The present study aimed to assess the incidence of the vitamin D receptor (VDR) gene polymorphism TaqI in patients with periodontitis, and the potential association of this polymorphism with the severity of the disease. This was a case-controlled study, which included 162 adults divided into two groups as follows: Case group (81 patients diagnosed with periodontitis) and control group (81 patients without periodontitis). Venous blood was obtained from each sample from which DNA was extracted. The gene polymorphism was determined using restricted fragment length polymorphism-PCR and DNA sequencing to identify endonuclease restrictions in exon 9 (TaqI). The data were analyzed using an independent samples t-test. VDR gene polymorphisms were detected in periodontitis cases with TT (86.4%), Tt (12.4%) and tt (1.2%) genotypes. DNA sequencing confirmed a change in the sequence of the VDR gene nucleotides in patients with periodontitis. The data indicated that the severity of periodontal tissue damage may be influenced by changes in the nucleotide sequence.
vitamin D receptorperiodontal diseaseDNA amplificationTaqIgenotypeFunding: The present study was supported by the Ministry of Research, Technology, and Higher Education of the Republic of Indonesia (grant no. 1109/D3/PL/2010).Introduction
Periodontitis is one of the most common inflammatory diseases affecting the tissues supporting teeth and it is characterized by progressive resorption of the alveolar bone (1-3). Periodontitis is also one of the primary causes of loss of teeth in adults, and it can affect an individual's quality of life if left untreated (4-6). Periodontitis is initiated by bacterial plaque on the tooth surface and can be caused by multiple factors, such as an imbalance of periodontal pathogens, host immunity and other environmental, local and systemic factors (7,8). The majority of studies on this topic have emphasized on the role of genetic factors in disease pathogenesis, and on their ability to influence the unique reaction that characterizes the susceptibility of each individual (1,5). Approximately 50% of the clinical severity of periodontitis may be associated with host genetics (3,8). However, the genetic effects may differ among different ethnicities due to the diversity of the subjects in a population (3,7). Therefore, understanding of the pathophysiology of this disease from a genetic standpoint is essential for its early detection and diagnosis.
Over the past decade, considerable efforts have been made to identify the influence of various genetic factors, such as genes that code for IL-1(9), TNF-α (10), IL-10(11), IL-4(12), IL-4 receptor-α (13), Fc γ receptor (14), CD-14(15) and the vitamin D receptor (VDR). The genetic predispositions associated with these genes are considered to affect the severity of different diseases (16,17). VDR, in particular, is a promising candidate in periodontitis since it affects both bone metabolism and immunological function (4,18). This receptor is present in various cell types and can act as a transcriptional regulator (2). It is located on chromosome 12 q and has 14 exons, 6 of which are located on the 5'region that is not translated (1a-1f) (7,18). The untranslated 3'region of the VDR gene comprises a polymorphism cluster in TaqI, ApaI and BsmI (19,20). If the function of VDR is affected by the polymorphisms of the VDR gene, the contribution of these variants is considered critical for the pathogenesis of systemic diseases related to bone tissues, such as periodontal disease (19,20).
Several studies have attempted to elucidate an association between the presence of VDR gene polymorphisms and the pathogenesis of certain diseases. A series of characterized VDR gene polymorphisms, including those for the FokI, ApaI, TaqI and BsmI genes have been previously reported (2,3,5). To date, an association has been found between the susceptibility to periodontal disease and a certain number of single-candidate gene polymorphisms (21). Other studies have also shown a connection between periodontal disease and vitamin D levels (2,22,23). Although extensive evidence has been obtained, the majority of the studies were only focused on the investigation of the association between periodontitis and the VDR gene polymorphism (2,21-23). In the present study, DNA sequencing and restricted fragment length polymorphism (RFLP)-PCR analysis were used to further examine the changes in nucleotide arrangement of the VDR gene. The identification of genetic variants linked to the increased susceptibility to certain diseases may be key to the development and advancement of preventive medicine. Therefore, the aim of the present study was to investigate possible correlations between the VDR gene polymorphisms, specifically in exon 9 (TaqI), and the severity of periodontitis. This study was a case-controlled study and the subjects were recruited from a Makassar-based population in Indonesia.
