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. 2025 Apr 10;25:510. doi: 10.1186/s12903-025-05860-3

Oral health behaviours and metabolic syndrome: mediation effect of lifestyle habits

Mizuki Saito 1, Yoshihiro Shimazaki 1,✉, Saori Yoshii 2, Tetsuhito Kojima 2
PMCID: PMC11983727  PMID: 40211264

Abstract

Background

Recent studies have reported an association between toothbrushing frequency and systemic health. Plaque control, achieved through frequent brushing, is known to prevent dental caries and periodontal disease, potentially reducing the risk of systemic diseases. However, individuals with good oral health behaviours may also exhibit healthier lifestyle habits which could impact systemic health. In examining the relationship between oral health behaviours and systemic health, it is important to consider the influence of factors that mediate the relationship between them. This study conducted mediation analyses to evaluate the extent to which lifestyle habits and periodontal status mediate the relationship between oral health behaviours and systemic health.

Methods

Health examinations, including dental assessments, were performed on 15,579 individuals at the Aichi Health Promotion Foundation. Of these, 12,540 participants aged 40–74 years were included in the analysis. Mediation analyses were conducted using the number of metabolic syndrome (MS) components as the outcome variable, oral health behaviours (regular dental visits, use of interdental brushes or dental floss, and toothbrushing frequency) as exposure variables, lifestyle habits (smoking, drinking, exercise, and eating habits) and periodontal status as mediators, and age and sex as covariates.

Results

Regular dental visits showed significant total and indirect effects on MS, although no significant direct effect was observed. The use of interdental brushes or dental floss and toothbrushing frequency demonstrated significant total, direct and indirect effects on MS. Exercise habits, eating habits and periodontal status were significant mediators in the relationship between regular dental visits and MS. These mediators also significantly influenced the associations between both the use of interdental brushes or dental floss and toothbrushing frequency with MS.

Conclusion

The relationship between oral health behaviours and MS is mediated by lifestyle habits and periodontal status. Among the mediating variables tested in this study, the indirect effects of diet and exercise habits tended to be stronger than the indirect effect of periodontal disease. Oral health behaviours may influence systemic health through their impact on lifestyle habits.

Keywords: Oral health behaviour, Metabolic syndrome, Lifestyle habit, Mediation analysis

Background

Oral diseases such as dental caries, periodontal disease, and tooth loss are the most common diseases, affecting nearly half of the world’s population. The prevalence of oral diseases is increasing due to population growth, the aging of the population, and increased tooth retention [1]. The most basic and important factor in preventing oral diseases is good oral health behaviours, including brushing one’s teeth. However, toothbrushing alone cannot completely remove plaque, which is a primary cause of periodontal disease and dental caries [2, 3]. Furthermore, more frequent toothbrushing does not necessarily lead to better oral hygiene. A study investigating the relationship between plaque removal frequency and periodontal status revealed that the periodontal condition of those who did not brush their teeth daily was poor, but there was no difference in the periodontal condition of those who brushed their teeth daily, even if the frequency of daily brushing increased [4].

Periodontal disease and tooth loss are risk factors for various chronic conditions, including metabolic syndrome (MS) [5–8]. Tooth loss is a risk factor for malnutrition and frailty [9, 10], periodontal disease is a risk factor for diabetes and cardiovascular disease [11, 12], and oral disease affects systemic health [11, 12]. Recent studies have reported an association between toothbrushing frequency and systemic health outcomes [13–16]. A follow-up study involving middle-aged Japanese individuals found that those who brushed their teeth three times a day had a significantly lower risk of developing MS compared to those who brushed only once a day or less [13]. Similarly, a potential link between toothbrushing frequency and non-alcoholic fatty liver disease has been suggested [16].

Good oral health behaviours may lead to good oral health and reduced risk of systemic disease. Even if an association between toothbrushing frequency and systemic health status is observed, it cannot be explained entirely by oral health status. Individuals who brush their teeth more frequently, or who use interdental brushes and dental floss, are likely to be more conscious of their overall health. Studies have shown that frequent toothbrushing is associated with lower smoking rates; indeed, smokers are less likely to visit the dentist regularly compared to non-smokers [17]. Moreover, individuals who brush their teeth more frequently tend to have healthier eating habits and are less likely to be obese [18]. Lifestyle has a strong influence on the development of the non-communicable diseases such as MS and fatty liver [19, 20], and the impact of periodontitis compared to lifestyle is considered small. Thus, the association between toothbrushing frequency and systemic health may be better explained by the presence of healthy lifestyle behaviours, such as regular exercise and a balanced diet, which positively influence systemic health.

In examining the relationship between oral health behaviours and systemic health, it is important to consider the existence and influence of factors that mediate the relationship between them. In this study, mediation analyses were conducted to evaluate the extent to which lifestyle factors and periodontal status mediate the relationship between MS as an indicator of systemic health and oral health behaviours, such as toothbrushing frequency, use of interdental brushes or dental floss, and regular dental visits.

Methods

Study design and participants

This was a cross-sectional observational study. Between April 1, 2010, and March 31, 2011, a total of 15,579 individuals underwent health examinations, including dental examinations, at the Aichi Health Promotion Foundation. Among these, 12,540 individuals aged 40–74 years were included in this study.

Directed acyclic graph (DAG)

DAGs are used to illustrate assumptions about the relationships among variables. The assumptions take the form of edges going from one node to another. These edges are directed, as shown by a single arrowhead indicating their effect [21]. In this study, a DAG was used to identify a mediation model (Fig. 1). Table 1 provides the rationale for creating the directional pathways for the DAG shown in Fig. 1. The DAGitty online tool was used to check the DAG for consistency and validity. Lifestyle habits and periodontal status were considered mediators, and sex and age were considered covariates.

