch population. J Oral Facial Pain Headache. 2015;29:51–9. https://doi.org/10.11607/ofph.1324 published Online First: 2015/01/31.
Mundt T, Mack F, Schwahn C, Bernhardt O, Kocher T, Biffar R. Association between sociodemographic, behavioral, and medical conditions and signs of temporomandibular disorders across gender: results of the study of health in Pomerania (SHIP-0). Int J Prosthodont. 2008;21:141–8 published Online First: 2008/06/13.
Plesh O, Adams SH, Gansky SA. Temporomandibular joint and muscle disorder-type pain and comorbid pains in a national US sample. J Orofac Pain. 2011;25:190–8 published Online First: 2011/08/13.
Velly AM, Fricton J. The impact of comorbid conditions on treatment of temporomandibular disorders. J Am Dent Assoc (1939). 2011;142:170–2 published Online First: 2011/02/02.
Ries LG, Berzin F. Analysis of the postural stability in individuals with or without signs and symptoms of temporomandibular disorder. Braz Oral Res. 2008;22:378–83 published Online First: 2009/01/17.
Ries LG, Graciosa MD, Medeiros DL, Pacheco SC, Fassicolo CE, Graefling BC, Degan VV. Influence of craniomandibular and cervical pain on the activity of masticatory muscles in individuals with Temporomandibular Disorder. CoDAS. 2014;26:389–94 published Online First: 2014/11/13.
Fujimoto M, Hayakawa L, Hirano S, Watanabe I. Changes in gait stability induced by alteration of mandibular position. J Med Dent Sci. 2001;48:131–6 published Online First: 2002/08/06.
Sforza C, Tartaglia GM, Solimene U, Morgun V, Kaspranskiy RR, Ferrario VF. Occlusion, sternocleidomastoid muscle activity, and body sway: a pilot study in male astronauts. Cranio. 2006;24:43–9. https://doi.org/10.1179/crn.2006.008 published Online First: 2006/03/18.
Manchikanti L. Epidemiology of low back pain. Pain Physician. 2000;3:167–92 published Online First: 2006/08/15.
Shmagel A, Foley R, Ibrahim H. Epidemiology of Chronic Low Back Pain in US Adults: Data From the 2009–2010 National Health and Nutrition Examination Survey. Arthritis Care Res. 2016;68:1688–94. https://doi.org/10.1002/acr.22890 published Online First: 2016/10/27.
Maher C, Underwood M, Buchbinder R. Non-specific low back pain. Lancet (London, England). 2017;389:736–47. https://doi.org/10.1016/s0140-6736(16)30970-9 published Online First: 2016/10/18.
Herman PM, Broten N, Lavelle TA, Sorbero ME, Coulter ID. Health Care Costs and Opioid Use Associated With High-impact Chronic Spinal Pain in the United States. Spine. 2019;44:1154–61. https://doi.org/10.1097/brs.0000000000003033 published Online First: 2019/08/03.
Wiesinger B, Malker H, Englund E, Wanman A. Does a dose-response relation exist between spinal pain and temporomandibular disorders? BMC Musculoskelet Disord. 2009;10:28. https://doi.org/10.1186/1471-2474-10-28 published Online First: 2009/03/04.
Wiesinger B, Malker H, Englund E, Wanman A. Back pain in relation to musculoskeletal disorders in the jaw-face: a matched case-control study. Pain. 2007;131:311–9. https://doi.org/10.1016/j.pain.2007.03.018 published Online First: 2007/04/27.
Storm C, Wanman A. Temporomandibular disorders, headaches, and cervical pain among females in a Sami population. Acta Odontol Scand. 2006;64:319–25. https://doi.org/10.1080/00016350600801915 published Online First: 2006/09/02.
Walczynska-Dragon K, Baron S, Nitecka-Buchta A, Tkacz E. Correlation between TMD and cervical spine pain and mobility: is the whole body balance TMJ related? Biomed Res Int. 2014;2014:582414. https://doi.org/10.1155/2014/582414 published Online First: 2014/07/23.
Visscher CM, Lobbezoo F, de Boer W, van der Zaag J, Naeije M. Prevalence of cervical spinal pain in craniomandibular pain patients. Eur J Oral Sci. 2001;109:76–80 published Online First: 2001/05/12.
De Laat A, Meuleman H, Stevens A, Verbeke G. Correlation between cervical spine and temporomandibular disorders. Clin Oral Investig. 1998;2:54–7 published Online First: 2004/10/20.
Garrigos-Pedron M, Elizagaray-Garcia I, Dominguez-Gordillo AA, Del-Castillo-Pardo-de-Vera JL, Gil-Martinez A. Temporomandibular disorders: improving outcomes using a multidisciplinary approach. J Multidiscip Healthc. 2019;12:733–47. https://doi.org/10.2147/jmdhS178507 published Online First: 2019/10/01.
Kim L, Kim JA, Kim S. A guide for the utilization of Health Insurance Review and Assessment Service National Patient Samples. Epidemiol Health. 2014;36:e2014008. https://doi.org/10.4178/epih/e2014008 published Online First: 2014/08/01.
