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Saudi Journal of Medicine & Medical Sciences logoLink to Saudi Journal of Medicine & Medical Sciences
. 2023 Jul 15;11(3):219–228. doi: 10.4103/sjmms.sjmms_128_23

Predictors of Caries Risk among Egyptian Children Attending Pediatric Dental Clinics at a University Hospital

Rabaa Mahmoud Aboubakr 1,, Doaa Mohsen Alkhadragy 1, Mai Monuir El Said Okda 1, Hadeer Wael Mohamed Rady 1, Rasha Mokhtar Elnagar 2,3
PMCID: PMC10393090  PMID: 37533660

Abstract

Background:

Dental caries is the most prevalent dental disease. The external validity of the available caries risk assessment (CRA) tools is not established, especially among pediatric population.

Objectives:

To assess caries risk using the caries management by risk assessment (CAMBRA) protocol among Egyptian children aged 3–12 years and suggest variables that could potentially be used to develop a simpler CRA model.

Materials and Methods:

For this cross-sectional study, we recruited 320 children aged 3 to <6 years (Group I) and 320 children aged 6–12 years (Group II). CAMBRA was used to collect data about disease indicators, biological and environmental factors, and protective factors among study participants. Each child was examined clinically to collect data about past caries experiences and to measure plaque scores.

Results:

The risk of caries was high in 92.5% of Group I and 83.4% of Group II participants. The overall dmft was 5.71 ± 3.18 for Group I and 4.78 ± 2.53 for Group II. In Group I, a significant positive relation was found between the overall mean caries risk score and past caries experience (dmft; r = 0.344, P < 0.001) and mean plaque index (r = 0.463, P < 0.001). In Group II, a significant positive relation was found between the overall mean caries risk score and dmft score (r = 0.511, P < 0.001), S. mutans count (r = 234, P < 0.001), Lactobacilli count (r = 0.316, P < 0.001), and plaque index (r = 0.463, P < 0.001). Participants’ age, parents’ education, and parents’ occupation had a negative significant effect on the overall mean caries risk score.

Conclusion:

This study suggests predictors that can be used in the development of a new CRA model for children aged 3–12 years.

Keywords: Child, dental caries, dental caries susceptibility, Egypt, risk assessment

INTRODUCTION

The American Academy of Pediatric Dentistry (AAPD) recognizes early childhood caries as a significant chronic disease, resulting from an imbalance between multiple risk and protective factors over time.[1] When pathological factors overcome the preventive factors, dental hard tissue break down occurs, which can lead to pain and tooth loss.[2] Risk assessment may be a useful tool in caries prevention and management. It can be used as a strategy for improving the efficiency and effectiveness of preventive procedures and programs. Better and more cost-effective treatment can be provided by using risk assessment rather than providing treatments independent of the individual’s risk.[3] To identify those at risk, several caries risk assessment (CRA) models have been developed such as the AAPD Caries-risk Assessment Form, Cariogram, the American Dental Association model, and the caries management by risk assessment (CAMBRA) protocol.[4]

CAMBRA was developed at the University of California, San Francisco (UCSF), in 2003, and has been updated several times based on clinical outcomes.[5-8] Risk is measured by several factors that contribute to caries progression or reversal: clinical observations, preventive factors, biological and environmental risk factors, and the clinical judgment of the care provider.[6,8] In CAMBRA, separate forms are used for CRA for two age ranges: aged 0 to <6 years and aged ≥6 years through adulthood. The caries risk level is classified by health care workers as low, moderate, high, or extremely high/extreme, depending on factors involved in the management of caries.[7] Recently, CRA has become the basis of preventive and minimal invasive approaches to caries management.[9,10] Worldwide, caries risk has been assessed using different CRA tools, but CAMBRA is most commonly used.[11] However, some of CAMBRA’s items such as 5000 ppm F toothpaste, F varnish in the past 6 months, 0.05% sodium fluoride mouth rinse daily, and 0.12% chlorhexidine gluconate mouth rinse daily 7 days monthly, cannot be generalized in all countries because of differences in individuals’ health awareness and socioeconomic levels. As stated by Young and Featherstone,[12] protocols and forms should be easy to understand and apply in clinical practice for successful caries management by risk assessment. In addition, there is a need for use of unified models across countries and similar studies to enable direct comparisons, and thus help provide consolidated data. In Egypt, there is insufficient evidence about the feasibility of using CAMBRA as a CRA tool among children.[13] Therefore, this study was conducted to collect data about the distribution of caries risk among Egyptian preschool- and school-aged children, and potentially suggest variables for developing a simpler CRA model that can easily be adopted universally.

MATERIALS AND METHODS

Study design, setting, and participants

This cross-sectional study was conducted in the Pediatric Department of the Faculty of Dentistry at Mansoura University, Mansoura, Egypt, between June 01 and September 30, 2022.

The study was conducted after obtaining approval from the Ethics Committee of the Faculty of Dentistry at Mansoura University. Legal guardians of the study participants were informed about the aim and specific objectives of the research and the value of their children’s participation. Furthermore, they were informed that participation was voluntary and that the children’s identities would be kept anonymous and confidential. Written informed consent was collected from parents/legal guardians prior to the data collection stage.

Sample size and group allocation

Oral screening was carried out for 5324 children who attended the pediatric dental clinic during the study period, of which 4320 children fulfilled the study criteria, which were being aged 3–12 years, free from systemic diseases or disabilities, and parents providing consent for participation. The eligible children (4320) were categorized into two groups: Group I (aged 3 to <6 years: 2592) and Group II (aged 6–12 years: 1728). The presumed population proportion was based on the reported prevalence of dental caries in Egypt: for Group I, it was considered as 61.4%,[14] and for Group II, as 60%.[15] An online sample size calculator was used to calculate the required sample (https://www.calculator.net/sample-size-calculator.html): with a 95% confidence level, 5% margin of error, the final subsample size for each group was calculated as 320 children for Group I and 305 children for Group II. Subsequently, a simple random sampling technique was used to recruit 320 children in each group (N = 640) [Figure 1].

