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J Dent Res. Nov 2010; 89(11): 1198–1202.
PMCID: PMC2954250
NIHMSID: NIHMS212837

Taste Genes Associatedwith Dental Caries

Abstract

Dental caries is influenced by a complex interplay of genetic and environmental factors, including dietary habits. Previous reports have characterized the influence of genetic variation on taste preferences and dietary habits. We therefore hypothesized that genetic variation in taste pathway genes (TAS2R38, TAS1R2, GNAT3) may be associated with dental caries risk and/or protection. Families were recruited by the Center for Oral Health Research in Appalachia (COHRA) for collection of biological samples, demographic data, and clinical assessment of oral health, including caries scores. Multiple single-nucleotide polymorphism (SNP) assays for each gene were performed and analyzed by transmission disequilibrium test (TDT) analysis (FBAT software) for three dentition groups: primary, mixed, and permanent. Statistically significant associations were seen in TAS2R38 and TAS1R2 for caries risk and/or protection.

Keywords: dental caries, taste preference, genetic association, taste pathway genes

Introduction

Dental caries is the most prevalent childhood and chronic disease worldwide. Caries occurrence and progression are known to be influenced by a complex interplay of both environmental and genetic factors, with numerous contributing factors having been identified, including bacterial flora, dietary habits, fluoride exposure, oral hygiene, salivary flow, salivary composition, and tooth structure. The importance of genetic factors in caries is supported by twin studies that have estimated that 40-60% of caries susceptibility is genetically determined (Boraas et al., 1988; Conry et al., 1993; Bretz et al., 2005, 2006; Wang et al., 2010). There is also strong support, from animal model studies, for a genetic component to caries (Liu et al., 1998; Shuler, 2001; Nariyama et al., 2004).

To date, there have been few studies on the association of specific genes with human caries. Tuftelin was found to be associated with caries (Slayton et al., 2005), as well as Ameloblastin (Deeley et al., 2008). Given the strong evidence of a genetic component to dental caries, the discovery of additional genes and pathways may greatly improve the identification of individuals at risk and enhance the implementation of targeted preventive strategies at the critical stage before onset of caries.

Given the influence of dietary habits on dental caries, we hypothesized that taste pathway genes, such as genes for taste preference, might influence caries risk. Although taste preferences based on chemical tastants have been proven useful for the assessment of dietary habits, this approach has been hampered by numerous difficulties and is limited to a point in time that may not represent an individual’s lifelong dietary habits. A genetics approach provides an opportunity for better discrimination between genetic and environmental components.

Therefore, in the current study, we investigated markers within the genes for “taste receptor, type-2, member 38” (TAS2R38), “taste receptor, type-1, member 2” (TAS1R2), and “guanine nucleotide binding protein, alpha transducing-3” (GNAT3) for associations with dental caries in a large cohort of families from Appalachia. Our ultimate goal is to use these results to develop targeted intervention strategies for dental caries based on specific environmental modifications, in the context of specific genetic backgrounds such as taste preferences.

Materials & Methods

Study participants were drawn from the ongoing oral health etiology studies of the Center for Oral Health Research in Appalachia (COHRA), a partnership between the University of Pittsburgh and West Virginia University. As previously described (Polk et al., 2008), a family recruitment approach identified eligible resident households with at least one biological parent-child pair including a child between ages 1 and 18 living in the same household, regardless of caries status. Exclusion criteria included individuals with neurological impairment, a severe physical handicap, psychosis, and families with either of the parent-child pair having a reduced ability to form blood clots or resist infection. The COHRA study population includes a range of socio-economic status (median annual household income less than $25,000), and is fairly representative of the general Appalachian population, which ranks very low compared with the rest of the nation in terms of many oral health measures and access to oral health care (Grembowski et al., 1987; Janes et al., 1999; Purnell, 1999). Statistical analysis was limited to Caucasian families due to the small non-Caucasian sample size and potential complications of genetic heterogeneity. After receiving informed consent approved by the institutional review boards of both universities, COHRA ascertains representative families from West Virginia and Pennsylvania, and applies a full range of oro-dental, behavioral, and microbiological assessments (Polk et al., 2008). Each participant also provided a sample for DNA extraction (blood, buccal tissue, mouthwash, or saliva). See Table 1 for the characteristics of the study participants, all of whom were members of COHRA families.

