Our objective was to develop and perfect a model for the assessment of risk of dental caries onset in children. Even though dental caries prevalence in children is continuing to decline, there is still a significant minority for whom it is a problem. In this study, we sought to ascertain whether a set of variables selected in a previous cross-sectional study could be used to differentiate between caries-free six-year-olds who would or would not subsequently present with clinically-detectable caries. A total of 472 caries-free six-year-olds--286 from a fluoridated community and 186 from a fluoride-deficient community--was selected. Clinical examinations for DMFS, dental fluorosis, and plaque were conducted. Stimulated whole saliva was collected for analysis of mutants streptococci, lactobacilli, total viable flora, and fluoride, calcium, and phosphate concentrations. A questionnaire was used for collection of demographic data as well as information on prior fluoride exposure, dietary habits, and oral hygiene practices. By means of linear discriminant analyses, it was possible to predict correctly which children would develop caries within six to 12 months (sensitivity) in 82.8% of cases and which children would not develop caries during that period (specificity) in 82.4% of cases.

Although the prevalence of dental caries is continuing to decline, it still affects a majority of the US population and can be a serious problem for those afflicted. The objective of this project was to develop and perfect a model for assessment of risk of dental caries onset in children. In the first study, reported herein, a set of clinical, microbiological, biochemical, and socio-demographic variables was identified that distinguished, with an acceptable level of sensitivity and specificity, between children who had no previous caries experience and children who had high caries levels. A total of 313 children--age 12-15 years, 140 from a fluoridated community and 173 from a fluoride-deficient community--was selected on the basis of previous caries experience, either zero DMFS or high DMFS (> or = 6 in the fluoridated or > or = 8 in the fluoride-deficient community). Clinical exams for DMFS, dental fluorosis, and plaque were conducted. Stimulated whole saliva was collected for analysis of mutans streptococci, lactobacilli, total viable flora, and fluoride concentration. A questionnaire was used for collection of demographic data as well as information on prior fluoride exposure, dietary habits, and oral hygiene practices. By means of discriminant analyses, with use of seven key clinical and laboratory variables, it was possible for zero-DMFS subjects to e classified correctly (specificity) in 77.6% of cases in the fluoridated community and in 86.1% of cases in the fluoride-deficient community. High-caries subjects were classified as such (sensitivity) in 79.3% and 88.1% of cases, respectively.

The present study was undertaken to evaluate the effect of a twice-daily topical application of a 0.05% NaF mouthrinse on de- and remineralization in the oral cavities of subjects suffering from radiation-induced hyposalivation. Six subjects each wore a bonded intra-oral appliance containing a sound and a demineralized human enamel slab for four weeks. During that period, the subjects used 0.05% NaF rinses, twice daily, instead of the 1.1% NaF gel that had previously been a part of their preventive regimen. Salivary flow rates, plaque pH profiles following a 10% sucrose rinse, S. mutans and lactobacillus counts, fluoride clearance, and enamel microhardness were determined during the study. Sound enamel samples displayed no evidence of demineralization, and the previously demineralized enamel showed remineralization in the outer 50 microns in three of the six subjects. The results suggest that a twice-daily oral rinse with 0.05% NaF can prevent demineralization and enhance remineralization in subjects with radiation-induced hyposalivation.

An epidemiologic investigation to reliably identify caries-susceptible subjects by microbiological and chemical assessment of plaque and saliva is currently in progress. As part of that study, the numerical relationships of mutans streptococci, lactobacilli and total viable microflora in plaque and saliva among 12- to 15-year-old children in a fluoridated community were determined. Paraffin-stimulated whole saliva and pooled dental plaque were collected. Each sample was suspended in reduced transport fluid, chilled on ice, and assayed. The bivariate normal distribution was found to be a suitable model for the distribution of the pairs [numbers of bacteria in plaque (log₁₀), numbers of bacteria in saliva (log₁₀)]. Statistically significant positive correlations were found between numbers of mutans streptococci in plaque and saliva, and between lactobacilli in plaque and saliva.