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ORIGINAL RESEARCH article

Front. Pediatr., 28 July 2020
Sec. General Pediatrics and Pediatric Emergency Care
Volume 8 - 2020 | https://doi.org/10.3389/fped.2020.00419

Enamel and Dentin Caries Risk Factors of Adolescents in the Context of the International Caries Detection and Assessment System (ICDAS): A Longitudinal Study

Ketian Wang1,2 Liangyue Pang1,2 Cancan Fan1,2 Tianqiang Cui3 Lixia Yu1,2 Huancai Lin1,2*
  • 1Department of Preventive Dentistry, Guanghua School of Stomatology, Hospital of Stomatology, Sun Yat-sen University, Guangzhou, China
  • 2Guangdong Provincial Key Laboratory of Stomatology, Sun Yat-sen University, Guangzhou, China
  • 3Foshan Stomatology Hospital, Foshan, School of Stomatology and Medicine, Foshan University, Foshan, China

Objective: The objective of this study was to identify risk factors for enamel and dentin caries in adolescents.

Method: This 1-year longitudinal study was conducted in 2018 and 2019; 13- to 14-year-old adolescents were recruited. The merged International Caries Detection and Assessment System (ICDAS) was used to identify caries. The relationships between the caries increment and variables were analyzed with a zero-inflated negative binomial (ZINB) regression model.

Results: A total of 1,016 participants completed the assessment. The ZINB analysis found that individuals with caries at baseline were more likely to develop new dentin caries. Females, or individuals who had a high cariostat score had an increased likelihood of having a high ΔD4-6MFT score. Among the caries-free adolescents at baseline, females, or individuals who consumed snacks once or more than once a day were more likely to develop caries. Individuals from one-child families, who used fluoride toothpaste, and who had a high saliva buffering capability (pH≥4.25) had an increased likelihood of a low ΔD1-6MFT score.

Conclusion: The results suggest that there are some specific risk factors of initiating of enamel caries in adolescents, including the frequency of snack consumption, sex, saliva buffering capability, fluoride toothpaste usage and belonging to a one-child family. In all adolescents, most of whom have enamel caries, the dentin caries risk factors were past caries experience, cariostat score and sex.

Introduction

Although preventive strategies have been implemented for decades, dental caries remain a major public health problem, especially in developing countries (1). Adolescence is a period in which the risk for dental caries remains especially high (2). The global caries prevalence was approximately 50% among 12–15-year-old adolescents and over 70% among 17-year-old adolescents (3). In China, the prevalence of caries among 12-year-old children has increased from 28.9 to 38.5% in the last decade (4, 5). These numbers have raised concerns about caries experience among adolescents. Adolescence is a vital life stage in which children begin to develop self-performed oral health habits instead of relying solely on parental supervision (6). Dental caries may lead to pain and swelling and affect early permanent dentition development in adolescents, potentially drastically reducing their quality of life (7). Therefore, it is important to adopt some intervention measures for the early prevention of caries among teenagers.

Caries risk assessment is known to be an essential element in the planning of preventive and therapeutic strategies (8). As one of the most common chronic, infectious and multifactor diseases among children and adults (9), dental caries have a complicated etiology model consisting of demographic factors, socioeconomic factors, oral health-related behaviors, and biological factors (10). These factors have been applied in some caries assessment systems (11, 12); however, few were targeted at adolescents, and the caries phenotypes were not distinguished in these assessment systems. Some cross-sectional studies have been performed to investigate the risk indicators for dental caries among Chinese adolescents (13, 14), but there is a lack of evidence of the risk factors according to longitudinal studies.

Due to (1) the high increasing caries rate, (2) critical stage for self-behavior formation, and (3) unique social and psychological needs (15), the primary objective of this study was to investigate the caries risk factors in adolescents in South China by conducting a 1-year longitudinal study, specifying the risk factors without the effect of past caries experience.

Methods

Ethical Approval

The study was approved by the Ethical Review Committee of Guanghua School of Stomatology, Sun Yat-Sen University (ERC-[2018]01). Written informed consent was obtained from each participant's guardian before the baseline and follow-up assessments. A verbal assent was obtained from each of the participants.

Subjects

The baseline data were collected from March to April 2018 in Foshan. Foshan is a medium-sized city in Guangdong Province in southern China, with a population of 7.6 million. The gross domestic product (GDP) was CNY 124,324 (USD 18,018) per capita in 2017 (16). The water fluoride concentration is 0.16 mg/L (17).

In total, twenty independent variables were investigated in this study. PASS 11.0.7 (NCSS, LLC) was applied to calculate the sample size. The Poisson regression model was used. The significance level was set at 0.05, with a power of 0.8, assuming a 20% non-response rate; thus, the total sample size was calculated as at least 953 participants.

A multistage cluster sampling technique was employed. The size for each cluster was calculated by the following formula (18):

r=Z2VR2R+Z2V

The calculated sample size (R) was 953, with a standard error set at 8% (Δ = 8%*2) and a confidence interval of 95% (Z = 1.96). According to the data from the 4th National Oral Health Survey in China, the variation coefficient (V) should be 1.53 (4). Hence, the cluster size should be 186 and the cluster number was 6 (953/186). Among 39 middle schools in Foshan in 2018, six of them were randomly sampled. Four grade seven classes were randomly sampled from each of the 6 schools as the class size was ~45 in Foshan schools. All the students in these classes whose parents were Han Chinese and permanent residents in Foshan were recruited for this study. Those who reported systematic illness or antibiotic use in the preceding 2 weeks were excluded.

For the longitudinal evaluation at the 1-year follow-up (2019), all adolescents who completed the assessments at baseline were invited to participate in a follow-up assessment.