Materials and methodsStudy population and data collection
The present study was a case-controlled study including patients who were enrolled at the Periodontology Department of the Dental Hospital, Hasanuddin University, Indonesia. The study protocol was approved by the Ethics Committee for Biomedical Research in Humans, Faculty of Medicine, Hasanuddin University (approval no. 0189/H.04.8.4.5.31/PP36-KOMETIK/2010, approval date 04/06/2010). The current study was performed in accordance with the Declaration of Helsinki (24). In total, 162 individuals were recruited, and they were divided into two groups: Case group, patients diagnosed with periodontitis (14 males and 67 females) and the control group, healthy patients without periodontitis (38 males and 43 females). The median age of the case group was 38 years (age range 25-60) and the median age of the control group was 34 years (age range 22-60). Determination of the sample size was based on the Lemeshow formula for the case-controlled study design. The actual odd ratio (OR) estimate was ~2. Consideration of OR=2 has been used in previous research studies; an OR of 2 obtained in these previous studies suggested that samples with VDR gene polymorphisms were 2x more likely to suffer from chronic periodontitis than those without VDR gene polymorphisms. Thus we used this as minimum standard to calculate our sample size (25,26). Since the number of populations was infinite (unknown) P2*=0.5 was used with a value of 0.05. The anticipated rate was 10% and the power of the test was 0.842.
The diagnostic criteria for the case group included patients diagnosed with periodontitis based on the New Classification of Periodontal Disease (2018) (27). The periodontitis stage in the present study was divided into three categories as determined previously (24). It was based on the clinical attachment loss (CAL) and probing pocket depth (PPD): Stage I, CAL 1-2 mm and maximum PPD ≤4 mm; stage II, CAL 3-4 mm and maximum PPD≤5 mm; and stages III and IV, CAL≥5 mm and PPD≥6 mm. The diagnostic criteria for the control group were healthy patients without periodontitis, which was defined by the absence of clinically detectable inflammation in the gingiva, such as an intact periodontium without a gingival recession and CAL, ‘salmon’ or ‘coral pink’ in color, firm in consistency and firmly attached to the underlying alveolar bone. The subjects that were suitable for the present study were included in the case and the control groups and were provided with the necessary information regarding the research procedure. They were asked to sign the relevant informed consent form for their agreement in participating in the study. The recruitment of the patients was performed for 1 year by two allocated researchers. The first researcher selected patients from the medical record and completed the information in the research form regarding age, sex, ethnicity, occupation, medical history and history of drugs used. Subsequently, a Professor in the Department of Periodontology performed the clinical examination for the diagnosis of periodontal disease and suggested whether or not each patient was suitable for inclusion in the study.
Inclusion and exclusion criteria
The inclusion criteria were: Indonesian patients, age range of 25-60 years, and had at least 20 teeth. The patients who exhibited 2 interproximal sites with CAL≥2 mm, and 6 interproximal sites with PPD≥4 mm were also included. The exclusion criteria were the following: Patients with systemic diseases, such as diabetes, tuberculosis, hepatitis or human immunodeficiency virus, as well as patients with smoking habits or had used prosthetics. Moreover, patients who were pregnant and/or breastfeeding were also excluded from the study.
Clinical examination
Patients who met the inclusion criteria received a comprehensive dental examination and a complete research chart was recorded. It is well established that important clinical signs of periodontitis include poor to moderate scores in the oral hygiene index-simplified (OHI-S), PPD and CAL (27,28), therefore these clinical signs were used to evaluate their influence on the incidence of VDR gene polymorphisms. Initially, the number of caries teeth, the number of edentulous and the OHI-S score (29) were assessed. Subsequently, scaling was performed on all subjects using an ultrasonic scaler. The clinical examination was performed to evaluate the PPD and the level of CAL. The measurements of PPD were made at 6 sites on each tooth according to the charting form used in the Department of Periodontology. The largest value from 6 tooth surfaces in each tooth was obtained for analysis. CAL was measured based on the distance from the cementoenamel junction to the base of the pocket. For analysis, interdental CAL at the site of the greatest loss was taken.
