Next Article in Journal
COVID-19 Mortality Rate and Its Incidence in Latin America: Dependence on Demographic and Economic Variables
Next Article in Special Issue
Oral Functions Are Associated with Muscle Strength and Physical Performance in Old-Old Japanese
Previous Article in Journal
Effects of the Action for Neutralization of Bullying Program on Bullying in Spanish Schoolchildren
Previous Article in Special Issue
Association between Physical Frailty Subdomains and Oral Frailty in Community-Dwelling Older Adults
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Assessment of Age-Related Changes on Masticatory Function in a Population with Normal Dentition

1
Department of Dentistry, The Graduate School, Yonsei University, Seoul 03722, Korea
2
Department of Advanced General Dentistry, College of Dentistry, Dankook University, Cheonan 31116, Korea
3
Department of Advanced General Dentistry, College of Dentistry, Yonsei University, Seoul 03722, Korea
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2021, 18(13), 6899; https://0-doi-org.brum.beds.ac.uk/10.3390/ijerph18136899
Submission received: 27 May 2021 / Revised: 22 June 2021 / Accepted: 25 June 2021 / Published: 27 June 2021
(This article belongs to the Special Issue Oral Frailty and Oral Health Management)

Abstract

:
This study aimed to investigate the influence of changes in age-related physiological muscular and dental factors on masticatory function. This study was conducted in 211 healthy participants divided into four different age groups: 20–45 years (Gr1); 45–60 years (Gr2); 61–70 years (Gr3); and ≥71 years (Gr4). For objective evaluation of masticatory function, the masticatory performance, bite force, posterior bite area (PBA), functional tooth units (FTUs), the number of remaining teeth, tongue pressure, masseter muscle thickness (MMT), and handgrip strength were examined. Food intake ability (FIA) and the Oral Health Impact Profile-14 score were assessed subjectively using questionnaires. A significant decrease in the number of remaining teeth, FTUs, handgrip strength, and FIA was found in Gr4, and a significant decrease in the tongue pressure, PBA, and bite force was found in those aged ≥61 years. In groups 1 and 3, an association of the PBA with masticatory performance was observed. However, there was no significant decreasing trend in the MMT with respect to masticatory performance with aging. With sufficient FTUs and posterior tooth support, although age-dependent decreases in the bite force, tongue pressure and handgrip strength were observed, masticatory performance was maintained. Establishing the PBA by improving occlusion through dental treatment is thought to be important for masticatory function.

1. Introduction

It is commonly understood that muscle weakness occurring in the elderly population could reduce tongue pressure and lip motor function. Although tooth loss, which may be experienced during the life cycle, is a disease and pathological phenomenon, it is observed more frequently in older populations, and masticatory function is weakened sequentially due to aging [1].
Masticatory function can be representatively expressed in terms of masticatory performance and masticatory ability. The evaluation of masticatory function includes objective methods used to measure an individual’s capacity and subjective methods used to measure an individual’s response [2]. In the objective evaluation of masticatory function, factors including the number of remaining teeth, occlusal strength, and perioral muscles are considered as the indicators of static masticatory function. Meanwhile, as an organically linked dynamic process, mastication could be assessed as masticatory performance to measure mastication efficiency. Such methods used to evaluate masticatory performance include the sieving method to test comminution with natural [3] or artificial test food [4], the use of two-colored wax to test mixing [5], and the use of glucose gummies to test shearing [6]. Subjective evaluation of masticatory function is conducted using questionnaires asking about the kinds of chewable food or chewing ability [7]. The level of oral health-related satisfaction can be assessed by the oral health-related quality of life (OHRQoL) determined using the Oral Health Impact Profile (OHIP) questionnaire, which deals with self-perceived oral and general health [8].
Numerous previous studies regarding the dependence of masticatory performance on the dental status have demonstrated the following: First, dental factors influence masticatory function [2,9,10,11,12]. Second, the bite force and occluding area, which are influenced by the number of teeth and functional tooth units (FTUs), are correlated with masticatory performance [13]. Third, age per se has no influence on masticatory performance [14].
Recent studies have reported the relationship between masticatory function and the oral motor system. The amount of total muscle decreases by approximately 40% between the ages of 20 and 80 years; thus, people may experience a loss of functional motor units with advancing age [15]. In a study related to age-related changes in perioral muscle, it was demonstrated that tongue strength is positively related to handgrip strength [16]. A study based on 60 healthy young adults reported that the maximum tongue pressure influenced masticatory performance [17]. According to a study in more than 260 participants, including those who wore dentures, there was a significant correlation between masticatory performance and handgrip strength, while there was no correlation between masticatory performance and tongue pressure in elderly individuals with occlusal support [18]. Another study measured the self-assessed food intake ability (FIA) in 512 people who were ≥60 years old and reported a strong correlation between the dental status and subjective masticatory ability [19].
The relationship between the perioral muscle and masticatory function in terms of aging has been studied; however, the mechanism of action between the two has not yet been fully understood, since few studies have addressed both subjective and objective masticatory function. Therefore, it is necessary to conduct objective and subjective investigations simultaneously by considering the age-related physiological changes in not only dental factors but also perioral muscular factors.
It is hypothesized that both subjective and objective masticatory function decreases with the aging process of skeletal and muscular strength. The purpose of this study was to explore the differences between subjective and objective masticatory function in different age groups and to investigate the influence of changes in age-related physiological muscular and dental factors on masticatory function. As a cross-sectional study based on healthy dentate individuals, this study aimed to offer age-specific baseline data with clinical value for evaluating masticatory function.

2. Materials and Methods

2.1. Participants

This study was conducted in patients who visited the Department of Advanced General Dentistry at Yonsei University Dental Hospital between August 2020 and December 2020. Measurements were collected from 220 healthy and independent individuals, based on the calculation of sample size using G*power 3.1 software (Kiel University, Kiel, Germany) with α as 0.05, power as 0.8, and 0.25 of effect size [20,21]. Participants who were capable of independent social activities without any general illness and had at least 26 remaining teeth, including fixed dental prostheses, were selected for this study to minimize the influence of both the physical and dental status on the outcome of the masticatory function assessment. The exclusion criteria were as follows: a systemic disease, such as a disorder of saliva secretion or neuromuscular function; cognitive impairment; moderate to advanced periodontitis; or arch relationship with malocclusion or occlusal trauma. Of the 220 participants, nine individuals with incomplete data sets (6 participants from Gr 3 and 3 from Gr 4) were excluded. Finally, 211 volunteers who met the inclusion criteria for this study were divided into two major groups as adults (≤60 years) and elderly individuals (>60 years) and assigned to four different age groups, as follows: group 1, 20–45 years (n = 51; mean age: 32.1 ± 7.4); group 2, 46–60 years (n = 54; mean age: 53.5 ± 4.2); group 3, 61–70 years (n = 45; mean age: 66.2 ± 2.8); and group 4, 71 years or older (n = 61; mean age: 77.4 ± 5.2). Participants were recruited through voluntary registration and given informed consent for their participation.

2.2. Study Design

Mastication function was assessed through objective and subjective measurements. The objective assessment of masticatory function was performed by evaluating the dental status through an oral examination and study model analysis, as well as examining dynamic and static masticatory function by measuring masticatory performance and dental status indicators, such as the number of FTUs and remaining teeth, tongue pressure, bite force, posterior bite area (PBA), handgrip strength, tooth wear and masseter muscle thickness (MMT) (see Figure A1). For the subjective assessment of masticatory function, FIA and OHRQoL were investigated using questionnaires. The whole process of all assessments was conducted by one researcher. The entire research protocol was conducted under the approval by Institutional Review Board of Yonsei University Dental Hospital (Approval number: 2–2020-0047).