Oral Health Questionnaires

Detailed information was obtained through a structured questionnaire completed by the adolescents with the guidance of their guardians. The questionnaire was mainly designed with reference to the Fisher-Owens conceptual model of influence on children's oral health (19). It consisted of three parts, as follows:

1) Demographic information: sex, age, residence, whether the child is an only child in his/her family and his/her primary caregiver;

2) Socioeconomic information: family income, caregivers' education levels, and whether they have dental insurance; and

3) Oral health-related behaviors: tooth brushing frequency, flossing habits, toothpaste containing fluoride or not, frequency of snack consumption, frequency of sweet drink consumption, and dental attendance experience.

The compulsory education is 9 years in China; thus, “9 years” was set as a threshold to distinguish the education of the caregivers in the variable “education of caregiver.” As to the categories in the variable “household monthly incoming,” according to the Foshan government, households with the lowest 20% annual average household income are classified into the low income group, while households with the highest 20% annual average household income are classified into the high income group (16). In 2017, the thresholds were 35,339.38 CNY (~3,000 CNY per month) for the low income group and 85,774.21 CNY (~7,000 CNY per month) for the high income group in Foshan (20).

Dental Examinations

Dental examinations were conducted under a portable light by three calibrated examiners, each of whom equipped with one recorder. A community periodontal index (CPI) explorer, a dental mirror sterile cotton swabs and compressed air were used during the dental examination. The procedure for all tests are shown in Figure 1. The Plaque Index was checked first. The Plaque Index (PlI) was recorded according to the Silness and Löe scale (21). After the teeth were brushed by the adolescent him/herself, the caries were examined. The merged International Caries Detection and Assessment System (ICDAS) criteria were used (22). All tooth surfaces were first examined with a wet surface and then re-examined after the teeth were dried with compressed air. Sterile cotton swabs were used during caries examination when debris remained on tooth surfaces. Teeth or surfaces filled and teeth or surfaces missing due to caries (extractions due to orthodontics or other reasons were not included, and a verbal confirmation was obtained from the examinee when unclear).

FIGURE 1
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Figure 1. The procedure for dental examination and other tests.

Three examiners attended a 12-h e-learning course on ICDAS before the study. To calculate the consistency of the inter-examiner reliability, 105 subjects were randomly chosen during the oral examination; they were re-examined by another examiner immediately after being examined by the first examiner (35 examinees from A to B, 35 examinees from B to C, and 35 examinees from C to A).

Decayed teeth were recorded as enamel caries (coded 1–3 in the ICDAS system, D1–3) or dentin caries (coded 4–6 in the ICDAS system, D4–6) (23). Filled surfaces and missing teeth due to caries (the reasons for missing teeth were obtained from the questionnaire) were also recorded (24).

The same three examiners who performed the baseline examinations performed the 1-year follow-up examinations. As in the baseline examinations, the caries were recorded as enamel or dentin caries according to the merged ICDAS. Filled surfaces and missing teeth due to caries were also recorded.

Similar to the baseline assessment, 105 subjects were randomly re-examined to calculate Cohen's kappa.

Plaque and Saliva Samples

Plaque samples were collected using the sterile swab included in the cariostat kit (GangDa Medical Technology Co. Ltd., Beijing, China). According to the cariostat kit instructions, the examiners scrubbed the buccal surfaces of the maxillary molars and mandibular incisors 3–5 times and immersed the swab into the culture medium ampule. The samples were incubated at 37°C for 48 h. The color of the culture medium was compared with the reference color on the color chart supplied with the cariostat kit. A score of “0” designates the lowest acidogenecity of oral microorganisms, while “3.0” represents the highest acidogenecity of oral microorganisms (25).

Whole saliva was collected after the students had rinsed their mouths with tap water. Unstimulated saliva was collected for 15 min. Students were asked to spit the saliva through a funnel into a scaled tube every 3 min. Then, the unstimulated saliva flow rate (ml/min) was calculated. The flow rate was recorded into “abnormal (<0.25)” or “normal (≥0.25)” (26).

The saliva buffering capability was measured according to the Ericsson method (27). One milliliter of saliva was added to 3 ml of 3.3 mmol HCl within 5 min after collection and then allowed to stand for 20 min to remove CO2. The final pH of the saliva was evaluated by an electrical pH meter. The buffering capability was recorded into “low” (<3.5), “moderate” (3.5–4.25) or “high” (≥4.25) (28).

Statistical Analysis

The data were analyzed by R 3.6.1 statistical software. Individuals with missing data were excluded from the analysis. The D1-3T/S, D4-6T/S, teeth or surfaces filled (FT/S) and teeth or surfaces missing due to caries (MT/S) were calculated both at baseline and at the 1-year follow-up. The following indices were calculated:

ΔD1-6MFT=(D4-6Tfollow-up-D4-6Tbaseline)                            +(D1-3Tfollow-up-D1-3Tbaseline)                            +(FTfollow-up—FTbaseline)                            +(MTfollow-up—MTbaseline)ΔD4-6MFT=(D4-6Tfollow-up—D4-6Tbaseline)                            +(FTfollow-up—FTbaseline)                            + (MTfollow-up—MTbaseline)

For categorical variables, chi-square tests were used to test the association of caries experience with the variables studied. The Mann-Whitney U test or Kruskal-Wallis H test was employed to study the distribution of decayed, missing, and filled teeth (ΔDMFT) scores according to different variables. For continuous variables, logistic regression was used to test the association of caries experience with the variables, and negative binominal regression was employed to study the distribution of ΔDMFT scores. Independent variables with p < 0.50 in the binary analysis were included as covariates in the multivariate analysis.

For the multivariate analyses, the Poisson model, negative binomial model and zero-inflated model were considered to study the relationships between the ΔDMFT scores and the selected variables. Vuong's test was employed to choose an appropriate model. Backward stepwise selection was used to filter the variables in the multivariate regression analysis.

