Abstract
Background
Mouth breathing (MB) and incompetent lip seal (ILS) are common oral dysfunctions with potential repercussions for dentofacial development, systemic health, and psychological well-being. Although related, MB and ILS represent distinct conditions: ILS denotes difficulty maintaining lip closure at rest, whereas MB concerns the route of respiration. Despite growing recognition of their physical impacts, few studies have examined how MB and ILS are related to psychological stress in young adults.
Methods
A cross-sectional study was conducted among 567 Japanese university students aged 18–27 years using a self-administered questionnaire. The survey included 53 items on oral conditions, lifestyle habits, and nasal symptoms, and 29 items from Section B of the Brief Job Stress Questionnaire to assess psychological stress. Exploratory factor analysis (EFA) was used to identify latent constructs. Extreme Gradient Boosting (XGBoost) was applied to classify high-stress individuals and highlight important predictors, while direct and indirect associations among ILS, MB, nasal disease, and stress were examined using structural equation modeling (SEM).
Results
EFA extracted five latent factors: nasal disease, ILS and MB, oral hygiene and bad breath, condition of the teeth and gums, and lip dryness. XGBoost achieved moderate predictive performance (accuracy = 0.69, F1 = 0.74), with top predictors corresponding to ILS- and MB-related items (“Do you sleep with your mouth open?” and “Is your mouth often open during the day?”). SEM indicated that nasal disease had a direct association with stress, whereas ILS and MB indirectly influenced stress through oral symptoms such as lip dryness and bad breath. Lip dryness also showed a direct path to stress, suggesting its dual role as both a symptom and a potential stressor.
Conclusion
ILS and MB are associated with higher stress levels in young adults primarily through indirect pathways involving oral discomfort. Lip dryness may mediate this relationship. Their partial independence from nasal disease supports the view that ILS and MB are distinct but interrelated conditions. These findings highlight the need for early screening and integrated management of oral and nasal function to promote psychological well-being.
Supplementary Information
The online version contains supplementary material available at https://doi.org/10.1186/s12903-026-08030-1.
Keywords: Incompetent lip seal, Mouth breathing, Stress, Young adults, Oral function, Nasal disease, Structural equation modeling, Machine learning, AI (artificial intelligence)
Introduction and background
In recent years, increasing attention has been paid to the effects of mouth breathing (MB) and an incompetent lip seal (ILS) on oral function and overall health [1–15]. MB and ILS are common oral dysfunctions that can adversely affect dentofacial development and overall well-being. In this study, MB is defined as habitual airflow predominantly through the mouth at rest or during sleep and ILS as the inability to maintain a relaxed, closed-lip posture at rest without perioral muscle strain. Although related, MB and ILS are distinct: ILS refers to resting lip competence, whereas MB is related to the route of breathing. They often co-occur but are not necessarily present simultaneously. Clarifying these constructs is essential for accurately interpreting their health associations.
Previous studies have shown that MB and ILS can negatively affect various oral health domains, including malocclusion [1, 5], periodontal disease [6], and dental caries [7], as well as systemic outcomes such as sleep-disordered breathing and poor sleep quality [8, 9], aggravated allergic symptoms [10], and impaired physical development [11, 12]. Studies from the 1990s and 2000s first identified the local oral consequences of MB, such as gingival inflammation and open-bite malocclusion [4, 6]. Subsequent investigations expanded this view to include systemic and developmental effects in children [1, 5]. More recent systematic reviews have synthesized these findings, highlighting that mouth breathing and an incompetent lip seal can influence not only craniofacial morphology but also psychosocial and behavioral outcomes [3, 16]. These developments illustrate the growing recognition that oral dysfunctions have multifactorial impacts extending beyond the oral cavity.
While traditional research into oral health has focused on physical and functional issues, such as mastication, speech, and pain [1, 2], the psychological and emotional consequences of oral dysfunction remain underexplored. In Japan, Developmental Insufficiency of Oral Function (DIOF) has recently gained formal recognition as a pediatric diagnostic framework encompassing screening, assessment, and management of oral dysfunctions—including ILS and MB—within clinical and public-health practice [15]. This context underscores growing attention to MB/ILS as targets for screening and early preventive care, and motivates studying their relevance beyond childhood into young adulthood. Our previous studies examined how ILS and MB affect children’s oral and systemic health, contributing to the formal recognition of DIOF and the development of assessment tools, such as lip-closure strength tests [11–14]. These investigations have laid the groundwork for exploring how oral dysfunction influences mental well-being and oral-health-related quality of life (OHRQoL) in later developmental stages.
However, compared with functional and morphological outcomes, fewer epidemiological studies have evaluated how ILS and MB relate to psychological stress, a key dimension of OHRQoL. Importantly, a recent meta-analysis demonstrated that chronic sleep loss can significantly impair emotional regulation and increase vulnerability to stress and mood disturbances [17]. Thomson et al. reported an association between emotionality and OHRQoL [18]. Recent literature has also highlighted a bidirectional relationship between stress and oral health—psychological distress may exacerbate oral symptoms (e.g., dryness, discomfort), while symptomatic oral states may, in turn, increase perceived stress [16, 19]. However, large-sample, quantitative examinations of whether MB and ILS are associated—directly or indirectly—with stress in young adults remain limited. Consequently, despite heightened attention to these issues due to the establishment of DIOF [15], existing research still lacks comprehensive analyses of how MB and ILS directly affect stress and OHRQoL in adults who have completed their growth phase.