2.2.1. Objective Assessment

Dental Status

FTUs, the number of remaining teeth and tooth wear were examined. All participants belonged to Eichner index A, with four posterior support zones [22]. Tooth wear was determined by examining the tooth wear of the study model. When patterns of attrition, including facets, were observed in the region over one of the four quadrants, including (pre)molars. Tooth wear was coded as follows: tooth wear = 1; no tooth wear = 0. To prove intra-examiner reliability, the same examiner re-performed the assessment of tooth wear of 80 pairs of study models without referencing the prior data and the Cohen’s Kappa value was calculated as an excellent agreement (k = 0.822) [23]. FTUs were recorded by counting the number of occluding posterior tooth pairs. With the existence of a pair of opposing teeth in both the upper and lower arches, the molar area (excluding the 3rd molar) was recorded as 2 FTUs, and the premolar area was recorded as 1 FTU. Therefore, full dentition could also be indicated as 12 FTUs [9].

Masticatory Performance

Masticatory performance was determined by measuring the amount of dissolved glucose. For this test, a specifically designed 2 g-gummy containing dissolvable glucose (Gurucolum, GC, Tokyo, Japan) was used. The amount of dissolved glucose after the chewing exercise was measured using a specifically designed device (Glucosensor GS-2, GC, Tokyo, Japan), presenting the masticatory performance in numerical values. Participants were asked to chew the glucose-containing gummy for 20 s in their habitual chewing pattern, to rinse their mouth with 10 mL of purified water and to spit everything in their mouth, including the purified water, jelly, and saliva, onto a filter in a cup. The glucose-containing solution that was collected after filtering the comminuted jelly particles was mixed carefully with a brush and then coated onto the sensor chip. The value indicated by the measuring device was recorded.

Tongue Pressure

With regard to tongue pressure, although the forces applied during dynamic oral function for eating cannot be measured, the pressure loaded on the anterior region of the tongue has been used as an indicator of the tongue muscle strength with the consideration that it reflects the reserve capacity of the tongue [24]. The tongue pressure was measured using a probe (TPM-01, JMS, Hiroshima, Japan) consisting of a plastic catheter and a balloon. The participant was asked to sit on a chair, to hold the wing part of the probe connected to a balloon with his/her incisor teeth, to locate the balloon in the anterior palatal region, and to compress the balloon as powerfully as possible onto the palate for approximately 7 s. The measurement was repeated three times, and the mean value of the three records was used.

Bite Force and Occluding Bite Area

The bite force, which is the strength of force exerted from the coordination of the masticatory muscles and occluding teeth, was measured using a pressure-sensitive sheet (97 μm) [25]. The participant was asked to sit on a chair with the Frankfort horizontal plane parallel to the floor and the head in a relaxed state and to bite the sheet at the maximal inter-cuspal position with his/her maximum occlusal force for three seconds. The pressure measurement film was analyzed with a Bite force analyzer (Dental Prescale 50H, GC, Tokyo, Japan) [26,27]. In the analysis, the total bite force and the posterior and anterior occlusal contact areas were measured using Occluser 709 software (Occluser 709, GC, Tokyo, Japan).

Handgrip Strength

The handgrip strength has been used simply as an indicator of whole-body mass [28]. The participant was asked to stand up and to grab and squeeze the hand dynamometer (Takei handheld dynamometer, Japan) with his/her maximum power. The measurement was repeated three times for each hand, and the mean values were calculated and used.

Masseter Muscle Thickness (MMT)

The MMT is a useful index related to the strength of the masseter muscle [29], and it can be measured using an ultrasonic device. The values measured in the middle region during contraction of the left and right masseter muscles were used in this study, and the mean values of the measurements obtained from 3 points in the anterior, middle, and posterior regions of one cross-sectional image were used (Minisono, Alpinion, Anyang, Korea) [30]. Measurements were performed at the middle region, in which the outer fascia of the muscle and bony structure on the lateral side of the mandible are present, based on a report indicating that this site yields the best reproducibility [30,31].

2.2.2. Subjective Assessment

Food Intake Ability (FIA) Questionnaire (14 Items)

Masticatory ability was evaluated by asking the participants to complete a questionnaire listing 14 kinds of food ranging from soft and easy-to-chew food to hard food. Fourteen kinds of food included among the 30 kinds of food used in a previous study were included [25]. A five-point Likert scale was used, with a higher score indicating a better masticatory ability, as follows: 1 point (cannot chew at all); 2 points (difficult to chew); 3 points (cannot say either way); 4 points (can chew some); and 5 points (can chew well). (Figure 1).

OHIP-14

The OHIP questionnaire has been widely used as one of the most common questionnaires for evaluating self-satisfaction with OHRQoL. The OHIP-14 evaluates seven items, including functional limitation, pain, psychological discomfort, physical disability, psychological disability, social disability, and handicap, with a four-point Likert scale (0 = never, 1 = hardly ever, 2 = occasionally, 3 = fairly often, and 4 = very often). The lower the total score is, the better the OHRQoL [32].

2.3. Statistical Analysis

A normal data distribution for each variable in the age groups was confirmed using the Shapiro-Wilk test (see Table A1). One-way ANOVA and chi-square tests were used to investigate the significance of differences among age groups. The p for trends in masticatory function with increasing age was tested by simple linear regression or the Mantel-Haenszel chi-square test. Multiple comparisons were performed using Tukey’s test. Bivariate correlation coefficients were calculated to examine correlations among variables by Pearson’s correlation analysis. Multiple linear regression analysis was carried out to test the association of each explanatory variable with the outcome variable after controlling for the other variables. Variables associated with masticatory performance and FIA in the univariate analysis were chosen as independent variables for multivariate analysis (see Tables S1 and S2). A value of p < 0.05 was considered to indicate statistical significance. All data were analyzed using the statistical software R, version 4.0.4 (R Foundation for Statistical Computing, Vienna, Austria).

3. Results

3.1. Differences in Masticatory Function among Different Age Groups

The dental status and demographic characteristics of each age group are presented in Table 1. The results of the analysis of masticatory function for each age group are shown in Table 2. The number of remaining teeth (p = 0.007), FTUs (p < 0.001), PBA (p < 0.001), bite force (p < 0.001), tongue pressure (p < 0.001), and handgrip strength (p < 0.001) significantly decreased with increasing age. There were significant decreases in the number of remaining teeth (p = 0.007), FTUs (p < 0.001), and handgrip strength (p < 0.001) in group 4. Significant decreases in tongue pressure (p < 0.001), PBA (p < 0.001), and bite force (p < 0.001) were observed in group 3, reaching the lowest value in group 4. The number of patients without tooth wear was significantly higher among group 1 than among those in the other age groups. The MMT, anterior bite area (ABA) and OHIP-14 score showed no significant differences in any age group. Masticatory performance, which is an objective assessment of masticatory function, presented no significant intergroup differences with increasing age, while FIA, which is a subjective assessment of masticatory function, showed a significantly decreasing trend with increasing age, reaching the lowest value in group 4. (see Figure A2).