Table 1.
Characteristics of Study Population

The caries assessments were performed by trained dental professionals (dentists and dental hygienists) who were calibrated periodically across all sites. Intraclass correlation coefficient (ICC) analysis was applied to quantify the consistency of caries assessments among and within the examiners. Note that very high concordance rates were observed for both inter-examiner reliability (ICC between 0.86 and 0.99) and intra-examiner reliability (ICC > 0.99).

Each tooth was identified as either permanent or primary, and each surface on each tooth was scored as decayed, missing due to caries, or filled. We calculated the standard decayed, filled, teeth/surface scores dfs/dft (Drury et al., 1999) for primary teeth to avoid misidentification of unerupted teeth in children, and DMFT/DMFS for permanent teeth using the cavitated enamel and dentin lesion definition. Three groupings of individuals were used for analysis: “primary” = individuals with only primary teeth (caries score dft/dfs); “mixed” = individuals with at least one primary tooth and at least one permanent tooth (caries scores dft+DMFT and dfs+DMFS); and “permanent” = individuals with only permanent teeth (caries scores DMFT/DMFS). For analysis, we dichotomized the original dft/DMFT caries scores by caries status [assigning 0 values for individuals with no caries (dft/DMFT = 0) and 1 for individuals with any caries (dft/DMFT > 0)].

DNA Sample Preparation

Subject genomic DNA was extracted from either blood, buccal tissue, or mouthwash with the Gentra Puregene kit (Qiagen, Valencia, CA, USA) or from saliva by means of the Oragene DNA Self Collection kit (DNA genotek, Ottawa, ON, Canada). A participant’s DNA was extracted according to standard manufacturer protocols and quantified with the Taqman RNaseP Detection Reagent (Applied Biosystems, Carlsbad, CA, USA) for standardization to 2 ng/µL.

Genotyping Methods

Genotyping for TAS2R38-SNP(1-3) (rs713598, rs1726866, rs10246939), TAS1R2-SNP(1-2) (rs4920566, rs9701796), and GNAT3-SNP(1-2) (rs2074674, rs6962693) with Taqman SNP Genotyping Assays (Applied Biosystems) in 5-µL reactions with 4.5 ng DNA was amplified on a Tetrad PTC 225 thermocycler (MJ Research, Waltham, MA, USA). Genotype amplification detection and analysis were performed on the ABI 7900HT with ABI SDS software (Applied Biosystems). See Table 2 for SNP details. The error rate of additional SNP assays, genotyped in triplicate under identical conditions and confirmed with a separate method utilizing restriction site alterations, revealed a 0.4% genotyping discrepancy rate (data not shown).

Table 2.
Candidate Gene Markers Studied

Statistical Analysis

We used the transmission disequilibrium test (TDT) to assess association in the presence of linkage disequilibrium between the SNPs and the dental caries phenotypes. The Family Based Association Test (FBAT), an extension of the TDT (Laird et al., 2000; Rabinowitz and Laird, 2000; Horvath et al., 2001) was used for both SNP and haplotype analyses (haplotypes are patterns of alleles within multiple SNPs that are together on the same chromosome strand in an individual). To detect allelic associations with both caries risk and caries protection, we evaluated each caries score twice, first assessing transmission patterns to the individuals affected with caries (to detect risk alleles), and second assessing transmission to individuals with no caries (for protection). The default threshold for statistical significance was applied (i.e., p-values ≤ 0.05). All reported SNP genotypes were in Hardy-Weinberg Equilibrium.

Results

We analyzed dental records for 496 people in primary, 562 in mixed, and 1391 in permanent dentition (Table 1). The average ages for these 3 dentition groups were 3.4, 9.8, and 29.4 yrs, respectively. The male-to-female ratios were comparable for both primary and mixed dentition, while there were substantially more females in the permanent dentition group. The summary statistics of the dft/DMFT and dfs/DMFS scores are also listed, showing the median dft/DMFT and dfs/DMFS increasing with the average age of the 3 study group categories (Table 1).

Analysis of our data revealed a significant association of the G, G, and C individual alleles representing the P, A, and V amino acid substitutions in the TAS2R38 gene with protection from caries in the “primary” group (p = 0.007, 0.03, 0.01, respectively) (Table 3). Haplotype analysis supported these findings, with significant association of GGC, GGX, and XGC (X representing any nucleotide) haplotypes in the “primary” group with caries protection (p = 0.005, 0.004, 0.02) (Table 4). The corresponding opposing haplotypes CAT and CAX were significantly associated in the “primary” group with caries risk (0.02, 0.03, respectively), which verified the validity of our findings (Table 4). Analysis of 2 SNPs in the TAS1R2 gene revealed significant association of the C allele of the TAS1R2-SNP2 in the “mixed” group for both caries protection (p = 0.03) and caries risk (p = 0.02) (Table 3). No statistically significant results were found in the permanent group (results not shown in detail).

