Abstract
The antigens of the Duffy blood group system (DARC) act as a receptor for the interleukin IL-8. IL-8 plays an important role in the pathogenesis of chronic periodontitis due to its chemotactic properties on neutrophils. The aim of this study was to investigate a possible association of Duffy blood group gene polymorphisms with the -353T>A, -845T>C and -738T>A SNPs of the IL8 gene in chronic periodontitis. One hundred and twenty-four individuals with chronic periodontitis and 187 controls were enrolled. DNA was extracted using the salting-out method. The Duffy genotypes and IL8 gene promoter polymorphisms were investigated by PCR-RFLP. Statistical analyses were conducted using the Chi square test with Yates correction or Fisher's Exact Test, and the possibility of associations were evaluated by odds ratio with a 95% confidence interval. When analyzed separately, for the Duffy blood group system, differences in the genotype and allele frequencies were not observed between all the groups analyzed; and, in nonsmokers, the -845C allele (3.6% vs. 0.4%), -845TC genotype (7.3% vs. 0.7%) and the CTA haplotype (3.6% vs. 0.4%) were positively associated with chronic periodontitis. For the first time to our knowledge, the polymorphisms of erythroid DARC plus IL8 -353T>A SNPs were associated with chronic periodontitis in Brazilian individuals. In Afro-Brazilians patients, the FY*02N.01 with IL8 -353A SNP was associated with protection to chronic periodontitis.
Introduction
The Duffy blood group system is composed of five antigens, also called the Duffy antigen receptor chemokines (DARC), which occur as membrane glycoproteins [1-3]. These antigens are present on red blood cells (RBCs) and endothelial cells lining the post-capillary venules in most tissues, except the brain, where the Duffy antigen is expressed in Purkinje cells [4].
Besides being a receptor of the Plasmodium vivax and knowlesi malarial parasites [5], HIV-1 [6] and molecules such as tetraspanin CD82 [7], DARC is also a high-affinity receptor for the CXC class of pro-inflammatory chemokines, such as IL-8, and CC, including monocyte chemoattractant protein-1 (MCP-1), macrophage inflammatory protein-1 (MIP) and regulated and normal T cell expressed and secreted (RANTES) [8]. Unlike typical chemokine receptors, DARC does not activate the intracellular signaling cascade linked to protein G, a key event in the signaling of cell migration, because it lacks the highly conserved Asp-Arg-Tyr (DRY) motif in the second intracellular loop of the protein, and is therefore considered a silent receptor [9,10].
The main antigens of the Duffy blood group system, Fya and Fyb, are encoded by two allele forms of the FY gene, the FY*01 and FY*02 alleles respectively, which differ by a single base substitution at nucleotide 125 [11]. This substitution of an amino acid in the amino-terminal domain of the protein does not affect the binding affinity of chemokines [12]. Most West Africans and two-thirds of Afro-Americans do not express Fya or Fyb on the surface of RBCs (the Fy(a−b−) phenotype) due to a homozygous nucleotide base change in the 5´ untranslated region of the FY gene, -67T>C, which is also called the GATA-1 box mutation. The genotype found in these individuals is FY*02N.01/FY*02N.01 [11,13-15]. The rare allele, FY*02M.01, characteristic of Caucasians, encodes a weak expression of Fyb in RBCs due to two polymorphisms in exon 2 of the FY gene (265C>T and 298G>A) [16]. In Brazil, due to the miscegenation of Afro-Brazilians, Brazilian Indians and Europeans, these polymorphisms are also found in other ethnic groups [17].
Recent studies have shown that the adsorption of IL-8 onto RBCs by DARC leads to an increased recruitment of leukocytes from the blood to the tissue compared to individuals without DARC on the RBCs. This is because DARC removes the "desensitizing" plasma chemokines (free circulating IL-8 binds to neutrophils and prevents their chemotaxis) and indirectly improves the coding signal of IL-8 on the surface of endothelial cells (via immobilization by glycosaminoglycans) at predestined sites to recruit neutrophils [18].
IL-8 is responsible for inducing chemotaxis and mediates the activation and migration of neutrophils into tissues from a peripheral blood [18]. The IL8 gene is located on chromosome 4q13-q21 (GeneBank accession number M28130) and more than 70 single nucleotide polymorphism (SNPs) have been identified. The expression levels of a protein may be modulated by genetic polymorphisms in regulatory regions of the gene, mainly the promoter regions, and the IL8 -353 T>A (rs4073) SNP has been shown to regulate IL-8 levels after stimulation with lipopolysaccharide (LPS) [19]: IL-8 production was highest to AA group, least to TT group and intermediated to AT group at same time. Furthermore, -353 T>A -738 T>A and -845 T>C formed a haplotype in the IL8 gene [20] and linkage disequilibrium was observed between the -845 and -738 SNPs and -738 and -353 SNPs [21].