3.2. Bivariate Correlations with Variables

The level of correlation was interpreted based on the correlation coefficient, as follows: negligible (0–0.3); weak (0.3–0.5); moderate (0.5–0.7); strong (0.7–0.9); and very strong (≥0.9) [33]. In all age groups, a significant, strong positive correlation was found between the number of remaining teeth and FTUs (Gr1: r = 0.96, Gr2: r = 0.87, Gr3: r = 0.94, and Gr4: r = 0.89, p < 0.001, respectively) and between the PBA and bite force (Gr1: r = 0.73, Gr2: r = 0.96, Gr3: r = 0.93, and Gr4: r = 0.84, p < 0.001, respectively). In addition, a significant, weak to moderate positive correlation was found between the MMT and bite force (Gr1: r = 0.45, Gr2: r = 0.48, Gr3: r = 0.44, and Gr4: r = 0.56, p < 0.01, respectively), between the MMT and PBA (Gr1: r = 0.52, Gr2: r = 0.45, Gr3: r = 0.45, and Gr4: r = 0.53, p < 0.01, respectively), and between the handgrip strength and tongue pressure (Gr1: r = 0.56, Gr2: r = 0.43, Gr3: r = 0.53, and Gr4: r = 0.47 p < 0.01, respectively) in all age groups. The MMT and handgrip strength showed a decreasing correlation with increasing age (Gr1: r = 0.74, Gr2: r = 0.52, Gr3: r = 0.54, and Gr4: r = 0.43, p < 0.01, respectively), indicating a strong to weak correlation with significance. Only group 3 presented a significant, strong correlation (r = −0.8) of FIA with the OHIP-14 score, while the other groups showed a weak negative correlation with significance (Gr1: r = −0.45, Gr2: r = −0.42, and Gr4: r = −0.49, p < 0.01, respectively). A significant correlation of age with dental factors and muscle factors was only observed in group 4, and age and tongue pressure showed a significant, moderate negative correlation (r = −0.5, p < 0.01). (Table 3).

3.3. Multiple Linear Regression Analysis with Masticatory Performance

In groups 1 and 3, the PBA (Gr1 and Gr3: p = 0.044) was significantly associated with masticatory performance. In groups 2 and 4, however, no significant relationship was found between masticatory performance and any of the independent variables. The OHIP-14 score (p = 0.014) was also significantly associated with masticatory performance in group 1. (Table 4).

3.4. Multiple Linear Regression Analysis with Food Intake Ability

In all age groups, a significant association between FIA and the OHIP-14 score (p < 0.001, respectively) was observed. In addition, a significant relationship was found with FTUs (p = 0.002) in group 2 and with tongue pressure (p = 0.047) in group 3. (Table 5).

3.5. Stepwise Multiple Linear Regression Analysis with Handgrip Strength

In all age groups, tongue pressure (Gr1: p = 0.002, Gr2: p = 0.024, Gr3: p = 0.002, and Gr4: p < 0.001) was significantly associated with handgrip strength. Moreover, a significant relationship was observed with the MMT (Gr1: p < 0.001; Gr2 and Gr3: p = 0.001) in all age groups except group 4. (Table 6).