Table 3.
FBAT Single SNP Association Analyses on 2 Taste Preference Genes
Table 4.
Haplotype Association Analyses for TAS2R38 in Primary Dentition

Discussion

In spite of the many methodological challenges, studies have demonstrated the importance of dietary habits, nutritional status, and chemically determined taste sensitivity with respect to caries risk (Bretz et al., 2006). We have taken advantage of the growing knowledge of the genetic components of taste preference and dietary habits to investigate the association of taste receptors and pathways with caries, resulting in evidence for association of TAS2R38 and TAS1R2 genotypes and/or haplotypes with caries.

The haplotypes of 3 SNPs representing the corresponding amino acid substitutions (A49P, A262V, V296I) in TAS2R38 have been well-characterized for their influence on the bitter taste sensitivity to specific classes of chemicals, including PROP (propylthiouracil) and PTC (phenylthiocarbamide). The proline, alanine, and valine combination (PAV) represented by the nucleotides (GGC) is associated with bitter sensitivity or “supertasters”, while the alanine, valine, and isoleucine combination (AVI) represented by the nucleotides (CAT) is associated with bitter insensitivity or “non-tasters”. Additional intermediate taster haplotypes, including AAV (CGC) and AAI (CGT), are more rare (Drayna, 2005). Supertasters have been associated with an increased density of anterior fungiform taste papillae and increased sensitivity to a wide variety of taste and oral sensations, including sweetness, mouth-feel, fats, and oral irritation (reviewed in Tepper, 2008). Analysis of our data revealed a significant association of the G, G, and C individual alleles representing the P, A, and V substitutions of supertasters with caries protection in the “primary” group. This is further supported by the similar association of the GGC, GGX, and XGC haplotypes. In addition, the CAT haplotype representing the AVI non-taster and CAX haplotype were associated with caries risk. This suggests a role for this gene in caries that may act through influences on dietary habits that then result in differing cariogenic and/or nutritional status.

These results are particularly interesting, considering that phenotypic inversions and other age-related biological responses have been characterized for TAS2R38 haplotypes or chemically determined bitter sensitivity, including correlations to food preferences, liking, and use, including sweet preferences. It has been shown that bitter sensitivity of the TAS2R38 supertaster haplotype declines with age, including a substantial transition during puberty (Bell and Tepper, 2006). While studies in adults have been inconsistent in correlating bitter sensitivity to sweet sensitivity, a study in preschool children (3.5-4.5 yrs) demonstrated that correlation of PROP determined supertaster children with increased sweet sensitivity, but, strikingly, these supertasters were sweet “likers” and consumed more sweet foods and beverages (Keller and Tepper, 2004). In another study, the supertaster haplotype of children (5-10 yrs) was similarly correlated to increased sweet sensitivity, liking, and consumption, while the mothers had no correlation to sweet preference (Mennella et al., 2005). However, the counterintuitive association of the supertaster genotype/haplotype as protective in presumably sweet-liking children suggests that the mechanism is more complex than sugar consumption.

Consumption of fruits and vegetables, especially cruciferous vegetables, has been associated with reduced risk of cancer, with bitterness indicated as the primary reason for avoidance (Drewnowski and Gomez-Carneros, 2000; Murillo and Mehta, 2001). In adults, studies investigating the relationship of bitter sensitivity to cruciferous vegetable preferences have been varied (reviewed in Tepper, 2008). The most consistent relationship appears in studies with preschool children, including two studies showing that preschool non-tasters gave broccoli higher ‘liking’ ratings and consumed more bitter vegetables than preschool supertasters (Keller et al., 2002; Bell and Tepper, 2006).