Results

General Information

A total of 1,087 adolescents were invited, and 1,055 completed the baseline survey. The baseline response rate was 97.06%. A total of 1,016 adolescents completed all evaluations in the longitudinal study (a 96% follow-up rate). Among them, 591 were boys, and 425 were girls. The mean age at baseline was 13.19 ± 0.40 years. Thirty-nine children were lost to follow-up primarily because they transferred schools, were absent from school on the follow-up day, or were unwilling to attend the follow-up examination. Figure 2 displays a flowchart describing the subjects in this study.

FIGURE 2
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Figure 2. Flowchart of the survey.

The Cronbach's alpha of the questionnaire was 0.75, indicating good reliability. For the inter-examiner reliability of the caries examinations, the Cohen's kappa values were 0.85 (Examiner A vs. B), 0.83 (Examiner B vs. C) and 0.91 (Examiner C vs. A) at baseline. The Cohen's kappa values were 0.80 (Examiner A vs. B), 0.78 (Examiner B vs. C), and 0.86 (Examiner C vs. A) at the 1-year follow-up assessment.

The dentin caries prevalence rate was 36.2%; when enamel caries were included, the rate was 87.8% at baseline. At the 1-year follow-up, the caries prevalence rate was 91.5% (enamel and dentin caries) and 49.6% (dentin caries). The incidence rate for dentin caries was 37.0%. When enamel caries were included, the incidence rate was 47.6%. The mean ΔD1-6MFT was 1.41 ± 2.06, and the mean ΔD4-6MFT was 1.08 ± 1.85. Table 1 shows the profile of caries in the studied population.

TABLE 1
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Table 1. Mean caries experience and severity at tooth and surface levels at baseline and one-year follow-up assessments.

All Participants

For all participants, the distribution of the ΔD4-6MFT scores was positively skewed, with a skewness of 2.1 (Figure 3). Table 2 shows the results of the binary analysis. Independent variables with p < 0.50 in the binary analysis were submitted to further multivariate analysis. As a result, household monthly income and dental flossing were excluded from the model.

FIGURE 3
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Figure 3. Increase in dentin caries (ΔD4-6MFT) of all participants (n = 1,016).

TABLE 2
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Table 2. Incidence proportion and rank of median D4−6MFT scores among independent variables (n = 1,016).

The result of Vuong's test showed that the zero-inflated negative binomial (ZINB) model was the best model to fit the data (p < 0.001). After the multivariate analysis, variables with a P < 0.05 were retained in the models. The ΔD4-6MFT score was related to sex (p = 0.001, IRR = 0.732, 95% CI: 0.663–0.945) and cariostat score (p = 0.012, IRR = 1.182, 95% CI: 1.037–1.347). In the zero-inflated part, individuals with past dentin caries experience had an increased likelihood of having an increment in D4-6MFT score (p < 0.001, OR = 1.765, 95% CI: 1.343–2.321) (Table 3).

TABLE 3
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Table 3. Dentin caries risk factors of all participants.

Caries-Free Group

There were 129 individuals who were caries free (D1-6MFT = 0) at baseline. After 1 year, 6 patients missed the follow-up assessment. Among the remaining 123 individuals, 57 (46.3%) adolescents were still caries free. The 123 individuals were categorized as the caries-free group. The mean ΔD1-6MFT was 1.54 ± 2.12, and the mean ΔD4-6MFT was 0.07 ± 0.43 (ranging from 0 to 3). Only four individuals developed dentin caries; thus, the enamel caries and dentin caries were both included in the analysis of the caries-free group, where the ΔD1-6MFT score was treated as the dependent variable.

Figure 4 shows the distribution of the ΔD1-6MFT score of the caries-free population, which was positively skewed, with a skewness of 2.00. As in the analysis of all participants, the caregivers, household monthly income, frequency of toothbrushing and orthodontic appliances were excluded after the binary analysis yielded p-values over 0.5 for these variables in all binary tests (Table 4).

FIGURE 4
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Figure 4. Increase in enamel and dentin caries (ΔD1-6MFT) of caries-free group (n = 123).

TABLE 4
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Table 4. Incidence proportion and rank of median D1−6MFT scores among independent variables (n = 123).

For the multivariate analysis, the result of Vuong's test showed that the ZINB model was also the best model to fit the data (P = 0.049). In the zero-inflated portion, the result shows that male individuals (p = 0.001 OR = 0.223, 95% CI: 0.089–0.558) and individuals who ate snacks not every day (p = 0.013 OR = 0.387, 95% CI: 0.175–0.853) had a decreased likelihood of having an increment in D1-6MFT score (Table 5). The ΔD1-6MFT score was related to belonging to a one-child family (p = 0.030, IRR = 0.606, 95% CI: 0.385–0.954) and the use of fluoride toothpaste (p = 0.047, IRR = 0.632, 95% CI: 0.401–0.995). In addition, compared with individuals with a low saliva buffering capability (pH < 3.5), individuals with a high saliva buffering capability (pH ≥ 4.25) had a low ΔD1-6MFT score (p = 0.025, IRR = 0.563, 95% CI: 0.341–0.931).

TABLE 5
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Table 5. Enamel and dentin caries risk factors of caries-free group.

Discussion

With the broadening of understanding and the definition of dental caries, the focus of caries detection, diagnosis, and management has shifted from advanced caries to initial caries (29); thus, the merged ICDAS criteria were employed in this study. ICDAS was designed to identify the clinical stages of the caries process (22). In the present study, enamel caries and dentin caries were both evaluated. For all participants, only the increase in dentin caries was considered, mainly for two reasons. First, most adolescents in this study had at least one enamel caries lesion at baseline, and only 8.5% children were “truly caries free” at the 1-year follow-up assessment; hence it would be meaningless to investigate enamel caries risk factors in the whole population. In addition, to allow for comparison with the results of other studies that have used the World Health Organization WHO criteria, the D4-6 threshold for caries, which is considered closest to the WHO criteria, was employed (30). The increase in enamel caries was analyzed in the caries-free population.