Figure 1.

Figure 1

Flowchart showing study design and sample selection

Examiners training and calibration

Clinical examination was carried out by three clinical instructors in the Departments of Pediatric Dentistry and Dental Public Health. Although the examiners were well-trained in measuring oral hygiene and dental caries indexes, their skill was calibrated after a period of training on the assigned indexes. For training, each examiner practiced the examination on a group of 10 children for 2 days (n = 20). After two days, every examiner independently examined the same group of 20 children and compared their findings with those of the other examiners in the team; the inter-examiner reliability was >86%, which was considered good.[16] Regarding intra-examiner reliability, each examiner examined a group of 25 subjects twice, with a time interval of at least 30 minutes between examinations; the intraclass correlation coefficient was >93%; which was considered excellent based on Fleiss.[17]

Data collection

The participants’ risk for caries was assessed for both groups using CAMBRA.[18] These risk assessment forms enable investigators to collect data about disease indicators, biological and environmental factors, and protective factors. Any disease indicator listed on the forms was scored +3, any item related to biological and environmental factors was scored +2, and any item related to protective factors was scored −1. For Group I, overall scores of −4 to −1 indicated minimal risk for caries, 0 to 3 moderate risk, 4 to 13 high risk, and 14 to 18 extremely high risk. For Group II, overall scores of −8 to −2 indicated minimal risk for caries, −1 to 2 moderate risk, 3 to 17 high risk, and 18 to 30 extremely high risk.[19]

In addition, social indicators such as parents’ education levels and occupations were used to evaluate the socioeconomic levels of the participating children.[20,21]

Clinical examination

The oral examination was conducted in the pediatric dental clinic in regular dental chairs using artificial light. To assess the oral hygiene of children in Group II, the examiner used the Silness and Loe plaque index,[21] wherein a score of <1 indicates minimal risk for future caries and a score of >2 indicates elevated risk, while scores 1–2 indicated moderate risk. To assess the oral hygiene of children in Group I, plaque was determined to be present (score of 1) or absent (score of 0) based on the eruption date of teeth specified in the plaque index. To assess dental caries in primary/permanent teeth, examiners used indexes of decayed/Decayed, missing/Missed, and filled/Filled primary/permanent teeth/Tooth (dmft/DMFT) index.[22] A Community Periodontal Index (CPI) probe was used to detect dental caries using criteria of the World Health Organization for the diagnosis of dental caries.[22] A dmft/DMFT score of ≤1 indicated insignificant risk for dental caries, and a score of ≥6 indicated elevated risk for future caries, while scores more than 2 to 5 indicated moderate risk.

Salivary parameters

Children in Group II were instructed to refrain from eating or drinking for 1 hour before salivary sample collection. They were seated in a relaxed, upright position and given equal pieces of paraffin pellets (Paraffin pellets, Ivoclar Vivadent Marketing Ltd., Gurugram, India). They were instructed to chew for 30 s and then swallow the collected saliva, and then continue chewing for 5 min, spitting out the collected saliva every 1 min into 15-mL graduated test tubes. To calculate the stimulated salivary flow rate (SSFR) in milliliters per minute, the amount of collected saliva was divided by 5.[23] A SSFR of ≥1 mL/min indicates insignificant risk, and an SSFR of ≤0.5 mL/min indicates elevated risk for future caries.[23]

Bacterial isolation

The salivary samples were transported on the same day as collected to the Microbiology Diagnostic and Infection Control Unit at the Medical Microbiology and Immunology Department, Faculty of Medicine, Mansoura University, for microbiological testing. Two selective culture media were used: Lactobacillus MRS agar (Titan Biotech Ltd., Rajasthan, India) for isolation of Lactobacillus species and BD DIFCOTM Mitis Salivarius Agar 500 g (Becton, Dickinson and Company, Sparks, MD, USA) for isolation of Streptococcus mutans. All culture plates were incubated anaerobically at 37°C for 48 h. The bacterial colonies were identified according to their morphological and biochemical characteristics.[24,25] The bacterial count was conducted with an automated cell counter (Biotec Laboratory Equipment, Alexandria, Egypt), with a bacterial count of >106 colony-forming units (CFU) for S. mutans[26] and >105 CFU for Lactobacillus indicated elevated risk for future dental caries.[13]

Statistical analysis

To analyze the data, SPSS version 20.0 (IBM Corp. Chicago, IL, USA) was used. Standard descriptive statistics such as means, standard deviations, and frequencies were calculated to determine the characteristics of the sample. To compare two or more means, the Mann–Whitney U and Kruskal–Wallis tests were used for nonparametric data, and independent two-sample t test and one-way analysis of variance was used for normally distributed data. To examine the correlations between at least two continuous variables, we used Pearson’s correlation coefficient for normally distributed data and Spearman’s coefficient for nonparametric data. We performed linear regression analysis to determine the effect of significant predictors on dependent variables. The confidence interval was set at 95%, and P value <0.05 was considered statistically significant.

RESULTS

The mean ages of study participants were 5.04 ± 0.91 years in group I and 8.34 ± 1.48 years in group II. Both groups had more boys than girls. Of the parents, none had postgraduate degrees; parents with middle-level education predominated in both groups I (58.4%) and II (58.1%), as did parents with nonskilled occupations (70.9% and 60.3%, respectively) [Table 1].

Table 1.