Other taste and dietary preferences also correlate with bitter sensitivity, including bitter citrus, cheese, and carbonated beverages (reviewed in Tepper, 2008). Interestingly, comparison of two independent studies of preschool female non-tasters and female college students, respectively, suggested an inversion with age in dietary fat consumption (Yackinous and Guinard, 2002; Keller and Tepper, 2004). It is possible that the association of TAS2R38 with caries in the primary dentition may reflect biological processes that change with age, a greater influence of social and cultural influences on adult habits, or a combination of both. While this association is supported by the consistency in the genotype and haplotype associations and could be explained by age-related processes, the potential for undetected association in the mixed and permanent dentitions exists. A larger study group and additional statistical models may be needed to identify associations in these groups, especially if the phenotypic effect is smaller. Additionally, the focus of this analysis on genetic factors does not account for the potential of environmental confounders.

In addition to the influences of the TAS2R38 receptor on taste preferences and dietary habits, a specific sweet receptor has been identified as a heterodimer of the TAS1R2 and TAS1R3 gene products. Analysis of our data revealed a significant association of the C allele of TAS1R2-SNP2 with both caries risk and protection in the “mixed” group. The absence of additional supporting genotype or haplotype association suggests caution in excluding these associations as potential type I errors. However, it is possible that the C allele is interacting with additional SNPs that were not genotyped in our study and are associated separately with caries risk or protection.

In summary, our results have identified two genes important in taste-sensing that are associated with dental caries risk and/or protection. These results highlight the importance of understanding the role of taste preferences in caries and the utility of a genetics approach that overcomes the methodological challenges of laboratory taste preference assessment and reported dietary habits. Ultimately, the characterization of genes involved in taste preference and their genetic association with caries will contribute to greater screening of susceptible individuals and inform intervention strategies. Studies have shown that dietary intervention strategies in infants can have some level of influence on food acceptance (Mennella et al., 2008). It is possible that different intervention strategies may prove more productive for individual subgroups of taste receptor genotypes and thereby contribute to early and targeted dental caries prevention.

Acknowledgments

We thank the field staffs of the data collection and coordination sites, and the participating community health care organizations, including the Camden-on-Gauley Medical Center, Community Health Clinic of Nicholas County, Cornerstone Care Clinic, McKean County Dental Center, Richwood Area Community Hospital, Summersville Memorial Hospital, and the Webster County Memorial Hospital. We appreciate the assistance of the GORGE Connection Rural Health Education Partnership Board, the Webster-Nicholas Rural Health Education Consortium Board, the West Virginia Rural Health Education Partnerships program, and the numerous individuals and social service agencies that helped develop both this study and the Center for Oral Health Research in Appalachia. We also thank Barbara Dilettuso, Alena Kureichyk, and Dr. Alexandre Vieira for their support.

Footnotes

This study was supported by a grant from the National Institute of Dental and Craniofacial Research (R01-DE014899). Additional support was provided by the University of Pittsburgh School of Dental Medicine, the West Virginia School of Dentistry, and the West Virginia Eberly College of Arts and Sciences. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institute of Dental and Craniofacial Research, or the National Institutes of Health.

The authors declare no potential conflicts of interest with respect to the authorship and/or publication of this article.