The DMFT index is the count of decayed, missing and filled teeth and it is commonly used in epidemiological surveys. The DMFT count is often overdispersed, with excess zero counts. To address this type of distribution, Lewsey and Thomson applied ZINB regression models to fit the data (31). In the present study, Vuong's test showed that the ZINB regression model fit the data of this study better than other common statistical models. Thus, ZINB regression analysis was employed to analyse the effects of the independent variables.

The results showed that the higher the individual cariostat score is, the higher the possible ΔD4-6MFT score he or she could have. Developed by Shimono, the cariostat test is a colorimetric test that determines the acidogenecity of oral microorganisms in plaque through changes at a pH of 7 (32). The color changes from blue (scores 0, pH of 6.1 ± 0.3) to yellow (scores 3.0, pH of 4.0 ± 0.3). Cariostat has the ability to determine the acidogenecity of the bacteria without being affected by the amount of the microorganism colony (32). The higher the cariostat score, the higher the acidogenecity of the oral microorganisms. Therefore, the result found in the present study reveals a significant relationship between the composition of biofilm colonized on tooth surfaces and the increase in caries. Biofilm with active acidproductive and aciduric bacteria is a risk factor for dentin caries, which is consistent with previous studies (33). Cariostat has been proven to be a valid caries predictor in children (25). Unlike other chair-side cariogenic microbiology tests, such as Dentocult SM or Dentocult LB (which are no longer produced), cariostats assess the bacteria in dental plaques rather than in saliva. This results in increased accuracy because cariogenic bacteria work in the form of plaque on tooth surfaces.

Nevertheless, the results showed that the cariostat score was not a predictor for enamel caries when analyzing the caries free group, where most individuals developed only enamel caries. This result could be because the early stage of caries is less affected by bacteria with comparatively low acid-producing capability, whereas the cariostat test works by testing the activity of acid-producing bacteria in the biofilm (34). Hence, a potential limitation of the cariostat test is that it does not show good prediction performance in the early stage of caries.

Another risk factor identified in the whole population was sex; the results showed that females were more likely to have higher ΔD4-6MFT scores than males. In addition, in the caries-free population, females were more likely to develop new caries than males. A similar phenomenon has been observed in some other populations (35). The reason for the sex difference in caries development was inconclusive. The different salivary composition and flow rate, dietary habits, genetic variations, early eruption of teeth, and particular social roles in families were the most common factors explaining the consistent trend of higher caries rates in females than in males (36, 37).

It is not surprising to find that past caries experience was the only risk factor for the onset of new dentin caries in the whole population. As observed in other populations (38, 39), past caries experience was the strongest predictor of new dentin caries. However, it is not an ideal approach, as it is not conducive to the early prevention of dental caries. A 2-years cohort study reported not only that moderate and severe caries were associated with caries incidence but also that the initial caries were associated with caries incidence (40). To determine the initial factors for caries onset, only individuals whose D1-6MFT score was “0” were included in the further analysis.

Our results showed that in addition to sex, the frequency of snack consumption was another risk factor for the onset of enamel and dentin caries (mostly enamel caries) in the caries-free population. Snack consumption has gained an increasing role as a risk indicator for caries development in children (41, 42); even non-sweet snacks are potentially cariogenic due to their content of extensively hydrolysed starch (43). In the present study, individuals eating snacks every day had a higher risk of caries because it extends the duration of acid production and exposure, thereby tipping the scale toward the development of caries (44). Diet has been recognized as a caries risk factor in various models explaining the etiology of dental caries (4547). Recently, Meyer-Lueckel et al. introduced a pathogenesis model of caries based on the ecological plaque hypothesis, where a greater role has been assigned to sugar in the etiology (48). They hold the view that caries is a disease of civilizations that consume a greater amount of sugar, which was not the case throughout most of human history (49). Furthermore, the frequent consumption of fermentable carbohydrates causes a pathological shift in the oral microflora, leading to an increase in cariogenic bacteria (50). Therefore, it is meaningful to advocate less snack consumption in adolescents to prevent dental caries.

In the negative binomial portion, individuals from one-child families or who used fluoride toothpaste were likely to have relatively low ΔD1-6MFT scores. These results were consistent with those in previous studies (35, 51). Fluoride can help the hydroxyapatite remineralization process, and it is most abundant in the outer layers of enamel, which explains why individuals using fluoride toothpaste were likely to have less enamel caries (52). Currently, there is no fluoride tap water in mainland China, and for most places like Foshan in South China, the water fluoride concentration was low (<0.30 mg/L) (53). As a result, it is critical to promote clinical and personal fluoride usage among children. Additionally, in this study, individuals with a high saliva buffering capability (pH ≥ 4.25) were likely to have a lower ΔD1-6MFT score than those with a low saliva buffering capability (pH < 3.5), implicating of saliva buffering tests to distinguish risk adolescents. Saliva buffering fast check kits, are now provided by some manufacturers, like the “Saliva-check” by GC, and “CRT buffer” by Ivoclar. These kits can quickly test the saliva buffering capability and easily be used by non-professional practitioners. These kits make it possible to to check the saliva buffering capability for both clinical and public health use in future.