4. Discussion

In this study, the influence of oral motor system and dental factors on the masticatory function on the basis of aging were investigated and the difference between subjective and objective masticatory function in different age groups was explored. To our knowledge, this is the first study to address this subject.
A trend of significant decreases in tongue pressure (p < 0.001) and handgrip strength (p < 0.001) with aging was observed in this study. An obvious decrease in tongue pressure was found in groups 3 and 4, whereas an obvious decrease in handgrip strength was seen in group 4 compared with the other groups. A significant correlation between handgrip strength and tongue pressure in all age groups was found in this study (Gr1: r = 0.56, Gr2: r = 0.43, Gr3: r = 0.53, and Gr4: r = 0.47, p < 0.01, respectively). In group 4, a moderate correlation between age and tongue pressure (r = −0.5) and a weak correlation between age and handgrip strength (r = −0.31) were found. This is consistent with the results reported in previous studies. Human age-related muscle atrophy begins at approximately the age of 25 years and accelerates after approximately the age of 60 [34]. Likewise, in the tongue muscle, fatty infiltration and amyloid deposition increase with aging, resulting in a decrease in muscle fibers and ultimately a decrease in tongue pressure [28]. Hara et al. conducted age-specific research in 980 people, including denture wearers, and reported very similar patterns of reduction in tongue pressure and handgrip strength with aging in both sexes and more drastic reductions in the elderly group than in the adult group. Tongue pressure has been considered to be influenced by skeletal muscle mass and muscle power in adults [34]; hence, changes in perioral muscle, such as those indicated by changes in tongue pressure, could potentially be predicted using handgrip strength, which is easy to measure.
Some previous studies have reported tongue pressure as a significant factor in measuring masticatory performance [17,35]. Another study reported no association of tongue pressure with masticatory performance [18], which is consistent with the results of this study. Despite similarities in the dental status, the different results among these studies could be due to the different assessment methods and subject selection criteria. The present study adopted the assessment of shearing ability as a method for measuring masticatory performance. According to Yamada et al.’s study [36] on masticatory performance in young dentate adults, there was no significant correlation between shearing ability and tongue function, but masticatory performance assessed using shearing ability showed a significant correlation with both the occlusal force and occlusal contact area, which are results similar to those of the present study.
Meanwhile, a previous study on the relation between oral motor function and masticatory performance in elderly individuals highlighted the importance of tongue function in masticatory performance by using a color-changeable chewing gum to assess the masticatory performance [37]. Measurement of mixing ability assisted by tongue and lip function can allow a more efficient analysis of masticatory performance in elderly individuals with decreased tongue pressure and clarify the relationship between tongue pressure and masticatory performance.
The correlation between the handgrip strength and MMT decreased from strong (r = 0.736) in group 1 to weak (r = 0.425) in group 4, and no significant change was observed in the intergroup comparison of the MMT. This result is interpreted to indicate the value of the handgrip strength, which represents the decreasing strength of muscles in general with aging, while the MMT is maintained throughout life in subjects with normal dentition. If only considering the result of the Pearson correlation analysis, it might be concluded that the handgrip strength can be assessed instead of the force exerted by the oral musculature. As an additional analysis, multiple linear regression analysis with the handgrip strength indicated that the handgrip strength method could be substituted with the tongue pressure and MMT in subjects <71 years old (p < 0.001), whereas in group 4, it could be substituted with the tongue pressure (p < 0.001) but not the MMT.
The bite force was decreased (p < 0.001) with aging, and a significant decrease was found in those aged ≥61 years. The significant correlation between the MMT and bite force in all subjects (r = 0.456, p < 0.001) (see Table A2) is consistent with the result of a previous study reporting a significant association (r = 0.41, p < 0.001) between the cross-section of the masseter muscle and bite force. That study also reported the masseter muscular strength as a major contributing factor of bite force in adults [3]. One hypothesis in this study was that the bite force is positively related to the MMT and that these two variables decrease with aging; however, it was rejected, as the change in the MMT with aging was not significant (p = 0.72). The reason why the MMT did not decrease with aging decreases in bite force can be deduced. The masseter muscle predominantly consists of type 1 fibers, which are mainly associated with masseter muscle atrophy caused by muscle disuse [29,38]. The elderly participants in this study retained a sufficient number of functioning teeth; therefore, the influence of disuse due to tooth loss did not lead to atrophy of the masseter muscle or physiological muscle changes with aging. Previous studies have reported that the thickness of the masseter muscle is reduced by tooth loss [29], with edentulous patients showing significantly thinner masseter muscles than dentate patients [39]. Under edentate conditions, therefore, the MMT might be decreased by reduced masticatory function.
The PBA can be considered as a factor associated with bite force. A strong correlation was found between the PBA and bite force in this study (r range: 0.73–0.96). Previous studies directly comparing the PBA and bite force could not be found; most studies have compared each of them with masticatory performance. Ikebe el al. reported that the association of bite force with masticatory performance was significant and that the decrease in masticatory performance was significant in Eichner index B rather than in Eichner index A, suggesting the importance of the posterior occlusal contact of the remaining dentition [40].
In the regression analysis of masticatory performance, a significant association with the PBA rather than bite force was found in groups 1 and 3. In a previous study, where masticatory performance was measured using the sieving method in 30 patients with 28 teeth, the occlusal contact area was reported as the most pivotal determinant of masticatory performance, followed by the maximum bite force [41]. The authors also reported better masticatory performance with larger occlusal contact areas and stronger premolar bite force. In this study, with participants retaining sufficient FTUs over the threshold level [10] affecting masticatory function, the area of occlusion, such as the PBA, had more influence on masticatory performance than the bite force.
An extremely high (r range: 0.87–0.96) correlation was found between the number of remaining teeth and FTUs. In addition, a trend of a significant decrease with aging was observed in the number of remaining teeth (p = 0.007) and FTUs (p < 0.001). However, the participants of this study were limited to healthy dentate patients, and a difference in the number of teeth <1 was considered to be a small difference; hence, the number of teeth was not considered to cause any significant difference in the results or play a role as a confounding factor in this study. Hatch et al. stated that the number of FTUs and bite force influenced masticatory performance and that the number of FTUs was the most crucial factor [3]. Many studies have suggested that >20 teeth and >8 FTUs are sufficient to maintain masticatory function and that <5 FTUs is the threshold for indicating a problematic dental functional status [2,10,14,19,42]. Because the inclusion criteria of this study were over the threshold suggested above (26 teeth and 10 FTUs on average), it was inferred that there was no change in masticatory performance with aging. Statistically, the results also showed that masticatory performance was not associated with age as an independent variable in the regression analysis in any age group. In conclusion, with a good dental status, such as a sufficient number of FTUs, although age-dependent decreases in muscular factors, such as tongue pressure and handgrip strength, and occlusal factors, such as PBA and bite force, were also observed, masticatory performance was maintained with aging. Establishment of the occlusal contact area could thus be important for improving masticatory performance through restorative dental treatment.
The PBA obtained by quantifying the posterior occlusal area and tooth wear was analyzed with respect to masticatory performance among the age groups. With aging, the rate of tooth wear increased, but the PBA decreased, whereas no change in masticatory performance was observed. By regarding the tooth wear parameter as a characteristic of the increased occlusal area of worn teeth, it was investigated whether an increase in tooth wear can lead to an increase in masticatory performance. In the univariate regression analysis in this study, none of the age groups presented a significant relation between the influence of tooth wear and masticatory performance. This is consistent with the result of a recent report on the effect of tooth wear on masticatory performance, suggesting no significant relationship between tooth wear severity in the post-canine area and masticatory performance [43]. Hence, tooth wear was not considered to have an influence on masticatory performance in this study. However, tooth wear was assessed as a nominal variable, as the area of the wear itself could not be analyzed as a continuous variable. In future studies, a continuous parametrization of the degree of tooth wear using a tooth wear index will be helpful for obtaining a clear understanding.
Food intake ability (FIA), as a parameter of the subjective masticatory function evaluation, significantly decreased with aging, which is different from the trend in masticatory performance, which did not present a significant change in the objective masticatory function evaluation. However, similar to masticatory performance, an association between FIA and age was not found on regression analysis in any age group. Furthermore, a correlation between masticatory performance and FIA was not observed in any of the age groups, which is also consistent with the results of previous studies that have reported either almost no or a very weak correlation between the self-assessed masticatory ability and masticatory performance [2]. Masticatory function can be subjectively evaluated using combined factors, such as physical, psychological, and social factors; hence, it may be difficult to obtain results that are consistent with those of objective evaluations.
As a subjective assessment, the OHIP can be used to evaluate dental health from the view of the patient, and a high OHRQoL can reflect a favorable dental environment with high-quality dental prostheses or dentures. In the multiple linear regression, a significant relationship between FIA and the OHIP-14 score was found in all age groups in this study (p < 0.001). Similarly, Fueki et al. compared the OHIP score and patients’ perception of chewing ability assessed using a questionnaire on food intake and reported a significant, moderate relation between them [44]. Meanwhile, FIA showed inconsistent relationships with other variables, such as significant associations with the number of FTUs in group 2 and tongue pressure in group 3. It can be inferred that other factors not investigated in this study may affect FIA.
This study can provide the age-specific baseline data for clinical use regarding masticatory function. However, there are several limitations such as sample size, uneven gender distribution, and in particular difficulty in selecting participants due to poly-medication in the elderly over 60 years in this study. Longitudinal studies based on a larger number of participants are recommended to avoid sample size bias and to generalize the relations among the parameters with respect to masticatory performance and FIA. Investigations on the correlation between the PBA and tooth wear as well as on the perioral musculature function reflecting tongue and lip movement are needed for further research.

5. Conclusions

This study demonstrates that masticatory function is related to many factors (Figure 2). Static masticatory function, except for the masseter muscle thickness (MMT), decreased with aging. However, a decrease in masticatory performance with aging was not observed, and the influence of tongue pressure on food intake ability (FIA) could not be generalized. From the perspective of subjective masticatory function, FIA was associated with OHIP-14 score, which was related to OHRQoL. Even if age-related factors, including the number of remaining teeth, posterior bite area (PBA), handgrip strength, and tongue pressure, decreased with aging, dynamic masticatory function, i.e., masticatory performance, was maintained throughout life as long as the PBA was established. In conclusion, the establishment of posterior occlusal support is important in oral rehabilitation for masticatory function in the elderly.

Supplementary Materials

The following are available online at https://0-www-mdpi-com.brum.beds.ac.uk/article/10.3390/ijerph18136899/s1, Table S1: Multiple linear regression analysis of factors associated with masticatory performance, Table S2: Multiple linear regression analysis of factors associated with food intake ability

Author Contributions

Conceptualization, B.-Y.J.; Methodology, B.-Y.J., R.-M.D. and S.K.; Investigation, L.Y.; Data curation, S.-A.J.; Formal analysis, S.K.; Writing-original draft preparation, S.K.; Visualization, S.K.; Writing-review and editing, B.-Y.J.; Funding acquisition, B.-Y.J. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by the National Research Foundation of Korea (NRF) grant funded by the Korean government (MSIT) (grant number 2020R1A2C2004893).

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Institutional Review Board of Yonsei University Dental Hospital (Approval number: 2–2020-0047).

Informed Consent Statement

Informed consent was obtained from each subject involved in the study.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this study.

