BioMed Research International
Volume 2017 (2017), Article ID 4096316, 7 pages
https://doi.org/10.1155/2017/4096316

Research Article

Association between Single Nucleotide Polymorphisms in Vitamin D Receptor Gene Polymorphisms and Permanent Tooth Caries Susceptibility to Permanent Tooth Caries in Chinese Adolescent

Miao Yu,1,2 Qian-Zhou Jiang,² Zhe-Yi Sun,¹ Yuan-Yuan Kong,² and Zhi Chen¹

¹The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) and Key Laboratory of Oral Biomedicine Ministry of Education, School and Hospital of Stomatology, Wuhan University, Wuhan, China
²Key Laboratory of Oral Medicine, Guangzhou Institute of Oral Disease, Stomatology Hospital of Guangzhou Medical University, Guangzhou 510140, China

Correspondence should be addressed to Zhi Chen; zhichen@whu.edu.cn

Received 24 July 2017; Accepted 22 October 2017; Published 12 November 2017

Academic Editor: Hai-Feng Pan

Copyright © 2017 Miao Yu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract.

Purpose. Dental caries is a multifactorial infectious disease. In this study, we investigated whether single nucleotide polymorphisms (SNPs) in vitamin D receptor (VDR) gene were associated with susceptibility to permanent tooth caries in Chinese adolescents. Method. A total of 200 dental caries patients and 200 healthy controls aged 12 years were genotyped for VDR gene polymorphisms using the PCR-restriction fragment length polymorphism (PCR-RFLP) assay. All of them were examined for their oral and dental status with the WHO criteria, and clinical information such as the Decayed Missing Filled Teeth Index (DMFT) was evaluated. Genomic DNA was extracted from the buccal epithelial cells. The four polymorphic SNPs (Bsm I, Taq I, Apa I, and Fok I) in VDR were assessed for both genotypic and phenotypic susceptibilities. Results. Among the four examined VDR gene polymorphisms, the increased frequency of the CT and CC genotype of the Fok I VDR gene polymorphism was associated with dental caries in 12-year-old adolescent, compared with the controls ( = 17.813, ). Moreover, Fok I polymorphic allele C frequency was significantly increased in the dental caries cases, compared to the controls ( = 14.144, , OR = 1.730, 95% CI = 1.299–2.303). However, the other three VDR gene polymorphisms (Bsm I, Taq I, and Apa I) showed no statistically significant differences in the caries groups compared with the controls. Conclusion. VDR-Fok I gene polymorphisms may be associated with susceptibility to permanent tooth caries in Chinese adolescent.

1. Introduction

Dental caries is a polyfactorial infectious disease involving interplay between environmental factors and multiple genetic factors. Despite more than 100 years of continued prevention of this disease, caries is still a major oral problem throughout the world, affecting 60%–90% of schoolchildren [1]. As the economy is booming and sugar consumption is increasing in China, caries is nowadays the most popular oral disease in China [2].

The microbiological and environmental factors causing dental caries have been extensively studied. However, cariogenic microbial and environmental exposures are not sufficient to explain susceptibility to caries. Host susceptibility is highlighted by potential genetic factors for caries risk. More than 20 candidate genes have been reported, including enamel formation genes, immune response genes, and genes related to saliva, taste, and others [3].

Enamel is a hard and highly mineralized substance covering tooth crown and protects the tooth as a barrier. There were potential associations between genes responsible for enamel formation and susceptibility to caries. Previous studies suggest that the variation in genes encoding enamelin, tuftelin, and amelogenin may be related to susceptibility to dental caries [4, 5]. Recently, gene-linkage analysis suggests that several enamel-forming related genes may contribute to susceptibility to caries in different ethnic populations including Korean [6], Brazilian [7], and Japanese [8]. In contrast, Gasse et al. found that SNPs of in amelogenin gene are not associated with susceptibility to caries [9]. No association between mannose-binding lectin (MBL) and dental caries was proven in Chinese children [10] nor between amelogenin X (AMELX) gene and caries susceptibility in Polish children [11].