An interesting finding in this study is that the variables regarding oral hygiene, including the plaque index and teeth brushing frequency, were found to be negatively correlated with caries development. Oral hygiene was not a caries risk factor in this population. The failure of oral hygiene in prediction among this population could due to their genetic background. Strömberg et al. indicated that individuals with a specific genetic background may develop more caries from bad oral hygiene than individuals with other genetic backgrounds (54). Hence, variables such as PlI and tooth brushing frequency could still be predictable in other populations with different genetic backgrounds.

Adolescence is a vital life stage where children begin to develop self-performed oral health habits instead of relying solely on parental supervision. Ostberg et al. reported that children's oral health-related behaviors will change significantly during adolescence (6). Adolescents at baseline were all at their first year in middle school, when they started to “gain more freedom” in oral health behaviors (e.g., less brushing teeth or eating more snacks without parent's supervision). Furthermore, evidences from other longitudinal research indicate a significantly high rate of caries progression in 11–16-year-olds (45, 46). As a result, though remained free of caries until adolescence, it is still possible for individuals in caries free group to developed dental caries lesions in 1-year follow up. However, in the present study X-ray was not applied in the caries detection, and some proximal initial caries could have been missed. As a result, the results of the “caries-free group” still need to be seen with caution.

The present evidence shows that dental caries, when including enamel caries, could be very prevalent with a prevalence rate of over 80% among most populations aged 12–15 years, as was our population (5557). The reason for a high prevalence rate could be insufficient awareness of initial caries in most adolescents, their guardians and even clinical dentists. It was suggested that approximately half of the initial proximal lesions in 15-year-old adolescents progress to cavitated lesions at the age of 20 (58). Preventing the onset and development of enamel caries deserves more attention. According to the International Caries Classification and Management System (ICCMS™), the caries activity judgement is a practical tool in clinical management of caries lesions (59). The treatment decision routine with lesion activity judgement has been proven reliable in daily clinical practice. Additionally, the unique potential of activity judgement makes it a research tool for exploring transition patterns of caries lesions in response to different interventions. Most valuably, caries activity judgement in the planning and organization of dental public health services can provide information about the amount of active non-cavitated lesions indicated for non-operative treatment (60). Nevertheless, the information about lesion activities was not recorded in our data, which could be a weakness of this study. The main reason why caries lesion activities were not evaluated is that the lesion activity could change with time, and the activity of some enamel caries could change without substantial progression. The change could be mercurial, under which circumstance a shorter follow-up interval (usually 3 months or shorter) should be set. The present study design was not able to monitor the activity change throughout the year. Future studies with a shorter follow-up interval should be conducted to explore the transition patterns of caries lesions.

In many developed countries, the level of dental caries experience has declined in the past few decades (61). The incidence density was estimated as 0.5–0.7 per year per person (count by D3MFT, represented as D4-6MFT in this study) in an ecological time-trend study in adolescents aged 12–18 years in Norway (62). The incidence density of 2,848 adolescents in another 4-years cohort study in Sweden was estimated as 0.5 per year per person (count by D4-6S) (63). In the present study, the incidence density was 1.08 (count by D4-6MFT). This number should be higher than those in adolescents in Norway and Sweden. Although the caries prevalence rate in China is lower than that in developed countries (1), it shows a growing trend, and the incidence is also higher than those in developed countries. The observed high incidence of caries could mainly be the result of inadequate awareness of public health in China. Benefitting from rapid economic development, children are consuming more sugars than 10 years ago; nevertheless, few dental public health measures have been applied, whereas they have been applied for decades in developed countries. Therefore, in China more public health resources must be devoted to caries.

The increase in caries in the studied adolescents was higher than those in developed countries, indicating more that dental public health resources are necessary. Our results suggest that past caries experience is still the strongest predicator for dentin caries. Female individuals and individuals with a high cariostat score tended to develop more dentin caries. These factors are suitable for distinguishing high-risk individuals. After excluding the influence of past caries experience, the frequency of snack consumption, sex, saliva buffering capability, fluoride toothpaste usage, and belonging to a one-child family were risk factors of dental caries. As a result, advocating less snack consumption and promoting fluoride toothpaste could help to prevent caries; meanwhile, sex, saliva buffering capability, and number of children in the family should be indicators for distinguishing the high-risk individuals. However, the result should be treated with caution because no X-ray was applied in the caries detection; thus, the proximal initial caries could have been missed, and a multistage cluster sampling technique was adopted, which could amplify the sampling error. These limitations could cause some bias in the result.

Data Availability Statement

The datasets generated for this study are available on request to the corresponding author.

Ethics Statement

The studies involving human participants were reviewed and approved by Ethical Review Committee of Guanghua School of Stomatology, Sun Yat-Sen University. Written informed consent to participate in this study was provided by the participants' legal guardian/next of kin.

Author Contributions

HL substantially contributed to conception and design of this study. KW, LP, CF, TC, and LY contributed to acquisition, analysis, and interpretation of data. KW drafted the manuscript. LP, CF, TC, LY, and HL revised the manuscript for important intellectual content critically. All authors gave final approval to this article, and all agreed to be accountable for all aspects of the work in ensuring that questions relating to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Funding

The present study was supported by the National Natural Science Foundation of China (no. 81570967) and China's Forth National Oral Health Epidemiology Survey (no. 201502002).

Conflict of Interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

We gratefully acknowledge the assistance of the staff at the Preventive Dentistry at the Hospital of Stomatology of Sun Yat-Sen University and the staff at Foshan Stomatology Hospital for their assistance during the oral examination and sample collection process. All of them agreed on the manuscript submission.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fped.2020.00419/full#supplementary-material

References

1. Oral health. Available online at: https://www.who.int/news-room/fact-sheets/detail/oral-health (accessed December 1, 2019).

2. Adolescent Oral Health Care. Available online at: https://www.aapd.org/research/oral-health-policies–recommendations/adolescent-oral-health-care/ (accessed January 16, 2020).