This study aimed to clarify the structural relationships between ILS, MB, oral symptoms, nasal disease, and psychological stress in a sample of young adults. Exploratory factor analysis (EFA) was used to identify latent constructs, Extreme Gradient Boosting (XGBoost) to highlight features related to higher stress, and structural equation modeling (SEM) to test direct and indirect associations—particularly whether MB and ILS are related to stress via oral symptoms such as lip dryness and bad breath. Throughout, we avoid causal claims and interpret the paths as associations consistent with the cross-sectional design.
Materials and methods
Study design
This was a cross-sectional study investigating the associations among ILS, MB, nasal disease, and psychological stress in young Japanese adults.
Participants and data collection
A total of 567 Japanese university students aged 18–27 years (302 male and 265 female) participated in the study. Participants were recruited through university mailing lists and online announcements at two institutions: a women’s junior college in Gifu Prefecture and a university in Tokyo. After excluding incomplete or inconsistent responses, 567 valid datasets were analyzed. Data were collected between 2020 and 2022, during the COVID-19 pandemic. All participants were therefore described as “healthy,” meaning that they did not report any chronic or acute illness and were attending regular university activities without medical restrictions. The survey was anonymous and self-administered, covering items on oral conditions, lifestyle habits, nasal symptoms, and stress. All participants completed an anonymous online questionnaire (Google Forms) after reading an electronic consent statement describing the study purpose, details about voluntary participation, and data handling procedures. Only those who provided informed consent could access the questionnaire.
The self-administered questionnaire consisted of 10 items on medical history and 43 items assessing oral health status, lifestyle habits, and nasal symptoms (53 items total). These items were adapted from previously published large-scale surveys of oral function in Japanese children and adolescents [11–14]—only the wording was modified from caregivers reporting on their child’s behaviors (e.g., “Is your child…?”) to participants reporting on themselves (e.g., “Are you…?” or “Do you…?”) while preserving the original content and intent of each question. By applying the same items to participants aged 18–27 years, we aimed to explore whether ILS and MB persist into young adulthood, thereby informing the potential need for early intervention. Although formal psychometric validation has not yet been conducted, content validity was supported by referencing prior research and through expert consensus within the study team. The complete English wording of all 53 items is provided in Table 1 and Supplementary File 1.
Table 1.
Questionnaire items on systemic disease history, oral conditions, lifestyle habits, and nasal symptoms
| Item no. | Question item |
|---|---|
| Medical history of systemic diseases | |
| Q1 | Have you ever been diagnosed with asthma? |
| Q2 | Have you ever been diagnosed with atopic dermatitis? |
| Q3 | Have you ever been diagnosed with allergic rhinitis? |
| Q4 | Have you ever been diagnosed with adenoid hypertrophy? |
| Q5 | Have you ever been diagnosed with bronchitis? |
| Q6 | Have you ever been diagnosed with otitis media? |
| Q7 | Have you ever been diagnosed with hay fever? |
| Q8 | Do you catch a cold more than twice a year? |
| Q9 | Do you have a fever over 38 °C more than twice a year? |
| Q10 | Do you get swollen tonsils more than twice a year? |
| Lifestyle habits and oral status | |
| Q11 | Do you get tired easily? |
| Q12 | Are you a good riser? |
| Q13 | Are you good at exercising? |
| Q14 | Are you a restless sleeper? |
| Q15 | Do you have round shoulders? |
| Q16 | Does your nose become stuffed easily during the day? |
| Q17 | Does your nose become stuffed easily while sleeping? |
| Q18 | Do you sneeze often? |
| Q19 | Do you often have a runny nose? |
| Q20 | Do you often have a nosebleed? |
| Q21 | Do you often have a sore throat? |
| Q22 | Do you often fail to listen? |
| Q23 | Are you a habitual snorer? |
| Q24 | Is your mouth often dry? |
| Q25 | Do people tell you that you have bad breath in the morning? |
| Q26 | Do people tell you that you have bad breath during day? |
| Q27 | Is your mouth often open during the day? |
| Q28 | Do you sleep with your mouth open? |
| Q29 | Can you keep your mouth closed for about 1 min? |
| Q30 | Do you have an overbite? |
| Q31 | Do you have an underbite? |
| Q32 | Do you have an anterior open bite? |
| Q33 | Can you speak clearly? |
| Q34 | Are your lips often chapped? |
| Q35 | Are your lips thick? |
| Q36 | Is your upper lip turned upward? |
| Q37 | Are your teeth visible between your upper and lower lips? |
| Q38 | Are your lips droopy? |
| Q39 | Are your lips often cracked? |
| Q40 | Are your gums often swollen? |
| Q41 | Are your gums easily stained? |
| Q42 | Are your teeth easily stained? |
| Q43 | Do you often have canker sores? |
| Q44 | Do you have tartar build-up? |
| Q45 | Do your meals consist of small servings? |
| Q46 | Do you prefer soft food? |
| Q47 | Do you drink water during meals? |
| Q48 | Do you eat fast? |
| Q49 | Are you a picky eater? |
| Q50 | Do you chew food well? |
| Q51 | Are you a noisy eater? |
| Q52 | Do you keep your mouth closed when you eat? |
| Q53 | Do you have food left in your mouth for a long time? |
This self-administered questionnaire included 10 items on the medical history of systemic diseases and 43 items on lifestyle habits, oral condition, and nasal symptoms
Items Q1–Q10 were rated on a two-point scale (yes/no), while Q11–Q53 were rated on a four-point scale (yes, maybe yes, maybe no, no)
Items related to medical history were recorded on a two-point scale (yes/no), whereas oral health, lifestyle, and nasal symptoms were rated on a four-point scale: yes, maybe yes, maybe no, and no). All participants provided informed consent before participation. The first page of the Google Form included an explanation of the study as well as an informed consent statement. The study was conducted in accordance with the Declaration of Helsinki. Participants who agreed were permitted to access and complete the questionnaires. This study was approved by the Ethics Review Committee of the Ogaki Women’s Junior College (approval no. R2-2) and the Institute of Science Tokyo (Approval No. 2024307).
