Next Article in Journal
Exploring Lifestyle Factors and Treatment Adherence among Older Adults with Hypertension Attending a Mobile Health Unit (MHU) in a Rural Area of Central Portugal
Previous Article in Journal
Changes in the Progression of Chronic Kidney Disease in Patients Undergoing Fecal Microbiota Transplantation
Previous Article in Special Issue
Effect of a Multifaceted Intervention on Children’s Body Image and the Mediating Role of Body Image in Changes in Adiposity Indicators
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Brief Report

The Associations between Snack Intake and Cariogenic Oral Microorganism Colonization in Young Children of a Low Socioeconomic Status

1
Eastman Institute for Oral Health, University of Rochester Medical Center, Rochester, NY 14642, USA
2
Dental Department, King Fahad University Hospital, Imam Abdulrahman Bin Faisal University, Dammam 31441, Saudi Arabia
3
Department of General Dental Practice, College of Dentistry, Health Science Center, Kuwait University, P.O. Box 24923, Kuwait City 13110, Kuwait
4
Department of Biostatistics and Computational Biology, University of Rochester Medical Center, Rochester, NY 14642, USA
5
School of Nursing, University of Rochester, Rochester, NY 14642, USA
*
Author to whom correspondence should be addressed.
Nutrients 2024, 16(8), 1113; https://doi.org/10.3390/nu16081113
Submission received: 21 March 2024 / Revised: 3 April 2024 / Accepted: 8 April 2024 / Published: 10 April 2024
(This article belongs to the Special Issue Diet, Lifestyle and Chronic Disease in Early Life)

Abstract

:
Cariogenic microorganisms are crucial pathogens contributing to the development of early childhood caries. Snacks provide fermentable carbohydrates, altering oral pH levels and potentially affecting microorganism colonization. However, the relationship between snack intake and cariogenic microorganisms like Candida and Streptococcus mutans in young children is still unclear. This study aimed to assess this association in a prospective underserved birth cohort. Data from children aged 12 to 24 months, including oral microbial assays and snack intake information, were analyzed. Sweet and non-sweet indices based on the cariogenic potential of 15 snacks/drinks were created. Mixed-effects models were used to assess the associations between sweet and non-sweet indices and S. mutans and Candida carriage. Random forest identified predictive factors of microorganism carriage. Higher non-sweet index scores were linked to increased S. mutans carriage in plaques (OR = 1.67, p = 0.01), potentially strengthening with age. Higher sweet index scores at 12 months were associated with increased Candida carriage, reversing at 24 months. Both indices were top predictors of S. mutans and Candida carriage. These findings underscore the associations between snack intake and cariogenic microorganism carriage and highlight the importance of dietary factors in oral health management for underserved young children with limited access to dental care and healthy foods.

1. Introduction

Early childhood caries (ECC), which is recognized as the most prevalent chronic childhood disease, disproportionately affects up to 70% of preschool children from socioeconomically disadvantaged backgrounds in both developing and industrialized countries [1,2]. ECC can lead to long-term consequences to children’s health, such as pain during eating or drinking, difficulties in biting and chewing, and reduced appetite, potentially resulting in weight loss. Among the various factors contributing to early childhood caries, cariogenic microorganisms play a crucial role. Streptococcus mutans (S. mutans) is a well-established contributor due to its acidogenic and aciduric capabilities, as well as its role in forming the extracellular matrix, which is an essential component for dental plaque [3,4]. Another emerging cariogenic pathogen is Candida albicans, which has been found in high levels in children with early childhood caries [5,6]. C. albicans also exhibits acidogenic and aciduric properties [7,8]. Additionally, C. albicans has been found to be positively correlated with S. mutans carriage [9], possibly due to its ability to increase S. mutans in biofilms through a unique adhesive interaction mediated by extracellular polysaccharide formation. This interaction may lead to more severe caries when a person is co-infected with S. mutans [10,11,12].
A variety of dietary factors have also been linked to ECC. Research indicates that the sugar content, micronutrient composition, and frequency of eating can influence oral pH properties, buffering capacity, and enamel health [13]. Snack intake has emerged as a critical contributor to the elevated risk of ECC, given the significant increase in snacking frequency and energy intake among young children in recent decades [14,15,16,17]. Sweets and desserts continue to be the primary components of snacks in children [14], and the relationship between snack intake and ECC may be partially attributed to the ability of sugary snacks to modulate the presence and colonization of cariogenic oral microorganisms. These snacks with a high sugar content provide fermentable carbohydrates that stimulate bacterial growth and alter the pH levels in the oral environment, thereby promoting bacterial biofilm formation [18,19]. There, snack intake, particularly those rich in sugars, may play a role in fostering the growth of cariogenic microorganisms and contributing to the development of ECC.
Several studies have investigated the associations between sugary snacks and S. mutans carriage in young children, yielding mixed results [19,20,21,22,23,24,25]. However, there are gaps in our understanding, particularly regarding the relationships between snack intake and other cariogenic microorganisms, such as Candida. Additionally, while sugary snacks have been extensively studied, the individual effects of low- or non-sugary snacks have been largely overlooked. However, previous studies have indicated a link between eating frequency, which includes both sugary and non-sugary foods, and S. mutans carriage [20,25]. To address these knowledge gaps, this study aimed to assess the associations between snack intake, including snacks of high and low sugar content, and cariogenic microorganisms, including S. mutans and Candida, in a prospective cohort of young children from low socioeconomic backgrounds.