3. Petersen PE, Bourgeois D, Ogawa H, Estupinan-Day S, Ndiaye C. The global burden of oral diseases and risks to oral health. Bull World Health Organ. (2005) 83:661–9.

PubMed Abstract | Google Scholar

4. Quan JK, Wang XZ, Sun XY, Yuan C, Liu XN, Wang X, et al. Permanent teeth caries status of 12- to 15-year-olds in China: findings from the 4th National Oral Health Survey. Chin J Dent Res. (2018) 21:181–93. doi: 10.3290/j.cjdr.a41080

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Sun X, Bernabé E, Liu X, Gallagher JE, Zheng S. Determinants of catastrophic dental health expenditure in China. PLoS ONE. (2016) 11:e0168341. doi: 10.1371/journal.pone.0168341

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Ostberg A-L, Jarkman K, Lindblad U, Halling A. Adolescents' perceptions of oral health and influencing factors: a qualitative study. Acta Odontol Scand. (2002) 60:167–73. doi: 10.1080/000163502753740197

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Weber M, Bogstad Søvik J, Mulic A, Deeley K, Tveit AB, Forella J, et al. Redefining the phenotype of dental caries. Caries Res. (2018) 52:263–71. doi: 10.1159/000481414

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Cagetti MG, Bontà G, Cocco F, Lingstrom P, Strohmenger L, Campus G. Are standardized caries risk assessment models effective in assessing actual caries status and future caries increment? a systematic review. BMC Oral Health. (2018) 18:123. doi: 10.1186/s12903-018-0585-4

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Benjamin RM. Oral health: the silent epidemic. Public Health Rep. (2010) 125:158–9. doi: 10.1177/003335491012500202

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Zukanović A. Caries risk assessment models in caries prediction. Acta Med Acad. (2013) 42:198–208. doi: 10.5644/ama2006-124.87

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Featherstone JDB, Chaffee BW. The evidence for caries management by risk assessment (CAMBRA®). Adv Dent Res. (2018) 29:9–14. doi: 10.1177/0022034517736500

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Bratthall D, Petersson GH. Cariogram – a multifactorial risk assessment model for a multifactorial disease. Community Dent Oral Epidemiol. (2005) 33:256–64. doi: 10.1111/j.1600-0528.2005.00233.x

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Hu J, Jiang W, Lin X, Zhu H, Zhou N, Chen Y, et al. Dental caries status and caries risk factors in students ages 12–14 years in Zhejiang, China. Med Sci Monit. (2018) 24:3670–8. doi: 10.12659/MSM.907325

PubMed Abstract | CrossRef Full Text | Google Scholar

14. Kung AYH, Zhang S, Zheng LW, Wong GHM, Chu CH. Oral health status of chinese paediatric and adolescent oncology patients with chemotherapy in Hong Kong: a pilot study. Open Dent J. (2015) 9:21–30. doi: 10.2174/1874210601509010021

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Baker SR, Mat A, Robinson PG. What psychosocial factors influence adolescents' oral health? J Dent Res. (2010) 89:1230–5. doi: 10.1177/0022034510376650

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Foshan Municipal Bureau of Statistics. Statistical Communique of 2017. National Economic and Social Development of Foshan City - China Statistics Information Network. Statistical Communique of 2017. National Economic and Social Development of Foshan City - China Statistics Information Network. (2018). Available online at: http://www.tjcn.org/tjgb/19gd/35445.html (accessed January 11, 2019).

17. Foshan Water Conservancy Bureau. Foshan Municipal Water Affairs Bureau - Foshan City Water Supply Monthly Announcement (June 2017). Foshan Municipal Water Affairs Bureau - Foshan City Water Supply Monthly Announcement (June 2017). (2017). Available online at: http://www.fswater.gov.cn/zhengwu/ywxx/gongshui/gs_szgb/201707/t20170714_6258352.html (accessed January 11, 2019).

18. Thompson SK. Adaptive cluster sampling. J Am Stat Assoc. (1990) 85:1050–9. doi: 10.1080/01621459.1990.10474975

CrossRef Full Text | Google Scholar

19. Fisher-Owens SA, Gansky SA, Platt LJ, Weintraub JA, Soobader M-J, Bramlett MD, et al. Influences on children's oral health: a conceptual model. Pediatrics. (2007) 120:e510–20. doi: 10.1542/peds.2006-3084

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Foshan Statistics Bureau. Foshan Statistical Yearbook 2017. Foshan People's Government Portal. (2018). Available online at: http://www.foshan.gov.cn/gzjg/stjj/tjnj_1110962/content/post_1705913.html (accessed March 29, 2020).

21. Löe H. The gingival index, the plaque index and the retention index systems. J Periodontol. (1967) 38:610–6. doi: 10.1902/jop.1967.38.6.610

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Pitts NB, Ekstrand KR, ICDAS Foundation. International Caries Detection and Assessment System (ICDAS) and its International Caries Classification and Management System (ICCMS) - methods for staging of the caries process and enabling dentists to manage caries. Community Dent Oral Epidemiol. (2013) 41:e41–52. doi: 10.1111/cdoe.12025

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Aidara AW, Pitts N, Ottolenghi L, Senakola E, Bourgeois D. Comparison between measurements of tooth decay with an International Caries Detection and Assessment system method versus the decayed, missing, and filled teeth method. Int J Contemp Dent. (2016) 7:9.