Fig. 1.

Fig. 1

Directed acyclic graph

Table 1.

Description of rationale for pathways shown in the base DAG

Node from Directionality of pathway Node to Rationale
Oral health behaviours Towards mediator

Lifestyle habits

 Drinking

 Smoking

 Exercise

 Eating

People with poor oral health behaviour are more likely to have poor lifestyle habits. Those who brush their teeth less frequently and those who do not visit the dentist are more likely to have drinking and smoking habits [17, 22]. Those who visit the dentist regularly and brush their teeth frequently are more likely to have healthy exercise and eating habits [23, 24].
Oral health behaviours Towards mediator Periodontal status Toothbrushing and the use of an interproximal device helps prevent periodontal disease [25]. Oral health instructions and professional plaque control can help prevent periodontal disease.
Oral health behaviours Towards outcome Metabolic syndrome Toothbrushing and the use of an interproximal device helps prevent metabolic syndrome [26].

Lifestyle habits

 Drinking

 Smoking

 Exercise

 Eating

Towards outcome Metabolic syndrome Lifestyle factors such as drinking, smoking, exercise, and diet strongly influence the incidence and progression of metabolic syndrome [20].
Periodontal status Towards outcome Metabolic syndrome Chronic inflammation caused by periodontitis may be associated with metabolic syndrome [6].

Exposure variables

Oral health behaviours were evaluated as exposure variables. These behaviours were assessed using a self-administered questionnaire that inquired about regular dental visits, daily toothbrushing frequency, and the use of interdental brushes or dental floss.

Outcome

The primary outcome was the total number of MS components met by each participant, as determined from the results of health examinations. The Japanese criteria for MS components were used [27], which included the following: waist circumference ≥ 85 cm for males and ≥ 90 cm for females; blood pressure ≥ 130/85 mmHg; triglyceride level ≥ 150 mg/dL or high-density lipoprotein cholesterol level < 40 mg/dL; and blood glucose level ≥ 110 mg/dL. Participants using medication for dyslipidaemia, hypertension, or diabetes mellitus, or with a history of such medications, were classified as meeting the corresponding criteria.

Mediators

Periodontal status and lifestyle habits, such as smoking, drinking, exercise, and eating behaviours, were examined as mediators. Lifestyle information was obtained via a self-administered questionnaire [28]. Responses were categorised as follows:

  • Smoking: Current, past, or never.

  • Drinking: Everyday, sometimes, or never.

  • Exercise habits: Exercising at least twice a week (yes, no), engaging in walking-equivalent activity for at least 1 hour per day (yes, no), and walking at a fast pace (yes, no).

  • Eating habits: Low intake of vegetables and seaweed (yes, no); frequent consumption of sweetened drinks (yes, no); preference for eating meat rather than fish (yes, no); eating snacks after dinner ≥ 3 times/week (yes, no); eating dinner just before bedtime ≥ 3 times/week (yes, no); and frequent consumption of fried foods (yes, no).

Periodontal status was assessed through dental examinations using the Community Periodontal Index (CPI) [29]. Each participant’s oral cavity was divided into sextants, and 10 representative teeth (11, 16, 17, 26, 27, 31, 36, 37, 46, and 47) were examined. Measurements were conducted at six sites per tooth (mesiobuccal, midbuccal, distobuccal, distolingual, midlingual, and mesiolingual) using a CPI probe (YDM, Tokyo, Japan). CPI codes were defined as follows:

  • Code 0: Healthy.

  • Code 1: Bleeding on probing.

  • Code 2: Calculus detected on probing.

  • Code 3: Periodontal pockets 4–5 mm.

  • Code 4: Periodontal pockets ≥ 6 mm.

  • Code X: Sextants without target teeth.

The highest CPI code per participant, excluding sextants classified as Code X, was used as the individual CPI score. Twelve calibrated dentists (inter-examiner kappa ≥ 0.5) conducted the examinations under reflected light on dental chairs.

Covariates

Age and sex were included as covariates in the analysis.

Statistical analysis

Participants with missing data or those whose periodontal status was unknown (all sextants classified as Code X) were excluded. Toothbrushing frequency was categorised into three groups: ≤ 1 time/day, 2 times/day, and ≥ 3 times/day. Periodontal status was categorised as follows: healthy (CPI codes 0–2), moderate periodontitis (CPI code 3), and severe periodontitis (CPI code 4).

Exercise habits were quantified based on “yes” responses to the three exercise-related questions. Similarly, eating habits were evaluated based on “yes” responses to the six dietary-related questions. Table 2 shows the operationalisation of each variable. The association between the number of MS components and each variable was assessed using chi-squared tests for categorical variables and analysis of variance (ANOVA) for continuous variables.

Table 2.

Operationalisation of the variables

Definition Assessment Response options
Outcome
 Metabolic syndrome The total number of MS components met Waist circumference, blood pressure, triglyceride level or high-density lipoprotein cholesterol level, and blood glucose level Five-point scale from 0 to 4.
Exposure variable
 Regular dental visits Do you visit the dentist regularly? Two-step evaluation (Yes / No).
 Toothbrushing frequency Daily tooth brushing frequency How many times do you brush your teeth daily? Three-point scale (≤ 1 time/day, 2 time/day, or ≥ 3 time/day).
 Use of interdental brush or dental floss Do you use dental floss or interdental brushes? Two-step evaluation (Yes / No).
Mediators
 Drinking Current drinking habit Do you drink alcohol? Three-point scale (every day, sometimes, or never).
 Smoking Smoking habit Do you smoke cigarettes (including electronic cigarettes)? Three-point scale (current, past, or never).
 Exercise Number of “yes” responses to three questions about exercise habits

Walking or equivalent physical activity for at least one hour per day in daily life.