Demographic characteristics of study participants (N=320)

Demographic characteristics Group I, n (%) Group II, n (%)
Gender
 Male 162 (50.6) 177 (55.3)
 Female 158 (49.4) 143 (44.7)
Parent’s education
 No education 98 (30.6) 100 (31.3)
 Middle-level education 187 (58.4) 186 (58.1)
 University education 35 (10.9) 34 (10.6)
Parent’s occupation
 Nonskilled 227 (70.9) 193 (60.3)
 Semiskilled 58 (18.1) 93 (29.1)
 Skilled 35 (10.9) 34 (10.6)

n – Number of participating children in Group I and II

Risk of caries

Of the 320 participants in Group I, 296 (92.5%) demonstrated high risk of caries, while the remaining 24 (7.5%) demonstrated moderate risk [Figure 2]. Of the 320 participants in group II, 267 (83.4%) demonstrated high risk of caries, 21 (6.6%) moderate risk, and 32 (10%) low caries risk.

Figure 2.

Figure 2

Distribution of risk levels among study participants

In Group I, the total mean dmft score was 5.71 ± 3.18, with 5.3% of the children having a score of 1 and 1.3% a score of 20. In Group II, the overall mean dmft score was 4.78 ± 2.53, with 9.4% of the children having a score of 1, while 0.9% had a score of 11. In Group II, the mean DMFT was 0.61 ± 0.94, with 66.6% of the children having a score of 0 and 0.9% having 4 [Figures 3 and 4]. About 37.8% of the children in Group I had plaque, which was scored as present (1) or absent (0). The overall mean plaque score in group II was 1.59 ± 0.82, with a score of 3 found in 3.1% of the children; only 0.6% of the children demonstrated a score of 0 [Figure 5].

Figure 3.

Figure 3

Distribution of dmft scores among study participants. dmft – decayed, missing, and filled tooth

Figure 4.

Figure 4

Distribution of DMFT scores among study participants (Group II). DMFT – Decayed, Missing, and Filled tooth

Figure 5.

Figure 5

Distribution of plaque scores among study participants

In Group I, the caries risk level was high for similar proportions of boys (49.8%) and girls [50.2%; Table 2]. Of the parents of the children at high risk, a majority (59.7%) had a middle-level education, and a majority (73.6%) had nonskilled occupations. Among the children in Group II, a higher caries risk level was more characteristic of boys (57.3%) than girls (42.7%). Of the parents of the children at high risk, a majority (55.8%) had a middle-level education, and a majority (61.4%) had nonskilled occupations.

Table 2.

Risk levels among study participants

Demographic characteristics Group I Group II


Low caries risk Moderate caries risk, n (%) High caries risk, n (%) Low caries risk, n (%) Moderate caries risk, n (%) High caries risk, n (%)
Gender
 Male - 15 (62.5) 147 (49.8) 10 (31.3) 7 (33.3) 153 (57.3)
 Female - 9 (37.5) 148 (50.2) 22 (68.8) 14 (66.7) 114 (42.7)
Parent’s education
 No education - 4 (16.7) 94 (31.9) 3 (9.4) 6 (28.6) 91 (34.1)
 Middle-level education - 10 (41.7) 176 (59.7) 22 (68.8) 15 (71.4) 149 (55.8)
 University education - 10 (41.7) 25 (8.5) 7 (21.9) 0 27 (10.1)
Parent’s occupation
 Nonskilled - 9 (37.5) 217 (73.6) 11 (34.4) 18 (85.7) 164 (61.4)
 Semiskilled - 5 (20.8) 53 (18) 14 (43.8) 3 (14.3) 76 (28.5)
 Skilled - 10 (41.7) 25 (8.5) 7 (21.9) 0 27 (10.1)
 Totala - 24 (7.5) 296 (92.5) 32 (10) 21 (6.6) 267 (83.4)

aPercentages in this row reflect the total number of children in each group

Among children in Group I, the overall mean caries risk score was 8.61; the mean caries risk score was slightly higher for girls (8.86) than for boys [8.35; Table 3]. The parents’ education levels and occupations differed significantly (P < 0.001) regarding overall mean risk score: among all socioeconomic indicators, the overall mean caries risk score was highest for children whose parents had no education (9.42) and for those whose parents had nonskilled occupations (9.24). Among dmft scores, children with mean dmft scores >6 had the highest mean caries risk score (9.66). Furthermore, children whose teeth exhibited plaque had a higher overall mean caries risk score (10.37) than children without plaque (7.54).

Table 3.

Relation between overall mean caries risk score and demographic and clinical characteristics of Group I

Participant’s characteristics Mean risk score Comments
Overall mean risk score 8.61±2.97
Gender
 Male 8.86±3.04
 Female 8.35±2.88
 Independent samples t-test 1.541 (P<0.124)
Parent’s education level
 No education (a) 9.42±3.08 (a) vs. (c): P<0.001*,#
 Middle-level education (b) 8.66±2.69 (b) vs. (c): P<0.001*,#
 University education (c) 6.09±2.72
 One-way ANOVA 13.61 (P<0.001*)
Parent’s occupation
 Nonskilled (d) 9.24±2.79 (d) vs. (f): P<0.001*,#
 Semiskilled (e) 7.67±2.73 (e) vs. (f): P<0.001*,#
 Skilled (f) 6.09±2.72
 One-way ANOVA 14.37 (P<0.001*)
Dental caries experience
 DMFT
  <1 (g) 4.88±1.99 (g) vs. (i): P<0.001*,#
  1–6 (h) 8.30±2.96 (h) vs. (i): P<0.001*,#
  >6 (i) 9.66±2.52
 One-way ANOVA 9.70 (P<0.001*)
Plaque index
 Present 10.37±2.43
 Absent 7.54±2.75
 Independent samples t-test 9.612 (P<0.001*)