Google Scholar

24. Banting D, Eggertsson H, Ekstrand KR, Ferreira-Zandoná A, Ismail AI, Longbottom C, et al. Rationale and evidence for the international caries detection and assessment system (ICDAS II). Ann Arbor. (2005) 1001:48109–1078. doi: 10.17096/jiufd.38691

CrossRef Full Text | Google Scholar

25. Nishimura M, Oda T, Kariya N, Matsumura S, Shimono T. Using a caries activity test to predict caries risk in early childhood. J Am Dent Assoc. (2008) 139:63–71. doi: 10.14219/jada.archive.2008.0022

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Ericsson Y. Clinical investigations of the salivary buffering action. Acta Odontol Scand. (1959) 17:131–65. doi: 10.3109/00016355908993928

CrossRef Full Text | Google Scholar

29. Gomez J. Detection and diagnosis of the early caries lesion. BMC Oral Health. (2015) 15:S3. doi: 10.1186/1472-6831-15-S1-S3

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Bhoopathi RH, Patil PU, Kamath BV, Gopal D, Kumar S, Kulkarni G. Caries detection with ICDAS and the WHO criteria: a comparitive study. JCDR. (2017) 11:ZC09 12. doi: 10.7860/JCDR/2017/29017.10929

CrossRef Full Text | Google Scholar

31. Lewsey JD, Thomson WM. The utility of the zero-inflated Poisson and zero-inflated negative binomial models: a case study of cross-sectional and longitudinal DMF data examining the effect of socio-economic status. Community Dent Oral Epidemiol. (2004) 32:183–9. doi: 10.1111/j.1600-0528.2004.00155.x

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Rodis OMM, Ji Y, Matsumura S, Shimono T, Okazaki Y. Comparison of plaque samples and saliva samples using the CAT21 test ® (Cariostat method). Pediatr Dent J. (2005) 15:6–9. doi: 10.1016/S0917-2394(05)70023-9

CrossRef Full Text | Google Scholar

33. Aas JA, Griffen AL, Dardis SR, Lee AM, Olsen I, Dewhirst FE, et al. Bacteria of dental caries in primary and permanent teeth in children and young adults. J Clin Microbiol. (2008) 46:1407–17. doi: 10.1128/JCM.01410-07

CrossRef Full Text | Google Scholar

34. Parisotto TM, Steiner-Oliveira C, Duque C, Peres RCR, Rodrigues LKA, Nobre-dos-Santos M. Relationship among microbiological composition and presence of dental plaque, sugar exposure, social factors and different stages of early childhood caries. Arch Oral Biol. (2010) 55:365–73. doi: 10.1016/j.archoralbio.2010.03.005

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Martinez-Mier EA, Zandona AF. The impact of gender on caries prevalence and risk assessment. Dent Clin North Am. (2013) 57:301–15. doi: 10.1016/j.cden.2013.01.001

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Ferraro M, Vieira AR. Explaining gender differences in caries: a multifactorial approach to a multifactorial disease. Int J Dent. (2010) 2010: 649643. doi: 10.1155/2010/649643

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Richards VP, Alvarez AJ, Luce AR, Bedenbaugh M, Mitchell ML, Burne RA, et al. Microbiomes of site-specific dental plaques from children with different caries status. Infect Immun. (2017) 85:e00106-17. doi: 10.1128/IAI.00106-17

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Dou L, Luo J, Fu X, Tang Y, Gao J, Yang D. The validity of caries risk assessment in young adults with past caries experience using a screening cariogram model without saliva tests. Int Dental J. (2018) 68:221–6. doi: 10.1111/idj.12378

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Fernando S, Kumar S, Bakr M, Speicher D, Lea R, Scuffham PA, et al. Children's untreated decay is positively associated with past caries experience and with current salivary loads of mutans Streptococci; negatively with self-reported maternal iron supplements during pregnancy: a multifactorial analysis. J Public Health Dent. (2019) 79:109–15. doi: 10.1111/jphd.12301

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Guedes RS, Piovesan C, Ardenghi TM, Emmanuelli B, Braga MM, Mendes FM. Presence of initial caries lesions as a risk factor for caries in preschool children: a cohort study. Caries Res. (2018) 52:32–41. doi: 10.1159/000479824

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Holloway PJ, Moore WJ. The role of sugar in the aetiology of dental caries: 1. sugar and the antiquity of dental caries. J Dent. (1983) 11:189–90. doi: 10.1016/0300-5712(83)90182-3

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Marsh PD. Microbial ecology of dental plaque and its significance in health and disease. Adv Dental Res. (1994) 8:263–71. doi: 10.1177/08959374940080022001

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Milgrom P, Reisine S. Oral health in the United States: the post-fluoride generation. Annu Rev Public Health. (2000) 21:403–36. doi: 10.1146/annurev.publhealth.21.1.403

PubMed Abstract | CrossRef Full Text | Google Scholar

44. Marshall TA, Broffitt B, Eichenberger-Gilmore J, Warren JJ, Cunningham MA, Levy SM. The roles of meal, snack, and daily total food and beverage exposures on caries experience in young children. J Public Health Dent. (2005) 65:166–73. doi: 10.1111/j.1752-7325.2005.tb02807.x

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Mejàre I, Källestål C, Stenlund H. Incidence and progression of approximal caries from 11 to 22 years of age in sweden: a prospective radiographic study. Caries Res. (1999) 33:93–100. doi: 10.1159/000016502

PubMed Abstract | CrossRef Full Text | Google Scholar

46. Hintze H. Approximal caries prevalence in Danish recruits and progression of caries in the late teens: a retrospective radiographic study. Caries Res. (2001) 35:27–35. doi: 10.1159/000047427

PubMed Abstract | CrossRef Full Text | Google Scholar

47. Keyes PH. Recent advances in dental caries research. bacteriology. bacteriological findings and biological implications. Int Dent J. (1962) 12:443–64.

Google Scholar

48. Fejerskov O. Changing paradigms in concepts on dental caries: consequences for oral health care. Caries Res. (2004) 38:182–91. doi: 10.1159/000077753

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Featherstone JDB. The caries balance: contributing factors and early detection. J Calif Dent Assoc. (2003) 31:129–33.