Stress assessment
Psychological and physical stress reactions were assessed using Section B of the English version of the new Brief Job Stress Questionnaire (BJSQ) developed by Japan’s Ministry of Health, Labour and Welfare [20, 21]. Section B comprises 29 items covering five psychological domains (vigor, anger/irritability, fatigue, anxiety, and depression) and one physical domain (somatic complaints) (Table 2).
Table 2.
Items from Section B of the Brief Job Stress Questionnaire (BJSQ) and their subscales
| Question item | Scale | |
|---|---|---|
| Q1 | I have been very active | Vigor (reverse scored) |
| Q2 | I have been full of energy | Vigor (reverse scored) |
| Q3 | I have been lively | Vigor (reverse scored) |
| Q4 | I have felt angry | Anger/irritability |
| Q5 | I have been inwardly annoyed or aggravated | Anger/irritability |
| Q6 | I have felt irritable | Anger/irritability |
| Q7 | I have felt extremely tired | Fatigue |
| Q8 | I have felt exhausted | Fatigue |
| Q9 | I have felt weary or listless | Fatigue |
| Q10 | I have felt tense | Anxiety |
| Q11 | I have felt worried or insecure | Anxiety |
| Q12 | I have felt restless | Anxiety |
| Q13 | I have been depressed | Depression |
| Q14 | I have thought that doing anything was a hassle | Depression |
| Q15 | I have been unable to concentrate | Depression |
| Q16 | I have felt gloomy | Depression |
| Q17 | I have been unable to handle work | Depression |
| Q18 | I have felt sad | Depression |
| Q19 | I have felt dizzy | Physical Stress Reaction (Somatic complaints) |
| Q20 | I have experienced joint pains | Physical Stress Reaction (Somatic complaints) |
| Q21 | I have experienced headaches | Physical Stress Reaction (Somatic complaints) |
| Q22 | I have had a stiff neck and/or shoulders | Physical Stress Reaction (Somatic complaints) |
| Q23 | I have had lower back pain | Physical Stress Reaction (Somatic complaints) |
| Q24 | I have had eyestrain | Physical Stress Reaction (Somatic complaints) |
| Q25 | I have experienced heart palpitations or shortness of breath | Physical Stress Reaction (Somatic complaints) |
| Q26 | I have experienced stomach and/or intestinal problems | Physical Stress Reaction (Somatic complaints) |
| Q27 | I have lost my appetite | Physical Stress Reaction (Somatic complaints) |
| Q28 | I have experienced diarrhea and/or constipation | Physical Stress Reaction (Somatic complaints) |
| Q29 | I haven’t been able to sleep well | Physical Stress Reaction (Somatic complaints) |
Items were categorized based on the original structure of the Brief Job Stress Questionnaire (BJSQ), following the official classification of stress responses recommended by the Ministry of Health, Labour and Welfare of Japan [16, 22]
Psychological Stress Response (Positive): Vigor (Items 1–3; reverse scored)
Psychological Stress Response (Negative): Anger/Irritability (Items 4–6), Fatigue (Items 7–9), Anxiety (Items 10–12), Depression (Items 13–18)
Physical Stress Response: Somatic complaints (Items 19–29)
This classification also aligns with common international frameworks for stress and mental health research (e.g., emotional reactions, fatigue, somatic complaints)
Vigor (Items 1–3) was reverse scored so that higher scores indicate greater stress, aligning the direction of scoring with the other negative stress response items
This procedure is consistent with the original scoring method of the BJSQ, in which high vigor represents low stress
Participants rated each item on a four-point Likert scale (1 = strongly disagree to 4 = strongly agree). The Vigor subscale (items 1–3) was reverse scored so that higher total scores uniformly reflected higher stress levels. This procedure aligns with the BJSQ’s original scoring guidelines, which define high vigor as low stress and therefore requires reversal when computing the total stress level.
The composite stress score was used as a continuous variable in SEM. For the machine learning analysis using XGBoost, the score was binarized at the median to classify the participants into high-stress (1) and low-stress (0) groups. This unified treatment of the total score is consistent with previous applications of the BJSQ and reflects its intended use as a comprehensive indicator of stress.
Statistical analysis
Exploratory factor analysis
EFA was conducted on 43 questionnaire items related to oral symptoms, lifestyle habits, and nasal conditions to extract latent variables. The maximum likelihood method with a promax rotation was used. The number of factors was determined according to the Kaiser-Guttman criterion (eigenvalues > 1) and scree plot inspection. Items with loadings exceeding 0.40 were retained. Factor structures were used to inform the subsequent SEM. The sample size (n = 567) exceeded the recommended minimum for factor analysis (10 participants per item).
Machine learning: XGBoost
To identify the predictors of high stress, an XGBoost classification model (XGBClassifier, random_state = 42) was developed. The input variables included all the questionnaire items. The dataset was randomly divided into training (80%) and testing (20%) subsets.
Hyperparameters, such as n_estimators, max_depth, and learning_rate, were optimized using a grid search with 3-fold cross-validation. The model performance was evaluated using precision, recall, F1-score, and feature importance. The results were reported for both high- and low-stress classes.