Appendix A

Table A1. The normality tests.
Table A1. The normality tests.
Age Groups Shapiro-WilkSkewnessKurtosis
p
20–45 (1)PBA0.1801.0021.031
ABA0.5962.2055.675
RT0.000−1.4410.670
FTUs0.000−1.4990.307
MP0.7760.158−0.487
BF0.8710.717−0.248
TP0.571−0.3990.263
HG0.0040.166−1.063
MMT0.2840.000−0.705
FIA0.000−2.9589.787
OHIP-140.0001.119−0.217
46–60 (2)PBA0.1620.6280.206
ABA0.0604.64823.767
RT0.000−1.9454.665
FTUs0.000−2.2114.066
MP0.3000.235−0.739
BF0.0680.541−0.299
TP0.621−0.281−0.137
HG0.0540.140−1.058
MMT0.5420.186−0.709
FIA0.000−2.5175.455
OHIP-140.0002.6127.587
61–70 (3)PBA0.0140.9921.106
ABA0.0006.60544.055
RT0.000−2.2765.426
FTUs0.000−1.8963.124
MP0.4040.5210.539
BF0.9051.0881.619
TP0.354−0.4990.805
HG0.3420.085−1.300
MMT0.3720.4300.316
FIA0.000−1.7652.114
OHIP-140.3541.4361.257
71+ (4)PBA0.6810.128−0.423
ABA0.0002.8999.808
RT0.000−0.491−0.329
FTUs0.000−0.740−0.102
MP0.662−0.154−0.014
BF0.4890.017−0.446
TP0.3600.1871.235
HG0.1970.336−0.404
MMT0.2420.2970.401
FIA0.000−1.6181.798
OHIP-140.0001.4161.215
RT: number of remaining teeth, FTUs: functional tooth units, MP: masticatory performance, HG: handgrip strength, PBA: posterior bite area, ABA: anterior bite area, BF: bite force, MMT: masseter muscle thickness, FIA: food intake ability, TP: tongue pressure.
Table A2. Pearson’s correlation coefficient in all subjects.
Table A2. Pearson’s correlation coefficient in all subjects.
AgeRTFTUsMPTPHGPBAABABFMMTFIAOHIP_14
Age1
RT−0.185 **1
FTUs−0.304 ***0.892 ***1
MP0.0030.0790.0921
TP−0.431 ***0.1320.156 *0.0941
HG−0.331 ***0.157 *0.155 *0.0990.570 ***1
PBA−0.279 ***0.252 ***0.303 ***0.306 ***0.342 ***0.423 ***1
ABA0.0390.0570.032−0.113−0.041−0.059−0.142 *1
BF−0.278 ***0.191 **0.230 ***0.287 ***0.324 ***0.422 ***0.870 ***−0.0731
MMT0.0350.0330.0020.193 **0.314 ***0.509 ***0.459 ***−0.0820.456 ***1
FIA−0.237 ***0.157 *0.253 ***0.170 *0.260 ***0.310 ***0.244 ***0.0250.268 ***0.160 *1
OHIP_140.0430.009−0.057−0.142 *−0.084−0.141 *−0.136 *0.002−0.158 *−0.112−0.518 ***1
p *** < 0.001, p ** < 0.01, p * < 0.05. RT: number of remaining teeth, FTUs: functional tooth units, MP: masticatory performance, HG: handgrip strength, PBA: posterior bite area, ABA: anterior bite area, BF: bite force, MMT: masseter muscle thickness, FIA: food intake ability, TP: tongue pressure.
Figure A1. Measuring devices for objective assessment in this study. (a) masticatory performance, GS-2. (b) tongue pressure, TPM-01 [45]. (c) bite force and occluding bite area, Dental Prescale and Occluser software program. (d) handgrip strength, Takei handheld dynamometer. (e) masseter muscle thickness, Minisono.
Figure A1. Measuring devices for objective assessment in this study. (a) masticatory performance, GS-2. (b) tongue pressure, TPM-01 [45]. (c) bite force and occluding bite area, Dental Prescale and Occluser software program. (d) handgrip strength, Takei handheld dynamometer. (e) masseter muscle thickness, Minisono.
Ijerph 18 06899 g0a1
Figure A2. Changes of the variable in masticatory function among age groups. (a) the number of remaining teeth. (b) functional tooth units. (c) handgrip strength. (d) FIA. (e) tongue pressure. (f) PBA. (g) bite force. (h) masticatory performance. (i) MMT. (j) OHIP-14.
Figure A2. Changes of the variable in masticatory function among age groups. (a) the number of remaining teeth. (b) functional tooth units. (c) handgrip strength. (d) FIA. (e) tongue pressure. (f) PBA. (g) bite force. (h) masticatory performance. (i) MMT. (j) OHIP-14.
Ijerph 18 06899 g0a2