Vitamin D (Vit D) plays a significant rule in enamel mineralization [12] and the level of Vit D in serum is proved to be associated with caries [13]. Vitamin D receptor (VDR) is regarded as a mediator for the effect of Vit D related biomineralization. VDR is involved in biomineralization during mineralized tissue development, such as bone and tooth enamel [14, 15]. It has been indicated that the VDR gene has multiple polymorphisms, including the following four single nucleotide polymorphisms (SNPs): Bsm I (rs1544410), Taq I (rs731236), Apa I (rs7975232), and Fok I (rs10735810) [16]. Studies have shown that VDR gene polymorphisms may affect susceptibility to various diseases, such as osteoarthritis, diabetes, cardiovascular disease, and tuberculosis [17], as well as susceptibility to oral diseases, such as periodontitis [18] and dental implant loss [19].

Concerning the incidence of dental caries, gene immune deficiency and inflammation alterations may contribute to host susceptibility and affect the course of caries [20], so we speculated that VDR gene polymorphisms might have relationship with dental caries. In the present study, four SNPs of VDR, Bsm I (rs1544410), Taq I (rs731236), Apa I (rs7975232), and Fok I (rs10735810), were genotyped with the restriction fragment length polymorphism (RFLP) analysis method, aiming to find association between dental caries and VDR gene polymorphisms in Chinese adolescents.

2. Materials and Methods

2.1. Study Subjects

Our research was approved by the Ethics Committee of Guangzhou Medical University. It was performed under the guidelines of the World Medical Association Declaration of Helsinki. Informed consents were acquired from all adolescents and their guardians.

Four hundred Chinese adolescents aged 12 were recruited from the same city district primary schools for this study. Twelve-year-old adolescents were chosen for their permanent teeth, including second molars which had already erupted. Only permanent teeth were considered when the deciduous teeth still exist. Subjects were categorized into two groups according to the Decayed Missing Filled Teeth (DMFT) Index: caries-free (DMFT index = 0) and caries experience (DMFT index > 0). Each group contained two hundred members. Information about oral hygiene levels and habits including bleeding on probing (BOP), Volpe Manhold Index scores (VM-value), and brushing habit of each individual were collected at the same time.

2.2. Sample Collection

Two dentists conducted the clinical examinations. They used a periodontal probe and dental mirror according to the criteria recommended by the WHO guidelines. The diagnostic criterion of caries lesions was determined by visual examination of tooth surfaces. Values of Cohen’s kappa for agreement were 0.90 between two dentists.

Buccal epithelial cells were obtained by rubbing the buccal mucosa with a swab. In accordance with the instructions of manufacturer, genomic DNA was extracted with the use of a commercial kit (Tiangen, Beijing, China) following the instructions of the manufacturer. Extracted DNA was aliquoted for each sample and stored at −20°C until PCR amplification.

2.3. SNP Selection and Genotyping

The primers to amplify the VDR gene were designed using Primer Premier 5 (Premier Biosoft Inter, Palo Alto, USA) and synthesized by Shanghai Chaoshi Co. (Shanghai, China). Four SNPs of VDR gene were analyzed: Apa I (rs7975232, located at intron 8, in the 3′ UTR), Bsm I (rs1544410, located at intron 8, in the 3′ UTR), Taq I (rs731236, located at intron 9, in the 3′ UTR), and Fok I (rs10735810, located at intron 2, at the first start codon). Genotyping was performed by the restriction fragment length polymorphism (RFLP) technique [21]. Table 1 presents the primers and their amplifying fragment lengths.

Table 1: The primers of vitamin D receptor (VDR) and band site of genotype.