Structural equation modeling
Based on the constructs identified by EFA and the key variables highlighted by XGBoost, an SEM was developed to evaluate the relationships between the latent variables (e.g., MB, ILS, nasal disease, and lip dryness) and psychological stress. The model included both direct and indirect paths. The model fit was evaluated using the following indices: Comparative Fit Index (CFI), Goodness of Fit Index (GFI), Adjusted Goodness of Fit Index (AGFI), Tucker-Lewis Index (TLI), Root Mean Square Error of Approximation (RMSEA), Akaike Information Criterion (AIC), and Bayesian Information Criterion (BIC). Statistical significance was set at p < 0.05.
Machine learning and SEM were performed using Python (version 3.12.6) in a Jupyter Notebook environment (version 7.3.2). The following libraries were used: pandas (version 2.1.1), numpy (version 1.25.2), scikit-learn (version 1.3.2), xgboost (version 3.0.0), and semopy (version 2.4.3). Differences were considered statistically significant in all analyses.
Results
Preliminary analysis: self-reported indicators of mouth breathing and incompetent lip seal
The mean age of the participants was 20.4 years (SD = 1.8). In this study, following previous research using pediatric and adolescent populations [11–14], we interpreted Question 27 (“Is your mouth often open during the day?”) as a self-reported indicator of ILS and MB. This approach is consistent with earlier studies that used this item to screen for ILS tendencies in large-scale surveys. From responses of “Yes” or “Maybe Yes,” 28.6% of participants were classified as having signs of ILS or MB (Fig. 1).
Fig. 1.

Self-reported frequency of mouth breathing and incompetent lip seal (ILS). Responses to the questionnaire item: “Is your mouth often open during the day?” representing participants' self-reports. Present indicates responses of “Yes” or “Maybe yes.”. Absent indicates responses of “No” or “Maybe no.”
Exploratory factor analysis
EFA extracted five latent factors from the 43 items: (1) nasal disease, (2) ILS and MB, (3) oral hygiene and bad breath, (4) condition of teeth and gums, and (5) lip dryness. Consequently, 23 of the 43 items were retained and classified into these five factors (Table 3). The Kaiser–Meyer–Olkin (KMO) measure was 0.792, and Bartlett’s test of sphericity yielded P < 0.001, confirming the adequacy of the sample for factor analysis. The cumulative contribution ratio was 49.7%. Items with factor loadings ≥ 0.40 were used to compute mean factor scores for subsequent analyses. These latent constructs were entered into the SEM as observed indicators.
Table 3.
Pattern matrix of the exploratory factor analysis
| Item no. | Factor 1 | Factor 2 | Factor 3 | Factor 4 | Factor 5 | |
|---|---|---|---|---|---|---|
| Question item | Disease of the nose | Incompetent lip seal Mouth breathing | Condition of teeth and gum | Bad breath | Lip Dryness | |
| Q16 | Does your nose become stuffed easily while sleeping? | 0.805 | ||||
| Q19 | Do you often have a nosebleed? | 0.790 | ||||
| Q17 | Do you sneeze often? | 0.732 | ||||
| Q18 | Do you often have a runny nose? | 0.674 | ||||
| Q37 | Are your teeth visible between your upper and lower lips? | 0.808 | ||||
| Q38 | Are your lips droopy? | 0.747 | ||||
| Q30 | Do you have an overbite? | 0.579 | ||||
| Q28 | Do you sleep with your mouth open? | 0.440 | ||||
| Q27 | Is your mouth often open during the day? | 0.407 | ||||
| Q42 | Are your teeth easily stained? | 0.646 | ||||
| Q44 | Do you have tartar build-up? | 0.596 | ||||
| Q40 | Are your gums often swollen? | 0.581 | ||||
| Q41 | Are your gums easily stained? | 0.454 | ||||
| Q26 | Do people tell you that you have bad breath during day? | 1.002 | ||||
| Q25 | Do people tell you that you have bad breath in the morning? | 0.626 | ||||
| Q34 | Are your lips often chapped? | 1.019 | ||||
| Q39 | Are your lips often cracked? | 0.419 |
Pattern matrix derived from exploratory factor analysis (EFA) using Promax rotation and maximum likelihood estimation
Items were grouped into five latent factors. Factor loadings > 0.4 were considered meaningful
Table 4 presents the factor correlation matrices. Factor 2 (ILS and MB) was the most strongly correlated with Factor 3 (r = 0.558), followed by Factors 5 (r = 0.349), 1 (r = 0.326), and 4 (r = 0.228). All correlation coefficients were statistically significant (p < 0.001).
Table 4.
Factor correlation matrix
| Factor 1 | Factor 2 | Factor 3 | Factor 4 | Factor 5 | |
|---|---|---|---|---|---|
| Disease of the nose | Incompetent lip seal/Mouth breathing | Condition of teeth and gums | Bad breath | Lip Dryness | |
| Factor 1 | 1 | 0.326*** | 0.367*** | 0.177*** | 0.284*** |
| Factor 2 | 1 | 0.558*** | 0.228*** | 0.349*** | |
| Factor 3 | 1 | 0.432*** | 0.410*** | ||
| Factor 4 | 1 | 0.197*** | |||
| Factor 5 | 1 |
***P < 0.001
Factor correlation matrix showing intercorrelations among the five latent constructs identified by EFA
All correlation coefficients are statistically significant (***p < 0.001)
Artificial intelligence-based machine learning: XGBoost
The XGBoost model classified the participants into high- and low-stress groups with an overall accuracy of 0.69. For the high-stress group, the model achieved a precision of 0.67, recall of 0.82, and F1-score of 0.74. For the low-stress group, precision was 0.76, recall was 0.59, and the F1-score was 0.66. These results indicate good predictive performance, particularly for identifying individuals at a high risk of stress. The detailed classification metrics are listed in Table 5.
Table 5.