2. Methods

2.1. Study Population

The current study is a subset of a parent prospective birth cohort study. The birth cohort was recruited from two university-affiliated clinics in upstate New York [26]. Pregnant women aged 18 years or older, eligible for New York State-supported medical insurance, and carrying a singleton fetus, were enrolled during the third trimester of pregnancy. Following birth, their full-term infants were also recruited for the birth cohort and assessed up to 24 months of age. Infants were excluded if they had a low birthweight (<2500 g), had Down syndrome, had orofacial deformity, or had received oral and/or systemic antifungal treatment before the baseline visit. A total of 160 infants were enrolled in the subsequent postnatal visits. For inclusion in the current study, infants had oral microbial data at 12, 18 or 24 months, as well as dietary assessment on snack intake at the same visits. A small number of records (n = 7 at 18 months and n = 10 at 24 months) without information on feeding method at 12 months were excluded from the current study (Figure 1).

2.2. Oral Sample Collection and Quantification

Oral samples, including saliva and plaque, were collected at each visit. All care providers were informed not to brush infants’ teeth or offer food 2 h before oral sample collection. Saliva samples were collected using SalivaBio Infant’s Swab (SIS) (Salimetrics, Inc., Carlsbad, CA, USA). Plague samples were collected using a standard dental scaler. Oral samples were stored on ice after collection and transferred to the lab within 2 h for microbiological assays. The methods used to identify and quantify Candida spp. and S. mutans have been previously described [9,27]. Briefly, S. mutans was isolated using Mitis Salivarius with Bacitracin selective medium by incubating it at 37 °C for 48 h and identified by colony morphology [28]. BBLTM CHROMagarTM Candida (BD, Sparks, MD, USA) was used to isolate Candida spp. by incubating it at 37 °C for 48 h. Colonies of S. mutans and Candida spp. including C. albicans, C. krusei, and C. glabrata, were counted and recorded as colony forming units (CFU). Additionally, C. albicans and S. mutans were further identified using the colony polymerase chain reaction (PCR) method.

2.3. Snack Data Collection

A questionnaire was administered at each visit to collect information on the child’s snack intake, including details on the amount and frequency of consumption of 15 common snacks and drinks, adapted from previous studies [29,30]. These snacks and drinks were categorized into a high or low cariogenic potential. Items, including chips, crackers, cookies, candy, soda or diet soda, dried fruit, ice cream, and fruit drink with sugar, were classified as high cariogenic potential and were summed to create a sweet index. Consumption of each snack/drink was assigned a score of “1”, while no consumption was assigned a score of “0”, according to previous studies [29,30]. The sweet index, representing intake of high-cariogenic snacks and drinks, ranged from 0 to 8. Items, including yogurt, dry cereal, fresh fruit, water, 100% juice, fruit drinks without sugar, and milk, were classified as low cariogenic potential and were summed to create a non-sweet index. The non-sweet index, indicating the intake of low-cariogenic snacks and drinks, ranged from 0 to 7. Sweet and non-sweet indices weighted by the amount and frequency of consumption were also assessed.

2.4. Covariates

Demographic information, oral hygiene practices, and feeding methods were obtained through questionnaires. Information on medications was extracted from medical records. Several variables were adjusted for in the analysis, including maternal education (high school or less vs. more than high school), infant sex, black race, white race, whether the father provided care to the infant (yes/no), tooth brushing practice (yes/no), exclusive breastfeeding at 12 months (0 = only solid food, 1 = breastfeeding exclusively; 2 = bottle feeding or both), history of antibiotics use until the time of visit (yes/no), and the number of erupted teeth. Plaque score and ECC were assessed at each visit by dentists in a dedicated examination room using standard dental examination equipment, materials and supplies [26]. Plaque score and ECC were also adjusted in the analysis.

2.5. Statistical Analysis

The presence of oral cariogenic microorganisms, including S. mutans and Candida, was the primary outcome. We hypothesized that both sweet and non-sweet indices were associated with the carriage of cariogenic microorganisms, including S. mutans and Candida. Mixed-effects models were conducted to assess the associations between sweet and non-sweet indices of snack intake and oral microorganism carriage at 12, 18, and 24 months of age. Additionally, the potential modification effect of time was evaluated by including an interaction term between the time of visit and snack indices in the models. Logistic regression models were used to assess the associations between sweet and non-sweet indices and oral microorganism carriage at each study visit. The relative importance of 30 demographic, oral hygiene practice, and diet factors in relation to the carriage of oral cariogenic microorganisms in prediction was determined using the random forest method. All statistical analyses were performed using STATA 18.0 (College Station, TX, USA).
Power analysis was conducted using G*Power 3.1 to determine adequate sample size for a cross-sectional logistic regression model. A mixed-effects model could potentially have higher power than correspondent cross-sectional logistic regression models due to its ability to account for within-subject correlations in a cohort study. Three effect sizes were assumed, corresponding to odds ratios of 1.2 (small effect size), 1.5 (medium effect size), and 3 (large effect size). With a significance level (p) set at 0.05, power at 80%, and an R-squared value of 0.2 between the predictor and other covariates, the sample sizes needed were calculated to be 482, 123, and 57, respectively, for the three effect sizes. According to this power analysis, our study had adequate power to identify a predictor with an odds ratio of 1.5 or more.

3. Results

3.1. Characteristics of the Child Cohort

In this study, the majority of the children were African Americans (>53%), and more than half of the mothers had a high school education or less (>54%) (Table 1). Additionally, a significant proportion of the children were not exclusively breastfed at 12 months of age (>84%). The sweet and non-sweet indices of snack intake showed an increasing trend with age (p < 0.001). Analysis of children’s saliva and plaque samples revealed the presence of S. mutans and Candida in early life. The prevalence of S. mutans carriage in both saliva and plaques increased significantly with age (p < 0.001), rising from 21% or more at 12 months to 50% or more at 24 months. However, there was no significant age-related increase in Candida carriage in saliva or plaques (p > 0.17).

3.2. Association between Snack Intake and Cariogenic Microorganism Carriage

The associations between sweet and non-sweet indices and the carriage of S. mutans and Candida in saliva and plaques among children aged 12 to 24 months were analyzed using the mixed-effect models (Table 2). Higher scores on the non-sweet index were associated with increased odds of S. mutans carriage in plaques (OR = 1.67, 95%CI: 1.14, 2.46). The weighted sweet and non-sweet indices had similar results to the non-weighted indices, except that the weighted non-sweet index scores were positively associated with Candida carriage in plaques (OR = 1.01, 95%CI: 1.00, 1.02) (Supplementary Table S1). The modification effect of time on the relationship between snack intake and cariogenic microorganism carriage is presented in Table 3. Significant interactions between the sweet index and the time of visit were found in the associations with Candida carriage in saliva and plaques. Specifically, higher sweet index scores at 12 months were associated with an increased risk of Candida carriage in saliva and plaques (Figure 2A,B), whereas this association reversed at 24 months. An interaction was also observed between the non-sweet index and the time of visit (p = 0.04) in the association with S. mutans carriage in plaques but not in saliva (Figure 2C). The positive associations between non-sweet index scores and S. mutans carriage in plaques seemed to strengthen with age (Figure 2D). The weighted sweet and non-sweet indices had similar results to the non-weighted indices, except that the association between weighted non-sweet index scores and S. mutans carriage in plaques was not modified by the time of visit. But the association between the weighted sweet index scores and S. mutans carriage in plaques was modified by the time of visit, with a positive association more prominent in the earlier visit (Supplementary Table S2).
The cross-sectional associations between sweet and non-sweet indices and the carriage of S. mutans and Candida in saliva and plaques among children at each study visit are presented in Supplementary Table S3. Higher sweet index scores were associated with a decreased risk of Candida carriage in saliva at 24 months of age (OR = 0.73, 95%CI: 0.55, 0.98). Higher non-sweet index scores were associated with an increased risk of S. mutans carriage in plaques at 18 months of age (OR = 3.18, 95%CI: 1.44, 7.01).

3.3. Rank of the Predictive Factors of Cariogenic Microorganism Carriage

The relative importance of 30 demographic, dental, and diet factors in relation to oral S. mutans and Candida carriage in prediction were determined using random forest. The sweet and non-sweet indices emerged as top-ranking factors for S. mutans carriage in both saliva and plaques between 12 and 24 months (Supplementary Figures S1 and S2). Among individual snacks, cookie intake ranked among the top five predictive factors for S. mutans carriage in saliva at 12 months, while yogurt intake was among the top five predictive factors for S. mutans carriage in plaques at 12 and 24 months. Similarly, the sweet and non-sweet indices were identified as top-ranking factors for Candida carriage in both saliva and plaques between 12 and 24 months (Supplementary Figures S3 and S4). Among individual snacks, cookie intake was among the top five predictive factors for Candida carriage in saliva and plaques at 18 months.

4. Discussion

In this study, conducted on a birth cohort from low socioeconomic backgrounds, higher scores on the non-sweet index were linked to increased odds of S. mutans carriage in plaques, with this positive association potentially strengthening with age. On the other hand, higher sweet index scores at 12 months were linked to an increased risk of Candida carriage in saliva and plaques, with this association reversed at 24 months. Results from random forest indicated both the sweet and non-sweet indices as top-ranking factors in prediction for the carriage of S. mutans and Candida, with specific snacks like cookies and yogurt intake also featuring prominently. These findings underline the importance of both sweet and non-sweet snack consumption in their association with the presence of cariogenic oral microorganisms during early childhood, particularly among socioeconomically disadvantaged populations.
Previous studies have presented mixed results regarding the association between sugar intake or sweetened food/beverages and the presence of S. mutans in saliva or plaques. Some studies have reported positive associations [19,20,22,25], while others found no association or low correlation [21,24]. In our cross-sectional analysis, a trend, albeit non-significant, of positive associations between sweet index scores and S. mutans carriage in saliva and plaques was observed at 12 and 18 months of age. This trend was also evident in the association between weighted sweet index scores and S. mutans carriage in saliva and plaques. Interestingly, several studies have also noted a positive relationship between eating or snacking frequency, including both sugary and non-sugary foods, and S. mutans carriage [20,23,25]. The study found a positive association between non-sweet index scores and S. mutans carriage in plaques, potentially strengthening with age. These results, along with previous research, suggests that snacks, regardless of sugar content, may contribute to S. mutans colonization. Additionally, certain snacks previously classified as low-cariogenic foods, such as dry cereal, may have a high sugar content [29]. The Environmental Working Group has reported that children’s cereals are more heavily loaded with added sugar compared to adult cereals [31]. These findings highlight the need for further investigation into the classification of the cariogenic potential of individual food and the specific mechanisms linking snack intake, particularly low- or non-sugary snacks, with the carriage of cariogenic microorganisms.
This study has uncovered a novel connection between sweet index scores (both weighted and non-weighted) and oral Candida carriage. At 12 months of age, positive associations were found between sweet index scores and increased risk of Candida carriage in saliva and plaques. But at 24 months of age, negative associations were identified. To our knowledge, no prior studies have examined the relationship between dietary intake and oral Candida carriage in children. Nonetheless, in vitro studies have indicated that sucrose can promote Candida growth and the formation of inter-kingdom biofilms between Candida and S. mutans [32,33]. However, the observed variation in the association between the sweet index and Candida carriage with age in this study warrants further investigation to elucidate the underlying mechanisms.
The longitudinal and random forest analyses conducted in this study emphasize the potential importance of sweet and non-sweet indices in relation to the oral carriage of cariogenic microorganisms, S. mutans and Candida, in early childhood. However, several limitations should be considered when interpreting the results. Firstly, the study only assessed the intake of common snacks and drinks, and the main meals consumed by the children were not assessed. Future studies should incorporate more comprehensive dietary assessment, such as a diet diary or repeated 24 h dietary recalls, to provide a holistic understanding of dietary influences on the oral microbiome. Additionally, this study did not explore the association between snack intake and the quantity of S. mutans and Candida in the oral cavity, as a significant number of children in the cohort were free from S. mutans or Candida carriage. Future research could investigate the relationship between dietary intake and S. mutans or Candida growth among young children who test positive for S. mutans or Candida carriage.

5. Conclusions

Findings from this study support the associations between snack intake and the presence of oral cariogenic microorganisms, S. mutans and Candida, in early childhood, underscoring the importance of considering dietary factors in oral health management for young children, particularly in underserved populations with limited access to dental care and healthy foods. Future research can expand on these findings by conducting more comprehensive dietary assessments and further elucidating the specific mechanisms by which different types of food and beverages influence the colonization of cariogenic microorganisms in order to inform targeted interventions.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/nu16081113/s1, Table S1. Associations between weighted snack intake and oral microorganism carriage from child aged 12 months to 24 months. Table S2. Interactions between weighted sweet/non-sweet indices and time of visit and their associations with oral microorganisms. Table S3. Cross-sectional analysis of the associations between snack indices and oral microorganism carriage. Figure S1. Rank of the predictive factors of S. mutans carriage in saliva by age. Figure S2. Rank of the predictive factors of S. mutans carriage in plaque by age. Figure S3. Rank of the predictive factors of Candida carriage in saliva by age. Figure S4. Rank of the predictive factors of Candida carriage in plaque by age.

Author Contributions

A.A., J.X. and Y.M. contributed to the conception, design, data acquisition, analysis, and interpretation, drafting and critically revising the manuscript; N.A. contributed to data acquisition and interpretation, drafting and critically revising the manuscript; S.M., H.X. and M.S. contributed to data analysis, data interpretation and critically reviewing the manuscript. All authors agree to be accountable for all aspects of the work. All authors have read and agreed to the published version of the manuscript.

Funding

This study is supported by National Institute of Dental and Craniofacial Research NIDCR K23DE027412 and NIDCR R01DE031025. The funding agencies had no role in the study design, data collection, analyses, decision to publish, or preparation of the manuscript.

Institutional Review Board Statement

The reported study was approved by the University of Rochester Research Subject Review Board (#4628, approval date: 18 August 2017).

Informed Consent Statement

All participants were informed of the study objects and protocols, and gave written consent prior to study activities.

Data Availability Statement

The original contributions presented in the study are included in the article/Supplementary Materials, further inquiries can be directed to the corresponding author.

Acknowledgments

We thank the participants and staff who contributed to the study.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Dye, B.A.; Hsu, K.L.; Afful, J. Prevalence and Measurement of Dental Caries in Young Children. Pediatr. Dent. 2015, 37, 200–216. [Google Scholar] [PubMed]
  2. Fleming, E.; Afful, J. Prevalence of total and untreated dental caries among youth: United States, 2015–2016. In NCHS Data Brief; no 307; National Center for Health Statistics: Hyattsville, MD, USA, 2018. [Google Scholar]
  3. Palmer, C.; Kent, R., Jr.; Loo, C.; Hughes, C.; Stutius, E.; Pradhan, N.; Dahlan, M.; Kanasi, E.; Arevalo Vasquez, S.; Tanner, A. Diet and caries-associated bacteria in severe early childhood caries. J. Dent. Res. 2010, 89, 1224–1229. [Google Scholar] [CrossRef] [PubMed]
  4. Manchanda, S.; Sardana, D.; Peng, S.; Lo, E.C.M.; Chandwani, N.; Yiu, C.K.Y. Is Mutans Streptococci count a risk predictor of Early Childhood Caries? A systematic review and meta-analysis. BMC Oral Health 2023, 23, 648. [Google Scholar] [CrossRef] [PubMed]
  5. de Carvalho, F.G.; Silva, D.S.; Hebling, J.; Spolidorio, L.C.; Spolidorio, D.M. Presence of mutans streptococci and Candida spp. in dental plaque/dentine of carious teeth and early childhood caries. Arch. Oral Biol. 2006, 51, 1024–1028. [Google Scholar] [CrossRef]
  6. Al-Ahmad, A.; Auschill, T.M.; Dakhel, R.; Wittmer, A.; Pelz, K.; Heumann, C.; Hellwig, E.; Arweiler, N.B. Prevalence of Candida albicans and Candida dubliniensis in caries-free and caries-active children in relation to the oral microbiota-a clinical study. Clin. Oral. Investig. 2016, 20, 1963–1971. [Google Scholar] [CrossRef] [PubMed]
  7. Samaranayake, L.P.; Hughes, A.; Weetman, D.A.; MacFarlane, T.W. Growth and acid production of Candida species in human saliva supplemented with glucose. J. Oral. Pathol. 1986, 15, 251–254. [Google Scholar] [CrossRef] [PubMed]
  8. Klinke, T.; Kneist, S.; de Soet, J.J.; Kuhlisch, E.; Mauersberger, S.; Forster, A.; Klimm, W. Acid production by oral strains of Candida albicans and Lactobacilli. Caries Res. 2009, 43, 83–91. [Google Scholar] [CrossRef] [PubMed]
  9. Xiao, J.; Moon, Y.; Li, L.; Rustchenko, E.; Wakabayashi, H.; Zhao, X.; Feng, C.; Gill, S.R.; McLaren, S.; Malmstrom, H.; et al. Candida albicans Carriage in Children with Severe Early Childhood Caries (S-ECC) and Maternal Relatedness. PLoS ONE 2016, 11, e0164242. [Google Scholar] [CrossRef] [PubMed]
  10. Gregoire, S.; Xiao, J.; Silva, B.B.; Gonzalez, I.; Agidi, P.S.; Klein, M.I.; Ambatipudi, K.S.; Rosalen, P.L.; Bauserman, R.; Waugh, R.E.; et al. Role of glucosyltransferase B in interactions of Candida albicans with Streptococcus mutans and with an experimental pellicle on hydroxyapatite surfaces. Appl. Environ. Microbiol. 2011, 77, 6357–6367. [Google Scholar] [CrossRef]
  11. Hwang, G.; Marsh, G.; Gao, L.; Waugh, R.; Koo, H. Binding Force Dynamics of Streptococcus mutans-glucosyltransferase B to Candida albicans. J. Dent. Res. 2015, 94, 1310–1317. [Google Scholar] [CrossRef]
  12. Koo, H.; Bowen, W.H. Candida albicans and Streptococcus mutans: A potential synergistic alliance to cause virulent tooth decay in children. Future Microbiol. 2014, 9, 1295–1297. [Google Scholar] [CrossRef]
  13. Zero, D. Recaldent™—Evidence for clinical activity. Adv. Dent. Res. 2009, 21, 30–34. [Google Scholar] [CrossRef]
  14. Dunford, E.; Popkin, B. 37 year snacking trends for US children 1977–2014. Pediatr. Obes. 2018, 13, 247–255. [Google Scholar] [CrossRef]
  15. Xue, H.; Maguire, R.L.; Liu, J.; Kollins, S.H.; Murphy, S.K.; Hoyo, C.; Fuemmeler, B.F. Snacking frequency and dietary intake in toddlers and preschool children. Appetite 2019, 142, 104369. [Google Scholar] [CrossRef]
  16. Evans, E.W.; Hayes, C.; Palmer, C.A.; Bermudez, O.I.; Cohen, S.A.; Must, A. Dietary intake and severe early childhood caries in low-income, young children. J. Acad. Nutr. Diet. 2013, 113, 1057–1061. [Google Scholar] [CrossRef]
  17. MacKeown, J.M.; Faber, M. Frequency of consumption of cariogenic food items by 4-month-old to 24-month-old children: Comparison between two rural communities in KwaZulu–Natal, South Africa. Int. J. Food Sci. Nutr. 2005, 56, 95–103. [Google Scholar] [CrossRef]
  18. Dotsey, R.P.; Moser, E.A.S.; Eckert, G.J.; Gregory, R.L. Effects of Cola-Flavored Beverages and Caffeine on Streptococcus mutans Biofilm Formation and Metabolic Activity. J. Clin. Pediatr. Dent. 2017, 41, 294–299. [Google Scholar] [CrossRef]
  19. Cornejo, C.F.; Soken, L.J.; Salgado, P.A.; Gliosca, L.A.; Squassi, A.F. Detection of Streptococcus mutans and Streptococcus sobrinus and Their Association with Oral Microbiome Stressors in 6–18-month-old Infants. Int. J. Clin. Pediatr. Dent. 2023, 16, 68–73. [Google Scholar] [CrossRef]
  20. Habibian, M.; Beighton, D.; Stevenson, R.; Lawson, M.; Roberts, G. Relationships between dietary behaviours, oral hygiene and mutans streptococci in dental plaque of a group of infants in southern England. Arch. Oral Biol. 2002, 47, 491–498. [Google Scholar] [CrossRef]
  21. Weber-Gasparoni, K.; Goebel, B.M.; Drake, D.R.; Kramer, K.W.; Warren, J.J.; Reeve, J.; Dawson, D.V. Factors associated with mutans streptococci among young WIC-enrolled children. J. Public. Health Dent. 2012, 72, 269–278. [Google Scholar] [CrossRef]
  22. Mohan, A.; Morse, D.E.; O’Sullivan, D.M.; Tinanoff, N. The relationship between bottle usage/content, age, and number of teeth with mutans streptococci colonization in 6–24-month-old children. Community Dent. Oral Epidemiol. 1998, 26, 12–20. [Google Scholar] [PubMed]
  23. Ingemansson Hultquist, A.; Lingström, P.; Bågesund, M. Risk factors for early colonization of mutans streptococci—A multiple logistic regression analysis in Swedish 1-year-olds. BMC Oral Health 2014, 14, 147. [Google Scholar] [CrossRef] [PubMed]
  24. Roeters, F.J.; van der Hoeven, J.S.; Burgersdijk, R.C.; Schaeken, M.J. Lactobacilli, mutants streptococci and dental caries: A longitudinal study in 2-year-old children up to the age of 5 years. Caries Res. 1995, 29, 272–279. [Google Scholar] [CrossRef] [PubMed]
  25. Wan, A.K.; Seow, W.K.; Purdie, D.M.; Bird, P.S.; Walsh, L.J.; Tudehope, D.I. A longitudinal study of Streptococcus mutans colonization in infants after tooth eruption. J. Dent. Res. 2003, 82, 504–508. [Google Scholar] [CrossRef]
  26. Alkhars, N.; Zeng, Y.; Alomeir, N.; Al Jallad, N.; Wu, T.T.; Aboelmagd, S.; Youssef, M.; Jang, H.; Fogarty, C.; Xiao, J. Oral Candida Predicts Streptococcus mutans Emergence in Underserved US Infants. J. Dent. Res. 2022, 101, 54–62. [Google Scholar] [CrossRef]
  27. Xiao, J.; Fogarty, C.; Wu, T.T.; Alkhers, N.; Zeng, Y.; Thomas, M.; Youssef, M.; Wang, L.; Cowen, L.; Abdelsalam, H.; et al. Oral health and Candida carriage in socioeconomically disadvantaged US pregnant women. BMC Pregnancy Childbirth 2019, 19, 480. [Google Scholar] [CrossRef] [PubMed]
  28. Little, W.A.; Korts, D.C.; Thomson, L.A.; Bowen, W.H. Comparative recovery of Streptococcus mutans on ten isolation media. J. Clin. Microbiol. 1977, 5, 578–583. [Google Scholar] [CrossRef] [PubMed]
  29. Chaffee, B.W.; Feldens, C.A.; Rodrigues, P.H.; Vítolo, M.R. Feeding practices in infancy associated with caries incidence in early childhood. Community Dent. Oral Epidemiol. 2015, 43, 338–348. [Google Scholar] [CrossRef]
  30. Peres, M.A.; Sheiham, A.; Liu, P.; Demarco, F.F.; Silva, A.E.; Assunção, M.C.; Menezes, A.M.; Barros, F.C.; Peres, K.G. Sugar Consumption and Changes in Dental Caries from Childhood to Adolescence. J. Dent. Res. 2016, 95, 388–394. [Google Scholar] [CrossRef]
  31. EWG. Children’s Cereals: Sugar by the Pound. 2014. Available online: https://www.ewg.org/research/childrens-cereals (accessed on 30 January 2024).
  32. Pizzo, G.; Giuliana, G.; Milici, M.E.; Giangreco, R. Effect of dietary carbohydrates on the in vitro epithelial adhesion of Candida albicans, Candida tropicalis, and Candida krusei. New Microbiol. 2000, 23, 63–71. [Google Scholar]
  33. Negrini, T.C.; Ren, Z.; Miao, Y.; Kim, D.; Simon-Soro, Á.; Liu, Y.; Koo, H.; Arthur, R.A. Dietary sugars modulate bacterial-fungal interactions in saliva and inter-kingdom biofilm formation on apatitic surface. Front. Cell. Infect. Microbiol. 2022, 12, 993640. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Participant flow diagram of the study.
Figure 1. Participant flow diagram of the study.
Nutrients 16 01113 g001
Figure 2. (A) The relationship between sweet index scores and predicted probability of Candida carriage in saliva at 12, 18, and 24 months. (B) The relationship between sweet index scores and predicted probability of Candida carriage in plaques at 12, 18, and 24 months. (C) The relationship between non-sweet index scores and predicted probability of S. mutans carriage in saliva at 12, 18, and 24 months. (D) The relationship between non-sweet index scores and predicted probability of S. mutans carriage in plaques at 12, 18, and 24 months. The blue line represents the relationship at 12 months and the blue area represents the confidence interval; the red line represents the relationship at 18 months and the red area represents the confidence interval; and the green line represents the relationship at 24 months and the green area represents the confidence interval.
Figure 2. (A) The relationship between sweet index scores and predicted probability of Candida carriage in saliva at 12, 18, and 24 months. (B) The relationship between sweet index scores and predicted probability of Candida carriage in plaques at 12, 18, and 24 months. (C) The relationship between non-sweet index scores and predicted probability of S. mutans carriage in saliva at 12, 18, and 24 months. (D) The relationship between non-sweet index scores and predicted probability of S. mutans carriage in plaques at 12, 18, and 24 months. The blue line represents the relationship at 12 months and the blue area represents the confidence interval; the red line represents the relationship at 18 months and the red area represents the confidence interval; and the green line represents the relationship at 24 months and the green area represents the confidence interval.
Nutrients 16 01113 g002
Table 1. Characteristics of the children (n = 123).
Table 1. Characteristics of the children (n = 123).
CharacteristicsPercentage or Mean (SD)
12 Months a
(n = 123)
18 Months a
(n = 97)
24 Months a
(n = 104)
Race__White24.4%23.7%24.0%
  __Black54.5%53.6%54.8%
Female51.2%50.5%51.9%
Maternal education (High school or less)56.1%54.6%55.8%
Dad as care provider43.1%48.5%45.2%
Exclusively breastfeeding at 12 months15.5%15.5%13.5%
History of antibiotics use12.2%16.5%18.3%
Tooth brushing66.7%92.8%99.0%
Number of erupted teeth 5.8 (2.7)13.2 (3.2)17.1 (1.9)
Plaque score0.24 (0.42)0.49 (0.63)0.63 (0.68)
ECC3.3%12.4%25.0%
Predictors
Snack__Sweet index2.1 (1.5)3.1 (1.7)3.6 (1.7)
Snack__Non-sweet index4.5 (1.4)5.2 (0.9)5.2 (1.1)
Outcomes
S. mutans carriage__saliva21.1%41.2%50.0%
S. mutans carriage__plaque21.7%36.1%56.7%
Candida carriage__saliva50.4%54.6%40.4%
Candida carriage__plaque25.8%23.7%29.8%
Note. a Percentage or mean (SD).
Table 2. Associations between snack intake and oral microorganism carriage from children aged 12 months to 24 months.
Table 2. Associations between snack intake and oral microorganism carriage from children aged 12 months to 24 months.
Sweet IndexNon-Sweet Index
OR95% CIpOR95% CIp
S. mutans carriage__saliva1.050.85, 1.290.681.060.80, 1.420.68
S. mutans carriage__plaque0.990.79, 1.250.951.671.14, 2.460.01
Candida carriage__saliva0.910.75, 1.090.311.130.89, 1.450.32
Candida carriage__plaque0.930.75, 1.160.540.810.61, 1.070.13
Note. Mixed-effects models were used to estimate the associations between sweet/non-sweet indices and oral microorganism carriage, respectively. Covariates adjusted in the models included maternal education, infant sex, infant race, dad as care provider, history of antibiotics use, tooth brushing, number of erupted teeth, exclusive breastfeeding at 12 months of age, plaque score, ECC, and time of visit. OR is odds ratio. CI is confidence interval. Bolded results are results that fulfill p < 0.05.
Table 3. Interactions between sweet/non-sweet indices and time of visit and their associations with oral microorganisms.
Table 3. Interactions between sweet/non-sweet indices and time of visit and their associations with oral microorganisms.
S. mutansCandida
SalivaPlaqueSalivaPlaque
OR (95%CI)pOR (95%CI)pOR (95%CI)pOR (95%CI)p
Sweet Index1.70 (0.80, 3.64)0.171.54 (0.66, 3.56)0.262.69 (1.34, 5.43)0.0062.80 (1.29, 6.09)0.01
Time1.12 (0.93, 1.35)0.221.16 (0.94, 1.42)0.171.17 (0.99, 1.38)0.061.17 (0.98, 1.40)0.04
Sweet Index × Time0.97 (0.94, 1.01)0.190.98 (0.94, 1.02)0.290.94 (0.91, 0.98)0.0020.94 (0.90, 0.98)0.004
Non-sweet Index0.64 (0.26, 1.60)0.340.45 (0.13, 1.56)0.211.37 (0.63, 2.95)0.431.25 (0.53, 2.95)0.62
Time0.86 (0.64, 1.16)0.340.74 (0.50, 1.09)0.261.02 (0.79, 1.32)0.861.11 (0.83, 1.47)0.49
Non-sweet index × Time1.03 (0.98, 1.08)0.251.08 (1.00, 1.16)0.040.99 (0.95, 1.03)0.620.97 (0.93, 1.02)0.30
Note. Mixed-effects models were used to estimate the interactions between sweet/non-sweet indices and time of visit, respectively. Covariates adjusted in the models included maternal education, infant sex, infant race, dad as care provider, history of antibiotics use, tooth brushing, number of erupted teeth, exclusive breastfeeding at 12 months of age, plaque score, and ECC. OR is odds ratio. CI is confidence interval. Bolded results are interaction results that fulfill p < 0.05.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Alkadi, A.; Alkhars, N.; Manning, S.; Xu, H.; Sohn, M.; Xiao, J.; Meng, Y. The Associations between Snack Intake and Cariogenic Oral Microorganism Colonization in Young Children of a Low Socioeconomic Status. Nutrients 2024, 16, 1113. https://doi.org/10.3390/nu16081113

AMA Style

Alkadi A, Alkhars N, Manning S, Xu H, Sohn M, Xiao J, Meng Y. The Associations between Snack Intake and Cariogenic Oral Microorganism Colonization in Young Children of a Low Socioeconomic Status. Nutrients. 2024; 16(8):1113. https://doi.org/10.3390/nu16081113

Chicago/Turabian Style

Alkadi, Ahmed, Naemah Alkhars, Samantha Manning, Hongzhe Xu, Michael Sohn, Jin Xiao, and Ying Meng. 2024. "The Associations between Snack Intake and Cariogenic Oral Microorganism Colonization in Young Children of a Low Socioeconomic Status" Nutrients 16, no. 8: 1113. https://doi.org/10.3390/nu16081113

APA Style

Alkadi, A., Alkhars, N., Manning, S., Xu, H., Sohn, M., Xiao, J., & Meng, Y. (2024). The Associations between Snack Intake and Cariogenic Oral Microorganism Colonization in Young Children of a Low Socioeconomic Status. Nutrients, 16(8), 1113. https://doi.org/10.3390/nu16081113

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

Article Metrics

Back to TopTop