SNP
Alleles
Primers
Fragment size (bp)
Digested fragment length (bp)

Bsm I
(rs1544410)
G/A
5′-ATACCTACTTTGCTGGTTTGC-3′ 
5′-AGCCCATCTCCATTCCTTG-3′
512
AA: 512
AG: 512, 315, 197
GG: 315, 197

Taq I
(rs731236)
T/C
5′-AGCAGAGCAGAGTTCCAAGCAGA-3′ 
5′-ATCTTGGCATAGAGCAGGTGGCT-3′
345
CC: 345
CT: 345, 260, 85
TT: 260, 85

Apa I
(rs7975232)
C/A
740
AA: 740
AC: 740, 535, 205
CC: 535, 205

Fok I
(rs10735810)
C/T
5′-AGCTGGCCCTGGCACTGACTCTGGCT-3′ 
5′-ATGGAAACACCTTGCTTCTTCTCCCTC-3′
265
CC: 265
CT: 265, 196, 69
TT: 196, 69

2.4. Statistical Analysis

Data for this study were analyzed with Statistical Package for the Social Sciences (SPSS) 18.0 statistical software (USA). A Hardy–Weinberg equilibrium assessment was performed. The difference in proportion of gender, age, and oral hygiene status between the caries group and the caries-free controls was compared by Chi-square test. The significance of allele, genotype frequency, and allele carriage rate differences between two groups were also evaluated by Chi-square test. The results were analyzed with 95% confidence interval (CI). Haploview4.2 (http://www.broadinstitute.org/haploview) was used to carry out linkage disequilibrium analysis (LD) and haplotype analysis. The values of LD were calculated with and displayed with confidence bounds. The significance of different haplotypes was offered by permutation tests. The p value < 0.05 was selected to define statistical significance.

3. Results

The distribution of gender and age in caries group and caries-free group was equipoised. The female to male ratio was 1 : 0.89 and 1 : 1.04 for healthy controls and dental caries adolescents, respectively. The mean age of caries-free group and dental caries adolescents was years and years, respectively. The gender and mean age between the two subjects was not significantly different ( value > 0.05). The data of BOP, VM-value, brushing time, and frequency of the two analyzed groups showed no significant difference ( value > 0.05). Table 2 illustrates the demographic characteristics of the analyzed groups.

Table 2: Demographic characteristics of the study subjects.

Cases
Controls

value

()
()

Mean age

Gender (%)

0.640
0.424

Female
98 (49)
106 (53)

Male
102 (51)
94 (47)

BOP (+)
28 (14.0)
23 (11.5)
0.562
0.454

VM-value (+)
41 (20.5)
36 (18.0)
0.402
0.526

Brushing time

    <3 min
171 (85.5)
165 (82.5)
0.700
0.413

    ≥3 min
29 (14.5)
35 (17.5)

Brushing frequency

    <2 times a day
95 (47.5)
91 (45.5)
0.161
0.688

    ≥2 times a day
105 (52.5)
109 (54.5)

Note. BOP: bleeding on probing; VM-value: Volpe Manhold Index scores.

Table 3 shows the distribution of genotypes and allele frequencies for Bsm I (rs1544410), Taq I (rs731236), Apa I (rs7975232), and Fok I (rs10735810) SNPs of VDR gene in the two analyzed groups. The results were fitted to a Hardy–Weinberg equilibrium ( value > 0.49).

Table 3: Summary of allele and genotype frequencies in 12-year-old adolescents.

VDR gene polymorphisms (rs number)
Total
Caries experience
()
Caries-free
()
X²
value
OR (95% CI)
Power (%)

Bsm I (rs1544410)
AA
0
0
0
0.448
0.503

AG
67 (16.75)
36 (18)
31 (15.5)

GG
333 (83.25)
164 (82)
169 (84.5)

Carriage of allele A
36 (18)
31 (15.5)
0.448
0.503
1.197 (0.707–2.026)

A
67 (8.375)
36 (9)
31 (7.75)
0.407
0.523
1.177 (0.713–1.944)
9.8

G
733 (91.625)
364 (91)
369 (92.25)

Taq I (rs731236)
CC
329 (82.25)
171 (85.5)
158 (79)
2.894
0.089

CT
71 (17.75)
29 (14.5)
42 (21)

