Abstract
Background
Early childhood caries (ECC) are particularly prevalent in disadvantaged populations, and socioeconomic factors are associated with the polarization of disease. A previous study showed that even within a homogenous low-income population disease is polarized, indicating that other factors apart from income may contribute to disease susceptibility.
Methods
This study used a hierarchical approach to identify factors associated with polarization of ECC in low-income subjects. This cross-sectional study was conducted retrospectively using a cohort of 244 children (aged 48–72 months) with family incomes not exceeding double the minimum wage (U.S. $8,208.00/year), living in neighborhoods on the outskirts of São Luís, Maranhão, Brazil. The sample was divided into three groups based on the Significant Caries (SiC) Index: no caries group, few caries group (mean 1.38 lesions), and a high caries group (mean 3.82 lesions). Hierarchical multinomial logistic regression analyses were performed based on a theoretical model.
Results
Twenty-eight (11.5%) of the 244 children presented with high caries. Age (p = 0.026; prevalence ratio (PR) = 1.10; 95% confidence interval (CI) 1.01–1.20) and frequency of sucrose consumption - p = 0.001; PR 4.65 (95% CI 1.83–11.84) were associated with increased risk of ECC.
Conclusions
In the high caries group, greater consumption of sucrose between main meals may explain why, in a group of children with homogenous social and health conditions, some had more caries than others.
Keywords: Early childhood caries, Public dental health, Diet, Epidemiology
Background
Early childhood caries (ECC) is a disease that involves development of one or more caries lesions, with or without cavitation, by the age of 71 months [1]. Epidemiological studies have indicated that ECC has a strong social element [2–4]. Indeed, higher prevalence in non-developed countries [5, 6] and in socioeconomically disadvantaged groups living in low, middle [2–4] and high-income countries [7, 8] have been documented.
Increased concentration of ECC within a specific group signifies a polarizing phenomenon, defined as a greater number of cases within a small segment of the population [9–11]. Polarization of caries has often been associated with socioeconomic deprivation in populations at social risk [9, 11–13]. This phenomenon may result from the non-homogenous distribution of strategies to control caries in populations, such as improvement in socioeconomic status and access to preventive dental care, fluoride, and dental education programs [9].
Polarization of ECC is well documented; the majority of young children are caries-free, and most carious lesions are concentrated in a small number of children [14–16]. The concentration of caries disease in a segment of the population has also been demonstrated in Brazil, in preschool [11] and school age children [9, 17]. The phenomenon is also associated with socioeconomic determinants in this population. In addition, polarization of caries disease has also been documented among Brazilian adolescents [10, 18] associated with skin color and the presence of tooth pain in the previous half year [10].
In a previous study involving children 18 to 42 months of age [19], we observed that caries disease was polarized in a population characterized by low socioeconomic status in the peripheral neighborhoods of São Luís, Maranhão Brazil. Given that socioeconomic factors have been associated with ECC risk and its polarization among children, it is important to understand what factors mediate susceptibility to the disease. Elucidation of these factors may reveal why, within a group of children who are all vulnerable, some have more caries than others.
Identifying modifiable proximal factors that mediate the association between socioeconomic status (SES) and ECC polarization may help design interventions to ameliorate the burden of this disease, especially among low-income groups. To the best of our knowledge, no previous study has explored proximal factors that may mediate the association between SES and caries polarization. The objective of this study was to use a hierarchical approach to identify factors associated with ECC polarization within a vulnerable low-income population.
Methods
Study design
This was a cross-sectional study nested within a cohort study of preschool children aged from 18 to 42-months, in which was evidenced caries polarization [19]. This study was conducted from March to September 2008 in the city of São Luís, Maranhão, Brazil. A convenience sample of children enrolled from community nurseries servicing low-income families, with incomes up to twice the Brazilian minimum wage (corresponding to U.S. $8,208.00/year) was selected. Four nurseries located in the poorest city district were sufficient to complete the sample size. All children attending these nurseries were invited to participate in the study.
A total of 260 parents signed informed consent forms for participation in the study. Exclusion criteria included the presence of debilitating systemic diseases, malnutrition, and antibiotic use that could interfere with colonization of Streptococcus mutans (SM) 30 days prior to the onset of the study. These factors were chosen because of their potential to influence the expression of caries.
Considering that this study used previously collected data, [19] ad hoc power analysis indicated that a sample of 226 children is able to detect a 2.5 prevalence ratio (PR), with an 80% test power and a 5% probability of type I error, assuming that 10% of children presented caries.