References

  • Bell KI, Tepper BJ. (2006). Short-term vegetable intake by young children classified by 6-n-propylthiouracil bitter-taste phenotype. Am J Clin Nutr 84:245-251 [PubMed]
  • Boraas JC, Messer LB, Till MJ. (1988). A genetic contribution to dental caries, occlusion, and morphology as demonstrated by twins reared apart. J Dent Res 67:1150-1155 [PubMed]
  • Bretz WA, Corby PM, Schork NJ, Robinson MT, Coelho M, Costa S, et al. (2005). Longitudinal analysis of heritability for dental caries traits. J Dent Res 84:1047-1051 [PMC free article] [PubMed]
  • Bretz WA, Corby PM, Melo MR, Coelho MQ, Costa SM, Robinson M, et al. (2006). Heritability estimates for dental caries and sucrose sweetness preference. Arch Oral Biol 51:1156-1160 [PubMed]
  • Conry JP, Messer LB, Boraas JC, Aeppli DP, Bouchard TJ., Jr (1993). Dental caries and treatment characteristics in human twins reared apart. Arch Oral Biol 38:937-943 [PubMed]
  • Deeley K, Letra A, Rose EK, Brandon CA, Resick JM, Marazita ML, et al. (2008). Possible association of amelogenin to high caries experience in a Guatemalan-Mayan population. Caries Res 42:8-13 [PMC free article] [PubMed]
  • Drayna D. (2005). Human taste genetics. Annu Rev Genomics Hum Genet 6:217-235 [PubMed]
  • Drewnowski A, Gomez-Carneros C. (2000). Bitter taste, phytonutrients, and the consumer: a review. Am J Clin Nutr 72:1424-1435 [PubMed]
  • Drury TF, Horowitz AM, Ismail AI, Maertens MP, Rozier RG, Selwitz RH. (1999). Diagnosing and reporting early childhood caries for research purposes. A report of a workshop sponsored by the National Institute of Dental and Craniofacial Research, the Health Resources and Services Administration, and the Health Care Financing Administration. J Public Health Dent 59:192-197 [PubMed]
  • Grembowski D, Conrad DA, Milgrom P. (1987). Dental care demand among children with dental insurance. Health Serv Res 21:755-775; erratum in Health Serv Res 22:367, 1987 [PMC free article] [PubMed]
  • Horvath S, Xu X, Laird NM. (2001). The family based association test method: strategies for studying general genotype-phenotype associations. Eur J Hum Genet 9:301-306 [PubMed]
  • Janes GR, Blackman DK, Bolen JC, Kamimoto LA, Rhodes L, Caplan LS, et al. (1999). Surveillance for use of preventive health-care services by older adults, 1995-1997. MMWR CDC Surveill Summ 48:51-88 [PubMed]
  • Keller KL, Tepper BJ. (2004). Inherited taste sensitivity to 6-n-propylthiouracil in diet and body weight in children. Obes Res 12:904-912 [PubMed]
  • Keller KL, Steinmann L, Nurse RJ, Tepper BJ. (2002). Genetic taste sensitivity to 6-n-propylthiouracil influences food preference and reported intake in preschool children. Appetite 38:3-12 [PubMed]
  • Laird NM, Horvath S, Xu X. (2000). Implementing a unified approach to family-based tests of association. Genet Epidemiol 19(Suppl 1):36-42 [PubMed]
  • Liu H, Deng H, Cao CF, Ono H. (1998). Genetic analysis of dental traits in 82 pairs of female-female twins. Chin J Dent Res 1:12-16 [PubMed]
  • Mennella JA, Pepino MY, Reed DR. (2005). Genetic and environmental determinants of bitter perception and sweet preferences. Pediatrics 115:e216-e222 [PMC free article] [PubMed]
  • Mennella JA, Nicklaus S, Jagolino AL, Yourshaw LM. (2008). Variety is the spice of life: strategies for promoting fruit and vegetable acceptance during infancy. Physiol Behav 94:29-38 [PMC free article] [PubMed]
  • Murillo G, Mehta RG. (2001). Cruciferous vegetables and cancer prevention. Nutr Cancer 41:17-28 [PubMed]
  • Nariyama M, Shimizu K, Uematsu T, Maeda T. (2004). Identification of chromosomes associated with dental caries susceptibility using quantitative trait locus analysis in mice. Caries Res 38:79-84 [PubMed]
  • Polk DE, Weyant RJ, Crout RJ, McNeil DW, Tarter RE, Thomas JG, et al. (2008). Study protocol of the Center for Oral Health Research in Appalachia (COHRA) etiology study. BMC Oral Health 8:18. [PMC free article] [PubMed]
  • Purnell L. (1999). Culturally competent care for traditional Appalachians. Imprint 46:56-59 [PubMed]
  • Rabinowitz D, Laird N. (2000). A unified approach to adjusting association tests for population admixture with arbitrary pedigree structure and arbitrary missing marker information. Hum Hered 50:211-223 [PubMed]
  • Shuler CF. (2001). Inherited risks for susceptibility to dental caries. J Dent Educ 65:1038-1045 [PubMed]
  • Slayton RL, Cooper ME, Marazita ML. (2005). Tuftelin, mutans streptococci, and dental caries susceptibility. J Dent Res 84:711-714 [PubMed]
  • Tepper BJ. (2008). Nutritional implications of genetic taste variation: the role of PROP sensitivity and other taste phenotypes. Annu Rev Nutr 28:367-388 [PubMed]
  • Wang X, Shaffer JR, Weyant RJ, Cuenco KT, DeSensi RS, Crout R, et al. (2010). Genes and their effects on dental caries (tooth decay) may differ between primary and permanent dentitions. Caries Res 44:277-284 [PMC free article] [PubMed]
  • Yackinous CA, Guinard JX. (2002). Relation between PROP (6-n-propylthiouracil) taster status, taste anatomy and dietary intake measures for young men and women. Appetite 38:201-209 [PubMed]

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