TT
0
0
0

Carriage of allele T
29 (14.5)
42 (21)
2.894
0.089
0.638 (0.379–1.073)

C
729 (91.125)
371 (92.75)
358 (89.5)
2.612
0.106
1.501 (0.915–2.462)
47.5

T
71 (8.875)
29 (7.25)
42 (10.5)

Apa I (rs7975232)
AA
57 (14.25)
33 (16.5)
24 (12)
2.898
0.235

AC
164 (41)
85 (42.5)
79 (39.5)

CC
179 (44.75)
82 (41.0)
97 (48.5)

Carriage of allele A
118 (59)
103 (51.5)
2.275
0.131
1.355 (0.913–2.012)

Carriage of allele C
167 (83.5)
176 (88)
1.657
0.198
0.69 (0.391–1.216)

A
278 (34.75)
151 (37.75)
127 (31.75)
3.175
0.075
1.304 (0.974–1.745)
43.1

C
522 (65.25)
249 (62.25)
273 (68.25)

Fok I (rs10735810)
CC
151 (37.75)
86 (43.0)
65 (32.5)
17.813
0.000

CT
182 (45.5)
96 (48.0)
86 (43.0)

TT
67 (16.75)
18 (9)
49 (24.5)

Carriage of allele C
182 (91)
151 (75.5)
17.229
0.000
3.281 (1.834–5.870)

Carriage of allele T
114 (57)
135 (67.5)
4.692
0.03
0.638 (0.425–0.959)

C
484 (60.5)
268 (67)
216 (54)
14.144
0.000
1.730 (1.299–2.303)
97.1

T
316 (39.5)
132 (33)
184 (46)

Significant differences were detected in the frequencies of Fok I genotype between the caries group and the caries-free group. In particular, the frequency of Fok I’s TT genotype was obviously lower in the caries experience group than that in the controls (9% versus 24.5%, resp.). We also found a lower carriage rate of allele T (57% in the caries group versus 67.5% in the controls, value = 0.03) and a higher carriage rate of allele C (91% versus 75.5%, value ≤ 0.001) in the caries group, compared to the caries-free controls. The odds ratio of the carriage of allele C reached 3.281, which showed a strong relationship between allele C of Fok I and caries group (OR > 3). We found that the frequency of allele C was markedly higher, while the frequency of allele T was significantly lower in the caries cases compared to the caries-free controls.

By contrast, for the other three VDR gene SNPS (Bsm I, Taq I, and Apa I), the genotypes and allele frequencies (G/A, T/C, and C/A, resp.) showed no statistically significant differences between the caries group and the control group.

All these four SNPs showed strong evidence of recombination when we performed LD analysis on data of caries and caries-free group or caries-free group only. The linkage between Taq I and Bsm I reached an uninformative status, an intermediate state from strong recombination to strong linkage disequilibrium, when LD analysis was carried out on data of caries group only (Figure 1).

(a)

(b)

(c)

Figure 1: LD analysis of SNPs in caries and caries-free group. LD plot of SNPs Taq I (rs731236), Apa I (rs7975232), Bsm I (rs1544410), and Fok I (rs10735810) in caries and caries-free group (a), caries-free group only (b), and caries group only (c). All these four SNPs showed strong recombination of each other (block in white) in both caries and caries-free group (a) and caries-free group only (b), while linkage of Taq I (rs731236) and Bsm I (rs1544410) reached a higher level (block in gray, ) in caries group only.

Haplotypes of these four SNPs were presented in an order based on the physical location of these four SNPs. The haplotypes TCGT and TAAC showed a significant difference between the cases and controls since their values were far less than 0.05. But when we put these data into 999-time permutation tests, only haplotype TCGT and SNP Fok I still had significant difference between the cases and controls (Table 4).

Table 4: Haplotype analysis and permutation tests.