Data collection
The mothers or caregivers were interviewed using a structured questionnaire that was tested in a pilot study involving 25 mothers or caregivers. The questionnaire included demographic and social variables (mother’s age, mother’s years of education, family income), mother-child data (if the mother has untreated cavities of caries or not), who stays at home with the child, previous information about oral health (if she received information about oral health care by a dentist or by health professional), previous child hospitalization, antibiotic use in the last year by the child, child visits to the dentist, nighttime breastfeeding after 1 year and child oral hygiene practices (when teeth brushing started, who brushes the child’s teeth and daily toothbrush frequency).
A 24-hour food recall was used to acquire information about participants’ dietary habits (use of a night bottle and frequency of sucrose consumption between main meals in the form of juice, baby formula, snacks, and sweets). On a separate day, a dental surgeon assessed the visible plaque index (VPI) of each participant under natural light in the knee-to-knee position. To calculate VPI, a score corresponding to the sum of tooth sides with clinically visible plaque in relation to the total number of tooth sides present was determined [20].
The same examiner determined the number of teeth with carious decay, with extraction completed or indicated, and with fillings apparent by surface examination (dmfs index) for each child using a dental mirror (n° 5) and an exploratory probe with a rhombus point, as recommended by the World Health Organization [21]. The clinical exam was repeated one week later in 10% of the study population to evaluate intra-examiner agreement (kappa = 0.91). To identify the group of children in which caries disease was polarized, the Significant Caries (SiC) Index, adapted for deciduous teeth corresponding to the third of the sample with highest dmfs scores, was used [22].
To detect SM contamination, 1.7 mL of non-stimulated saliva was collected by pressing a sterile swab on the sublingual zone and dorsal tongue of each child until the swab was saturated (~5 seconds in each area). Each saliva sample was diluted in saline solution (0.9% NaCl) to produce decimal dilutions. Aliquots (0.1 mL) of each dilution were spread onto Mitis salivarius-bacitracin agar plates and incubated in a 5% CO2 chamber for 48 hours. After incubation, the number of colony-forming units (CFUs) was counted on each plate with >10 colonies. A single examiner, who did not have knowledge of patients’ caries status, performed the microbial counts in duplicate using a digital colony counter (model CP 600 Plus, Phoenix).
Theoretical model
A hierarchical theoretical model with the following eight blocks was employed: 1) age of child in months; 2) socioeconomic and demographic factors; 3) mother’s past history of caries (if the mother has untreated cavities of caries or not); 4) child’s health status; 5) dietary child habits; 6) child oral hygiene data; 7) VPI; and 8) level of SM contamination in the saliva (Figure 1).
Age was considered a potentially confounding factor, so the model was adjusted for this variable, which represented the block furthest from the outcome. This variable was added as a continuous variable.
The second block included socioeconomic and demographic variables as distal factors in the theoretical model since they can influence all variables in subsequent blocks. Were included in this block mother’s age in years, mother’s years of education (<8, 8–11, or >11), family income (<1 minimum wage, 1 minimum wage (U.S. $4,104.00/year), or >1 minimum wage), who stayed at home with the child when she/he was not in day care (the mother, others), and whether the mother or caregiver received information about oral health (yes or no) [19].
The health variable included for the mother in the third block, which may mediate the association between socioeconomic variables and childhood caries, was previous history of caries, self-reported by the mother. She reported if she had untreated cavities of caries or not at the time of interview (yes, no).
Health variables for the child were included in the fourth block since they may mediate the association between the variables included in the previous blocks and childhood caries. The following variables were used: previous child hospitalization reported by the mother or caregiver (0, 1, or ≥2 times), antibiotic use in the last year (yes, no), and whether the child had already visited the dentist (yes, no).
In the fifth block, dietary practices were included, assuming that these variables may be influenced by socioeconomic and demographic factors, and by mother and child health variables. The variables in this block were: nighttime breastfeeding after 1 year (yes, no), use of a night bottle (yes, no), and frequency of sucrose consumption between main meals in the form of juice, baby formula, snacks, and sweets (≤3 or >3 times/day).
Oral hygiene practices may be moderator variables of the association between diet and ECC, so they were included in the sixth block as follows: when teeth brushing started (0–6 months, 7–12 months, after 12 months), who does the brushing (the child alone, the caregiver), and the number of times a day the child’s teeth are brushed (up to 1 time, ≥2 times).