Classification report of the XGBoost model
| Class | Precision | Recall | F1-score | Support |
|---|---|---|---|---|
| 0 (Low Stress) | 0.76 | 0.59 | 0.66 | 70 |
| 1 (High Stress) | 0.67 | 0.82 | 0.74 | 72 |
Performance metrics of the XGBoost classifier distinguishing high-stress and low-stress individuals
Precision, recall, F1-score, and support (sample size per class) are reported for each group
Among the top features contributing to the classification were “Is your mouth often open during the day?” (Q27), “Do you sleep with your mouth open?” (Q19), “Do you often have nasal congestion during sleep?” (Q7), and “Are your lips dry?” (Q40), all of which relate to ILS, MB, or associated nasal/oral symptoms.
These findings suggest that self-reported oral dryness, mouth opening, and poor sleep were common characteristics of students with higher stress levels. Although the predictive accuracy was moderate, it provides useful screening insight rather than clinical diagnostic precision, highlighting the potential for questionnaire-based identification of high-stress individuals.
Structural equation modeling
The final SEM model comprised three latent constructs—Nasal Disease (Q7, Q16), ILS/MB (Q25, Q37, Q44, Q52), and Lip Dryness (Q34, Q39)—and one observed variable (Stress level). The model showed an acceptable fit (Table 6). The final path diagram is shown in Fig. 2.
Table 6.
Fit indices for the final structural equation model (SEM), indicating good model fit
| Fit Index | Value |
|---|---|
| CFI (Comparative Fit Index) | 0.952 |
| GFI (Goodness of Fit Index) | 0.915 |
| AGFI (Adjusted Goodness of Fit Index) | 0.86 |
| NFI (Normed Fit Index) | 0.915 |
| TLI (Tucker-Lewis Index) | 0.921 |
| RMSEA (Root Mean Square Error of Approximation) | 0.045 |
| AIC (Akaike Information Criterion) | 45.835 |
| BIC (Bayesian Information Criterion) | 145.663 |
| LogLik (Log-Likelihood) | 0.082 |
Fig. 2.

Path diagram of the final structural equation model. Values on the arrows represent unstandardized regression coefficients (B) with corresponding P-values. ILS = Incompetent Lip Seal. Model fit indices for this model are presented in Table 6
The following significant structural paths were identified:
Nasal Disease → ILS/MB (B = 0.175, p = 0.01).
ILS/MB → Lip Dryness (B = 1.189, p < 0.001).
Lip Dryness → Stress Level (B = 3.506, p = 0.01).
Nasal Disease → Stress Level (B = 1.684, p = 0.05).
ILS/MB → Stress Level (B = 1.366, p = 0.04).
These results indicate that nasal disease exerts both direct and indirect effects on psychological stress.
The indirect pathway is mediated through ILS/MB and Lip Dryness, suggesting that oral dysfunctions may contribute to increased stress via both nasal and oral mechanisms. Notably, the item “Do you keep your mouth closed when you eat?” (Q52) showed a non-significant loading (p = 0.16), indicating a weak association with the ILS/MB construct in this model.
Discussion
Oral dysfunction and its link to stress
This study investigated the associations among ILS, MB, nasal disease, and psychological stress in young Japanese adults using a combined analytical approach of EFA, machine learning (XGBoost), and SEM. The SEM results revealed that nasal disease exerted both direct and indirect effects on psychological stress. Indirect effects were mediated through ILS/MB and lip dryness, indicating that oral dysfunctions may contribute to psychological burden via both nasal and oral pathways.
Although ILS/MB themselves were not directly linked to stress in the analyses, the structural model demonstrated that their impact operates primarily through oral symptoms such as lip dryness, tartar, and bad breath. These findings suggest that subjective oral discomfort serves as a key pathway connecting oral dysfunction to stress, consistent with previous studies reporting that oral dryness and nasal obstruction are associated with fatigue, irritability, and sleep disturbances [18, 19]. This highlights the importance of early recognition of oral symptoms even among healthy young adults. However, because of the cross-sectional nature of this study, causality cannot be inferred.
Integration of EFA, XGBoost, and SEM
A key methodological strength of this study was the integration of traditional psychometric and modern data-driven approaches. EFA summarized questionnaire items into interpretable latent constructs representing oral, nasal, and lifestyle domains, clarifying the internal structure of the data. XGBoost, a machine learning model capable of detecting nonlinear and interaction effects, supported the validity of the EFA-derived constructs by identifying top predictors—such as lip dryness, mouth opening, and sleep quality—that corresponded closely to the “oral symptom” and “MB/ILS” factors.
Furthermore, XGBoost highlighted individual items (e.g., sleep quality, bad breath) that were not dominant in the factor solution, suggesting that machine learning can complement EFA by detecting item-specific and nonlinear associations with stress. SEM then integrated these findings into a unified model, demonstrating direct and indirect pathways from nasal disease to stress via ILS/MB and lip dryness.
Although the classification performance of XGBoost was moderate (accuracy = 0.69, F1 = 0.74), these values are acceptable for exploratory behavioral research and provide supplementary evidence supporting the robustness of the SEM findings. From a clinical standpoint, the model’s ability to identify key behavioral indicators—such as habitual mouth opening and oral dryness—is considered meaningful. These behavioral indicators are observable in routine dental or pediatric examinations and may provide practical cues for early detection and intervention in stress-related oral dysfunction among young adults. This three-step approach—EFA for structure, XGBoost for feature relevance, and SEM for relational validation—provides a comprehensive framework applicable to other psychosomatic domains in dental and behavioral research.