(a)

Haplotype
Freq.
Case, control ratio counts
Case, control frequencies

value

TCGC
0.309
132.7 : 267.3, 114.7 : 285.3
0.332, 0.287
1.901
0.168

TCGT
0.25
80.3 : 319.7, 119.5 : 280.5
0.201, 0.299
10.259
0.0014

TAGC
0.197
89.7 : 310.3, 67.9 : 332.1
0.224, 0.170
3.758
0.0525

TAGT
0.088
35.0 : 365.0, 35.4 : 364.6
0.087, 0.088
0.003
0.9596

TCAT
0.05
21.9 : 378.1, 18.4 : 381.6
0.055, 0.046
0.312
0.5764

CAGT
0.03
12.1 : 387.9, 12.1 : 387.9
0.030, 0.030
0
0.9992

CCGC
0.018
7.6 : 392.4, 6.5 : 393.5
0.019, 0.016
0.088
0.7669

CCGT
0.017
4.1 : 395.9, 9.2 : 390.8
0.010, 0.023
1.979
0.1595

TAAC
0.013
9.4 : 390.6, 1.2 : 398.8
0.023, 0.003
6.391
0.0115

(b) #999 permutations performed

Name

Permutation value

TCGT
10.259
0.016

Fok I (rs10735810)
8.544
0.026

TAAC
6.391
0.0581

TAGC
3.758
0.3033

Apa I (rs7975232)
3.175
0.4765

Taq I (rs731236)
2.612
0.6056

CCGT
1.979
0.7217

TCGC
1.901
0.7598

Bsm I (rs1544410)
0.407
0.998

TCAT
0.312
0.998

TAGT
0.003
1

CAGT
0
1

CCGC
0.088
1

4. Discussion

Dental caries is a polyfactorial infectious disease involving interplay between environmental factors and multiple genetic factors. To rule out the effects of environmental factors in these two groups we compared, we collected information about oral hygiene levels and oral habits of each individual in cases and controls. There were no significant differences between case group and control group among these several factors (Table 2). This result offered support to the hypothesis that the differences of caries experience between cases and controls were possibly associated with genetic factors.

VDR gene polymorphisms are important factors for normal enamel development [12] and have been shown to contribute to susceptibility to various immune diseases [22]. Variations in human VDR gene lead to phenotypically diverse inherited enamel malformations [15]. Considering the role of the VDR gene in enamel formation, we hypothesized a possible contribution between VDR gene polymorphisms and dental caries. Our results support the hypothesis that susceptibility of Chinese adolescent to caries of permanent teeth was associated with the genotype frequency of the Fok I SNP.

Four SNPs of VDR, Bsm I (rs1544410), Taq I (rs731236), Apa I (rs7975232), and Fok I (rs10735810) were genotyped by the restriction fragment length polymorphisms analysis method in our study. Previous studies suggested that the distribution of VDR polymorphisms could have different patterns in different ethnicity [21, 23–26]. In this study, we failed to find any incidence of AA genotype for Bsm I and TT genotype for Taq I in Chinese adolescents. The most common genotype for each of the polymorphisms was GG for Bsm I (83.25%), CC for Taq I (82.25%), CC for Apa I (44.75%), and CT for Fok I (45.5%). The general distribution of VDR gene polymorphisms in our study showed similar pattern with previous study of Chinese population [21] but was different to those on African Americans [24], Turks [25], and Jordanians [26]. These consistency and inconsistency of our results with previous studies presented extra evidences to the existence of distribution specificity of VDR gene polymorphisms based on ethnicity and also suggested that the population we collected in this study could represent characteristics of Chinese to some extent.

Our findings showed that the susceptibility of Chinese adolescents to permanent tooth caries was associated with the genotype frequency of Fok I. The frequency of allele C was obviously higher in cases compared with the caries-free controls. The odds ratio of carriage of allele C reached 3.281, suggesting that allele C seems to be a risk factor of caries experience. The increased frequency of genotypes CT and CC were also found in caries group, while the genotype TT and allele T frequency were found to be significantly reduced in the caries group compared with the caries-free controls. These findings indicated that the allele T of Fok I appeared to be a protective factor for the caries experience, as the odd ratio and 95%CI of carriage rate of allele T was 0.638 (0.425–0.959) <1. In contrast, for the other three VDR genes (Apa I, Bsm I, and Taq I), the genotypes and allele frequencies (C/A, G/A, and T/C, resp.) showed no statistically remarkable differences between the caries group and the control group.