In the seventh block, whether a visible biofilm was present (<15% presence of visible plaque or ≥15%) was recorded assuming that this variable may be influenced by both hygiene and dietary practices.
In the final block the level of SM contamination in the saliva (<105 or ≥105 CFU – colony-forming units) was included as a biological variable nearest to the outcome that might be influenced by all variables in the previous blocks.
Statistical analyses
Multinomial logistic regression using forward selection and guided by a hierarchical approach was used [19, 23]. We evaluated possible associations between risk factors and ECC using a series of models, which allowed for the modeling of the dependent variable, structured as polytomous data divided according to three SiC categories (caries-free, few caries, high caries). The estimated coefficients were expressed as prevalence ratios (PRs) and their 95% confidence intervals were also calculated.
The hierarchical modeling started with the first block. The variables of the first block were adjusted simultaneously for each other and only those variables whose p value was <0.10 entered in subsequent models. Then variables of the second block were adjusted simultaneously for each other and for the variables whose p value was <0.10 in the previous step. The significance of each variable was considered at the time of entry into the model (p value <0.05). All other blocks were then added in succession following the same procedure.
All statistical analyses were performed using the STATA 10.0 program (Stata Corp., College Station, TX). Collinear variables were evaluated using the variance inflation factor.
Ethical aspects
The ethics committee of the University Hospital of the Federal University of Maranhão (Universidade Federal do Maranhão, UFMA) (case 33104-1251/2007) approved the study. The parents or legal representatives of each child that participated in the study read and signed informed consent forms. All children needing dental treatment were referred to the pediatric dental clinical of the UFMA.
Results
Among the 260 children whose parents signed informed consent forms, 16 (6.2%) were excluded from the study because they did not complete all steps of the investigation. In our final analyses, we used data from 244 children. In this study, ECC prevalence was 32%. Mean dmfs index was 0.42 and the standard deviation (SD) was 0.69 in the whole sample. Separating the dmfs index into their components, only the component cavity was observed in our sample.
According to the SiC index, the high caries group (more than three caries lesions) included 28 children (mean 3.82 lesions, SD 0.45). The few lesions group (1-3 caries lesions) contained 49 children (mean 1.38 lesions, SD 0.49). A distribution of explanatory variables according to caries group is shown in Table 1.
Table 1.
Variables | Caries free group N (%) | Few lesions group N (%) | High caries group N (%) |
---|---|---|---|
Family Income (minimum wages) | |||
<1 | 55 (65) | 19 (23) | 10 (12) |
1 | 75 (68) | 22 (20) | 14 (13) |
> 1 | 30 (79) | 5 (13) | 3 (8) |
Mother’s years of education | |||
< 8 | 37 (59) | 16 (25) | 10 (16) |
8 a 11 | 64 (72) | 15 (17) | 10 (11) |
> 11 | 59 (73) | 15 (18) | 7 (91) |
Who stayed at home with the child when s/he was not in day care | |||
The mother | 80 (68) | 24 (20) | 13 (11) |
Others | 80 (69) | 22 (19) | 14 (12) |
Whether the mother or caregiver had received information about oral health | |||
No | 68 (71) | 18 (19) | 9 (9) |
Yes | 93 (67) | 28 (20) | 18 (137) |
Mother’s history of caries | |||
No | 68 (69) | 21 (22) | 9 (9) |
Yes | 92 (68) | 25 (19) | 18 (13) |
Number of previous child hospitalizations | |||
0 | 90 (67) | 27 (20) | 18 (13) |
1 | 55 (71) | 15 (20) | 7 (9) |
≥2 times | 16 (73) | 4 (18) | 2 (9) |
Whether they had already visited the dentist | |||
No | 135 (67) | 44 (22) | 22 (11) |
Yes | 26 (79) | 2 (6) | 5 (15) |
Antibiotic use in the last year | |||
No | 107 (70) | 26 (17) | 19 (13) |
Yes | 54 (66) | 20 (24) | 8 (10) |
Nighttime breastfeeding after 1 year | |||
No | 125 (66) | 45 (24) | 20 (10) |
Yes | 38 (78) | 4 (8) | 7 (14) |
Use of a night bottle | |||
No | 117 (65) | 40 (22) | 23 (13) |
Yes | 44 (82) | 6 (11) | 4 (7) |
Frequency of sucrose consumption between main meals | |||
≤ 3 | 145 (72) | 42 (21) | 15 (7) |
>3 times | 22 (55) | 6 (15) | 12 (30) |
When teeth brushing started (months) | |||
0 - 6 | 19 (86) | 3 (14) | 0 (0) |
7 a 12 | 69 (69) | 16 (16) | 15 (15) |
> 12 | 73 (65) | 27 (24) | 12 (11) |
Who does the teeth brushing | |||
The child alone | 17 (49) | 14 (40) | 4 (11) |
The caregiver | 144 (72) | 32 (16) | 23 (11) |
The number of times a day their teeth are brushed | |||
up to 1 | 15 (58) | 7 (27) | 4 (15) |
≥2 | 146 (70) | 39 (19) | 23 (11) |
Visible biofilm | |||
<15% | 58 (79) | 11 (15) | 4 (6) |
≥ 15% | 112 (64) | 38 (22) | 24 (14) |
Streptococcus mutans contamination in the saliva | |||
<105 CFU* | 104 (69) | 28 (19) | 17 (11) |
≥ 10 5 CFU* | 63 (66) | 21 (22) | 11 (12) |
Total** | 167 (100) | 49 (100) | 28 (100) |
*CFU: colony-forming units **umbers may not add to total because of missing values.