Mediating role of oral symptoms
The mediating role of oral symptoms, particularly lip dryness, deserves special consideration. Lip dryness is known to reflect physiological mechanisms such as dehydration, increased oral airflow, and mucosal inflammation caused by habitual mouth opening [4, 7, 10]. These symptoms may increase self-perceived discomfort, thereby contributing to stress perception. Previous studies have also shown that psychological stress can itself exacerbate oral dryness, possibly through sympathetic activation or salivary-gland suppression [23, 24]. This bidirectional relationship may explain why oral symptoms are both consequences and mediators of stress. The indirect pathway observed in this study—Nasal Disease → ILS/MB → Lip Dryness → Stress—therefore highlights the importance of maintaining proper lip seal and nasal breathing to prevent secondary psychological strain. Our results are consistent with reports in children showing that MB and ILS are associated with emotional and behavioral problems [12–14, 25], suggesting that oral function and mental state are closely intertwined throughout development.
Comparison with previous research in children
Previous pediatric studies have demonstrated that MB and ILS are associated with oral dysfunctions such as malocclusion, gingival inflammation, and reduced salivary flow [5, 6, 13, 14]. Saitoh et al. [13] reported that children with habitual mouth opening had higher rates of oral dryness and irritability, while Inada et al. [12] found that preschool children with ILS exhibited lower lip-closure force and reduced oral moisture. These studies focused mainly on morphological or developmental aspects during childhood. The present study extends this line of research to young adults, a population in which such investigations are limited.
Our results suggest that, despite the completion of major craniofacial growth, functional habits such as MB and ILS may persist as behavioral tendencies, manifesting as subjective oral symptoms rather than overt structural changes. This continuity supports the notion that ILS and MB represent long-term behavioral patterns rather than transient developmental immaturities.
Moreover, studies in adults have reported associations between oral dryness and heightened psychological stress or poor sleep quality [9, 23, 24]. For example, Fujimoto et al. [23] observed that university students with MB reported higher perceived stress and fatigue, consistent with our finding that oral dryness mediated the link between MB/ILS and stress.
Compared with earlier pediatric research that primarily addressed dental morphology or airway obstruction, the present study provides novel evidence for psychophysiological mechanisms underlying oral dysfunction in adulthood. Collectively, these comparisons indicate that, although the mechanical consequences of MB/ILS (e.g., malocclusion) diminish with age, their psychological consequences—oral discomfort and stress vulnerability—may persist. This highlights the need for longitudinal approaches spanning from childhood to young adulthood to fully understand the developmental trajectory of oral dysfunction and its psychosocial correlates.
Interestingly, the items “Do you keep your mouth closed when you eat?” (Q52) and “Are you a noisy eater?” (Q51) showed non-significant loadings in both the factor analysis and SEM in the present study, and neither was associated with stress. In contrast, previous surveys in preschool and primary school children extracted “not closing the mouth while eating” as a key factor reflecting oral dysfunction [12, 13]. From a functional perspective, failure to close the mouth while eating should affect chewing efficiency and swallowing, often accompanied by noisy eating [12, 13]. The discrepancy between children and young adults may be explained by the difference in respondents—parents for children versus self-reports for adults. While parents are likely to notice such behaviors because they are visually apparent and socially concerning, young adults may not recognize them as functional issues. This difference suggests that behaviors that parents find worrisome in children may go unnoticed by individuals themselves in adulthood. Therefore, early parental recognition and intervention during childhood are essential for preventing persistent mouth-opening and noisy-eating habits into adulthood. Improvements in ILS and MB are generally achieved through orthodontic or behavioral interventions rather than occurring spontaneously [25]. This emphasizes the need for proactive management to prevent the persistence of these oral dysfunctions and their psychological impacts.
Methodological considerations and limitations
This study had several methodological advantages, including a large sample size (n = 567) suitable for both EFA and SEM, and the combined use of psychometric and data-driven analyses. However, several limitations should be acknowledged. First, because this was a cross-sectional study, causal relationships cannot be inferred. Second, all data were self-reported, and subjective judgments (e.g., self-assessment of ILS or MB) may not fully correspond to objective clinical measures. This self-report bias may have introduced misclassification errors, potentially attenuating true associations between oral dysfunction and stress. Third, the survey was conducted between 2020 and 2022 during the COVID-19 pandemic, and participants’ stress levels or oral behaviors may have been affected by social restrictions and prolonged mask wearing. Fourth, participants were recruited from two universities located in different regions (Tokyo and Gifu Prefecture); although many students lived independently in dormitories or apartments, regional and lifestyle differences may still have influenced stress perception or oral habits. Finally, the questionnaire was adapted from instruments validated in children [11–14] and has not yet undergone psychometric validation for young adults; confirmatory factor analysis and longitudinal reliability testing are warranted in future research.
Moreover, although the machine learning model demonstrated good classification performance, the lack of external validation using independent samples limited the robustness of the results. Future studies should incorporate external datasets to verify the predictive utility of this model. Furthermore, as the participants were university students, they may represent a socioeconomically advantaged segment of the young adult population, which could limit the generalizability of the findings to other demographic groups.
In addition, because the questionnaire relied on self-reported awareness, certain habitual or unconscious behaviors—such as resting mouth opening—may not have been fully captured. Unlike pediatric studies that commonly use caregiver- or clinician-reported observable behaviors, subjective self-assessment in young adults may lead to imprecision in measurement. This limitation could have attenuated factor loadings in the exploratory factor analysis and resulted in relatively conservative effect sizes in the structural equation model. Therefore, the observed associations should be interpreted with caution, and may not be generalizable to other populations. Future studies in young adults could complement subjective self-assessment with assessments of observable behaviors by healthcare providers. Comparison of subjective and objective assessments could then help confirm the validity of the scale.