It is notable that the minor allele frequency (MAF) of Bsm I and Taq I was extremely low in CHB base on HapMap project since MAF of Bsm I was 0.022 and Taq I was 0.011 (http://hapmap.ncbi.nlm.nih.gov/). This could explain why we failed to find any incidence of AA genotype for Bsm I and TT genotype for Taq I. These results also suggested that the number of samples needed to finally confirm the association between Bsm I, Taq I and caries susceptibility could be hundred times of the sample amount in our study. HapMap project data showed that Apa I had a much higher MAF (0.321), but the power on Apa I in our data merely reached 43.1%, which means that our data on Apa I had greater possibility of being a false negative result, while power on Fok I reached a 97.1% strong level (Table 3). Apa I, Bsm I, and Taq I could have potential association with caries susceptibility, but our data cannot offer a positive support to this hypothesis.

A recent study of dental caries in northwestern Chinese population indicated that Taq I could act as a caries risk factor in middle-age adults [27], which seemed to be a challenge to our data. But firstly, the power on Taq I in our data was not strong enough to reject false negative. On the other hand, China is a multinational country with 55 ethnic minorities and the majority Han people, and many of the ethnic minorities are living in relatively remote areas of China such as the southwest and northwest of China. So, the detailed composition of northwestern Chinese population could be much more complex than ours. This might partially explain the inconsistency.

In LD analysis, all these four SNPs showed very strong evidence of recombination except for Taq I and Bsm I in caries group data. However, the linkage of Taq I and Bsm I in caries group still did not reach the level of strong LD. Haplotype analysis and further permutation tests revealed that haplotypes TCGT and Fok I each were more likely to have association with exposure factor, while the haplotype TCGT seemed to be a protective one for its frequency was higher in caries-free group.

It has not been clear about the mechanism of VDR polymorphisms acting to caries susceptibility. VDR takes part in regulating the expression of genes related to immune response, calcium homeostasis, and cellular differentiation and proliferation [28]. In VDR gene, the SNPs Apa I, Bsm I, and Taq I are situated at the corresponding 3′UTR genomic DNA region, indicating that it was impossible for these three SNPs to result in the variation of the protein structure of VDR [29]. This might be the mechanical reason that SNPs Apa I, Bsm I, and Taq I reveal no significant relationship with the risk of dental caries in our study. On the other hand, SNP Fok I is lying in the exon 4 of VDR gene and locating in the start codon of VDR isoforms 1 and 2. It is made up of a T-to-C change with the occurrence of an initiation codon (ATG). An alternative start site would be utilized once the C variant exists; it might produce VDR protein of different sizes [28, 30]. This was consistent with our haplotype analysis result as the protective haplotype TCGT had T of Fok I not C. However, 3′UTR was also related to mRNA including the mRNA localization and stability and also the translation efficiency [31].

This study is the first to analyze the association between VDR gene polymorphisms and the susceptibility of Chinese school adolescents to caries in permanent teeth. Our findings suggest that Fok I could be a potential risk factor for caries in this specific population group. This finding may contribute to our knowledge of dental caries in terms of etiology and treatment course.

Ethical Approval

This study was approved by the Ethics Committee of Guangzhou Medical University (Resolution nos. 2013-03, 2014-05, 2015-11, and 2015-09) and is in accordance with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.

Consent

The guardians of all adolescents included in the study gave their written consent for clinical examination and oral swab collection.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Acknowledgments

Our research was supported by Grant-in-Aid from Guangdong Provincial Department of Science and Technology (Grant nos. 2014-807 and 2015-110-51), Health and Family Planning Commission of Guangdong Province (Grant no. A2016506), and the Bureau of Health of the Guangzhou Municipality (Grant no. 20161A010092).

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