*Statistically significant at P<0.05; #Multiple comparison (with Bonferroni test) – Statistically significant differences between three educational levels, as well as occupation categories and DMFT scores. DMFT – Decayed, missing and filled teeth

The overall mean caries risk score among children aged 6 to 12 years was 7.29. The mean risk score for girls (7.28) was almost equal to that for boys (7.30). These scores were higher among children whose parents had no education (8.96) and those whose parents had semiskilled occupations (7.85) compared with children in the other categories. About caries and plaque, the mean risk scores were highest among children with dmft scores >6 (10.09), SSFRs <0.5 (8.17), and plaque indexes of <2 (9.56). Regarding bacteria, the mean risk score was highest for children with S. mutans counts of >106 (9.78) and Lactobacilli counts of >105 [11.44; Table 4].

Table 4.

Relation between overall risk scores and demographic and clinical characteristics of Group II

Participant’s characteristics Mean risk score Comments
Overall mean risk score 7.29±4.39
Gender
 Male 7.28±3.71
 Female 7.30±5.11
 Mann–Whitney U-test 11.580 (P<0.088)
Parent’s education level
 No education (a) 8.96±4.44 (a) vs. (c):
 Middle-level education (b) 6.85±4.23 P<0.001* (b) vs. (c):
 University education (c) 4.74±3.26 P<0.001*
 Kruskal–Wallis test 5.79 (P<0.055)
Parent’s occupation
 Nonskilled (d) 7.47±4.19 (d) vs. (f): P<0.001*
 Semiskilled (e) 7.85±4.84 (e) vs. (f): P<0.001*
 Skilled (f) 4.74±3.26
 Kruskal–Wallis test 0.901 (P<0.637)
Dental caries experience
 DMFT
  <1 (g) 2.00±3.05 (g) vs. (i): P<0.001*,#
  1–6 (h) 6.02±2.95 (h) vs. (i): P<0.001*,#
  >6 (i) 10.09±3.60
 One-way ANOVA 98.822 (P<0.001*)
Plaque index
 <1 (j) 3.91±3.31 (j) vs. (k): P<0.001*
 1–2 (k) 9.01±4.23 (j) vs. (l): P<0.001*
 >2 (l) 9.56±2.99
 Kruskal–Wallis test 77.441 (P<0.001*)
Overall bacterial counts
Streptococcus mutans (m) vs. (n):
  <105 (m) 4.85±3.52 P<0.006* (m) vs. (o):
  105–106 (n) 5.38±2.44 P<0.001*
  >106 (o) 9.78±4.24
  Kruskal–Wallis test 20.336 (P<0.001*)
Lactobacilli (P) vs. (q): P<0.001*
  <104 (p) 4.46±3.75 (P) vs. (r): P<0.001*
  104–105 (q) 6.60±3.42
  >105 (r) 11.44±4.09
  Kruskal–Wallis test 43.597 (P<0.001*)
Salivary flow rate
 <0.5 (s) 8.17±4.58 (s) vs. (t): P<0.03*
 0.5–1 (t) 6.18±2.99 (s) vs. (u): P<0.003*
 >1 (u) 3.28±2.71
 Kruskal–Wallis test 11.105 (P<0.004*)

*Statistically significant at P<0.05; #Multiple comparison (with Bonferroni test) – Statistically significant differences between three DMFT categories; ®Pairwise comparison. DMFT – Decayed, missing and filled teeth

Correlation and linear regression analyses

In Group I, a significant positive relation was found between the overall mean caries risk score and past caries experience (dmft; r = 0.344, P < 0.001) and mean plaque index (r = 0.463, P < 0.001). In Group II, a significant positive relation was found between the overall mean caries risk score and each of the following: DMFT (r = 0.511, P < 0.001), S. mutans count (r = 234, P < 0.001), Lactobacilli count (r = 0.316, P < 0.001), and plaque index (r = 0.463, P < 0.001) [Table 5].

Table 5.

Relation between overall mean caries risk score and participant’s characteristics

Participant’s characteristics r (P)

Group I (Pearson correlations) Group II (Spearman’s coefficient)
Age −0.121 (0.03*) 0.026 (0.644)
Gender −0.086 (0.124) 0.096 (0.088)
Parent’s education −0.288 (<0.001*) −0.127 (0.024*)
Parent’s occupation −0.361 (<0.001*) −0.052 (0.351)
Past caries experience 0.344 (<0.001*) 0.511 (<0.001*)
Streptococcus mutans count - 0.234 (<0.001*)
Lactobacilli count - 0.316 (<0.001*)
Salivary flow rate - 0.141 (0.012*)
Plaque index 0.463 (<0.001*) 0.462 (<0.001*)

*Correlation is significant at the P<0.05 (two-tailed). r – The correlation coefficient

According to the linear regression model with all five predictors, R2 = 0.383, F (2.348) = 39.024, P < 0.000, both dmft and mean plaque scores had significant positive regression weights, which indicated that increasing dmft scores and plaque scores were expected to increase overall mean caries risk scores [Table 6]. Participants’ age, parents’ education, and parents’ occupation had a negative significant effect on overall mean caries risk score, which indicates that increases in these variables had less effect on the overall mean caries risk score (i.e. reduced the caries risk level). Furthermore, plaque scores had the highest main effect on the overall mean caries risk score (B = 2.224) followed by past caries experience (B = 1.585) [Table 6].

Table 6.