Lightly sweaty exercise for at least 30 minutes a day, at least twice a week, for at least one year.

Walking speed is faster than that of the same sex at the same age.

Four-point scale from 0 to 3.
 Eating Number of “yes” responses to six questions about eating habits

Vegetables and seaweed are not eaten very often.

Drink juice daily.

Eats more meat (beef and pork) than fish.

Snacking after dinner at least 3 times a week.

Eating dinner within 2 hours before bedtime at least 3 times a week.

Eats fried foods frequently.

Seven-point scale from 0 to 6.
 Periodontal status Community Periodontal Index Code 1: healthy, code 2: calculus detected on probing, code 3: periodontal pockets 4-5 mm, and code 4: periodontal pockets ≥ 6 mm. Three-point scale (code 0-2, code 3, and code 4).

Parallel mediation analyses were performed with the number of MS components as the outcome, oral health behaviours as exposure variables, lifestyle habits and periodontal status as mediators, and age and sex as covariates. Model 4 from the PROCESS macro for SPSS was used for mediation analysis. The 95% confidence interval (CI) of the mediating effect was estimated using 5,000 bootstrap samples. Each oral health behaviour was analysed individually. Statistical analyses were conducted using SPSS version 28.0 (IBM Corp., Armonk, NY, USA) and the Hayes PROCESS macro version 4.2. A p-value < 0.05 was considered statistically significant. This study was reported according to A Guideline for Reporting Mediation Analyses.

Results

Of the 15,579 people who underwent health examinations during the study period, 12,540 participants aged 40–74 years were eligible for the study. After excluding 71 participants whose CPI code was X, the final analysis included 12,469 individuals. Regarding the number of MS components, the number of participants with 0, 1, 2, 3, and 4 components was 2,201 (17.7%), 3,875 (31.7%), 3,104 (24.9%), 2,359 (18.9%), and 930 (7.5%), respectively. For the analysis involving toothbrushing frequency, 10,048 participants were included, excluding those with missing data regarding toothbrushing frequency.

Table 3 shows the characteristics of the study participants according to the number of met criteria for MS components. Use of interdental brushes or dental floss, toothbrushing frequency, drinking habit, smoking habit, periodontal status, exercise habit, eating habit, sex, and age were significantly associated with the number of met criteria for MS components.

Table 3.

Characteristics of participants according to the number of metabolic syndrome component

Number of metabolic syndrome components
0 (n =2,201) 1 (n = 3,875) 2 (n = 3,104) 3 (n = 2,359) 4 (n = 930) p-value
Exposure variable
 Regular dental visit n (%)
  No 1,564 (71.1) 2,727 (70.4) 2,231 (71.9) 1,737 (73.6) 658 (70.8) 0.079
  Yes 637 (28.9) 1,148 (29.6) 873 (28.1) 622 (26.4) 272 (29.2)
 Use of interdental brush or dental floss
  No 1,660 (75.4) 2,883 (74.4) 2,418 (77.9) 1,904 (80.7) 764 (82.2) < 0.001
  Yes 541 (24.6) 992 (25.6) 686 (22.1) 455 (19.3) 166 (17.8)
 Toothbrushing frequencya
  < 1 time/day 256 (14.3) 685 (21.8) 682 (27.5) 597 (31.7) 260 (34.8) < 0.001
  2 time/day 1,111 (62.1) 1,874 (59.5) 1,408 (56.8) 1,082 (57.4) 407 (54.4)
  > 3 time/day 423 (23.6) 590 (18.7) 387 (15.6) 205 (10.9) 81 (10.8)
Mediator variable
 Drinking habit
  Never 842 (38.3) 1,456 (37.6) 990 (31.9) 701 (29.7) 254 (27.3) < 0.001
  Sometimes 730 (33.2) 1,203 (31.0) 907 (29.2) 704 (29.8) 292 (31.4)
  Everyday 629 (28.6) 1,216 (31.4) 1,207 (38.9) 954 (40.4) 384 (41.3)
 Smoking habit
  Never 1,204 (54.7) 1,818 (46.9) 1,108 (35.7) 693 (29.4) 241 (25.9) < 0.001
  Past 481 (21.9) 1,009 (26.0) 1,070 (34.5) 929 (39.4) 428 (46.0)
  Current 516 (23.4) 1,048 (27.0) 926 (29.8) 737 (31.2) 261 (28.1)
 Periodontal status
  Healthy 1,278 (58.1) 1,905 (49.2) 1,223 (39.4) 847 (35.9) 327 (35.2) < 0.001
  Moderate periodontitis 713 (32.4) 1,451 (37.4) 1,374 (44.3) 1,074 (45.5) 422 (45.4)
  Severe periodontitis 210 (9.5) 519 (13.4) 507 (16.3) 438 (18.6) 181 (19.5)
Mean (SD)
Exercise habit 0.7 (0.8) 0.7 (0.8) 0.7 (0.8) 0.6 (0.8) 0.6 (0.7) 0.002
Eating habit 1.1 (1.1) 1.1 (1.1) 1.2 (1.1) 1.3 (1.1) 1.3 (1.1) < 0.001
Covariates
 Sex n (%)
  Men 1,184 (53.8) 2,546 (65.7) 2,590 (83.4) 2,129 (90.3) 877 (94.3) < 0.001
  Women 1,017 (46.2) 1,329 (34.3) 514 (16.6) 230 (9.7) 53 (5.7)
Mean (SD)
 Age 48.3 (7.2) 51.7 (8.1) 53.6 (8.4) 54.5 (8.3) 55.1 (8.0) < 0.001

Abbreviation: SD Standard deviation

an = 10,048

Tables 4 and 5 show the results of mediation analyses in which the number of met criteria for MS components was the outcome; regular dental visits, use of interdental brushes or dental floss, and toothbrushing frequency were the exposure variables; drinking, smoking, exercise, eating habits, and periodontal status were the mediators; and age and sex were the covariates.