References

  1. Lamster, I.B.; Asadourian, L.; Del Carmen, T.; Friedman, P.K. The aging mouth: Differentiating normal aging from disease. Periodontology 2000 2016, 72, 96–107. [Google Scholar] [CrossRef] [PubMed]
  2. van der Bilt, A. Assessment of mastication with implications for oral rehabilitation: A review. J. Oral Rehabil. 2011, 38, 754–780. [Google Scholar] [CrossRef] [PubMed]
  3. Hatch, J.P.; Shinkai, R.S.A.; Sakai, S.; Rugh, J.D.; Paunovich, E.D. Determinants of masticatory performance in dentate adults. Arch. Oral Biol. 2001, 46, 641–648. [Google Scholar] [CrossRef]
  4. Wintergerst, A.M.; Hernández-Sánchez, F. Masticatory performance parameters for young adults with “normal” occlusion. Cranio 2019, 37, 317–322. [Google Scholar] [CrossRef] [PubMed]
  5. Sato, H.; Fueki, K.; Sueda, S.; Sato, S.; Shiozaki, T.; Kato, M.; Ohyama, T. A new and simple method for evaluating masticatory function using newly developed artificial test food. J. Oral Rehabil. 2003, 30, 68–73. [Google Scholar] [CrossRef]
  6. Uesugi, H.; Shiga, H. Relationship between masticatory performance using a gummy jelly and masticatory movement. J. Prosthodont. Res. 2017, 61, 419–425. [Google Scholar] [CrossRef] [PubMed]
  7. Takagi, D.; Watanabe, Y.; Edahiro, A.; Ohara, Y.; Murakami, M.; Murakami, K.; Hironaka, S.; Taniguchi, Y.; Kitamura, A.; Shinkai, S.; et al. Factors affecting masticatory function of community-dwelling older people: Investigation of the differences in the relevant factors for subjective and objective assessment. Gerodontology 2017, 34, 357–364. [Google Scholar] [CrossRef]
  8. Locker, D.; Matear, D.; Stephens, M.; Lawrence, H.; Payne, B. Comparison of the GOHAI and OHIP-14 as measures of the oral health-related quality of life of the elderly. Community Dent. Oral Epidemiol. 2001, 29, 373–381. [Google Scholar] [CrossRef] [PubMed]
  9. Käyser, A.F. Shortened dental arches and oral function. J. Oral Rehabil. 1981, 8, 457–462. [Google Scholar] [CrossRef]
  10. Ueno, M.; Yanagisawa, T.; Shinada, K.; Ohara, S.; Kawaguchi, Y. Masticatory ability and functional tooth units in Japanese adults. J. Oral Rehabil. 2008, 35, 337–344. [Google Scholar] [CrossRef]
  11. Singh, K.A.; Brennan, D.S. Chewing disability in older adults attributable to tooth loss and other oral conditions. Gerodontology 2012, 29, 106–110. [Google Scholar] [CrossRef]
  12. Boretti, G.; Bickel, M.; Geering, A.H. A review of masticatory ability and efficiency. J. Prosthet. Dent. 1995, 74, 400–403. [Google Scholar] [CrossRef]
  13. Ikebe, K.; Morii, K.; Matsuda, K.I.; Nokubi, T. Discrepancy between satisfaction with mastication, food acceptability, and masticatory performance in older adults. Int. J. Prosthodont. 2007, 20, 161–167. [Google Scholar]
  14. Ikebe, K.; Matsuda, K.I.; Kagawa, R.; Enoki, K.; Yoshida, M.; Maeda, Y.; Nokubi, T. Association of masticatory performance with age, gender, number of teeth, occlusal force and salivary flow in Japanese older adults: Is ageing a risk factor for masticatory dysfunction? Arch. Oral Biol. 2011, 56, 991–996. [Google Scholar] [CrossRef] [PubMed]
  15. Hiramatsu, T.; Kataoka, H.; Osaki, M.; Hagino, H. Effect of aging on oral and swallowing function after meal consumption. Clin. Interv. Aging 2015, 10, 229. [Google Scholar] [CrossRef] [Green Version]
  16. Buehring, B.; Hind, J.; Fidler, E.; Krueger, D.; Binkley, N.; Robbins, J. Tongue strength is associated with jumping mechanography performance and handgrip strength but not with classic functional tests in older adults. J. Am. Geriatr. Soc. 2013, 61, 418–422. [Google Scholar] [CrossRef] [PubMed]
  17. Fujita, Y.; Ichikawa, M.; Hamaguchi, A.; Maki, K. Comparison of masticatory performance and tongue pressure between children and young adults. Clin. Exp. Dent. Res. 2018, 4, 52–58. [Google Scholar] [CrossRef] [Green Version]
  18. Morita, K.; Tsuka, H.; Kato, K.; Mori, T.; Nishimura, R.; Yoshida, M.; Tsuga, K. Factors related to masticatory performance in healthy elderly individuals. J. Prosthodont. Res. 2018, 62, 432–435. [Google Scholar] [CrossRef]
  19. Zhang, Q.; Witter, D.J.; Bronkhorst, E.M.; Creugers, N.H. The relationship between masticatory ability, age, and dental and prosthodontic status in an institutionalized elderly dentate population in Qingdao, China. Clin. Oral Investig. 2019, 23, 633–640. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  20. Faul, F.; Erdfelder, E.; Buchner, A.; Lang, A.G. Statistical power analyses using G* Power 3.1: Tests for correlation and regression analyses. Behav. Res. Methods 2009, 41, 1149–1160. [Google Scholar] [CrossRef] [Green Version]
  21. Cohen, J. Statistical Power Analysis for the Behavioral Sciences; Academic Press: London, UK, 2013. [Google Scholar]
  22. Ikebe, K.; Matsuda, K.I.; Murai, S.; Maeda, Y.; Nokubi, T. Validation of the Eichner index in relation to occlusal force and masticatory performance. Int. J. Prosthodont. 2010, 23, 521–524. [Google Scholar]
  23. Landis, J.R.; Koch, G.G. The Measurement of Observer Agreement for Categorical Data. Biometrics 1977, 33, 159–174. [Google Scholar] [CrossRef] [Green Version]
  24. Tsuga, K.; Yoshikawa, M.; Oue, H.; Okazaki, Y.; Tsuchioka, H.; Maruyama, M.; Yoshida, M.; Akagawa, Y. Maximal voluntary tongue pressure is decreased in Japanese frail elderly persons. Gerodontology 2012, 29, e1078–e1085. [Google Scholar] [CrossRef]
  25. Kim, B.I.; Jeong, S.H.; Chung, K.H.; Cho, Y.K.; Kwon, H.K.; Choi, C.H. Subjective food intake ability in relation to maximal bite force among Korean adults. J. Oral Rehabil. 2009, 36, 168–175. [Google Scholar] [CrossRef]
  26. Takeshima, T.; Fujita, Y.; Maki, K. Factors associated with masticatory performance and swallowing threshold according to dental formula development. Arch. Oral Biol. 2019, 99, 51–57. [Google Scholar] [CrossRef] [PubMed]
  27. Iwasaki, M.; Yoshihara, A.; Sato, N.; Sato, M.; Minagawa, K.; Shimada, M.; Nishimuta, M.; Ansai, T.; Yoshitake, Y.; Ono, T.; et al. A 5-year longitudinal study of association of maximum bite force with development of frailty in community-dwelling older adults. J. Oral Rehabil. 2018, 45, 17–24. [Google Scholar] [CrossRef]
  28. Machida, N.; Tohara, H.; Hara, K.; Kumakura, A.; Wakasugi, Y.; Nakane, A.; Minakuchi, S. Effects of aging and sarcopenia on tongue pressure and jaw-opening force. Geriatr. Gerontol. Int. 2017, 17, 295–301. [Google Scholar] [CrossRef]