Laboratory analysis
Venous blood (0.5-1 ml) samples were obtained from all subjects in both groups for laboratory analysis. The DNA from the peripheral leukocytes was extracted and purified using the Boom method (30). The analysis was performed in the Laboratory of Immunology and Molecular Biology, Faculty of Medicine, Hasanuddin University (Makassar, Indonesia). The gene polymorphisms were determined based on endonuclease restriction in exon 9 of the examined VDR gene using RFLP-PCR and direct sequencing.
Amplification by PCR
In all subjects, VDR gene polymorphisms were detected in exon 9 using the following specific primers: Forward, 5'-CTGGGGAGCGGGGAGTATGAAGGA-3' and reverse, 5'-GGGTGGCGGCAGCGGATGTA-3' (https://omim.org/entry/601769). DNA amplification was conducted for RFLP using the TaqI restriction enzyme. The PCR amplification was performed using 32 cycles, consisting of denaturation for 1 min at 94˚C, annealing for 1.5 min at 59˚C, and extension for 2 min at 72˚C. Following the completion of 32 cycles, the samples were heated at 72˚C for 7 min. The amplification products were analyzed by agarose gel electrophoresis.
RFLP-PCR analysis
Following amplification, 5 µl PCR amplification products and 2 µl loading buffer were mixed and loaded onto 1.5% agarose gels along with ethidium bromide. The gel was soaked in a container with Tris borate EDTA buffer, and subsequently, electrophoresis was performed at a steady voltage of 80 V for 1 h. The gel was removed and observed under UV light. The fragment bands observed at different distances from the sample indicated genotypic differences of the VDR gene polymorphism. The differences were marked with the letter t (a restriction area is present) or the letter T (no restriction area is present). The genotypes based on the bands of the agarose gels were classified as follows: i) TT: Absence of fragment sizes at 1,398 bp; ii) Tt: Presence of fragment sizes at (946 + 452 bp) and 1,398 bp and iii) tt: Presence of fragment sizes at 946 bp and 452 bp.
DNA sequencing
In all obtained samples, direct sequencing was performed by Macrogen, Inc. Sequencing confirmed the changes in the nucleotide base arrangement in exon 9 of the VDR gene.NCBI BLAST was used to analyze the sequencing results.
Statistical analysis
SPSS version 11.5 (SPSS, Inc.) was used for data analysis. The mean ± SD were calculated for all descriptive variables. An independent samples t-test was performed to detect phenotypic differences in subjects with periodontitis. P<0.05 was considered to indicate a statistically significant difference. Hardy-Weinberg equilibrium was verified manually using a standard calculation formula (31).
ResultsDistribution and characteristics of the subjects
In total, the data were collected for 162 patients from the Dental Hospital, Hasanuddin University. The age was known for all 162 patients. The detailed characteristics of the subjects are shown in Table I. Based on the independent samples t-test, it was found that both edentulous and OHI-S were significantly higher is the case group compared with the control groups (P<0.05; Table I). This difference indicated that patients with periodontitis exhibited worse oral hygiene than healthy patients without periodontitis.
VDR gene polymorphism
The VDR gene polymorphism consists of the following three genotypes: TT (1 band), tt (2 bands), and Tt (3 bands) (Fig. 1A and B). The TT genotype (1,398 bp) indicated no fragment sizes, whereas fragment sizes of 946, 452 and 1,398 bp were obtained for the Tt genotype and fragment sizes of 946 and 452 bp for the tt genotype. The genotype distribution of the VDR gene in the case and control groups is highlighted in Table II. It was noted that the case group exhibited a higher percentage of the TT genotype (86.4%) compared with either the Tt (12.3%) or the tt (1.2%) genotypes. The control group had a TT genotype percentage of 98.8%, a Tt genotype percentage of 1.2%, and an absence of the tt genotype. Both case and control groups exhibited a genotype distribution within the Hardy-Weinberg equilibrium [p2+2pq+q2=1; (0.96)2+2 (0.96) (0.04)+(0.04)2=1.0016].
The comparison between the VDR genotype of the subjects with periodontitis was based on the mean value of OHI-S, PPD and CAL (Table III). The results confirmed that the mean of OHI-S was higher for the patients with periodontitis and the TT genotype (mean score, 2.71) than that of the patients with periodontitis and the Tt/tt genotype (mean score, 2.12). However, the difference was not statistically significant (P>0.05). Both the PPD status and CAL were higher for the Tt/tt genotype (PPD mean score, 5.14; CAL mean score, 4.41) compared with those of the TT genotype (PPD mean score, 3.52; CAL mean score, 2.80). Both of these parameters indicated significant differences, with P-values of 0.006 and 0.001, respectively.
Polymorphism analysis of the VDR gene by sequencing
DNA sequencing confirmed a change in the sequence of the VDR gene nucleotides (Fig. 2). The data indicated the sequencing results of the three genotypes. The nucleotide sequence for the tt genotype at codon 352 was altered compared with that of the initial sequence of AGGTCGA (Fig. 2A and B); the final sequence was: AGGCCGA (Fig. 2C). This indicated a nucleotide substitution from T to C (GTC to GCC) due to the change in the amino acid valine (coded by GTC) to alanine (coded by GCC).
Discussion
The aim of the present study was to identify the presence of the VDR gene polymorphisms in patients with periodontitis (32). Subsequently, the VDR gene polymorphism was assessed as a risk factor associated with periodontitis between patients with periodontitis and healthy subjects (33). The present study examined the change in the nucleotide sequence of the VDR gene to explore the potential association of the VDR gene polymorphism with the severity of the disease. Limited studies have been performed utilizing DNA sequencing for the identification of genetic variants that are linked to susceptibility to periodontitis. In addition, to the best of our knowledge, the present study is the first study in this context conducted in Indonesia.
Current research conducted in the field of periodontology has particularly focused on the influence of genetic factors on individual susceptibility to periodontitis (34-36). The tendency for early-onset periodontitis can be inherited with either an autosomal recessive or autosomal dominant trait (37,38). In the present study, it was found that the frequency of the Tt and tt genotypes (t allele) was lower than that of the TT genotype (T allele) in both periodontitis and healthy subjects. This result is reasonable owing to the fact that the population in Makassar, Indonesia, as a part of the Asian race, has a minor presentation of the Tt and tt genotypes in the VDR gene. A similar result was noted in a study by Zmuda et al (39) that reported a frequency of the Tt and tt genotypes of only 2% in Asians, 5% in African Americans and 17% in Caucasians. In accordance with these findings, two previous studies conducted by Sun et al (37) and Tachi et al (25) also reported that the t allele was present in only 4% of a Chinese ethnic group and in 11% of a Japanese ethnic group. Moreover, a small distribution of the t alleles in the Asian race was also noted by Wang et al (40); only in 5% of the population examined.
The differences in the frequency of the genotypes or alleles in a population can be explained by the following concept: All polymorphisms begin as mutations occurring as a result of DNA damage. As the frequency of the allele increases in the population, the mutation is converted to a polymorphism (41,42). The difference in the allele frequencies between ethnicities tends to be influenced by evolutionary processes and genetic traits of a single population. Similar association studies regarding VDR polymorphisms and periodontal disease have been performed in other ethnic populations and races (34,43,44). A study by Borges et al (45) reported an OR of 4.57 for the association between VDR and periodontitis in a Brazilian population. In 2004, de Brito et al (26) also reported that the genotype and haplotype of the VDR gene polymorphism may be associated with the incidence of periodontal disease. The corresponding OR values were 2.41 and 4.32, respectively. Similarly, Brett et al (46) demonstrated an association between VDR gene polymorphism and periodontitis in the Caucasian race. Similarly, Tachi et al (25) reported an OR value as high as 2.3 in the Japanese population.
In our previous study, an OR value of 12.57 was noted indicating that subjects with VDR gene polymorphisms exhibited a 12.57-fold higher probability of suffering from periodontitis than those without VDR gene polymorphism (33). This is expected considering that the VDR gene is involved in various processes ranging from bone metabolism to the regulation of the immune response. The fundamental etiology of periodontitis is inflammation caused by bacterial infection, which promotes alveolar bone resorption; therefore, the VDR gene appears to be an optimal candidate for predicting periodontitis susceptibility. Previously published studies demonstrated that VDR plays an important role in trabecular bone compared with its role in cortical bone (26,46). Moreover, the variation in the VDR allele is responsible for the variation in bone mineral density (BMD) (26,46). VDR, which is involved in controlling calcium and phosphate concentrations in the blood, is disrupted by the presence of variations in the DNA sequence or the presence of polymorphisms, resulting in a decrease in BMD across the body, including the mandible and maxilla (47). A decrease in jaw bone density will increase the alveolar porosity by altering the trabecular pattern, which will eventually increase the bone resorption rate following the invasion of periodontal pathogens (46,48).
In the current study, the clinical features of periodontal tissue damage accompanying periodontitis were investigated by examining the periodontitis phenotype. The results indicated that patients with periodontitis who had the Tt/tt genotype exhibited a higher severity of periodontal tissue damage than those with the TT genotype. It was assumed that the Tt/tt genotype of exon 9 of the VDR gene affected mRNA stability or decreased the expression levels of mRNA of osteoblast-associated genes. This would decrease osteoblast function and increase osteoclast function, thereby leading to severe alveolar trabecular bone resorption. These findings are in accordance with a previous study conducted by Sun et al (37) who demonstrated that the presence of the t allele in the VDR TaqI may be a risk indicator for the susceptibility to early-onset periodontitis. Tachi et al (25) supported the findings of Sun et al (37) by demonstrating that the incidence of the TaqI polymorphism was associated with the susceptibility of developing aggressive periodontitis. In another study, the incidence of the homozygous (tt) genotype of TaqI in patients with osteoporosis was significantly higher in the osteoporosis group compared with that of the control group (18).
In addition to assessing the incidence of the VDR gene polymorphism, the present study detected a change in the sequence of the nucleotides corresponding to the amino acid valine. The nucleotide substitution in exon 9 (TaqI) of the VDR gene results in the conversion of valine to alanine in patients with periodontitis. Another published study evaluated the levels of VDR gene expression in intron 8 and demonstrated that the detection of ApaI C/T single nucleotide polymorphism #rs731236 in patients with chronic periodontitis was an important factor that was often overlooked in the prevention of this disease (43). Accumulated evidence from the previously published systematic review and meta-analysis showed that VDR is a biological effector of vitamin D that controls bone metabolism and inflammatory gene expression (5). Accordingly, in another review, it was also found that genetic polymorphisms could modify gene expression or function. Therefore, they may affect biological pathways and the susceptibility of the subjects to a variety of diseases (49). The likely explanation for these observed associations is to assume the existence of a truly functional sequence variation to a different part of the gene, which is, to a certain extent, linked to an allele of the anonymous polymorphism explored (25,49). In the present study, it was assumed that the nucleotide change would likely affect the level of VDR gene expression, which subsequently influences the translation rate of the protein or causes certain changes in RNA stability and translation. This increased the susceptibility of subjects with the t allele to a low bone density phenotype. The present study showed that patients with the tt genotype had a higher PPD (8 mm) than those of the patients with the Tt and TT genotypes. Therefore, the findings of the present study emphasize on the assumption that patients with the tt genotype are susceptible to decreased bone density or decreased immune system function. Unfortunately, since this was not fully addressed in the current research, it is recommended to analyze these findings in future studies.
It is important to note that the present study has certain limitations such as the small sample size and consisted of individuals from a single center. Therefore, additional research is required to identify the specific pathogenesis of this disease and the functional significance of the polymorphisms of the VDR gene.
In conclusion, the findings of the present study suggested that the VDR gene polymorphism was associated with periodontitis in the Makassar-based population. Indirect evidence confirms that the severity of periodontal tissue damage may be a consequence of the presence of the t allele or the tt genotype.
Acknowledgements
We would like to thank Professor Bahruddin Talib (Department of Prosthodontics, Faculty of Dentistry, Hasanuddin University, Makassar, Indonesia) and Professor Budu (Department of Ophthalmology Faculty of Medicine, Hasanuddin University) for their valuable scientific support, as well as Professor Burhanuddin Daeng Pasiga (Department of Dental Public Health, Faculty of Dentistry, Hasanuddin University) for their expert support in data analysis.
Availability of data and materials
The datasets used and/or analyzed during the present study are available from the corresponding author on reasonable request.
Authors' contributions
NH, SO and EM conceived and designed the study, and wrote the original draft of the manuscript. MR and ASHY analyzed and interpreted the data, and edited the manuscript. TS and KLO assisted in the design of the study, curated the data, and reviewed and edited the manuscript. All authors have read and approved the final manuscript. NH, SO and MR confirm the authenticity of all the raw data.
Ethics approval and consent to participate
The present study was approved by the Ethics Committee for Biomedical Research in Humans, Faculty of Medicine, Hasanuddin University (approval no. 0189/H.04.8.4.5.31/PP36-KOMETIK/2010). All patients in the case and control groups provided informed consent prior to the initiation of the study. The experimental procedures were based on the Declaration of Helsinki.
Patient consent for publication
The patients provided written informed consent for the publication of any data and/or accompanying images.
Competing interests
The authors declare that they have no competing interests.
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VDR gene polymorphism. Restricted fragment length polymorphism-PCR in the (A) case group and (B) control group. VDR, vitamin D receptor.
DNA sequencing of the VDR genotype. Sequencing of the (A) TT, (B) Tt and (C) tt genotype. VDR, vitamin D receptor.
Clinicopathological characteristics of the recruited cohort.
Case, n=81
Control, n=81
Parameters
Mean
SD
Mean
SD
P-value
Age, year
38.9
9.24
37.61
11.82
0.443
Height, cm
155.53
6.55
157.33
7.33
0.101
Weight, kg
55.46
6.45
56.19
9.22
0.618
Body mass index, kg/m2
22.47
2.9
23.18
3.4
0.936
Edentulous
2.48
2.69
1.06
1.07
<0.001b
Caries
2.17
2.3
2.04
1.69
0.673
Oral hygiene index-simplified
2.63
0.96
2.29
0.69
0.011a
Probing pocket depth, mm
4.54
1.27
-
-
Stage I (≤4 mm)
4
0
Stage II (≤5 mm)
5
0
Stage III/IV (≥6 mm)
7.2
1.98
Clinical attachment loss, mm
3.02
1.48
-
-
Stage I (1 to 2 mm)
2
0
Stage II (3 to 4 mm)
3.55
0.54
Stage III/IV (≥6 mm)
5.91
1.16
aP<0.05,
bP<0.001.
Vitamin D receptor gene genotype frequency in the case and control groups.
Case
Control
Genotype
n
%
n
%
TT
70
86.42
80
98.77
Tt
10
12.35
1
1.23
tt
1
1.23
0
0
Total
81
100
81
100
Comparison of the Vitamin D receptor genotype in patients with periodontitis based on OHI-S, PPD and CAL.