Gauer RL, Semidey MJ. Diagnosis and treatment of Temporomandibular disorders. Am Fam Physician. 2015;91:378–86.
Wong YK, Cheng J. A case series of temporomandibular disorders treated with acupuncture, occlusal splint and point injection therapy. Acupunct Med. 2003;21:138–49 published Online First: 2004/01/27.
Austin PC. Balance diagnostics for comparing the distribution of baseline covariates between treatment groups in propensity-score matched samples. Stat Med. 2009;28:3083–107. https://doi.org/10.1002/sim.3697.
Cavalieri M. Geographical variation of unmet medical needs in Italy: a multivariate logistic regression analysis. Int J Health Geogr. 2013;12:27. https://doi.org/10.1186/1476-072x-12-27 published Online First: 2013/05/15.
Lee JY, Yun J. What Else Is Needed in the Korean Government's Master Plan for People With Developmental Disabilities? J Prev Med Public Health. 2019;52:200–4. https://doi.org/10.3961/jpmph.18.249 published Online First: 2019/06/06.
Quan H, Li B, Couris CM, Fushimi K, Graham P, Hider P, Januel J-M, Sundararajan V. Updating and validating the Charlson comorbidity index and score for risk adjustment in hospital discharge abstracts using data from 6 countries. Am J Epidemiol. 2011;173:676–82.
Charlson ME, Pompei P, Ales KL, MacKenzie CR. A new method of classifying prognostic comorbidity in longitudinal studies: development and validation. J Chronic Dis. 1987;40:373–83.
Quan H, Sundararajan V, Halfon P, Fong A, Burnand B, Luthi JC, Saunders LD, Beck CA, Feasby TE, Ghali WA. Coding algorithms for defining comorbidities in ICD-9-CM and ICD-10 administrative data. Med Care. 2005;43:1130–9 published Online First: 2005/10/15.
Iwai N, Dohi O, Naito Y, Inada Y, Fukui A, Takayama S, Ogita K, Terasaki K, Nakano T, Ueda T, Okayama T, Yoshida N, Katada K, Kamada K, Uchiyama K, Ishikawa T, Handa O, Takagi T, Konishi H, Yagi N, Itoh Y. Impact of the Charlson comorbidity index and prognostic nutritional index on prognosis in patients with early gastric cancer after endoscopic submucosal dissection. Dig Endosc. 2018;30:616–23. https://doi.org/10.1111/den.13051.
Kim YY, Lee JS, Kang HJ, Park SM. Effect of medication adherence on long-term all-cause-mortality and hospitalization for cardiovascular disease in 65,067 newly diagnosed type 2 diabetes patients. Sci Rep. 2018;8. https://doi.org/10.1038/s41598-018-30740-y.
Koh W, Kang K, Lee YJ, Kim MR, Shin JS, Lee J, Lee JH, Shin KM, Ha IH. Impact of acupuncture treatment on the lumbar surgery rate for low back pain in Korea: A nationwide matched retrospective cohort study. PLoS One. 2018;13:e0199042. https://doi.org/10.1371/journal.pone.0199042 published Online First: 2018/06/13.
Choi AR, Shin JS, Lee J, Lee YJ, Kim MR, Oh MS, Lee EJ, Kim S, Kim M, Ha IH. Current practice and usual care of major cervical disorders in Korea: A cross-sectional study of Korean health insurance review and assessment service national patient sample data. Medicine (Baltimore). 2017;96:e8751. https://doi.org/10.1097/md.0000000000008751 published Online First: 2017/11/18.
Austin PC. Using the standardized difference to compare the prevalence of a binary variable between two groups in observational research. COMMUN STAT-SIMUL C. 2009;38:1228–34.
Petersen LA, Normand SL, Daley J, McNeil BJ. Outcome of myocardial infarction in Veterans Health Administration patients as compared with medicare patients. N Engl J Med. 2000;343:1934–41. https://doi.org/10.1056/nejm200012283432606 published Online First: 2001/01/03.
Conway A, Rolley JX, Fulbrook P, Page K, Thompson DR. Improving statistical analysis of matched case-control studies. R Res Nurs Health. 2013;36:320–4. https://doi.org/10.1002/nur.21536 published Online First: 2013/02/15.
Dunnett CW. Pairwise multiple comparisons in the homogeneous variance, unequal sample size case. J Am Stat Assoc. 1980;75:789–95.
Andersen R. A behavioral model of families’ use of health services. A behavioral model of families’ use of health services; 1968.
Babitsch B, Gohl D, von Lengerke T. Re-revisiting Andersen’s Behavioral Model of Health Services Use: a systematic review of studies from 1998–2011. Psychosoc Med. 2012;9:Doc11. https://doi.org/10.3205/psm000089 published Online First: 2012/10/25.
Diehr P, Yanez D, Ash A, Hornbrook M, Lin DY. Methods for analyzing health care utilization and costs. Annu Rev Public Health. 1999;20:125–44. https://doi.org/10.1146/annurev.publhealth.20.1.125 published Online First: 1999/06/03.