  29. Yamaguchi, K.; Tohara, H.; Hara, K.; Nakane, A.; Yoshimi, K.; Nakagawa, K.; Minakuchi, S. Factors associated with masseter muscle quality assessed from ultrasonography in community-dwelling elderly individuals: A cross-sectional study. Arch. Gerontol. Geriatr. 2019, 82, 128–132. [Google Scholar] [CrossRef] [PubMed]
  30. Bertram, S.; Brandlmaier, I.; Rudisch, A.; Bodner, G.; Emshoff, R. Cross-sectional characteristics of the masseter muscle: An ultrasonographic study. Int. J. Oral Maxillofac. Surg. 2003, 32, 64–68. [Google Scholar] [CrossRef] [PubMed]
  31. Bakke, M.; Tuxetv, A.; Vilmann, P.; Jensen, B.R.; Vilmann, A.; Toft, M. Ultrasound image of human masseter muscle related to bite force, electromyography, facial morphology, and occlusal factors. Scand. J. Dent. Res. 1992, 100, 164–171. [Google Scholar] [CrossRef]
  32. Allen, F.; Locker, D. A modified short version of the oral health impact profile for assessing health-related quality of life in edentulous adults. Int. J. Prosthodont. 2002, 15, 446–450. [Google Scholar] [PubMed]
  33. Mukaka, M.M. Statistics corner: A guide to appropriate use of correlation coefficient in medical research. Malawi Med. J. 2012, 24, 69–71. [Google Scholar] [PubMed]
  34. Hara, K.; Tohara, H.; Kobayashi, K.; Yamaguchi, K.; Yoshimi, K.; Nakane, A.; Minakuchi, S. Age-related declines in the swallowing muscle strength of men and women aged 20–89 years: A cross-sectional study on tongue pressure and jaw-opening force in 980 subjects. Arch. Gerontol. Geriatr. 2018, 78, 64–70. [Google Scholar] [CrossRef] [PubMed]
  35. Sagawa, K.; Furuya, H.; Ohara, Y.; Yoshida, M.; Hirano, H.; Iijima, K.; Kikutani, T. Tongue function is important for masticatory performance in the healthy elderly: A cross-sectional survey of community-dwelling elderly. J. Prosthodont. Res. 2019, 63, 31–34. [Google Scholar] [CrossRef]
  36. Yamada, A.; Kanazawa, M.; Komagamine, Y.; Minakuchi, S. Association between tongue and lip functions and masticatory performance in young dentate adults. J. Oral Rehabil. 2015, 42, 833–839. [Google Scholar] [CrossRef] [PubMed]
  37. Kikutani, T.; Tamura, F.; Nishiwaki, K.; Kodama, M.; Suda, M.; Fukui, T.; Takahashi, N.; Yoshida, M.; Akagawa, Y.; Kimura, M. Oral motor function and masticatory performance in the community-dwelling elderly. Odontology 2009, 97, 38–42. [Google Scholar] [CrossRef]
  38. Ciciliot, S.; Rossi, A.C.; Dyar, K.A.; Blaauw, B.; Schiaffino, S. Muscle type and fiber type specificity in muscle wasting. Int. J. Biochem. Cell Biol. 2013, 45, 2191–2199. [Google Scholar] [CrossRef]
  39. Bhoyar, P.S.; Godbole, S.R.; Thombare, R.U.; Pakhan, A.J. Effect of complete edentulism on masseter muscle thickness and changes after complete denture rehabilitation: An ultrasonographic study. J. Investig. Clin. Dent. 2012, 3, 45–50. [Google Scholar] [CrossRef]
  40. Ikebe, K.; Matsuda, K.I.; Kagawa, R.; Enoki, K.; Okada, T.; Yoshida, M.; Maeda, Y. Masticatory performance in older subjects with varying degrees of tooth loss. J. Dent. 2012, 40, 71–76. [Google Scholar] [CrossRef] [PubMed]
  41. Lepley, C.R.; Throckmorton, G.S.; Ceen, R.F.; Buschang, P.H. Relative contributions of occlusion, maximum bite force, and chewing cycle kinematics to masticatory performance. Am. J. Orthod. Dentofac. Orthop. 2011, 139, 606–613. [Google Scholar] [CrossRef]
  42. Shao, Z.; Guo, X.; Zhang, Q.; Bronkhorst, E.M.; Zou, D.; Creugers, N.H. Masticatory efficiency in patients with partially dentate dentitions. J. Dent. 2018, 75, 41–47. [Google Scholar] [CrossRef] [PubMed]
  43. Sterenborg, B.A.; Kalaykova, S.I.; Loomans, B.A.; Huysmans, M.C.D. Impact of tooth wear on masticatory performance. J. Dent. 2018, 76, 98–101. [Google Scholar] [CrossRef]
  44. Fueki, K.; Yoshida, E.; Igarashi, Y. A structural equation model relating objective and subjective masticatory function and oral health-related quality of life in patients with removable partial dentures. J. Oral Rehabil. 2011, 38, 86–94. [Google Scholar] [CrossRef] [PubMed]
  45. Kamijo, Y.; Kanda, E.; Ono, K.; Maeda, K.; Yanai, A.; Honda, K.; Tsujimoto, R.; Yanagi, M.; Ishibashi, Y.; Yoshida, M. Low tongue pressure in peritoneal dialysis patients as a risk factor for malnutrition and sarcopenia: A cross-sectional study. Ren. Replace. Ther. 2018, 4, 23. [Google Scholar] [CrossRef]
Figure 1. FIA questionnaire on 14 food items.
Figure 1. FIA questionnaire on 14 food items.
Ijerph 18 06899 g001
Figure 2. Summary of the significant interrelationships in this study among various factors of masticatory function.
Figure 2. Summary of the significant interrelationships in this study among various factors of masticatory function.
Ijerph 18 06899 g002
Table 1. Demographic characteristics and dental status of the participants.
Table 1. Demographic characteristics and dental status of the participants.
Total20–45 (1)46–60 (2)61–70 (3)71+ (4)p
Subjects N (%) 211 (100)51 (24.2)54 (25.6)45 (21.3)61 (28.9)
Age 58 ± 17.932.1 ± 7.453.5 ± 4.266.2 ± 2.877.4 ± 5.2
Gender (%) amale95 (45.0)25 (49.0)26 (48.1)21 (46.7)23 (37.7)0.591
female116 (55.0)26 (51.0)28 (51.9)24 (53.3)38 (62.3)
a: Chi-square test.
Table 2. Assessment of the variables of masticatory function among age groups.
Table 2. Assessment of the variables of masticatory function among age groups.
Adult GroupElderly Grouppp for Trend b Posthoc
20–45 (1)46–60 (2)61–70 (3)71+ (4)
Number of Remaining teeth27.25 ± 1.5927.57 ± 1.0627.38 ± 1.1326.64 ± 1.450.002 *0.007 *2, 3 > 4
FTUs 11.59 ± 0.8011.67 ± 0.7311.39 ± 1.0910.75 ± 1.25<0.001 *<0.001 *1, 2, 3 > 4
Masticatory performance (mg/dL)186.94 ± 55.85199.70 ± 68.37179.93 ± 53.63188.11 ± 58.220.4150.674
Tongue Pressure (kPa)38.92 ± 10.9338.28 ± 10.5031.68 ± 7.8226.52 ± 9.74<0.001 *<0.001 *1, 2 > 3 > 4
Handgrip strength (Kg)31.14 ± 10.4928.22 ± 8.7127.56 ± 9.2921.44 ± 8.03<0.001 *<0.001 *1, 2, 3 > 4
Posterior bite area (mm2)25.03 ± 12.8721.84 ± 12.1618.36 ± 10.4516.54 ± 8.02<0.001 *<0.001 *1, 2 > 3,4
Anterior bite area (mm2)3.14 ± 2.384.34 ± 5.895.51 ± 17.363.43 ± 3.720.5480.794
Bite force (N) 942.95 ± 443.82858.41 ± 432.72700.93 ± 416.20659.85 ± 308.290.001 *<0.001 *1, 2 > 3,4
Masseter m. thickness (mm)13.19 ± 2.6713.62 ± 2.6513.07 ± 2.1813.38 ± 2.600.7170.959
Food intake ability68.73 ± 2.9367.50 ± 4.8965.98 ± 5.9965.51 ± 6.400.007 *0.001 *1 > 4
OHIP-14 4.53 ± 6.334.85 ± 8.215.69 ± 7.474.80 ± 6.130.8700.744
Tooth wear (%) a no49 (96.1)46 (85.2)18 (40.0)16 (26.2)<0.001 *<0.001 *
yes2 (3.9)8 (14.8)27 (60.0)45 (73.8)
mean ± SD, * p < 0.05. a: Chi-square test, b: p for trend by simple linear regression or Mantel-Haenzel chi-square test.
Table 3. Pearson’s correlation coefficient in each age group.