Significant predictors of caries risk among children aged <6 years

Variables Unstandardized coefficients Standardized coefficients (β) t P 95% CI for B


B SE Lower limit Upper limit
Age −0.532 0.148 −0.163 −3.600 <0.001* −0.822 −0.241
Parent’s education −0.693 0.325 −0.144 −2.132 0.034* −1.333 −0.054
Parent’s occupation −0.596 0.299 −0.136 −1.992 0.047* −1.185 −0.007
Past caries experience 1.585 0.258 0.303 6.147 <0.001* 1.078 2.093
Plaque score 2.224 0.279 0.364 7.960 <0.001* 1.674 2.774

*Statistically significant at P<0.05. Dependent variable: Overall mean caries risk score. B – Unstandardized coefficient; SE – Standard error; CI – Confidence interval

In terms of predictors of caries risk among children in Group I (according to the linear regression model with all three predictors, R2 = 0.359, F (2.221) =21.632, P < 0.000), dental caries experience, Lactobacilli count, and plaque index scores showed significant positive relations with overall mean caries risk score. This finding indicates that an increase in the value of these predictors produced an increase in the overall mean caries risk score. Dental caries experiences (dmft) had the greatest effect on overall mean caries risk score (B = 0.246, P < 0.000) [Table 7].

Table 7.

Significant predictors of caries risk among children aged ≥6 years

Variables Unstandardized coefficients Standardized coefficients (β) t P 95% CI for B


B SE Lower limit Upper limit
Past caries experiences 0.246 0.033 0.449 7.410 <0.001* 0.180 0.311
Lactobacilli count 0.081 0.033 0.137 2.463 0.014* 0.016 0.146
Plaque index 0.094 0.027 0.197 3.523 <0.001* 0.041 0.146

*Statistically significant at P<0.05. Dependent variable – Overall mean caries risk score. B – Unstandardized coefficient; SE – Standard error; CI – Confidence interval

DISCUSSION

Dental CRA, based on a child’s age, social/biological factors, protective factors, and clinical findings, should be a routine component of oral health-care examinations.[27] Therefore, an accurate measurement model for CRA is necessary to ensure that children are provided with the best possible dental services. The CAMBRA concept provides dentists with scientific, evidence-based solutions with which to treat dental caries disease.[28] However, similar to the other CRA models, this protocol has not been adequately validated, especially among children aged <6 years.[2] Therefore, the present study attempted to determine the caries risk among a sample of children aged 3–12 years using CAMBRA forms and suggest a new CRA model based on the study results.

In the present study, high risk of caries was reported among both Groups I and II participants. This was likely explained by the lower socioeconomic level of the participating children, as 89% (Group I) and 89.4% (Group II) of parents had no education or middle-level education. In addition, 70.9% (Group I) and 60.3% (Group II) of the parents had nonskilled occupations. In fact, this finding was consistent with that of Iqbal et al.,[29] who found that 85% of their participants were at a high risk for caries and the remaining were at moderate risk. They attributed their results to the recruitment of the study sample from a dental department where most participants were seeking dental treatment and not routine care. Sudhir et al.[30] and Rechmann et al.,[31] obtained similar results, wherein 58.33% and 53.7% of their study samples, respectively, were at high risk for caries. Their results could be attributed to the same reasons as that of the study by Iqbal et al.,[29] as they recruited their participants from public clinics. In contrast, Muhson et al.[32] reported moderate caries risk in 55.4% of their participants. A recent study conducted in Egypt[13] concluded that out of 52 participants, high and moderate risk children were equal (17 each).

In the present study, within groups, boys and girls had nearly equal mean caries risk scores, the younger children had higher scores than the older children. Of the children aged 6 to 12 years (Group II), boys were at higher risk for caries than girls. This could likely be explained as girls taking better care of their oral hygiene than boys.[33] Iqbal et al.[29] found that 86.6% of boys versus 83.3% of girls were at high risk for caries. In contrast, the risk for caries was similarly high in Group I for boys (49.8%) and girls (50.2%). In younger children (as in Group I), it is difficult to detect differences in oral health care between boys and girls, as both genders have similar level of commitment to oral hygiene instructions, as concluded by Pawlaczyk-Kamieńska et al.[34]

The findings of the present study indicate that sociodemographic factors such as parents’ education level and occupation, past caries experiences (mean dmft), and mean plaque scores were significant predictors of caries risk among children aged <6 years, and dental caries experience, mean plaque scores, and Lactobacilli count were considered significant predictors among children aged 6 to 12 years. These findings were consistent with those of Prasai Dixit et al.,[35] who concluded that a combination of microbial tests (S. mutans and Lactobacillus) and past caries experience in a CRA model, rather than various alternatives alone, was the most efficient method in determining which patients were at risk. Liu et al.[36] later found that baseline dental caries experience is a better predictor than results of salivary tests (S. mutans and Lactobacillus) in screening children for caries risk.[37] Similarly Lin et al.,[38] concluded that past dental caries experience was the best predictor for preschool children and school-age children/adolescents during CRA. Fernando et al.[39] and Kopycka-Kedzierawski et al.[40] demonstrated a highly positive correlation between past caries experience and future caries development.

For bacterial assessment, the study results support testing for only Lactobacillus, and not S. mutans, in caries prediction, in contrast to findings of other studies.[41,42] Earlier, de Camargo et al.[43] had found that S. mutans counts did not add any value in predicting caries when past caries experience was used as a caries predictor. In addition, Sounah and Madfa[44] demonstrated a significant correlation between S. mutans and Lactobacillus in carious tissue without significant differences between levels of S. mutans and Lactobacillus isolated from saliva samples. Similarly, Milgrom et al.[45] demonstrated that Lactobacillus is an important contributory bacterium in tooth decay, but its role in initiation of the lesion is not well supported. Furthermore, Kim et al.[46] demonstrated that S. mutans colonies as predictors of future caries were present in 50% of the general population and even smaller proportions of people with lower degrees of caries.

With regard to other predictors, the presence of dental plaque is associated with high risk for caries, as it is indicative of disease.[47] In addition, parents’ education and occupation levels were significantly related to dental caries risk among children aged <6 years in the present study. This could be attributed to the relation between parents’ educational level and oral health awareness, as children of parents who have better education levels tend to have better oral hygiene practices.[48] Thirunavukkarasu et al.[49] showed that all sociodemographic variables examined in their study (including parents’ occupations) were linked strongly and significantly to the caries risk profile. Ghasemianpour et al.[50] concluded that a higher level of parental education was negatively related to dental caries indexes in their study sample. Abbass et al.[51] demonstrated that dmft was inversely correlated with both socioeconomic status and parental education but did not indicate the importance of age or gender in CRA. These findings were corroborated by those of Naik et al.,[52] who reported no association between age or gender and CRA.

Cagetti et al.[53] conducted a systematic review to evaluate the power of the available CRA models in estimating caries risk according to the actual and future caries status. They concluded that scientific evidence of the usefulness of standardized CRA models was insufficient and recommended establishing newer options for the diagnosis of dental caries and therapy. In a later systematic review with the same purpose, Coelho et al.[2] recommended conducting further studies with adequate follow-up periods, using placebo controls, and testing the effect of every CAMBRA component individually. On the other hand, they stated that the protocol for children aged <6 years was not evaluated in any of the studies included in their review; therefore, this protocol could not be validated adequately. Thus, in this study we attempted to devise new CRA models for both age groups.

Limitations

Participants were recruited from Pediatric Dental Clinic at the Faculty of Dentistry in Mansoura University, a governmental institution in which most of the patients were from low socioeconomic backgrounds, and this may be the reason for the high risk of caries in a large proportion of participants. Therefore, further multi-centre studies from Egypt and elsewhere are required to validate the findings of this study.

CONCLUSION

This study suggested some predictors that can be used as a new model for CRA among children aged 3–12 years. For children aged <6 years, the model could comprise sociodemographic factors, dental caries experience, and dental plaque. For children aged 6–12 years, the model could comprise dental caries experience, Lactobacillus count, and dental plaque. However, further studies with larger samples are required to validate the predictive feasibility of such a model across different populations, as a simple unified model such as this can be used globally and would facilitate comparison of results between different countries and studies.

Ethical consideration

The study received ethical approval from the Ethics Committee of the Faculty of Dentistry, Mansoura University (Ref. no.: M28060722; date: May 4, 2022). Written informed consents were collected from parents/legal guardians prior to the data collection stage. In addition, the procedures followed were in accordance with the Declaration of Helsinki, 2013.

Data availability statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.

Peer review

This article was peer-reviewed by two independent and anonymous reviewers.

Author Contributions

Conceptualization: R.M.A.; Methodology: R.M.A., D.M.A., M.M.E., H.W.M., and R.M.E.; data analysis, R.M.A. and R.M.E.; writing – original draft preparation: R.M.A. and R.M.E.; writing – review and editing: R.M.A., D.M.A., M.M.E., H.W.M., and R.M.E.; supervision: R.M.A.

All authors have read and agreed to the published version of the manuscript.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

REFERENCES

  • 1.Policy on early childhood caries (ECC): Classifications, consequences, and preventive strategies. Pediatr Dent. 2016;38:52–4. [PubMed] [Google Scholar]
  • 2.Coelho A, Amaro I, Iunes T, Paula A, Marto CM, Saraiva J, et al. CAMBRA protocol efficacy: A systematic review and critical appraisal. Dent J (Basel) 2022;10:97. doi: 10.3390/dj10060097. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Suneja E, Suneja B, Tandon B, Philip N. An overview of caries risk assessment: Rationale, risk indicators, risk assessment methods, and risk-based caries management protocols. Indian J Dent Sci. 2017;9:210. [Google Scholar]
  • 4.Featherstone JD, Crystal YO, Alston P, Chaffee BW, Doméjean S, Rechmann P, et al. Acomparison of four caries risk assessment methods. Front Oral Health. 2021;2:656558. doi: 10.3389/froh.2021.656558. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Gannam CV, Chin KL, Gandhi RP. Caries risk assessment. Gen Dent. 2018;66:12–7. [PubMed] [Google Scholar]
  • 6.Machiulskiene V, Campus G, Carvalho JC, Dige I, Ekstrand KR, Jablonski-Momeni A, et al. Terminology of dental caries and dental caries management: Consensus report of a workshop organized by ORCA and cariology research group of IADR. Caries Res. 2020;54:7–14. doi: 10.1159/000503309. [DOI] [PubMed] [Google Scholar]
  • 7.Rechmann P, Chaffee BW, Rechmann BM, Featherstone JD. Caries management by risk assessment: Results from a practice-based research network study. J Calif Dent Assoc. 2019;47:15–24. [PMC free article] [PubMed] [Google Scholar]
  • 8.Chaffee BW, Cheng J, Featherstone JD. Baseline caries risk assessment as a predictor of caries incidence. J Dent. 2015;43:518–24. doi: 10.1016/j.jdent.2015.02.013. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Hanafy RM, Abdelmoniem SA. Impact of an oral health education program in Egyptian children with attention deficit hyperactivity disorder: A cross sectional study. Spec Care Dentist. 2022;42:252–6. doi: 10.1111/scd.12675. [DOI] [PubMed] [Google Scholar]
  • 10.Hallett KB. The application of caries risk assessment in minimum intervention dentistry. Aust Dent J. 2013;58(Suppl 1):26–34. doi: 10.1111/adj.12047. [DOI] [PubMed] [Google Scholar]
  • 11.Featherstone JDB, Crystal YO, Alston P, Chaffee BW, Doméjean S, Rechmann P, et al. A comparison of four caries risk assessment methods. Front Oral Health. 2021;2:656558. doi: 10.3389/froh.2021.656558. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Young DA, Featherstone JD. Caries management by risk assessment. Community Dent Oral Epidemiol. 2013;41:e53–63. doi: 10.1111/cdoe.12031. [DOI] [PubMed] [Google Scholar]
  • 13.Khallaf YS, Hafez S, Shaalan OO. Evaluation of ICCMS versus CAMBRA caries risk assessment models acquisition on treatment plan in young adult population: A randomized clinical trial. Clin Cosmet Investig Dent. 2021;13:293–304. doi: 10.2147/CCIDE.S318313. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Shalan H, Bakr R. Oral health status of preschool children in Egypt. Acta Sci Dent Sci. 2018;2:67–72. [Google Scholar]
  • 15.Mahmoud SA, El Moshy S, Rady D, Radwan IA, Abbass MM, Al Jawaldeh A. The effect of unhealthy dietary habits on the incidence of dental caries and overweight/obesity among Egyptian school children (a cross-sectional study) Front Public Health. 2022;10:953545. doi: 10.3389/fpubh.2022.953545. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Koo TK, Li MY. A guideline of selecting and reporting intraclass correlation coefficients for reliability research. J Chiropr Med. 2016;15:155–63. doi: 10.1016/j.jcm.2016.02.012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Wassmuth T, Sakata MS, Paula AM, Pereira WM, Ferreira LA, Rossi LP. Intra-examiner and inter-examiner reliability in the determination of angular measurements of the wrist using a smartphone application. Man Ther Posturol Rehabil J. 2020;18:1–6. [Google Scholar]
  • 18.Kutsch VK. Dental caries: An updated medical model of risk assessment. J Prosthet Dent. 2014;111:280–5. doi: 10.1016/j.prosdent.2013.07.014. [DOI] [PubMed] [Google Scholar]
  • 19.Borrell LN, Crawford ND. Socioeconomic position indicators and periodontitis: Examining the evidence. Periodontol 2000. 2012;58:69–83. doi: 10.1111/j.1600-0757.2011.00416.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.American Academy of Pediatric Dentistry. Guideline on caries-risk assessment and management for infants, children, and adolescents. Pediatr Dent. 2013;35:E157–64. [PubMed] [Google Scholar]
  • 21.García-Quintana A, Díaz S, Cova O, Fernandes S, Aguirre MA, Acevedo AM. Caries experience and associated risk factors in Venezuelan 6-12-year-old schoolchildren. Braz Oral Res. 2022;36:e026. doi: 10.1590/1807-3107bor-2022.vol36.0026. [DOI] [PubMed] [Google Scholar]
  • 22.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. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Hemadi AS, Huang R, Zhou Y, Zou J. Salivary proteins and microbiota as biomarkers for early childhood caries risk assessment. Int J Oral Sci. 2017;9:e1. doi: 10.1038/ijos.2017.35. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Ahirwar S, Gupta M, Gupta G, Singh V. Screening, isolation and identification of Lactobacillus species from dental caries of children. Int J Curr Microbiol Appl Sci. 2017;6:497–503. [Google Scholar]
  • 25.Salman HA, Senthilkumar R, Imran K, Selvam KP. Isolation and typing of Streptococcus mutans and Streptococcus sobrinus from caries-active subjects. Contemp Clin Dent. 2017;8:587–93. doi: 10.4103/ccd.ccd_610_17. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Wassel MO, Salman NS, Metwalli NE. A preliminarily Investigation on oral colonization and counts of Streptococcus mutans and Streptococcus mitis in a group of predentate infants in relation to some maternal and infant factors (a longitudinal observational study) Int J Clin Pediatr Dent. 2023;16:79–86. doi: 10.5005/jp-journals-10005-2486. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Guo L, Shi W. Salivary biomarkers for caries risk assessment. J Calif Dent Assoc. 2013;41:107–9. 112-8. [PMC free article] [PubMed] [Google Scholar]
  • 28.Rechmann P, Kinsel R, Featherstone JD. Integrating caries management by risk assessment (CAMBRA) and prevention strategies into the contemporary dental practice. Compend Contin Educ Dent. 2018;39:226–33. [PubMed] [Google Scholar]
  • 29.Iqbal A, Khattak O, Chaudhary FA, Onazi MA, Algarni HA, AlSharari T, et al. Caries risk assessment using the caries management by risk assessment (CAMBRA) protocol among the general population of Sakaka, Saudi Arabia-a cross-sectional study. Int J Environ Res Public Health. 2022;19:1215. doi: 10.3390/ijerph19031215. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Sudhir KM, Kanupuru KK, Fareed N, Mahesh P, Vandana K, Chaitra NT. CAMBRA as a tool for caries risk prediction among 12- to 13-year-old institutionalised children –A longitudinal follow-up study. Oral Health Prev Dent. 2016;14:355–62. doi: 10.3290/j.ohpd.a35621. [DOI] [PubMed] [Google Scholar]
  • 31.Rechmann P, Chaffee BW, Rechmann BM, Featherstone JD. Changes in caries risk in a practice-based randomized controlled trial. Adv Dent Res. 2018;29:15–23. doi: 10.1177/0022034517737022. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Muhson ZN, Thabit S, Al-Ward FS, Al Shatari SA. Caries risk assessment of a sample of children attending preventive specialized dental center in Al Resafa, Baghdad. J Baghdad Coll Dent. 2020;32:17–24. [Google Scholar]
  • 33.Abe M, Mitani A, Hoshi K, Yanagimoto S. Large gender gap in oral hygiene behavior and its impact on gingival health in late adolescence. Int J Environ Res Public Health. 2020;17:4394. doi: 10.3390/ijerph17124394. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Pawlaczyk-Kamieńska T, Torlińska-Walkowiak N, Borysewicz-Lewicka M. The relationship between oral hygiene level and gingivitis in children. Adv Clin Exp Med. 2018;27:1397–401. doi: 10.17219/acem/70417. [DOI] [PubMed] [Google Scholar]
  • 35.Prasai Dixit L, Shakya A, Shrestha M, Shrestha A. Dental caries prevalence, oral health knowledge and practice among indigenous Chepang school children of Nepal. BMC Oral Health. 2013;13:20. doi: 10.1186/1472-6831-13-20. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Liu JF, Hsu CL, Chen LR. Correlation between salivary mutans Streptococci, Lactobacilli and the severity of early childhood caries. J Dent Sci. 2019;14:389–94. doi: 10.1016/j.jds.2019.06.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Hebbal M, Ankola A, Metgud S. Caries risk profile of 12 year old school children in an Indian city using Cariogram. Med Oral Patol Oral Cir Bucal. 2012;17:e1054–61. doi: 10.4317/medoral.17880. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Lin YT, Chou CC, Lin YJ. Caries experience between primary teeth at 3-5 years of age and future caries in the permanent first molars. J Dent Sci. 2021;16:899–904. doi: 10.1016/j.jds.2020.11.014. [DOI] [PMC free article] [PubMed] [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. [DOI] [PubMed] [Google Scholar]
  • 40.Kopycka-Kedzierawski DT, Scott-Anne K, Ragusa PG, Cvetanovska M, Flint K, Feng C, et al. Social, psychological, and behavioral predictors of salivary bacteria, yeast in caries-free children. JDR Clin Trans Res. 2022;7:163–73. doi: 10.1177/2380084421999365. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Lif Holgerson P, Öhman C, Rönnlund A, Johansson I. Maturation of oral microbiota in children with or without dental caries. PLoS One. 2015;10:e0128534. doi: 10.1371/journal.pone.0128534. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Santos VR, Valdez RM, Danelon M, Souza JA, Caiaffa KS, Delbem AC, et al. Effect of S. mutans combinations with Bifidobacteria/Lactobacilli on biofilm and enamel demineralization. Braz Oral Res. 2021;35:e030. doi: 10.1590/1807-3107bor-2021.vol35.0030. [DOI] [PubMed] [Google Scholar]
  • 43.de Camargo ER, Canalle JB, Capozzoli R, Dos Santos TW, Ballini MB, Ferraz LF, et al. Contribution of Streptococcus Mutans virulence factors and saliva agglutinating capacity to caries susceptibility in children: A preliminary study. J Clin Pediatr Dent. 2018;42:188–94. doi: 10.17796/1053-4628-42.3.4. [DOI] [PubMed] [Google Scholar]
  • 44.Sounah SA, Madfa AA. Correlation between dental caries experience and the level of Streptococcus mutans and lactobacilli in saliva and carious teeth in a Yemeni adult population. BMC Res Notes. 2020;13:112. doi: 10.1186/s13104-020-04960-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Milgrom P, Horst JA, Ludwig S, Rothen M, Chaffee BW, Lyalina S, et al. Topical silver diamine fluoride for dental caries arrest in preschool children: A randomized controlled trial and microbiological analysis of caries associated microbes and resistance gene expression. J Dent. 2018;68:72–8. doi: 10.1016/j.jdent.2017.08.015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Kim D, Barraza JP, Arthur RA, Hara A, Lewis K, Liu Y, et al. Spatial mapping of polymicrobial communities reveals a precise biogeography associated with human dental caries. Proc Natl Acad Sci U S A. 2020;117:12375–86. doi: 10.1073/pnas.1919099117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Seow WK. Early childhood caries. Pediatr Clin North Am. 2018;65:941–54. doi: 10.1016/j.pcl.2018.05.004. [DOI] [PubMed] [Google Scholar]
  • 48.Chen L, Hong J, Xiong D, Zhang L, Li Y, Huang S, et al. Are parents'education levels associated with either their oral health knowledge or their children's oral health behaviors? A survey of 8446 families in Wuhan. BMC Oral Health. 2020;20:203. doi: 10.1186/s12903-020-01186-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Thirunavukkarasu A, Alotaibi AM, Al-Hazmi AH, ALruwaili BF, Alomair MA, Alshaman WH, et al. Assessment of oral health-related quality of life and its associated factors among the young adults of Saudi Arabia: A multicenter study. Biomed Res Int 2022. 2022:5945518. doi: 10.1155/2022/5945518. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 50.Ghasemianpour M, Bakhshandeh S, Shirvani A, Emadi N, Samadzadeh H, Moosavi Fatemi N, et al. Dental caries experience and socio-economic status among Iranian children: A multilevel analysis. BMC Public Health. 2019;19:1569. doi: 10.1186/s12889-019-7693-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Abbass MM, Mahmoud SA, El Moshy S, Rady D, AbuBakr N, Radwan IA, et al. The prevalence of dental caries among Egyptian children and adolescences and its association with age, socioeconomic status, dietary habits and other risk factors. A cross-sectional study. F1000Res. 2019;8:8. doi: 10.12688/f1000research.17047.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Naik SP, Moyin S, Patel B, Warad LP, Punathil S, Sudeep CB. Caries risk assessment of 12-13-year-old government and private school going children of Mysore city using Cariogram: A comparative study. J Int Soc Prev Community Dent. 2018;8:160–7. doi: 10.4103/jispcd.JISPCD_437_17. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.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. [DOI] [PMC free article] [PubMed] [Google Scholar]

Associated Data

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

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.


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