Strengths
Despite these limitations, this study had several notable strengths. It is one of the few investigations to examine the relationships among ILS, MB, and psychological stress in young adults. By integrating EFA, SEM, and machine learning (XGBoost), this study provides a multidimensional understanding of how oral and nasal factors are linked to stress. This mixed-method design enhances both the credibility and interpretability of the findings. Moreover, the inclusion of a relatively large and demographically diverse sample improves the generalizability of the results across different student populations.
Implications for practice and research
These findings highlight the potential long-term effects of early oral dysfunctions on mental health. Recognizing the signs of ILS and MB during childhood may allow for earlier behavioral and clinical interventions, potentially mitigating psychological consequences later in life. This underscores the importance of interdisciplinary collaboration among dentists, pediatricians, and otolaryngologists to promote comprehensive oral–nasal health from a young age. Furthermore, longitudinal and interventional research is needed to examine whether improving oral function and breathing habits can contribute to better psychological well-being across the lifespan.
Conclusion
This study demonstrated that ILS and MB in young adults are significantly associated with higher psychological stress. This association occurs primarily through indirect pathways involving oral symptoms such as bad breath, tartar accumulation, and lip dryness. Nasal disease was independently associated with stress, whereas MB and ILS showed a strong direct path to lip dryness regardless of nasal obstruction. This reinforced the need to address these conditions as distinct clinical entities. These findings, confirmed through SEM with a good model fit, highlight the importance of early screening and comprehensive intervention strategies targeting both oral and nasal health. Preventive efforts during childhood may be particularly effective and may benefit from interdisciplinary collaboration among dentists, pediatricians, and otolaryngologists. Although this cross-sectional study did not allow for causal inferences, it offered valuable insights into the mechanisms linking oral dysfunction and mental health. Future longitudinal and interventional studies are warranted to explore these pathways over time and evaluate the effectiveness of early behavioral or clinical interventions.
Supplementary Information
Acknowledgements
We would like to thank Editage (www.editage.jp) for English language editing.
Abbreviations
- ILS
Incompetent Lip Seal
- MB
Mouth breathing
- BJSQ
Brief Job Stress Questionnaire
- SEM
Structural equation model
- DIOF
Developmental Insufficiency of Oral Function
- OHRQoL
Oral-health-related quality of life
- EFA
Exploratory Factor Analysis
- CFI
Comparative Fit Index
- GFI
Goodness of Fit Index
- AGFI
Adjusted Goodness of Fit Index
- TLI
Tucker-Lewis Index
- RMSEA
Root Mean Square Error of Approximation
- AIC
Akaike Information Criterion
- BIC
Bayesian Information Criterion
Authors’ contributions
Yasutaka Kaihara: Principal investigator, conceptualization, designing the study, writing the manuscript, data collection, statistical analyses. Mitsue Nagamine: Conceptualization, designing the study, data collection, statistical analyses, support for interpreting the results, support for writing the manuscript, supervising the project. Ryunosuke Hasegawa: Statistical analyses, support with interpreting the results, assistance in manuscript preparation. Emi Inada: Conceptualization, designing the study, support for interpreting the results, support for writing the manuscript. Yukiko Nogami: Conceptualization, support for interpreting the results, data checking, visualization, revising it critically for important intellectual content. Yuki Kiyokawa: Data checking, validation, support for interpreting the results, revising it critically for important intellectual content. Daisuke Murakami: Conceptualization, data checking, supervising the project, revising it critically for important intellectual content. Issei Saitoh: Conceptualization, data checking, supervising the project, revising it critically for important intellectual content.
Funding
This study was supported by the Japan Society for the Promotion of Science (JSPS) KAKENHI Grant Number 23K09430 (Grant-in-Aid for Scientific Research (C)), (Funding recipient: Yasutaka Kaihara).
Data availability
The datasets generated and/or analyzed during the current study are not publicly available because of ethical restrictions, but are available from the corresponding author on reasonable request. Aggregated summary tables (i.e., the descriptive and analytic tables presented in the main manuscript) and the full questionnaire are included in this published article and its supplementary information files.
Declarations
Ethics approval and consent to participate
The study was conducted in accordance with the Declaration of Helsinki. It was approved by the Ethics Review Committee of the Ogaki Women’s Junior College (approval no. R2-2) and the Institute of Science Tokyo (Approval No. 2024307). All participants provided informed consent before participation. The first page of the Google Form included an explanation of the study as well as an informed consent statement.
Consent for publication
Not Applicable.
Competing interests
The authors declare no competing interests.
Footnotes
The original online version of this article was revised: the Table 4 was corrected.
Publisher’s note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Change history
7/21/2026
The original online version of this article was revised: the Table 4 was corrected.