Table 3. Pearson’s correlation coefficient in each age group.
Group AgeRTFTUsMPTPHGPBAABABFMMTFIAOHIP-14
20–45 (1)Age1−0.0100.0380.2290.2370.1800.158−0.052−0.0210.354 *0.0730.033
RT 10.962 ***−0.1720.0860.0710.310 *0.2380.2750.031−0.0970.219
FTUs 1−0.0910.0420.0320.339 *0.1810.297 *0.027−0.1080.146
MP 1−0.1870.1080.299 *−0.0330.2610.1740.128−0.356 *
TP 10.559 ***0.1350.2260.0290.402 **0.0680.038
HG 10.455 **0.1130.432 **0.736 ***0.327 *0.018
PBA 10.1180.730 ***0.519 ***0.194−0.092
ABA 10.2460.1050.1530.267
BF 10.449 **0.229−0.034
MMT 10.291 *0.083
FIA 1−0.449 **
OHIP14 1
46–60 (2)Age10.1370.0820.014−0.0770.1060.0540.1720.0340.098−0.126−0.058
RT 10.872 ***0.301 *−0.0850.0730.0850.1080.0370.0410.268 *0.132
FTUs 10.284 *−0.0320.0140.2020.1180.1660.0290.447 **0.084
MP 10.354 **0.1710.412 **−0.1760.420 **0.311 *0.230−0.030
TP 10.439 **0.342 *−0.1140.409 **0.372 **0.248−0.048
HG 10.261−0.1650.375 **0.522 ***0.129−0.133
PBA 1−0.269 *0.961 ***0.452 **0.251−0.167
ABA 1−0.186−0.326 *0.174−0.163
BF 10.477 ***.315 *−0.232
MMT 10.023−0.079
FIA 1−0.422 **
OHIP14 1
61–70 (3)Age1−0.271−0.256−0.103−0.016−0.096−0.135−0.109−0.2070.139−0.2160.152
RT 10.943 ***0.1690.0900.0090.0320.079−0.047−0.1970.199−0.074
FTUs 10.1940.050−0.0380.0840.078−0.021−0.2010.227−0.138
MP 10.0380.0360.301 *−0.2330.2680.0590.188−0.139
TP 10.531 ***0.095−0.0850.1800.307 *0.454 **−0.291
HG 10.183−0.0980.2050.541 ***0.370 *−0.282
PBA 1−0.2200.926 ***0.451 **0.139−0.043
ABA 1−0.175−0.162−0.0360.082
BF 10.442 **0.175−0.069
MMT 10.280−0.137
FIA 1−0.797 ***
OHIP14 1
71+ (4)Age1−0.391 **−0.304 *0.034−0.505 ***−0.316 *−0.322 *0.354 **−0.156−0.247−0.0100.174
RT 10.891 ***0.0680.0320.1620.396 **−0.1220.284 *0.1390.135−0.250
FTUs 1−0.002−0.0500.1040.392 **−0.2380.257 *0.0790.177−0.225
MP 10.0390.0850.2030.1060.1610.1380.136−0.117
TP 10.469 ***0.428 **−0.1030.329 **0.306 *0.061−0.112
HG 10.568 ***−0.0760.466 ***0.425 **0.274 *−0.234
PBA 1−0.1150.835 ***0.531 ***0.228−0.247
ABA 10.270 *0.2170.126−0.223
BF 10.556 **0.208−0.293 *
MMT 10.166−0.304 *
FIA 1−0.491 ***
OHIP14 1
p *** < 0.001, p ** < 0.01, p * < 0.05. RT: number of remaining teeth, FTUs: functional tooth units, MP: masticatory performance, HG: handgrip strength, PBA: posterior bite area, ABA: anterior bite area, BF: bite force, MMT: masseter muscle thickness, FIA: food intake ability, TP: tongue pressure.
Table 4. Multiple linear regression analysis of factors associated with masticatory performance.
Table 4. Multiple linear regression analysis of factors associated with masticatory performance.
Multivariate
Bβ95% CIpR2
20–45 (1)Age
Gender (M)
Gender (F)
RT
FTUs
TP
HG
PBA1.1640.2680.032–2.2960.044 *0.198
ABA
BF
MTM
FIA
OHIP-14−2.926−0.332−5.229–−0.6230.014 *
Tooth wear
45–60 (2)Age
Gender (M)
Gender (F)
RT−1.848−0.043−15.495–11.8000.7900.106
FTUs1.0150.018−16.639–18.6690.910
TP−0.170−0.032−0.943–0.6030.664
HG
PBA1.1460.219−0.308–2.5990.122
ABA
BF0.0120.087−0.026–0.0510.527
MTM0.4250.018−3.724–4.5740.840
FIA
OHIP-14
Tooth wear
61–70 (3)Age
Gender (M)
Gender (F)
RT
FTUs
TP
HG
PBA1.5470.3010.042–3.0530.044 *0.091
ABA
BF
MTM
FIA
OHIP-14
Tooth wear
71+ (4)Age
Gender (M)
Gender (F)
RT
FTUs
TP
HG
PBA
ABA
BF
MTM
FIA
OHIP-14
Tooth wear
B: partial regression coefficient; β: standardized partial regression coefficient; * p < 0.05. RT: number of remaining teeth, FTUs: functional tooth units, FIA: food intake ability, HG: handgrip strength, PBA: posterior bite area, ABA: anterior bite area, BF: bite force, MMT: masseter muscle thickness, TP: tongue pressure.
Table 5. Multiple linear regression analysis of factors associated with FIA.
Table 5. Multiple linear regression analysis of factors associated with FIA.
Multivariate
Bβ95% CIpR2
20–45 (1)Age
Gender (M)
Gender (F)
RT
FTUs
TP
HG0.0570.203−0.043–0.1560.2570.329
PBA
ABA
BF
MTM0.1980.180−0.194–0.5890.315
MP
OHIP-14−0.216−0.468−0.328–−0.104<0.001 *
Tooth wear
45–60 (2)Age
Gender (M)
Gender (F)
RT
FTUs4.3780.6561.758–6.9970.002 *0.447
TP
HG
PBA
ABA
BF0.0010.107−0.001–0.0040.356
MTM
MP
OHIP-14−0.262−0.440−0.394–−0.130<0.001 *
Tooth wear
61–70 (3)Age
Gender (M)
Gender (F)
RT
FTUs
TP0.1680.2200.002–0.3350.047 *0.691
HG0.0270.041−0.150–0.2030.761
PBA
ABA
BF
MTM
MP
OHIP-14−0.573−0.715−0.732–−0.414<0.001 *
Tooth wear
71+ (4)Age
Gender(M)
Gender(F)−3.674−0.280−7.627–0.2790.0680.310
RT
FTUs
TP
HG−0.020−0.025−0.265–0.2260.872
PBA
ABA
BF
MTM
MP
OHIP-14−0.483−0.462−0.720–−0.246<0.001 *
Tooth wear
B: partial regression coefficient; β: standardized partial regression coefficient; * p < 0.05. RT: number of remaining teeth, FTUs: functional tooth units, MP: masticatory performance, HG: handgrip strength, PBA: posterior bite area, ABA: anterior bite area, BF: bite force, MMT: masseter muscle thickness, TP: tongue pressure.
Table 6. Stepwise multiple linear regression analysis of handgrip strength in each group.
Table 6. Stepwise multiple linear regression analysis of handgrip strength in each group.
Group Dependent VariableIndependent VariableBS.Eβp-ValueF
(p-Value)
R2
1HGMMT2.3970.3800.6100.00039.838
(p < 0.001)
0.624
TP0.3010.0930.3140.002
2HGMMT1.3700.4020.4170.00113.273
(p < 0.001)
0.342
TP0.2350.1010.2840.024
3HGMMT1.7810.5170.4180.00116.513
(p < 0.001)
0.440
TP0.4790.1440.4030.002
4HGTP0.2280.0940.2770.01818.189
(p < 0.001)
0.385
PBA0.4500.1140.4500.000
B: unstandardized partial regression coefficient, β: standardized partial regression coefficient, which indicates the relative importance of each variable. HG: handgrip strength, PBA: posterior bite area, MMT: masseter muscle thickness, TP: tongue pressure.
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Kim, S.; Doh, R.-M.; Yoo, L.; Jeong, S.-A.; Jung, B.-Y. Assessment of Age-Related Changes on Masticatory Function in a Population with Normal Dentition. Int. J. Environ. Res. Public Health 2021, 18, 6899. https://0-doi-org.brum.beds.ac.uk/10.3390/ijerph18136899

AMA Style

Kim S, Doh R-M, Yoo L, Jeong S-A, Jung B-Y. Assessment of Age-Related Changes on Masticatory Function in a Population with Normal Dentition. International Journal of Environmental Research and Public Health. 2021; 18(13):6899. https://0-doi-org.brum.beds.ac.uk/10.3390/ijerph18136899

Chicago/Turabian Style

Kim, Seonhui, Re-Mee Doh, Leegang Yoo, Sol-Ah Jeong, and Bock-Young Jung. 2021. "Assessment of Age-Related Changes on Masticatory Function in a Population with Normal Dentition" International Journal of Environmental Research and Public Health 18, no. 13: 6899. https://0-doi-org.brum.beds.ac.uk/10.3390/ijerph18136899

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop