Next Article in Journal
Influence of Size and Maturity on Injury in Young Elite Soccer Players
Next Article in Special Issue
Morphometric Analysis of the Mandibular Canal, Anterior Loop, and Mental Foramen: A Cone-Beam Computed Tomography Evaluation
Previous Article in Journal
Physical Sports Activities and Exercise Addiction during Lockdown in the Spanish Population
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Salivary Characteristics, Individual Casual Parameters, and Their Relationships with the Significant Caries Index among Korean Children Aged 12 Years

1
Department of Pediatric Dentistry, School of Dentistry, Jeonbuk National University, Jeonju 54896, Korea
2
Department of Conservative Dentistry, School of Dentistry and Institute of Oral Bioscience, Jeonbuk National University, Jeonju 54896, Korea
3
Department of Pediatric Dentistry, School of Dentistry, Kyung Hee University, Seoul 02447, Korea
*
Author to whom correspondence should be addressed.
Jae-Hwan Kim and Mi-Ah Kim contributed equally as first authors.
Int. J. Environ. Res. Public Health 2021, 18(6), 3118; https://doi.org/10.3390/ijerph18063118
Submission received: 4 February 2021 / Revised: 15 March 2021 / Accepted: 16 March 2021 / Published: 18 March 2021
(This article belongs to the Collection Oral and Public Health)

Abstract

:
This study aimed to investigate the salivary characteristics and individual daily living patterns in Korean children aged 12 years and evaluate their relationships according to the significant caries (SiC) index. The study sample consisted of 52 healthy Korean children. The subjects were allocated into a low caries-affected (low CA) group and a high caries-affected (high CA) group, according to the SiC index. Children underwent a standardized oral examination, and parents completed the questionnaires. Stimulated salivary samples were collected to evaluate the salivary pH, salivary flow rate, and salivary levels of Mutans streptococci (MS) and Lactobacilli (LB). The low CA group did not significantly differ from the high CA group for salivary flow rate and salivary pH. However, there were significant differences in salivary MS levels between the two groups (p < 0.05). Among the individual casual parameters, the prevalence of a sugar-associated primary energy source between meals was significantly higher in the high CA group than in the low CA group (p < 0.05). Within the limitations of this study, different levels of salivary MS and the consumption of different foods were observed in the low CA and high CA groups. The implications of these findings should be considered for caries susceptibility.

1. Introduction

Increasing public awareness of oral health care has led to a need for dental caries risk indicators to prevent and manage this disease [1,2]. Dental caries is the most prevalent infectious dental disease, which has been the primary cause of premature tooth loss in children [3,4]. The etiology of dental caries involves complex interactions between multifactorial predisposing factors [5]. Therefore, several caries risk assessment methods, including visual inspection and polymerase chain reaction, have been developed to identify more reliable predisposing factors [6,7]. Among the possible predisposing microbiological factors, Mutans streptococci (MS) and Lactobacilli (LB) are the primary bacteria associated with dental caries initiation. They can convert sucrose into acids, reduce oral pH, and survive below a pH level of 5.5 (threshold value for tooth demineralization) [8].
Salivary characteristics are also associated with the initiation and progression of dental caries [9,10]. In the previous literature, low salivary flow rate and poor buffering capacity have been suggested as dental caries-activity indicators [11,12]. However, the reliability of these factors in healthy children remains controversial. Previous literature evaluated children with specific conditions, such as asthma, chronic malnutrition, or children who received dental management under general anesthesia [12,13,14]. Other studies conducted on healthy patients evaluated salivary rate, pH, and salivary buffering capacity without analyzing their relationship with caries activity and caries experience [15].
Recently, individual casual parameters have emerged as major predisposing factors for the initiation and progression of dental caries. Evidence suggests that diet (particularly a sugar habit) can lead to dental caries [16,17]. Recent prospective studies show that feeding practices, the consumption of sugar-incorporated beverages, and other socio-behavioral factors can be potential risk factors for dental caries in children [18,19,20]. Dental caries is the result of complex interactions between various predisposing factors. Therefore, early detection and prediction are beneficial in the management and prevention of dental caries. Determining reliable risk predictors is a practical approach to preventing dental caries. This study aimed to investigate the salivary characteristics and individual daily living patterns in Korean children aged 12 years and evaluate their influence on dental caries experience.

2. Materials and Methods

2.1. Subject Enrollment and Sample Collection

This study was conducted according to the guidelines of the Declaration of Helsinki and approved by the Ethics Committee of Jeonbuk National University (ID: 201501004). Fifty-seven healthy children (aged 12 years) in two classes in one elementary school near Chonbuk National University were recruited as study subjects. Of these, 4 students were excluded from data as they moved to another school and could not participate in the study. One student was excluded from the data set due to uncooperative behavior. Finally, 52 children were selected (26 boys and 26 girls). The children were instructed to abstain from any oral hygiene for 24 h before sample collection and directed to brush their teeth after breakfast, 2 h before the appointment. After tooth brushing, no food or drink was allowed until saliva sampling. Stimulated saliva samples (at least 3 mL) were collected from all children 2 h after tooth brushing by asking them to chew on a piece of paraffin wax and spit into a 50 mL sterile tube. The samples were kept on ice and immediately transferred to the laboratory. Salivary tests and microbial analysis were performed on the same day.
One pediatric dentist performed the intraoral examination using a plane mouth mirror, following the World Health Organization (WHO) recommendations for oral epidemiological surveys. The DMFT/dmft index was evaluated (D/d = decay, M/m = missing, F/f = filling, t/T = teeth, D/d = DMFT/dmft).

2.2. Questionnaire for Individual Casual Parameters

A self-reported questionnaire was used to assess individual casual parameters in the school environment before the oral examination. The questionnaire included the following 4 questions:
  • How many times do you brush your teeth in a day? (<3 times a day, ≥3 times a day)
  • How long does it take you to clean your teeth after a meal? (<3 min, ≤10 min, and >10 min)
  • How long do you brush your teeth for? (<3 min, ≥3 min)
  • What is your primary source of energy between meals? (chocolates, candies, snacks, fruits, or vegetables)
Regarding primary food intake between meals, we divided this into two categories: sugar-intake habit (chocolates, candies, and snacks) and no sugar-intake habit (fruits and vegetables).

2.3. Defining Experimental Groups

In the present study, we allocated the subjects to two experimental groups according to the significant caries index (SiC index) with some modifications [21]. We calculated the DMFT/dmft values as the sum of DMFT and dmft value in each participant. We calculated the sum of all the DMFT/dmft values and divided it by the total number of participants. Finally, the mean DMTF/dmft index (mean value = 2.73) was used as the modified SiC index. Experimental groups were as follows:
(i)
Low CA (low caries-affected) group: participants presented a DMFT/dmft index below the modified SiC index.
(ii)
High CA (high caries-affected) group: participants presented a DMFT/dmft index above the modified SiC index.

2.4. Salivary Flow Rate and Salivary pH

All participants were instructed to chew on a piece of wax to stimulate salivary flow. After 30 s, they expectorated the saliva into a 50 mL tube for 5 min. After the disappearance of the salivary froth, the secretion rate was estimated in mL per min.
The pH values of saliva samples were estimated with a colorimetric kit (Saliva-Check Buffer, GC EUROPE N.V., Leuven, Belgium), according to the manufacturer’s instructions. In brief, a pH strip was placed into the collected sample of resting saliva for 10 s. The color of the strip was compared to the testing chart.

2.5. Microbiological Analysis of Saliva

A caries risk test (CRT bacteria, Ivoclar Vivadent AG, Liechtenstein) was used to measure the levels of MS and LB. The samples were vortexed for 10 sec. A portion of the saliva was pipetted onto two agar plates, one for MS and one for LB. The plates were incubated for 48 h at 37 °C. The number of colony-forming units (CFU) per mL of saliva was calculated according to the reference model chart provided in the instruction manual. The manual indicated the levels of bacteria as “low” (<105 CFU/mL) or “high” (≥105 CFU/mL). We assigned scores from 0 to 2. First, we divided the low-level mark into two scores: 0 (when there were no or almost no CFUs) and 1 (<105 CFU/mL). The high-level mark corresponded to 2 (≥105 CFU/mL).

2.6. Statistical Analysis

Data were analyzed using the Statistical Package for the Social Sciences (SPSS) 12.0 software (SPSS Inc., Chicago, IL, USA) for statistical analysis. The Shapiro–Wilk test was used to confirm that data were not normally distributed. All variables were statistically evaluated using either the Mann–Whitney test or Chi-square test. Correlations among numerical variables were analyzed using Spearman’s correlation test. A p-value of <0.05 was considered statistically significant.

3. Results

Of the 52 child participants, the low CA group consisted of 31 children, and the high CA group consisted of 21 children. Table 1 compares the values of salivary parameters between the two groups. The low CA group showed a mean salivary pH of 6.75 ± 0.49 and a mean saliva flow rate of 0.64 ± 0.44; the high CA group showed a mean salivary pH of 6.65 ± 0.57 and a mean salivary flow rate of 0.73 ± 0.36. There were no significant differences in salivary markers between the two groups. Salivary microbiological tests showed that the salivary levels of MS in the high CA group were statistically higher than those in the low CA group (p < 0.05). However, there was no statistical difference in salivary levels of LB between the two groups (Figure 1).
Table 2 and Table 3 show the correlations among all salivary parameters evaluated for the low CA group and the high CA group, respectively. A positive correlation between salivary MS levels and salivary LB levels was found in both the low CA group and the high CA group.
Table 4 shows comparisons of individual casual parameters between the low CA group and the high CA group. Among the individual casual parameters, a sugar-associated primary energy source consumed between meals was significantly higher in the high CA group (p < 0.05).

4. Discussion

In the present study, salivary parameters and individual casual parameters according to the SiC index were evaluated in 12-year-old Korean healthy children. Dental caries is the consequence of shifts in the balance between pathologic and protective factors [22]. Generally, dental caries is caused by organic acids produced by oral bacteria involved in the fermentation of dietary carbohydrates [23]. Additionally, biophysicochemical characteristics of saliva are considered important protective factors [24]. Therefore, analysis of oral bacteria and salivary characteristics can aid the early diagnosis and management of dental caries.
Saliva has an important role in oral health maintenance. It contributes to the oral defense system and shows buffering ability, antimicrobial activity, and calcium phosphate delivery to protect teeth from pathological factors [15]. Previous literature demonstrates that low salivary flow rate and low salivary pH are responsible for high caries prevalence [25]. Moreover, a strong association of salivary flow rate and salivary pH with dental caries has been confirmed in studies performed on subjects with specific medical conditions, suggesting that medications may considerably reduce the salivary flow rate and affect caries risk in patients [26]. However, the findings of the present study are in contrast with the results obtained from previous studies. This comparison may have been affected by sample characteristics. The results could be affected as the present research recruited only healthy children. A similar study conducted in Mexican schoolchildren demonstrated that salivary flow rate did not help predict caries risk [27]. Within the limitations of the present study, salivary flow rate and salivary pH did not significantly affect the initiation and progression of dental caries, indicating the presence of other markers that influence the initiation and progression of dental caries.
Microorganisms play an important role in the initiation and progression of dental caries as constituents of dental plaque biofilms [28]. A previous study on salivary MS levels suggested that the early acquisition of MS is related to a high incidence of early childhood dental caries and future caries susceptibility [29]. We found that 12-year-old healthy Korean children with high salivary MS levels had significantly high DMFT/dmft index values, a finding which is consistent with the results of previous studies. Salivary LB levels are also considered potent contributors to dental caries progression [30]. However, increased salivary LB levels were not found in the high CA group when compared to the low CA group in the present study. This finding is consistent with several studies showing that LB levels had a limited relationship to caries incidence [31,32]. Otherwise, in the present study, salivary LB levels showed a positive correlation with salivary MS levels (Table 2 and Table 3), regardless of caries experience. Thus, salivary MS levels demonstrate a strong correlation with dental caries initiation and progression. Further, this finding supports the hypothesis that salivary LB levels affect dental caries initiation and progression as secondary invaders [33].
Healthy eating patterns and meticulous tooth brushing are associated with oral health maintenance [34,35]. In the present study, the frequency and duration of tooth brushing and lag time between meals and tooth brushing did not differ between the low CA group and the high CA group. Only the primary energy source between meals was significantly associated with previous caries experiences, a finding that correlates with previous studies. A direct relation between sugar intake and dental caries has been reported, as cariogenic bacteria grow in the presence of fermentable carbohydrates [36]. Previous literature suggested that higher chocolate and candy consumption are risk factors for dental caries development in both primary and permanent dentition, as they remain on the tooth surface for hours without providing any nutritional value [37,38,39].
The present study has several limitations. The study was cross-sectional in design with a small sample size affecting the generalizability of the results. However, difficulties in participant enrollment existed as several parents whose children were requested to participate in this study did not consent. Further, some children who consented initially refused to provide salivary samples. Moreover, the assessment of individual casual parameters was based on a self-reported questionnaire. Thus, the overestimation or underestimation of these parameters could be possible. Future studies with a larger sample size are required.

5. Conclusions

Dental caries experiences in 12-year-old healthy Korean children showed a significant association with salivary MS levels and dietary sugar intake. The results indicate that these parameters could be reliable predictive indicators of dental caries in healthy Korean children aged 12 years. Incorporating these parameters in tests conducted during annual in-school oral examination is also recommended. This approach could achieve the prediction and early detection of dental caries and improve oral health status in children.

Author Contributions

Conceptualization, J.-H.K. and O.H.N.; methodology, J.-H.K. and O.H.N.; formal analysis, Y.K.C.; data curation, J.-H.K. and M.-A.K.; writing—original draft preparation, O.H.N.; visualization, Y.K.C.; project administration, O.H.N.; funding acquisition, O.H.N. All authors have read and agreed to the published version of the manuscript.

Funding

This work was financially supported by the National Research Foundation of Korea (NRF), the grant funded by the Korean government (MSIT) (NRF-2020R1C1C1006937).

Institutional Review Board Statement

The study was conducted according to the guidelines of the Declaration of Helsinki, and approved by the Ethics Committee of Jeonbuk National University (ID: 201501004).

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

All relevant data are within the paper.

Conflicts of Interest

The authors declare no conflict of interest. The funders had no role in the study design, collection, analyses, or interpretation of data, the writing of the manuscript, or in the decision to publish the results.

References

  1. Featherstone, J.D. The science and practice of caries prevention. J. Am. Dent. Assoc. 2000, 131, 887–899. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  2. Featherstone, J.D. The caries balance: Contributing factors and early detection. J. Calif. Dent. Assoc. 2003, 31, 129–133. [Google Scholar] [PubMed]
  3. Marsh, P.D. Dental plaque as a biofilm and a microbial community—Implications for health and disease. BMC. Oral. Health. 2006, 6 (Suppl. 1), S14. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Balakrishnan, M.; Simmonds, R.S.; Tagg, J.R. Dental caries is a preventable infectious disease. Aust. Dent. J. 2000, 45, 235–245. [Google Scholar] [CrossRef]
  5. Fisher-Owens, S.A.; Gansky, S.A.; Platt, L.J.; Weintraub, J.A.; Soobader, M.J.; Bramlett, M.D.; Newacheck, P.W. Influences on children’s oral health: A conceptual model. Pediatrics 2007, 120, e510–e520. [Google Scholar] [CrossRef] [Green Version]
  6. Kim, J.; Kim, M.; Lee, D.; Baik, B.; Yang, Y.; Kim, J. Rapid Detection of Pathogens Associated with Dental Caries and Periodontitis by PCR Using a Modified DNA Extraction Method. J. Korean. Acad. Pediatr. Dent. 2014, 41, 292–297. [Google Scholar] [CrossRef]
  7. Park, K.; Kim, D.; Lee, D.; Kim, J.; Yang, Y.; Kim, J. Evaluation of Caries Status among Adolescents in Jeonju City with WHO Basic Methods, International Caries Detection and Assessment System II (ICDAS-II). J. Korean. Acad. Pediatr. Dent. 2016, 43, 382–390. [Google Scholar] [CrossRef]
  8. Anderson, P.; Hector, M.P.; Rampersad, M.A. Critical pH in resting and stimulated whole saliva in groups of children and adults. Int. J. Paediatr. Dent. 2001, 11, 266–273. [Google Scholar] [CrossRef]
  9. Ohrn, R.; Enzell, K.; Angmar-Mansson, B. Oral status of 81 subjects with eating disorders. Eur. J. Oral Sci. 1999, 107, 157–163. [Google Scholar] [CrossRef]
  10. Pedersen, A.M.; Reibel, J.; Nordgarden, H.; Bergem, H.O.; Jensen, J.L.; Nauntofte, B. Primary Sjogren’s syndrome: Salivary gland function and clinical oral findings. Oral. Dis. 1999, 5, 128–138. [Google Scholar] [CrossRef]
  11. Almstahl, A.; Kroneld, U.; Tarkowski, A.; Wikstrom, M. Oral microbial flora in Sjogren’s syndrome. J. Rheumatol. 1999, 26, 110–114. [Google Scholar] [PubMed]
  12. Johansson, I.; Saellstrom, A.K.; Rajan, B.P.; Parameswaran, A. Salivary flow and dental caries in Indian children suffering from chronic malnutrition. Caries. Res. 1992, 26, 38–43. [Google Scholar] [CrossRef] [PubMed]
  13. Alaki, S.M.; Ashiry, E.A.; Bakry, N.S.; Baghlaf, K.K.; Bagher, S.M. The effects of asthma and asthma medication on dental caries and salivary characteristics in children. Oral. Health. Prev. Dent. 2013, 11, 113–120. [Google Scholar] [CrossRef]
  14. Lin, Y.J.; Lin, Y.T. Influence of dental plaque pH on caries status and salivary microflora in children following comprehensive dental care under general anesthesia. J. Dent. Sci. 2018, 13, 8–12. [Google Scholar] [CrossRef]
  15. Bergman, B.; Ericson, G. Cross-sectional study of patients treated with removable partial dentures with special reference to the caries situation. Scand. J. Dent. Res. 1986, 94, 436–442. [Google Scholar] [CrossRef]
  16. Meyer, B.D.; Lee, J.Y. The Confluence of Sugar, Dental Caries, and Health Policy. J. Dent. Res. 2015, 94, 1338–1340. [Google Scholar] [CrossRef]
  17. Sheiham, A.; James, W.P. Diet and Dental Caries: The Pivotal Role of Free Sugars Reemphasized. J. Dent. Res. 2015, 94, 1341–1347. [Google Scholar] [CrossRef]
  18. Chaffee, B.W.; Feldens, C.A.; Rodrigues, P.H.; Vitolo, M.R. Feeding practices in infancy associated with caries incidence in early childhood. Community. Dent. Oral Epidemiol. 2015, 43, 338–348. [Google Scholar] [CrossRef] [Green Version]
  19. Park, S.; Lin, M.; Onufrak, S.; Li, R. Association of Sugar-Sweetened Beverage Intake during Infancy with Dental Caries in 6-year-olds. Clin. Nutr. Res. 2015, 4, 9–17. [Google Scholar] [CrossRef] [Green Version]
  20. Peltzer, K.; Mongkolchati, A.; Satchaiyan, G.; Rajchagool, S.; Pimpak, T. Sociobehavioral factors associated with caries increment: A longitudinal study from 24 to 36 months old children in Thailand. Int. J. Environ. Res. Public Health 2014, 11, 10838–10850. [Google Scholar] [CrossRef] [Green Version]
  21. Campus, G.; Solinas, G.; Maida, C.; Castiglia, P. The ’Significant Caries Index’ (SiC): A critical approach. Oral. Health. Prev. Dent. 2003, 1, 171–178. [Google Scholar]
  22. Featherstone, J.D. Caries prevention and reversal based on the caries balance. Pediatr. Dent. 2006, 28, 128–132. [Google Scholar] [PubMed]
  23. Marsh, P.D. Sugar, fluoride, pH and microbial homeostasis in dental plaque. Proc. Finn. Dent. Soc. Suom. Hammaslaak. Toim. 1991, 87, 515–525. [Google Scholar]
  24. Rovelstad, G.H.; Geller, J.H.; Cohen, A.H. Caries susceptibility tests, hyaluronidase activity of saliva and dental caries experience. J. Dent. Res. 1958, 37, 306–311. [Google Scholar] [CrossRef]
  25. Animireddy, D.; Reddy Bekkem, V.T.; Vallala, P.; Kotha, S.B.; Ankireddy, S.; Mohammad, N. Evaluation of pH, buffering capacity, viscosity and flow rate levels of saliva in caries-free, minimal caries and nursing caries children: An in vivo study. Contem. Clin. Dent. 2014, 5, 324–328. [Google Scholar] [CrossRef]
  26. Bardow, A.; Nyvad, B.; Nauntofte, B. Relationships between medication intake, complaints of dry mouth, salivary flow rate and composition, and the rate of tooth demineralization in situ. Arch. Oral. Biol. 2001, 46, 413–423. [Google Scholar] [CrossRef]
  27. Sanchez-Perez, L.; Golubov, J.; Irigoyen-Camacho, M.E.; Moctezuma, P.A.; Acosta-Gio, E. Clinical, salivary, and bacterial markers for caries risk assessment in schoolchildren: A 4-year follow-up. Int. J. Paediatr. Dent. 2009, 19, 186–192. [Google Scholar] [CrossRef]
  28. Marsh, P.D. Dental plaque as a microbial biofilm. Caries. Res. 2004, 38, 204–211. [Google Scholar] [CrossRef]
  29. Kohler, B.; Andreen, I.; Jonsson, B. The earlier the colonization by mutans streptococci, the higher the caries prevalence at 4 years of age. Oral. Microbiol. Immunol. 1988, 3, 14–17. [Google Scholar] [CrossRef] [PubMed]
  30. Rupf, S.; Merte, K.; Eschrich, K.; Kneist, S. Streptococcus sobrinus in children and its influence on caries activity. Eur. Arch. Paediatr. Dent. 2006, 7, 17–22. [Google Scholar] [CrossRef] [PubMed]
  31. Gudkina, J.; Brinkmane, A. The impact of salivary mutans streptococci and sugar consumption on caries experience in 6-year olds and 12-year olds in Riga. Stomatologija 2010, 12, 56–59. [Google Scholar] [PubMed]
  32. Slayton, R.L.; Cooper, M.E.; Marazita, M.L. Tuftelin, mutans streptococci, and dental caries susceptibility. J. Dent. Res. 2005, 84, 711–714. [Google Scholar] [CrossRef]
  33. Caufield, P.W.; Schon, C.N.; Saraithong, P.; Li, Y.; Argimon, S. Oral Lactobacilli and Dental Caries: A Model for Niche Adaptation in Humans. J. Dent. Res. 2015, 94, 110s–118s. [Google Scholar] [CrossRef] [PubMed]
  34. Bruno-Ambrosius, K.; Swanholm, G.; Twetman, S. Eating habits, smoking and toothbrushing in relation to dental caries: A 3-year study in Swedish female teenagers. Int. J. Paediatr. Dent. 2005, 15, 190–196. [Google Scholar] [CrossRef]
  35. Da Silveira, K.S.R.; Prado, I.M.; Abreu, L.G.; Serra-Negra, J.M.C.; Auad, S.M. Association among chronotype, dietary behaviours, and caries experience in Brazilian adolescents: Is there a behavioural pattern? Int. J. Paediatr. Dent. 2018, 28, 608–615. [Google Scholar] [CrossRef] [PubMed]
  36. Sheiham, A.; James, W.P. A reappraisal of the quantitative relationship between sugar intake and dental caries: The need for new criteria for developing goals for sugar intake. BMC. Public Health 2014, 14, 863. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  37. Almasi, A.; Rahimiforoushani, A.; Eshraghian, M.R.; Mohammad, K.; Pasdar, Y.; Tarrahi, M.J.; Moghimbeigi, A.; Ahmadi Jouybari, T. Effect of Nutritional Habits on Dental Caries in Permanent Dentition among Schoolchildren Aged 10–12 Years: A Zero-Inflated Generalized Poisson Regression Model Approach. Iran. J. Public Health 2016, 45, 353–361. [Google Scholar] [PubMed]
  38. Boka, V.; Trikaliotis, A.; Kotsanos, N.; Karagiannis, V. Dental caries and oral health-related factors in a sample of Greek preschool children. Eur. Arch. Paediatr. Dent. 2013, 14, 363–368. [Google Scholar] [CrossRef]
  39. Llena, C.; Forner, L. Dietary habits in a child population in relation to caries experience. Caries. Res. 2008, 42, 387–393. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Presentation of microbiological test. Salivary levels of Mutans streptococci (MS) and Lactobacilli (LB) were recorded as follows; 0 = no or almost no CFUs, 1 = <105 CFU/mL, and 2 = ≥105 CFU/mL. Low CA; low caries-affected, High CA; High caries-affected * = statistically significant difference between the low CA and the high CA group (Mann–Whitney test, p < 0.05)
Figure 1. Presentation of microbiological test. Salivary levels of Mutans streptococci (MS) and Lactobacilli (LB) were recorded as follows; 0 = no or almost no CFUs, 1 = <105 CFU/mL, and 2 = ≥105 CFU/mL. Low CA; low caries-affected, High CA; High caries-affected * = statistically significant difference between the low CA and the high CA group (Mann–Whitney test, p < 0.05)
Ijerph 18 03118 g001
Table 1. Comparison of salivary pH and salivary flow rate according to the significant caries index.
Table 1. Comparison of salivary pH and salivary flow rate according to the significant caries index.
Salivary ParametersLow CA 1High CA 2p-Value
Salivary pH6.75 ± 0.496.65 ± 0.570.651
Saliva flow rate0.64 ± 0.440.73 ± 0.360.112
1 Low CA = low caries-affected, 2 high CA = high caries-affected.
Table 2. Correlation coefficients of caries parameters in the low caries-affected group.
Table 2. Correlation coefficients of caries parameters in the low caries-affected group.
Salivary ParametersSalivary pHSalivary Flow RateMS 1LB 2
Salivary pH1
Salivary flow rate0.2881
MS−0.326−0.2141
LB−0.1950.3230.370 *1
1 MS = Mutans streptococci, 2 LB = Lactobacilli, * = statistically significant difference between corresponding parameters (Spearman’s correlation test, p < 0.05).
Table 3. Correlation coefficients of caries parameters in the high caries-affected group.
Table 3. Correlation coefficients of caries parameters in the high caries-affected group.
Salivary ParametersSalivary pHSalivary Flow RateMS 1LB 2
Salivary pH1
Salivary flow rate0.2651
MS−0.033−0.0551
LB−0.3570.1500.482 *1
1 MS = Mutans streptococci, 2 LB = Lactobacilli, * = statistically significant difference between corresponding parameters (Spearman’s correlation test, p < 0.05).
Table 4. Comparison of individual casual parameters by the significant caries index.
Table 4. Comparison of individual casual parameters by the significant caries index.
Individual Casual
Parameters
Low CA 1High CA 2p-Value
Frequency of tooth brushing
<3 times a day9 (29%)6 (28.6%)0.971
≥3 times a day22 (71%)15 (71.4%)
Lag time between meals and tooth brushing
<3 min13 (41.9%)7 (33.3%)0.435
<10 min8 (25.8%)9 (42.9%)
≥10 min10 (32.3%)5 (23.8%)
Tooth brushing duration
<3 min19 (61.3%)13 (61.9%)0.964
≥3 min12 (38.7%)8 (38.1%)
Primary source of energy between meals
Sugar intake19 (61.3%)19 (90.5%)0.02 *
No sugar intake12 (38.7%)2 (9.5%)
1 Low CA = low caries-affected, 2 high CA = high caries-affected, * = statistically significant difference between low CA and high CA groups (Chi-square test).
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, J.-H.; Kim, M.-A.; Chae, Y.K.; Nam, O.H. Salivary Characteristics, Individual Casual Parameters, and Their Relationships with the Significant Caries Index among Korean Children Aged 12 Years. Int. J. Environ. Res. Public Health 2021, 18, 3118. https://doi.org/10.3390/ijerph18063118

AMA Style

Kim J-H, Kim M-A, Chae YK, Nam OH. Salivary Characteristics, Individual Casual Parameters, and Their Relationships with the Significant Caries Index among Korean Children Aged 12 Years. International Journal of Environmental Research and Public Health. 2021; 18(6):3118. https://doi.org/10.3390/ijerph18063118

Chicago/Turabian Style

Kim, Jae-Hwan, Mi-Ah Kim, Yong Kwon Chae, and Ok Hyung Nam. 2021. "Salivary Characteristics, Individual Casual Parameters, and Their Relationships with the Significant Caries Index among Korean Children Aged 12 Years" International Journal of Environmental Research and Public Health 18, no. 6: 3118. https://doi.org/10.3390/ijerph18063118

APA Style

Kim, J. -H., Kim, M. -A., Chae, Y. K., & Nam, O. H. (2021). Salivary Characteristics, Individual Casual Parameters, and Their Relationships with the Significant Caries Index among Korean Children Aged 12 Years. International Journal of Environmental Research and Public Health, 18(6), 3118. https://doi.org/10.3390/ijerph18063118

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