Change history
7/23/2026
A Correction to this paper has been published: https://doi.org/10.1186/s12903-026-09273-8
References
- 1.Harari D, Redlich M, Miri S, Hamud T, Gross M. The effect of mouth breathing versus nasal breathing on dentofacial and craniofacial development in orthodontic patients. Laryngoscope. 2010;120:2089–93. [DOI] [PubMed] [Google Scholar]
- 2.Jefferson Y. Mouth breathing: adverse effects on facial growth, health, academics, and behavior. Gen Dent. 2010;58:18–25. [PubMed] [Google Scholar]
- 3.Ziętek M, Dąbrowska E, Romańska J. Mouth breathing and its consequences in children—a literature review. Pediatr Rep. 2022;14:83–91. 10.3390/pediatric14010012. [DOI] [Google Scholar]
- 4.Abreu RR, Rocha RL, Lamounier JA, Guerra AFM. Etiology, clinical manifestations and concurrent findings in mouth-breathing children. J Pediatr (Rio J). 2008;84:529–35. 10.2223/JPED.1844. [DOI] [PubMed] [Google Scholar]
- 5.Jung MH, Yang WS, Nahm DS. Maximum closing force of mentolabial muscles and type of malocclusion. Angle Orthod. 2010;80:72–9. 10.2319/020509-78.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Wagaiyu EG, Ashley FP. Mouthbreathing, lip seal and upper lip coverage and their relationship with gingival inflammation in 11–14 year-old schoolchildren. J Clin Periodontol. 1991;18:698–702. 10.1111/j.1600-051x.1991.tb00112.x. [DOI] [PubMed] [Google Scholar]
- 7.Uehara S, Takahashi O, Wada T. Association between mouth breathing and caries prevalence in Japanese preschool children. J Clin Pediatr Dent. 2012;36:267–70. [Google Scholar]
- 8.Trosman I, Trosman SJ, Wang J. Sleep-disordered breathing in children with mouth breathing. J Clin Sleep Med. 2014;10:1005–6. [Google Scholar]
- 9.Lee SH, Kim BG, Chung YS. The association between poor sleep quality and mouth breathing: a population-based study. Sleep Med. 2017;30:45–50. 10.1016/j.sleep.2016.06.019.28215262 [DOI] [Google Scholar]
- 10.Izuhara Y, Matsumoto H, Nagasaki T, Kanemitsu Y, Murase K, Ito I, et al. Mouth breathing, another risk factor for asthma: the Nagahama Study. Allergy. 2016;71:1031–6. 10.1111/all.12885. [DOI] [PubMed] [Google Scholar]
- 11.Nogami Y, Saitoh I, Inada E, Murakami D, Iwase Y, Kubota N, et al. Prevalence of an incompetent lip seal during growth periods throughout Japan: a large-scale, survey-based, cross-sectional study. Environ Health Prev Med. 2021;26:11. 10.1186/s12199-021-00933-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Inada E, Saitoh I, Kaihara Y, Murakami D, Nogami Y, Kiyokawa Y, et al. Factors related to mouth breathing syndrome in preschool children and the effects of incompetent lip seal: an exploratory study. Clin Exp Dent Res. 2022;8:1555–60. 10.1002/cre2.661. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Saitoh I, Inada E, Kaihara Y, Nogami Y, Murakami D, Kubota N, et al. An exploratory study of the factors related to mouth breathing syndrome in primary school children. Arch Oral Biol. 2018;92:57–61. 10.1016/j.archoralbio.2018.03.012 [DOI] [PubMed]
- 14.Saitoh I, Inada E, Kaihara Y, Nogami Y, Murakami D, Kubota N, et al. An exploratory study of the factors related to mouth breathing syndrome in primary school children. Arch Oral Biol. 2018;92:57–61. 10.1016/j.archoralbio.2018.03.012. [DOI] [PubMed] [Google Scholar]
- 15.Saitoh I, Inada E, Kaihara Y, Nogami Y, Murakami D, Ishitani N, et al. The relationship between lip-closing strength and the related factors in a cross-sectional study. Pediatr Dent J. 2017;27:115–20. [Google Scholar]
- 16.Japanese Association for Dental Science. Basic approach to developmental insufficiency of oral function. 2024. https://www.jads.jp/assets/pdf/basic/r06/document-240402-2.pdf. Accessed 17 June 2024 [in Japanese].
- 17.Hensel ALJ, Nicholson K, Anderson KK, Gomaa NA. Biopsychosocial factors in oral and systemic diseases: a scoping review. Front Oral Health. 2024;5:1378467. 10.3389/froh.2024.1378467. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Tomaso CC, Johnson AB, Nelson TD The effect of sleep deprivation and restriction on mood, emotion, and emotion regulation: three meta-analyses in one. Sleep. 2021;44:zsaa289. 10.1093/sleep/zsaa289. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Thomson WM, Lawrence HP, Broadbent JM, Poulton R. The impact of xerostomia on Oral Health-related quality of life among younger adults. Health Qual Life Outcomes. 2006;4:86. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Asiri A, Nazir MA, Alsharief M, Shahin S, Al-Ansari A, Al-Khalifa KS Effect of psychological distress on oral health: a cross-sectional study. BMC Oral Health. 2024;24:Article. 10.1186/s12903-024-05319-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Ministry of Health, Labour and Welfare. The brief Job stress questionnaire. 2015. https://kokoro.mhlw.go.jp/etc/pdf/stress-check_80_e.pdf. Accessed 10 Jul 2025.
- 22.Ando E, Kawakami N, Shimazu A, Shimomitsu T, Odagiri Y. Reliability and validity of the English version of the New Brief Job Stress Questionnaire. Presented at the 31st International Conference on Occupational Health; 2015 May 31–June 5. Seoul, Korea.
- 23.Fujimoto A, Tanaka K, Umeda T, Yamamoto M, Adachi R, Sato M, et al. Relationship between mouth breathing and perceived stress among university students. J Oral Rehabil. 2018;45:790–7. 10.1111/joor.12679.29972243 [DOI] [Google Scholar]
- 24.Matsuo K, Kuroda M, Shima M, Hori A. The association between dry mouth and perceived stress in adolescents. Clin Oral Investig. 2020;24:1527–35. [Google Scholar]
- 25.Sato K, Fujiwara T, Okada A. Incompetent lip seal as a contributing factor to oral dysfunction in children and adolescents. Int J Pediatr Otorhinolaryngol. 2021;143:110692. [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
The datasets generated and/or analyzed during the current study are not publicly available because of ethical restrictions, but are available from the corresponding author on reasonable request. Aggregated summary tables (i.e., the descriptive and analytic tables presented in the main manuscript) and the full questionnaire are included in this published article and its supplementary information files.