The results of the multinomial model of hierarchized regression are reported in Table 2. No collinear variables were identified. In block 1, the age of the child was significantly associated with ECC in the high caries group (p = 0.026; PR = 1.10; 95% CI 1.01–1.20) and this association in few caries group was found to be within the limit of significance (p = 0.054; PR = 1.06; 95% CI 1.00-1.12). In the second and third blocks, none of the variables were associated with the outcome. In the fourth block, having access to a dentist was an indicator of protection in the few caries group (p = 0.035; PR = 0.20; 95% CI 0.05–0.89) but not in the high caries group (p = 0.932). In the fifth block, nocturnal breastfeeding beyond the age of 1 year was in the limit of significance, as a borderline protective factor for the few caries group (p = 0.051; PR = 0.33; 95% CI 0.11–1.01). In this same block, the consumption of sucrose between main meals was significant (p = 0.001) in the high caries group, PR = 4.65 (95% CI 1.83–11.84) (Table 2).
Table 2.
Groups/Variables | Block 1 | Block 4 | Block 5 | Block 6 | ||||
---|---|---|---|---|---|---|---|---|
PR (95% CI) | p | PR (95% CI) | p | PR (95% CI) | p | PR (95% CI) | p | |
Few caries group | ||||||||
Age | 1.06 (1.00-1.12) | 0.054 | ||||||
Child has visited the dentist | ||||||||
No | 1 | |||||||
Yes | 0.20 (0.05-0.89) | 0.035 | ||||||
Frequency of sucrose consumption between main meals | ||||||||
≤3 | 1 | |||||||
>3 | 0.83 (0.28-2.42) | 0.732 | ||||||
Use of a night bottle | ||||||||
No | 1 | |||||||
Yes | 0.42 (0.16-1.08) | 0.073 | ||||||
Nighttime breastfeeding after 1 year | ||||||||
No | 1 | |||||||
Yes | 0.33 (0.11-1.01) | 0.051 | ||||||
Who does the teeth brushing | ||||||||
The child alone | 1 | |||||||
The caregivers | 0.27 (0.11-0.66) | 0.004 | ||||||
High caries group | ||||||||
Age | 1.10 (1.01-1.20) | 0.026 | ||||||
Child has visited the dentist | ||||||||
No | 1 | |||||||
Yes | 1.05 (0.36-3.09) | 0.932 | ||||||
Frequency of sucrose consumption between main meals | ||||||||
≤3 | 1 | |||||||
>3 | 4.65 (1.83-11.84) | 0.001 | ||||||
Use of a night bottle | ||||||||
No | 1 | |||||||
Yes | 0.57 (0.18-1.85) | 0.353 | ||||||
Nighttime breastfeeding after 1 year | ||||||||
No | 1 | |||||||
Yes | 1.38 (0.50-3.80) | 0.532 | ||||||
Who does the teeth brushing | ||||||||
The child alone | 1 | |||||||
The caregivers | 1.00 (0.25-4.02) | 0.998 |
PR prevalence ratio, CI confidence interval.
Only variables whose p value were < 0.10 were shown in the table and others described below were omitted. Results for each variable were shown only for the block at which the variable was entered first. Blocks 2, 3, 7 and 8 were not presented because no significant variables were kept at these blocks.
Block 1: adjusted for age.
Block 2: adjusted for variable kept in block 1(age) plus variables from block 2.
Block 3: adjusted for variable kept in block 1(age) plus variables from block 3.
Block 4: adjusted for variable kept in block 1(age) plus variables from block 4.
Block 5: adjusted for variable kept in block 1(age), variable selected from block 4 (child has visited the dentist) plus variables from block 5.
Block 6: adjusted for variable kept in block 1(age), variable selected from block 4 (child has visited the dentist), variables selected from block 5 (frequency of sucrose consumption between main meals, nighttime breastfeeding after 1 year, and use of a night bottle) plus variables from block 6.
Block 7: adjusted for variable kept in block 1(age), variable selected from block 4 (child has visited the dentist), variables selected from block 5 (frequency of sucrose consumption between main meals, nighttime breastfeeding after 1 year and use of a night bottle), variable selected from block 6 (who does the teeth brushing) plus variables from block 7.
Block 8: adjusted for variable kept in block 1(age), variable selected from block 4 (child has visited the dentist), variables selected from block 5 (frequency of sucrose consumption between main meals, nighttime breastfeeding after 1 year and use of a night bottle), variable selected from block 6 (who does the teeth brushing) plus variables from block 8.
In the sixth block, the variable of the mother or caregiver brushing the child’s teeth for them was a significant protective factor in the few caries group (p = 0.004; PR = 0.27; 95% CI 0.11–0.66) but was not significant in the high caries group. The biological variables in the seventh (VPI) and eighth blocks (S. mutans contaminated saliva) were not associated with childhood caries.
Discussion
This study revealed that high sucrose consumption was associated with caries polarization among children living in vulnerable social condition after controlling for confounding variables through a hierarchical approach.
The phenomenon of caries polarization among children has been associated with social deprivation [24]. However it has been shown that even in populations with homogenous social background caries tend to concentrate in certain population subgroups [9, 24]. Reasons for this are poorly understood. In the present study we showed that higher sugar consumption is possibly the factor that mediates the association between low SES and caries polarization.
Indeed, studies have indicated that low socioeconomic level can alter dietary patterns [25] so sugar consumption may be a pathway to the association between low family income and caries polarization, since both socioeconomic factors [3, 4] and sucrose consumption [4, 15, 18, 19, 25, 26] also present robust associations with ECC. It is possible that synergy between deprived social conditions and high-sugar dietary patterns may explain these findings.
In the present study, we used the SiC index to identify the high caries group as a proxy for disease polarization, showing a mean of 3.82 lesions. Other studies involving children up to five years of age showed a SiC value similar to ours, such as a SiC value of 4.14 in Mexican children [27] and of 4.09 in Sri Lankan children [12].
Ours results showed that age was associated with ECC, in the high caries groups, confirming results of previous studies indicating that caries severity increases with age [19, 28–32].
The demographic, economic, and social variables (income, schooling, health information) in the second level were not associated with ECC. These data differ from results of two prior studies [2, 3], which found that social variables were associated with ECC. This is likely explained by the homogeneity of social variables in the cohort included in this study. Although the homogeneity lessened the power of social variables, homogeneous social variables are desirable in a study investigating variables that explain polarization of ECC incidence to reduce confounding by SES.
In the few caries group, the non-polarization phenomenon may be attributable to several protective factors, including access to a dentist, being breastfed after the age of 1 year and teeth brushing by the mother. Thus, it seems that even in deprived low-income groups, access to health care, protective feeding practices and oral hygiene might buffer the deleterious effect of high sugar consumption on ECC.
Access to the dentist was protective factor only in the few caries group (PR = 0.20). It’s possible that children of high caries group may have gone to the dentist for restorative care or even due to toothache. In this sense, it has been shown that access to dental treatment among preschoolers occurs especially for emergency care [33].
Similarly, teeth brushing performed by the mother were also protective only for the few caries group (PR = 0.27). The high caries group may not have had adequate hygiene practices, resulting in higher DMFS scores.
Nocturnal breastfeeding after age 1 (PR = 0.33) was a protective factor of borderline significance in the group with few caries (p = 0.051). It is possible that the small sample size could have contributed to the borderline association between nocturnal breastfeeding and ECC observed in the group with few caries. In the high caries group, however, this practice was not found to protect from the disease, possibly because children with greater number of lesions had other deleterious dietary practices superimposed on breastfeeding, such as consumption of more sucrose. Others epidemiological studies failed to show that breastfeeding after age 1 were associated with ECC [34–36], including previous analysis of data involving the same population of children [19].
The fact that we used a convenience sample is a limitation to the external validity of this study’s findings. However, it is possible that our results could be extrapolated to other low SES populations living in similar conditions.
One of the strengths of our study is that since ECC is considered a social disease, studying a population with homogenous social and economic conditions favors the identification of factors that stratify risk within vulnerable groups and allows for better control of confounding factors. Furthermore, the use of a hierarchical model permitted us to evaluate mediation of more proximal factors on the association between distal variables such as SES and ECC.
Conclusion
In conclusion, higher sucrose consumption increases the likelihood of ECC in socially vulnerable children. Caries population prevention strategies based on teeth brushing and visits to a dentist seems not to be enough to reduce inequalities in oral health because they do not seem to be reaching the most vulnerable groups among the vulnerable. Another possible explanation is that these preventive practices are not sufficient to counterbalance the deleterious effect of high sugar consumption in the high-caries group of children. Public policies focused on warning about the risk of added sugars consumption might be an additional strategy to control ECC in these deprived low-income populations.
Acknowledgements
We thank FAPEMA (Fundação de Amparo à Pesquisa do Estado do Maranhão), Ministério da Saúde, and CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico) for financial support.
Footnotes
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
AMMN - drafted the manuscript, participated in the study design, performed the statistical analysis, and gave final approval of the version to be published. AAMS - made substantial contributions to the conception and design of the study, analysis of data, and gave final approval of the version to be published. CMCA - participated in the study design, performed the statistical analysis and gave final approval of the version to be published. FNH - made substantial contributions to the conception and design of the study, analysis of data, and gave final approval of the version to be published. CCCR - made substantial contributions to the conception and design of the study, acquisition, analysis and interpretation of data, and gave final approval of the version to be published. All authors read and approved the final manuscript.
Contributor Information
Ana Margarida Melo Nunes, Email: amarg@globo.com.
Antônio Augusto Moura da Silva, Email: aamouradasilva@gmail.com.
Claudia Maria Coelho Alves, Email: cmcoelhoa@gmail.com.
Fernando Neves Hugo, Email: fernandoneveshugo@gmail.com.
Cecilia Claudia Costa Ribeiro, Email: cecilia_ribeiro@hotmail.com.
References
- 1.American Academy of Paediatric Dentistry . Policy on Early Childhood Caries (ECC): Classification, consequences and preventive strategies. 2011. [PubMed] [Google Scholar]
- 2.Hallet KB, O’Rourke PK. Pattern and severity of early childhood caries. Community Dent Oral Epidemiol. 2006;34:25–35. doi: 10.1111/j.1600-0528.2006.00246.x. [DOI] [PubMed] [Google Scholar]
- 3.Livny A, Assali R, Sgan-Cohen HD. Early Childhood Caries among a Bedouin community residing in the eastern outskirts of Jerusalem. BMC Public Health. 2007;7(7):167–169. doi: 10.1186/1471-2458-7-167. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Mohhebbi SZ, Virtanem JT, Vahid-Golpayegani M, Vehkalahti MM. Feeding habits as determinants of early childhood caries in a population where prolonged breastfeeding is the norm. Community Dent Oral Epidemiol. 2008;36:363–369. doi: 10.1111/j.1600-0528.2007.00408.x. [DOI] [PubMed] [Google Scholar]
- 5.Resini SD, Douglass JM. Psychosocial and behavioral issues in Early Childhood Caries. Community Dent Oral Epidemiol. 1998;26(suppl 32):32–44. doi: 10.1111/j.1600-0528.1998.tb02092.x. [DOI] [PubMed] [Google Scholar]
- 6.Prakash P, Subramania MP, 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(2):141–142. [PMC free article] [PubMed] [Google Scholar]
- 7.Stecksén-Blicks C, Borssén E. Dental caries, sugar-eating habits and toothbrushing in groups of 4-year-old children 1967-1997 in the city of Umea, Sweden. Caries Res. 1999;33(6):409–414. doi: 10.1159/000016544. [DOI] [PubMed] [Google Scholar]
- 8.Tomar SL, Reeves AF. Changes in the oral health of US children and adolescents and dental public health infrastructure since the release of the Healthy People 2010 Objectives. Acad Pediatr. 2009;9(6):388–395. doi: 10.1016/j.acap.2009.09.018. [DOI] [PubMed] [Google Scholar]
- 9.Narvai PC, Frazão P, Roncalli AG, Antunes JL. Dental caries in Brazil: decline, polarization, inequality and social exclusion. Rev Panam Salud Publica. 2006;19(6):385–393. doi: 10.1590/S1020-49892006000600004. [DOI] [PubMed] [Google Scholar]
- 10.Hugo FN, Vale GC, Ccahauana-Vásquez RA, Cypriano S, de Sousa ML. Polarization of dental caries among individuals aged 15 to 18 years. J Appl Oral Sci. 2007;14(4):253–258. doi: 10.1590/S1678-77572007000400003. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Ferreira SH, Béria JU, Kramer PF, Feldens EG, Feldens CA. Dental caries in 0-to-5-year old Brazilian children prevalence, severity and associated factors. Int J Paediatric Dent. 2007;17:289–296. doi: 10.1111/j.1365-263X.2007.00831.x. [DOI] [PubMed] [Google Scholar]
- 12.Perera PJ, Abeyweera NT, Fernando MP, Warnakulasuriya TD, Ranathunga N. Prevalence of dental caries among a cohort of preschool children living in Gampaha district, Sri Lanka: a descriptive cross sectional study. BMC Oral Health. 2012;12:49. doi: 10.1186/1472-6831-12-49. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Eckert GJ, Jackson R, Fontana M. Sociodemographic variation of caries risk factors in toddlers and caregivers. Int J Dentistry. 2010;2010:593487. doi: 10.1155/2010/593487. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Dimitrova M, Kukleva MP, Kondeva VK. A study of polarization in 1, 2 and 3 year-old children. Folia Med (Plovdiv) 2000;42(3):55–59. [PubMed] [Google Scholar]
- 15.Declerck D, Leroy R, Martens L, Lesajfre E, Garcia-Zattera MJ, Vanden Broucke S, Debyser M, Hoppenbrouers K. Factors associated with prevalence and severety of caries experience in preschool children. Community Dent Oral Epidemiol. 2008;36:168–178. doi: 10.1111/j.1600-0528.2007.00385.x. [DOI] [PubMed] [Google Scholar]
- 16.Carvalho JC, Figueiredo MJ, Mestrinho HD. Caries trends in Brazilian non-privileged preschool children in 1996 and 2006. Caries Res. 2009;43:2–9. doi: 10.1159/000181151. [DOI] [PubMed] [Google Scholar]
- 17.Antunes JLF, Peres MA, de Campos Mello TR, Waldman EA. Multilevel assessment of determinants of dental caries experience in Brazil. Community Dent Oral Epidemiol. 2006;34:146–152. doi: 10.1111/j.1600-0528.2006.00274.x. [DOI] [PubMed] [Google Scholar]
- 18.Peres SH, de Carvalho FS, de Carvalho CP, Bastos JR, Lauris JR. Polarization of dental caries in teen-agers in the Southwest of the state of São Paulo,Brasil. Ciência & Saúde Coletiva. 2008;13(2):2155–2162. doi: 10.1590/S1413-81232008000900020. [DOI] [PubMed] [Google Scholar]
- 19.Nunes AMM, Alves CM, Araújo FB, Ortiz TM, Ribeiro MR, Silva AAM, Ribeiro CC. Association between prolonged breast-feeding and early childhood caries: a hierarchical approach. Community Dent Oral Epidemiol. 2012;40(6):542–549. doi: 10.1111/j.1600-0528.2012.00703.x. [DOI] [PubMed] [Google Scholar]
- 20.Ainamo J, Bay I. Problems and proposals for recording gingivitis and plaque. Int Dent J. 1975;25:229–235. [PubMed] [Google Scholar]
- 21.World Health Organization . Oral Health Surveys-Basic Methods. 4. Geneva: World Health Organization; 1997. [Google Scholar]
- 22.Nishi M, Bratthall D, Stjemswãrd J. How to calculate the Significant Caries Index (SiC Index) Sweden: University Malmo; 2001. WHO Collaborating Centre/Faculty of Odontology. [Google Scholar]
- 23.Victora CG, Huttly SR, Funchs SC, Olinto MT. The role of conceptual framework in epidemiological analysis: a hierarchical approach. Int J Epidemiol. 1997;26(1):224–227. doi: 10.1093/ije/26.1.224. [DOI] [PubMed] [Google Scholar]
- 24.Stromberg U, Holmn A, Magnusson K, Twetman S. Geo-mapping of time trends in childhood caries risk-a method for assessment of preventive care. BMC Oral Health. 2012;12:9. doi: 10.1186/1472-6831-12-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Okubo H, Miyake Y, Sasaki S, Tanaka K, Murakami K, Hirota Y. Dietary patterns in infancy and their associations with maternal socio-economic and lifestyle factors among 758 Japanese mother-child pairs: yhe Osaka Maternal and Child Health Study. Matern Child Nutr. 2014;10(2):213–225. doi: 10.1111/j.1740-8709.2012.00403.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Feldens CA, Giugliani ER, Duncan BB, Drachler ML, Vitolo MR. Long-term effectiveness of a nutritional program in reducing early childhood caries: a randomized trial. Community Dent Oral Epidemiol. 2010;38:324–332. doi: 10.1111/j.1600-0528.2010.00540.x. [DOI] [PubMed] [Google Scholar]
- 27.Zuñiga-Manríquez AG, Medina-Solis CE, Lara-Carrilo E, Márquez-Corona M, Robles-Bermeo NL, Scougall-Vilchis RJ, Maupomé G. Experience, Prevalence and severity of dental caries and its association with nutritional status in Mexican infants 17-47 months. Rev Invest Clin. 2013;65(3):228–236. [PubMed] [Google Scholar]
- 28.Azevedo TDPL, Bezerra ACB, Toledo OA. Feeding Habits and Severe Early Childhood Caries in Brazilian Preschool Children. Pediatric Dentistry. 2005;27:28–33. [PubMed] [Google Scholar]
- 29.Van Palenstein Helderman WH, Soe W, Vant’ Hof MA. Risk factors of early childhood caries in a Southeast Asian population. J Dent Res. 2006;85:85–88. doi: 10.1177/154405910608500115. [DOI] [PubMed] [Google Scholar]
- 30.Thitasomakul S, Thearmontree A, Piwat S, Chankankar O, Pithpornchaiyakul W, Teanpaisan R, Madyusoh S. A longitudinal study of early childhood caries in 9-to18-month-old Thai infants. Community Dent oral Epidemiol. 2006;34:429–436. doi: 10.1111/j.1600-0528.2006.00292.x. [DOI] [PubMed] [Google Scholar]
- 31.Finlayson TL, Ismail AI, Sohn W. Psychosocial factors and early childhood caries among low-income African-American children in Detroit. Community Dent Oral Epidemiol. 2007;35:439–448. doi: 10.1111/j.1600-0528.2006.00352.x. [DOI] [PubMed] [Google Scholar]
- 32.Oliveira LB, Sheiham A, Bonecker M. Exploring the association of dental caries with social factors and nutritional status in Brazilian preschool children. Eur J Oral Sci. 2008;116(1):37–43. doi: 10.1111/j.1600-0722.2007.00507.x. [DOI] [PubMed] [Google Scholar]
- 33.Carino KM, Shinada K, Kawaguchi Y. Early childhood caries in northern Philippines. Community Dent Oral Epidemiol. 2003;31:81–89. doi: 10.1034/j.1600-0528.2003.00010.x. [DOI] [PubMed] [Google Scholar]
- 34.Rosenblatt A, Zarzar P. Breast-feeding and early childhood caries: an assessment among Brazilian infants. Int J Paediatric Dentistry. 2004;14:439–445. doi: 10.1111/j.1365-263X.2004.00569.x. [DOI] [PubMed] [Google Scholar]
- 35.Kramer MS, Vanilovich I, Matush L, Bogdanovich N, Zhang X, Shisko G, Muller-Bolla M, Platt RW. The Effect of Prolonged and Exclusive Breast-feeding and Dental Caries in Early Scholl-Age Children. Caries Res. 2007;41:484–488. doi: 10.1159/000108596. [DOI] [PubMed] [Google Scholar]
- 36.Iida H, Auinger P, Billings RJ, Weitzman M. Association Between Infant Breastfeeding and early Childhood Caries in the United States. Pediatrics. 2007;120:944–952. doi: 10.1542/peds.2006-0124. [DOI] [PubMed] [Google Scholar]
Pre-publication history
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2458/14/988/prepub