Table 4.

Mediation analysis of each oral health behaviour on the number of metabolic syndrome component

Outcome variable: number of metabolic syndrome components
Coefficient SE 95% CI
Regular dental visita
 Total effect -0.051 0.022 -0.094, -0.008
 Direct effect -0.021 0.022 -0.064, 0.022
 Indirect effect -0.030 0.004 -0.037, -0.023
Use of interdental brush or dental flossa
 Total effect -0.094 0.024 -0.140, -0.048
 Direct effect -0.067 0.024 -0.113, -0.021
 Indirect effect -0.027 0.004 -0.034, -0.020
Toothbrushing frequencyb
 Total effect -0.173 0.018 -0.208, -0.139
 Direct effect -0.146 0.018 -0.181, -0.111
 Indirect effect -0.027 0.004 -0.035, -0.019

Abbreviations: SE Standard error, CI Confidence interval

an = 12,469

bn = 10,048

Table 5.

Indirect effect of each health behaviour on the number of metabolic syndrome components

Mediator Coefficient SE 95% CI
Regular dental visita Total −0.030 0.004 −0.037, −0.023
Drinking habit 0.000 0.0002 −0.0004, 0.001
Smoking habit −0.0002 0.001 −0.003, 0.002
Exercise habit −0.014 0.003 −0.019, −0.009
Eating habit −0.012 0.002 −0.017, −0.008
Periodontal status −0.004 0.001 −0.007, −0.002
Use of interdental brush or dental flossa Total −0.027 0.004 −0.034, −0.020
Drinking habit −0.0001 0.0003 −0.001, 0.001
Smoking habit −0.0001 0.001 −0.003, 0.003
Exercise habit −0.013 0.002 −0.018, −0.009
Eating habit −0.011 0.002 −0.015, −0.007
Periodontal status −0.003 0.001 −0.005, −0.0004
Toothbrushing frequencyb Total −0.027 0.004 −0.035, −0.019
Drinking habit 0.000 0.0002 −0.0004, 0.0004
Smoking habit 0.0004 0.003 −0.005, 0.005
Exercise habit −0.009 0.002 −0.013, −0.006
Eating habit −0.015 0.003 −0.020, −0.010
Periodontal status −0.003 0.001 −0.006, −0.002

Abbreviations: SE Standard error, CI Confidence interval

an = 12,469

bn = 10,048

Table 4 shows the total, direct and indirect effects of each oral health behaviour on MS. Regular dental visits had significant total and indirect effects on MS, with coefficients of − 0.051 (95% CI: − 0.094, − 0.008) and − 0.030 (95% CI: − 0.037, − 0.023), respectively. There was no significant direct effect of regular dental visits on MS. Use of interdental brushes or dental floss had significant total, direct, and indirect effects, with coefficients of − 0.094 (95% CI: − 0.140, − 0.048), − 0.067 (95% CI: − 0.113, − 0.021) and − 0.027 (95% CI: − 0.034, − 0.020), respectively. Toothbrushing frequency also had significant total, direct and indirect effects, with coefficients of − 0.173 (95% CI: − 0.208, − 0.139), − 0.146 (95% CI: − 0.181, − 0.111) and − 0.027 (95% CI: − 0.035, − 0.019), respectively.

Table 5 shows the indirect effects of each mediator on the association between each oral health behaviour and MS. Exercise habits, eating habits and periodontal status had significant indirect effects on the association between regular dental visits and MS, with coefficients of − 0.014 (95% CI: − 0.019, − 0.009), − 0.012 (95% CI: − 0.017, − 0.008) and − 0.004 (95% CI: − 0.007, − 0.002), respectively. Exercise habits, eating habits and periodontal status also had significant indirect effects on the association between the use of interdental brushes or dental floss and MS, with coefficients of − 0.013 (95% CI: − 0.018, − 0.009), − 0.011 (95% CI: − 0.015, − 0.007) and − 0.003 (95% CI: − 0.005, − 0.0004), respectively. Similarly, exercise habits, eating habits and periodontal status had significant indirect effects on the association between toothbrushing frequency and MS, with coefficients of − 0.009 (95% CI: − 0.013, − 0.006), − 0.015 (95% CI: − 0.020, − 0.010) and − 0.003 (95% CI: − 0.006, − 0.002), respectively.

Discussion

We found that lifestyle habits and periodontal status mediate the relationship between oral health behaviours and MS. The indirect effects through periodontal status were smaller than those observed through exercise and eating habits.

A strength of this study was its analysis of a large number of participants. The inclusion of varied and detailed questions about exercise and eating habits in the questionnaire allowed the results to reflect the participants’ lifestyle habits comprehensively. Additionally, this study provides valuable insights, as few prior studies have explored the lifestyle-mediated influence in the relationship between oral health behaviours and MS.

However, several limitations should be acknowledged. First, lifestyle habits were assessed through self-reported questionnaires, which are subjective and may not accurately represent the actual amount of exercise performed or food consumed. The questionnaire items used in this study are widely used in health examinations in Japan but have not been validated [28]. Second, the study was conducted in a specific region of Japan, limiting the generalisability of the findings. Third, data on socioeconomic factors, such as income and education—which are known to influence lifestyle and health status [30, 31]—were unavailable. Furthermore, the study population was biased toward men, as most participants were health examination attendees, predominantly employees undergoing annual workplace screenings. The associations observed in this study between oral health behaviours, lifestyle habits and MS may reflect confounding rather than true mediation. Although mediation analyses were performed using oral health behaviours as exposure variables and lifestyle habits as mediators to evaluate their effects on MS, the cross-sectional design of this study prevented establishing a temporal relationship or causation between oral health behaviours and MS.

Several studies have investigated the relationship between toothbrushing frequency and MS. A 3-year follow-up study reported that individuals brushing their teeth ≥ 3 times per day had a significantly lower risk of MS compared to those brushing ≤ 1 time per day [13]. Another follow-up study found that more frequent toothbrushing was associated with a lower risk of MS, with significant direct and indirect effects observed in mediation analyses using periodontal status as a mediator [15]. Consistent with these findings, this study demonstrated significant associations between toothbrushing frequency and MS, including both direct effects and indirect effects mediated by periodontal status, exercise habits, and eating habits.

This study extended the scope of previous research by including regular dental visits and the use of interdental brushes or dental floss as exposure variables in the mediation analysis. Few studies have examined the association of interdental cleaning devices with MS, and no previous studies have evaluated the relationship between regular dental visits and MS. In one study examining the relationship between oral health behaviours and MS components, individuals who did not use dental floss daily had higher risks of abdominal obesity, hypertension and hyperglycaemia [26, 32]. Similarly, this study found that individuals who used interdental brushes or dental floss and those who regularly visited dentists exhibited fewer MS components than those who did not. Mediation analyses revealed significant direct and indirect effects of interdental cleaning device use on MS, mediated by periodontal status, exercise habits, and eating habits. Regular dental visits, however, exhibited only indirect effects.

It is likely that individuals with good oral health behaviours are generally more health-conscious, leading to better lifestyle habits, such as regular exercise, healthier eating, and avoidance of smoking and excessive drinking [23]. For instance, those who regularly visit dentists and use interdental cleaning devices tend to have better eating habits, while frequent toothbrushing is associated with exercise habits and non-smoking behaviour. Consequently, oral health behaviours may influence MS via their association with lifestyle habits such as exercise and eating habits.

Given the close relationship between oral health behaviours and lifestyle habits, these behaviours may not only affect MS but also other lifestyle-related diseases. Although this study focused on MS as the outcome, previous studies have reported associations between toothbrushing frequency and non-alcoholic fatty liver disease, as well as with decreased renal function [16, 33]. Future research should explore further the relationship between oral health behaviours and other systemic diseases.

In this study, toothbrushing frequency and the use of interdental brushes or dental floss had both significant direct and indirect effects in relation to MS. Individuals who brush their teeth more frequently may have a more relaxed lifestyle, allowing them to manage their time and mental well-being effectively. Consequently, they might experience less stress in their daily lives. Since excessive stress and fatigue are recognised risk factors for lifestyle-related diseases, toothbrushing frequency and the use of interdental cleaning devices might exert a direct effect on MS. However, this study did not assess participants’ stress levels, leaving the relevance of this potential mechanism unclear.

Health literacy, self-efficacy, and adherence are associated with maintaining a healthy lifestyle. Those with high self-efficacy and health literacy are more likely to have a healthy lifestyle [34, 35]. Self-efficacy promotes adherence to lifestyle guidance [36], which in turn reduces mortality due to MS [37]. Similarly, those with good oral health are more likely to be health literate and more concerned about oral health. Those with higher self-efficacy have better gingival status [38]. Socioeconomic determinants such as education, occupation, and income are thought to influence psychological aspects, resulting in differences in lifestyle habits. Socioeconomic disparities also influence health outcomes [30, 31]. Individuals with higher education, better social status, and greater wealth tend to exhibit higher health awareness, adopt healthier lifestyle habits and, consequently, have a lower risk of disease compared to those with fewer resources [30]. Socioeconomic factors also affect oral health behaviours and lifestyle habits, including drinking, smoking, exercise and eating [31], potentially acting as confounding variables in the association between oral health behaviours and MS. Unfortunately, this study lacked data on socioeconomic factors and indices of phycological status, such as health literacy, self-efficacy, and adherence, and could not adjust for these variables in the analysis. This limitation may partly explain the significant direct effects of toothbrushing frequency and interdental cleaning device use on MS. Future research should incorporate socioeconomic factors into the analysis to understand more precisely their influence.

Numerous studies have reported associations between periodontitis and MS. An 8-year follow-up study found that individuals with poor periodontal health had a higher risk of developing MS [39]. Similarly, this study observed a significant association between periodontal status and MS. Chronic inflammation caused by periodontitis affects systemic health beyond the oral cavity [40], making periodontitis a recognised risk factor for MS. It is plausible that individuals with good oral health behaviours are less likely to develop MS due to their better periodontal health. However, in this study, the indirect effects of periodontal status on MS were smaller than those mediated by lifestyle habits, such as exercise and dietary practices.

Individuals with good oral health behaviours were also less likely to engage in drinking and smoking. Although drinking and smoking were significantly associated with MS in bivariate analyses, they did not demonstrate significant indirect effects as mediators in the relationship between oral health behaviours and MS. Smoking is a well-established risk factor for various lifestyle-related diseases [41–43]; however, it is also associated with weight loss, which may weaken its association with MS [44]. Furthermore, appropriate alcohol consumption is generally not harmful to health [45]. In this study, the lack of detailed data on the amount of alcohol consumed may have influenced the results, which did not show a significant association between drinking and MS.

Many studies have assessed the relationship between frequency of toothbrushing and systemic health but those studies considered lifestyle habits confounding factors. The originality of this study lies in the fact that we examined lifestyle habits as mediators in a mechanism by which oral health behaviours affect systemic health. However, the influence of lifestyle habits and oral health behaviours on oral and systemic health status is very complex. It is difficult to determine whether lifestyle habits are confounding or mediating factors. The mediating effect of lifestyle habits in this study is only one possible mechanism. Another interesting result is that the frequency of toothbrushing and the use of interdental cleaning devices had a direct effect on MS. It is possible that toothbrushing itself may serve as a light form of exercise and/or prevent snacking. However, it is unlikely that brushing the teeth more often or using an interdental brush will reduce the risk of MS. For those with poor oral health behaviour, it is important to provide health guidance that also leads to lifestyle improvement. Another reason for the direct effects observed in this study may be the influence of confounding factors that were not considered, such as socioeconomic factors. Possible methods that could be used in future studies include Bayesian estimation using prior distributions of lifestyle and socioeconomic determinants, and approaches such as structural analysis of covariance.

Conclusions

The relationship between oral health behaviours and MS is mediated by lifestyle habits and periodontal status. Among the mediating variables tested in this study, the indirect effects of diet and exercise habits tended to be stronger than the indirect effect of periodontal disease. Oral health behaviours may influence systemic health through their impact on lifestyle habits. For those with poor oral health behaviour, it is important to provide health guidance that also leads to lifestyle improvement.

Acknowledgements

We thank the study participants and those involved in administering the health examinations.

Abbreviations

MS

Metabolic syndrome

DAG

Directed acyclic graph

CPI

Community Periodontal Index

CI

Confidence interval

Authors’ contributions

MS contributed to conception, design, analysis, interpretation, and draft and critically revised the manuscript. YS contributed to conception, design, interpretation, and draft and critically revised the manuscript. SY contributed to conception, design, data acquisition, and critically revised the manuscript. TK contributed to conception, design, data acquisition, and critically revised the manuscript. All authors gave their final approval and agree to be accountable for all aspects of the work.

Funding

This work was supported by JSPS KAKENHI Grant Number JP22K10353 and JP23K16239.

Data availability

The data that support the findings of this study are available from the Aichi Health Promotion Foundation, but restrictions apply to the availability of these data, which were used under license for the current study, and so are not publicly available. Data are however available from the authors upon reasonable request and with permission of the Aichi Health Promotion Foundation.

Declarations

Ethics approval and consent to participate

Written informed consent to use health examination data for research was obtained from all participants. The Institutional Review Board (IRB) of Aichi Gakuin University School of Dentistry approved the study design, data-collection methods, and the procedure for obtaining informed consent (approval number 618). The study was conducted strictly in accordance with the relevant provisions of the World Medical Association Declaration of Helsinki. This study was reported according to the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) guidelines for reporting observational studies.

Consent for publication

Not applicable.

Competing interests

The authors declare no competing interests.

Footnotes

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Jepsen S, Blanco J, Buchalla W, Carvalho JC, Dietrich T, Dörfer C, Eaton KA, Figuero E, Frencken JE, Graziani F, et al. Prevention and control of dental caries and periodontal diseases at individual and population level: consensus report of group 3 of joint EFP/ORCA workshop on the boundaries between caries and periodontal diseases. J Clin Periodontol. 2017;44 Suppl 18:s85–s93. 10.1111/jcpe.12687. [DOI] [PubMed]
  • 2.Chapple IL, Van der Weijden F, Doerfer C, Herrera D, Shapira L, Polak D, Madianos P, Louropoulou A, Machtei E, Donos N, et al. Primary prevention of periodontitis: managing gingivitis. J Clin Periodontol. 2015;42 Suppl 16:S71–6. 10.1111/jcpe.12366. [DOI] [PubMed] [Google Scholar]
  • 3.Hagman J, Wide U, Werner H, Hakeberg M. Oral health and oral health behavior in young adults with caries disease. BDJ Open. 2021;7(1):28. 10.1038/s41405-021-00084-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Pinto TM, de Freitas GC, Dutra DA, Kantorski KZ, Moreira CH. Frequency of mechanical removal of plaque as it relates to gingival inflammation: a randomized clinical trial. J Clin Periodontol. 2013;40(10):948–54. 10.1111/jcpe.12135. [DOI] [PubMed]
  • 5.Zhu Y, Hollis JH. Associations between the number of natural teeth and metabolic syndrome in adults. J Clin Periodontol. 2015;42(2):113–20. 10.1111/jcpe.12361. [DOI] [PubMed] [Google Scholar]
  • 6.Jepsen S, Suvan J, Deschner J. The association of periodontal diseases with metabolic syndrome and obesity. Periodontol 2000. 2020;83(1):125–53. 10.1111/prd.12326. [DOI] [PubMed] [Google Scholar]
  • 7.Stöhr J, Barbaresko J, Neuenschwander M, Schlesinger S. Bidirectional association between periodontal disease and diabetes mellitus: a systematic review and meta-analysis of cohort studies. Sci Rep. 2021;11(1):13686. 10.1038/s41598-021-93062-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Sumayin Ngamdu K, Mallawaarachchi I, Dunipace EA, Chuang LH, Jafri SH, Shah NR, Jeong YN, Morrison AR, Bhatt DL. Association between periodontal disease and cardiovascular disease (from the NHANES). Am J Cardiol. 2022;178:163–8. 10.1016/j.amjcard.2022.05.028. [DOI] [PubMed] [Google Scholar]
  • 9.Zelig R, Goldstein S, Touger-Decker R, Firestone E, Golden A, Johnson Z, Kaseta A, Sackey J, Tomesko J, Parrott JS. Tooth Loss and Nutritional Status in Older Adults: A Systematic Review and Meta-analysis. JDR Clin Trans Res. 2022;7(1):4–15. 10.1177/2380084420981016. [DOI] [PubMed]
  • 10.Xu X, Zhao Y, Wu B, Pei Y, Gu D. Association between tooth loss and frailty among Chinese older adults: the mediating role of dietary diversity. BMC Geriatr. 2023;23(1):668. 10.1186/s12877-023-04355-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Genco RJ, Graziani F, Hasturk H. Effects of periodontal disease on glycemic control, complications, and incidence of diabetes mellitus. Periodontol 2000. 2020;83(1):59–65. 10.1111/prd.12271. [DOI] [PubMed] [Google Scholar]
  • 12.Sanz M, Marco Del Castillo A, Jepsen S, Gonzalez-Juanatey JR, D'Aiuto F, Bouchard P, Chapple I, Dietrich T, Gotsman I, Graziani F, et al. Periodontitis and cardiovascular diseases: Consensus report. J Clin Periodontol. 2020;47(3):268–88. 10.1111/jcpe.13189. [DOI] [PMC free article] [PubMed]
  • 13.Kobayashi Y, Niu K, Guan L, Momma H, Guo H, Cui Y, Nagatomi R. Oral health behavior and metabolic syndrome and its components in adults. J Dent Res. 2012;91(5):479–84. 10.1177/0022034512440707. [DOI] [PubMed] [Google Scholar]
  • 14.Su L, Liu W, Xie B, Dou L, Sun J, Wan W, Fu X, Li G, Huang J, Xu L. Toothbrushing, blood glucose and HbA1c: findings from a random survey in Chinese population. Sci Rep. 2016;6:28824. 10.1038/srep28824. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Tanaka A, Takeuchi K, Furuta M, Takeshita T, Suma S, Shinagawa T, Shimazaki Y, Yamashita Y. Relationship of toothbrushing to metabolic syndrome in middle-aged adults. J Clin Periodontol. 2018;45(5):538–47. 10.1111/jcpe.12876. [DOI] [PubMed]
  • 16.Kim JY, Park YM, Lee GN, Song HC, Ahn YB, Han K, Ko SH. Association between toothbrushing and non-alcoholic fatty liver disease. PLoS One. 2021;16(5):e0243686. 10.1371/journal.pone.0243686. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Wiener RC, Bhandari R, Trickett Shockey AK, Waters C. Dental care utilization among veterans by smoking status. Int J Dent. 2019;2019:3419805. 10.1155/2019/3419805. [DOI] [PMC free article] [PubMed]
  • 18.Fernandez de Grado G, Ehlinger V, Godeau E, Arnaud C, Nabet C, Benkirane-Jessel N, Musset AM, Offner D. Changes in tooth brushing frequency and its associated factors from 2006 to 2014 among French adolescents: results from three repeated cross sectional HBSC studies. PLoS One. 2021;16(3):e0249129. 10.1371/journal.pone.0249129. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Centis E, Marzocchi R, Di Domizio S, Ciaravella MF, Marchesini G. The effect of lifestyle changes in non-alcoholic fatty liver disease. Dig Dis. 2010;28(1):267–73. 10.1159/000282101. [DOI] [PubMed] [Google Scholar]
  • 20.Rus M, Crisan S, Andronie-Cioara FL, Indries M, Marian P, Pobirci OL, Ardelean AI. Prevalence and risk factors of metabolic syndrome: a prospective study on cardiovascular health. Medicina (Kaunas). 2023;59(10). 10.3390/medicina59101711. [DOI] [PMC free article] [PubMed]
  • 21.Hernán MA, Robins J. Causal inference: what if. Boca Raton: Chapman, Hall/CRC; 2020. [Google Scholar]
  • 22.Jordão LMR, Malta DC, Freire M. Clustering patterns of oral and general health-risk behaviours in Brazilian adolescents: findings from a national survey. Community Dent Oral Epidemiol. 2018;46(2):194–202. 10.1111/cdoe.12354. [DOI] [PubMed] [Google Scholar]
  • 23.Harada S, Akhter R, Kurita K, Mori M, Hoshikoshi M, Tamashiro H, Morita M. Relationships between lifestyle and dental health behaviors in a rural population in Japan. Community Dent Oral Epidemiol. 2005;33(1):17–24. 10.1111/j.1600-0528.2004.00189.x. [DOI] [PubMed]
  • 24.Virtanen JI, Muikku T, Similä T, Cinar AB, Pohjola V. Physical activity, BMI and oral health behaviour among adolescents: Finnish school health promotion study. Eur J Public Health. 2019;29(2):296–302. 10.1093/eurpub/cky193. [DOI] [PubMed] [Google Scholar]
  • 25.Drisko CL. Periodontal self-care: evidence-based support. Periodontol 2000. 2013;62(1):243–55. 10.1111/prd.12012. [DOI] [PubMed] [Google Scholar]
  • 26.Esfanjani MT, Gilani N, Esfanjani AT, Nourizadeh AM, Faramarzi E, Hekmatfar S. Are oral health behaviors associated with metabolic syndrome in the Azar cohort population? BMC Oral Health. 2023;23(1):370. 10.1186/s12903-023-03003-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Matsuzawa Y. Metabolic syndrome–definition and diagnostic criteria in Japan. J Atheroscler Thromb. 2005;12(6):301. 10.5551/jat.12.301. [DOI] [PubMed] [Google Scholar]
  • 28.Ministry of Health, Labour and Welfare. Standard health examination and health guidance program (2024 version). 2024. https://www.mhlw.go.jp/stf/seisakunitsuite/bunya/0000194155_00004.html. Accessed 3 Mar 2025.
  • 29.World Health Organization. Oral health surveys, basic methods. 4th ed. Geneva: World Health Organization; 1997. [Google Scholar]
  • 30.Stormacq C, Van den Broucke S, Wosinski J. Does health literacy mediate the relationship between socioeconomic status and health disparities? Integrative review. Health Promot Int. 2019;34(5):e1–17. 10.1093/heapro/day062. [DOI] [PubMed] [Google Scholar]
  • 31.Peres MA, Macpherson LMD, Weyant RJ, Daly B, Venturelli R, Mathur MR, Listl S, Celeste RK, Guarnizo-Herreño CC, Kearns C, et al. Oral diseases: a global public health challenge. Lancet. 2019;394(10194):249–60. 10.1016/s0140-6736(19)31146-8. [DOI] [PubMed] [Google Scholar]
  • 32.Kim YH, Kim DH, Lim KS, Ko BJ, Han BD, Nam GE, Park YG, Han KD, Kim JH, Cho KH. Oral health behaviors and metabolic syndrome: the 2008–2010 Korean National Health and Nutrition Examination Survey. Clin Oral Investig. 2014;18(5):1517–24. 10.1007/s00784-013-1112-2. [DOI] [PubMed] [Google Scholar]
  • 33.Hirano K, Shimbo T, Komatsu Y, Kobayashi D. Frequency of tooth brushing as a predictive factor for future kidney function decline. J Nephrol. 2022;35(1):191–9. 10.1007/s40620-021-00987-2. [DOI] [PubMed] [Google Scholar]
  • 34.Głąbska D, Guzek D, Groele B, Gutkowska K. Fruit and vegetable intake and mental health in adults: a systematic review. Nutrients. 2020;12(1). 10.3390/nu12010115. [DOI] [PMC free article] [PubMed]
  • 35.Bektas İ, Kudubeş AA, Ayar D, Bektas M. Predicting the healthy lifestyle behaviors of Turkish adolescents based on their health literacy and self-efficacy levels. J Pediatr Nurs. 2021;59:e20–5. 10.1016/j.pedn.2021.01.016. [DOI] [PubMed] [Google Scholar]
  • 36.Wittmann FG, Pabst A, Zülke A, Luppa M, Oey A, Boekholt M, Weise S, Fankhänel T, Kosilek RP, Brettschneider C, et al. Adherence to a lifestyle intervention - just a question of self-efficacy? Analysis of the AgeWell.de-intervention against cognitive decline. Alzheimers Res Ther. 2024;16(1):133. 10.1186/s13195-024-01499-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Niu M, Chen J, Hou R, Sun Y, Xiao Q, Pan X, Zhu X. Emerging healthy lifestyle factors and all-cause mortality among people with metabolic syndrome and metabolic syndrome-like characteristics in NHANES. J Transl Med. 2023;21(1):239. 10.1186/s12967-023-04062-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Allen F, Fan SY, Loke WM, Na TM, Keng Yan GL, Mittal R. The relationship between self-efficacy and oral health status of older adults. J Dent. 2022;122:104085. 10.1016/j.jdent.2022.104085. [DOI] [PubMed] [Google Scholar]
  • 39.Saito M, Shimazaki Y, Yoshii S, Takeyama H. Periodontitis and the incidence of metabolic syndrome: an 8-year longitudinal study of an adult Japanese cohort. J Clin Periodontol. 2024;51(1):54–62. 10.1111/jcpe.13881. [DOI] [PubMed] [Google Scholar]
  • 40.Hajishengallis G, Chavakis T. Local and systemic mechanisms linking periodontal disease and inflammatory comorbidities. Nat Rev Immunol. 2021;21(7):426–40. 10.1038/s41577-020-00488-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Sasco AJ, Secretan MB, Straif K. Tobacco smoking and cancer: a brief review of recent epidemiological evidence. Lung Cancer. 2004;45 Suppl 2:S3–9. 10.1016/j.lungcan.2004.07.998. [DOI] [PubMed] [Google Scholar]
  • 42.Christenson SA, Smith BM, Bafadhel M, Putcha N. Chronic obstructive pulmonary disease. Lancet. 2022;399(10342):2227–42. 10.1016/s0140-6736(22)00470-6. [DOI] [PubMed] [Google Scholar]
  • 43.Oshunbade AA, Yimer WK, Valle KA, Clark D 3rd, Kamimura D, White WB, DeFilippis AP, Blaha MJ, Benjamin EJ, O’Brien EC, et al. Cigarette smoking and incident stroke in Blacks of the Jackson Heart Study. J Am Heart Assoc. 2020;9(12):e014990. 10.1161/jaha.119.014990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Seeley RJ, Sandoval DA. Neuroscience: weight loss through smoking. Nature. 2011;475(7355):176–7. 10.1038/475176a. [DOI] [PubMed]
  • 45.Klatsky AL. Alcohol and cardiovascular diseases: where do we stand today? J Intern Med. 2015;278(3):238–50. 10.1111/joim.12390. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The data that support the findings of this study are available from the Aichi Health Promotion Foundation, but restrictions apply to the availability of these data, which were used under license for the current study, and so are not publicly available. Data are however available from the authors upon reasonable request and with permission of the Aichi Health Promotion Foundation.


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