PubMed Abstract | Google Scholar

50. Meyer-Lueckel H, Paris S, Ekstrand KR, Effenberger S. Caries management: science and clinical practice. In: Mohammad Alkilzy, et al. Meyer-Lueckel, Hendrik; Paris, Sebastian; Kim R. Ekstrand; managing editor. Susanne Effenberger, With Contributions. Stuttgart: Thieme. (2013). doi: 10.1055/b-002-85484

CrossRef Full Text | Google Scholar

51. Prakash P, Subramaniam P, Durgesh BH, Konde S. Prevalence of early childhood caries and associated risk factors in preschool children of urban Bangalore, India: a cross-sectional study. Eur J Dent. (2012) 6:141–52. doi: 10.1055/s-0039-1698943

PubMed Abstract | CrossRef Full Text | Google Scholar

52. Lacruz RS, Habelitz S, Wright JT, Paine ML. Dental enamel formation and implications for oral health and disease. Physiol Rev. (2017) 97:939–93. doi: 10.1152/physrev.00030.2016

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Luo W, Gao X, Zhang X. Geochemical processes controlling the groundwater chemistry and fluoride contamination in the Yuncheng Basin, China—an area with complex hydrogeochemical conditions. PLoS ONE. (2018) 13:e0199082. doi: 10.1371/journal.pone.0199082

PubMed Abstract | CrossRef Full Text | Google Scholar

54. Strömberg N, Esberg A, Sheng N, Mårell L, Löfgren-Burström A, Danielsson K, et al. Genetic- and lifestyle-dependent dental caries defined by the acidic proline-rich protein genes PRH1 and PRH2. EBioMedicine. (2017) 26:38–46. doi: 10.1016/j.ebiom.2017.11.019

PubMed Abstract | CrossRef Full Text | Google Scholar

55. Wang X, Shaffer JR, Weyant RJ, Cuenco KT, DeSensi RS, Crout R, et al. Genes and their effects on dental caries may differ between primary and permanent dentitions. Caries Res. (2010) 44:277–84. doi: 10.1159/000314676

PubMed Abstract | CrossRef Full Text | Google Scholar

56. Wu Y, Jansen EC, Peterson KE, Foxman B, Goodrich JM, Hu H, et al. The associations between lead exposure at multiple sensitive life periods and dental caries risks in permanent teeth. Sci Total Environ. (2019) 654:1048–55. doi: 10.1016/j.scitotenv.2018.11.190

PubMed Abstract | CrossRef Full Text | Google Scholar

57. Lambert MJ, Vanobbergen JSN, Martens LC, Visschere LMJD. Socioeconomic inequalities in caries experience, care level and dental attendance in primary school children in Belgium: a cross-sectional survey. BMJ Open. (2017) 7:e015042. doi: 10.1136/bmjopen-2016-015042

PubMed Abstract | CrossRef Full Text | Google Scholar

58. Isaksson H, Alm A, Koch G, Birkhed D, Wendt LK. Caries prevalence in Swedish 20-year-olds in relation to their previous caries experience. Caries Res. (2013) 47:234–42. doi: 10.1159/000346131

PubMed Abstract | CrossRef Full Text | Google Scholar

59. Ismail AI, Pitts NB, Tellez M, Authors of International Caries Classification Management System (ICCMS), Banerjee A, Deery C, et al. The International Caries Classification and Management System (ICCMSTM) an example of a caries management pathway. BMC Oral Health. (2015) 15(Suppl 1):S9. doi: 10.1186/1472-6831-15-S1-S9

PubMed Abstract | CrossRef Full Text | Google Scholar

60. Nyvad B, Baelum V. Nyvad criteria for caries lesion activity and severity assessment: a validated approach for clinical management and research. Caries Res. (2018) 52:397–405. doi: 10.1159/000480522

PubMed Abstract | CrossRef Full Text | Google Scholar

61. Pitts NB, Zero DT, Marsh PD, Ekstrand K, Weintraub JA, Ramos-Gomez F, et al. Dental caries. Nat Rev Dis Primers. (2017) 3:17030. doi: 10.1038/nrdp.2017.30

PubMed Abstract | CrossRef Full Text | Google Scholar

62. Haugejorden O, Birkeland JM. Ecological time-trend analysis of caries experience at 12 years of age and caries incidence from age 12 to 18 years: Norway 1985–2004. Acta Odontol Scand. (2006) 64:368–75. doi: 10.1080/00016350600856083

PubMed Abstract | CrossRef Full Text | Google Scholar

63. Källestål C, Fjelddahl A. A four-year cohort study of caries and its risk factors in adolescents with high and low risk at baseline. Swed Dent J. (2007) 31:11–25.

PubMed Abstract | Google Scholar

Keywords: caries, ICDAS, ZINB, adolescent, epidemic

Citation: Wang K, Pang L, Fan C, Cui T, Yu L and Lin H (2020) Enamel and Dentin Caries Risk Factors of Adolescents in the Context of the International Caries Detection and Assessment System (ICDAS): A Longitudinal Study. Front. Pediatr. 8:419. doi: 10.3389/fped.2020.00419

Received: 17 January 2020; Accepted: 18 June 2020;
Published: 28 July 2020.

Edited by:

Cynthia Yiu, The University of Hong Kong, Hong Kong

Reviewed by:

Manikandan Ekambaram, University of Otago, New Zealand
Bruno Emmanuelli, Universidade Regional Integrada Do Alto Uruguai e das Missões, Brazil

Copyright © 2020 Wang, Pang, Fan, Cui, Yu and Lin. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Huancai Lin, linhc@mail.sysu.edu.cn

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