Goncalves DAD, Dal Fabbro AL, Campos J, Bigal ME, Speciali JG. Symptoms of Temporomandibular disorders in the population: an epidemiological study. J Orofac Pain. 2010;24:270–8.
LeResche L. Epidemiology of temporomandibular disorders: implications for the investigation of etiologic factors. Crit Rev Oral Biol Med. 1997;8:291–305. https://doi.org/10.1177/10454411970080030401.
De Rossi SS, Greenberg MS, Liu F, Steinkeler A. Temporomandibular Disorders Evaluation and Management. Med Clin North Am. 2014;98:1353. https://doi.org/10.1016/j.mcna.2014.08.009.
Bueno CH, Pereira DD, Pattussi MP, Grossi PK, Grossi ML. Gender differences in temporomandibular disorders in adult populational studies: a systematic review and meta-analysis. J Oral Rehabil. 2018;45:720–9. https://doi.org/10.1111/joor.12661.
Lee JW, Yang SI, Kim KH. A study on influential factors on satisfaction with the use of medical services by the qualified recipients of medical aid. J Digital Convergence. 2014;12:289–97.
Balasubramaniam R, de Leeuw R, Zhu H, Nickerson RB, Okeson JP, Carlson CR. Prevalence of temporomandibular disorders in fibromyalgia and failed back syndrome patients: a blinded prospective comparison study. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2007;104:204–16. https://doi.org/10.1016/j.tripleo.2007.01.012 published Online First: 2007/05/08.
Walczynska-Dragon K, Baron S. The biomechanical and functional relationship between temporomandibular dysfunction and cervical spine pain. Acta Bioeng Biomech. 2011;13:93–8 published Online First: 2012/02/22.
Rantala MA, Ahlberg J, Suvinen TI, Nissinen M, Lindholm H, Savolainen A, Kononen M. Temporomandibular joint related painless symptoms, orofacial pain, neck pain, headache, and psychosocial factors among non-patients. Acta Odontol Scand. 2003;61:217–22 published Online First: 2003/10/30.
Cuccia A, Caradonna C. The relationship between the stomatognathic system and body posture. Clinics (Sao Paulo, Brazil). 2009;64:61–6 published Online First: 2009/01/15.
Simsek S, Yagci N, Senol H. Prevalence of and risk factors for low back pain among healthcare workers in Denizli. Agri J Turkish Soc Algology. 2017;29:71–8. https://doi.org/10.5505/agri.2017.32549.
Kawaguchi M, Matsudaira K, Sawada T, Koga T, Ishizuka A, Isomura T, Coggon D. Assessment of potential risk factors for new onset disabling low back pain in Japanese workers: findings from the CUPID (cultural and psychosocial influences on disability) study. BMC Musculoskelet Disord. 2017;18. https://doi.org/10.1186/s12891-017-1686-y.
Malta DC, Oliveira MM, Andrade S, Caiaffa WT, Souza MFM, Bernal RTI. Factors associated with chronic back pain in adults in Brazil. Revista De Saude Publica. 2017;51:9s. https://doi.org/10.1590/s1518-8787.2017051000052 published Online First: 2017/06/08.
Kuntz B, Hoebel J, Fuchs J, Neuhauser H, Lampert T. Social inequalities in the prevalence of chronic back pain among adults in Germany. Bundesgesundheitsbl Gesundheitsforsch Gesundheitsschutz. 2017;60:783–91. https://doi.org/10.1007/s00103-017-2568-z published Online First: 2017/05/19.
This study was supported by the Research Institute of Korean Medicine Policy. The authors thank In-Hyuk Ha, the Director of Jaseng Spine and Joint Research Institute, who reviewed the overall content of this paper. He is the traditional Korean medicine doctors and specialists in the field of musculoskeletal diseases, including Hang-woo Nam, Won-sang Park, and Ju-won Kim, provided suggestions regarding the ICD 10 code that should be chosen for the spinal pain.
This research received no external funding.
Ethics approval and consent to participate
Due to the retrospective nature of this study, which utilized data with encrypted personal information, it was granted an exemption in writing by the Institutional Review Board of Jaseng Hospital of Korean Medicine in Seoul, Korea (JASENG 2018–09-007). All authors read the Helsinki Declaration and followed the guidelines in this study.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Prevalence of spinal pain in cases and controls according to TMD grade.
Prevalence of spinal pain for each level in cases and controls according to TMD Grade. spinal1, spinal pain grade 1; spinal2, spinal pain grade 2; spinal3, spinal pain grade 3.
Medical Service Use of TMD Patients.
Post hoc test for outcome differences between TMD grades.
About this article
Cite this article
Kim, D., Ko, SG., Lee, EK. et al. The relationship between spinal pain and temporomandibular joint disorders in Korea: a nationwide propensity score-matched study. BMC Musculoskelet Disord 20, 631 (2019). https://doi.org/10.1186/s12891-019-3003-4