Due to its chemotactic properties on neutrophils, IL-8 plays an important role in the pathogenesis of chronic periodontitis [22], a disease characterized by a destructive inflammatory process that affects the tissues of the tooth.
Polymorphisms of the FY gene may lead to reduced or even absent DARC expression on RBCs, while IL8 single nucleotide polymorphisms (SNPs) affect IL-8 production. Thus, examining these polymorphisms may contribute to the understanding of the immunopathogenesis underlying chronic periodontitis.
Methods
Sample selection
This study involved individuals from the north and northwest regions of the state of Paraná, southern Brazil. A total of 311 individuals were selected from those who sought dental treatment in the dental clinics of the Maringa State University (UEM) and Dental School of Inga (UNINGÁ) from January 2012 to September 2012. Males and females aged over 18 years and from all ethnic groups and with at least 20 teeth in the buccal cavity participated in this study. Individuals with acute infections or lactations and those who were pregnant were not included. After taking the patient’s history, clinical periodontal examinations were conducted by two examiners. Clinical parameters of probing depth and clinical insertion level were examined at six sites (mesiovestibular, vestibular, distovestibular, mesiolingual, lingual and dentilingual) of each tooth, as was bleeding on probing. After the periodontal examination, participants were categorized into two different groups: the chronic periodontitis group (n = 124) composed of individuals who had at least 5 sites in different teeth with periodontal pockets larger than or equal to 5 mm and clinical insertion level values greater than or equal to 3 mm; and the control group (n = 187), formed by individuals who did not have sites with reduced clinical insertion level values, displayed a probing depth of less than 4 mm and exhibited no bleeding on probing.
Information on the patient’s ethnic background, presence of other diseases such as diabetes, and smoking were obtained by interviewing the individual (anamnesis).
Ethics Information
All individuals who agreed to participate in this research were informed about the nature of the study and signed an informed consent form. This study was approved by the Human Research Ethics Committee of the Maringa State University (UEM - No. 719/2011, 02/12/2011).
Sample collection and DNA extraction
To extract the DNA, the buffy coat was obtained from the 4 mL of peripheral blood collected in EDTA by centrifugation (210 g for 15 min). The DNA was extracted using the salting-out method. The concentration and quality of the DNA were analyzed by optical density in a Thermo Scientific Nanodrop 2000® apparatus (Wilmington, USA).
Genotyping of the Duffy blood group system
The FY polymorphisms, including the SNPs 125 G>A (FY*01/FY*02), 265 C>T, 298 G>A (FY*02M.01) and the GATA-1 box mutation −67T>C (FY*02N.01), were determined by polymerase chain reaction–restriction fragment length polymorphism (PCR–RFLP), as previously described by Castilho et al. [23], and described in the Table 1.
Table 1. PCR-RFLP: primers, cycling conditions and enzymes used to the genotyping of the Duffy blood group system.
| SNP | Primer sequence (GenBank: S76830.1) | Restriction enzyme | Fragments after enzymatic digestion (bp) |
|---|---|---|---|
| *125G>A (rs12075) | 5′-tccccctcaactgagaactc-3′ | BanI | (G) 86 + 96 + 210 |
| 5′-catggcaccgtttggttcag-3′ | (A) 86+ 306 | ||
| *265C>T (rs34599082) | 5′-tccccctcaactgagaactc-3′ | MspAI | (C) 85 + 119 |
| 5′-catggcaccgtttggttcag-3′ | (T) 85 + 119 + 161 | ||
| *298G>A (rs13962) | 5′-tccccctcaactgagaactc-3′ | MwoI | (G) 86 + 96 + 210 |
| 5′-catggcaccgtttggttcag-3′ | (A) 86+ 306 | ||
| **-67T>C (rs2814778) | 5′-caacatctgtgtaccctg-3′ | StyI | (T) 81 + 108 |
| 5′-catggcaccgtttggttcag-3′ | (C) 61 + 81 + 108 |
Cycling conditions: * 95°C, 15’; 35 cycles (94°C, 20”; 62°C, 20”; 72°C, 20”) and 72°C, 10’
** 95°C, 15’; 35 cycles (94°C, 20”; 62°C, 20”; 72°C, 20”) and 72°C, 10’
Analysis of IL8 promoter polymorphisms
Polymorphisms of the IL8 promoter region were investigated by PCR-RFLP: the -845T>C and -353T>A SNPs were studied using an adapted procedure of Rovin et al. [20], and the -738T>A SNP was determined using the method of Heinzmann et al. [24] and Lee et al. [25], described in the Table 2.
Table 2. PCR-RFLP: primers, cycling conditions and enzymes used to identify polymorphisms in the IL8 promoter region.
| SNP | Primer sequence (GenBank:28130) | Restriction enzyme | Fragments after enzymatic digestion (bp) |
|---|---|---|---|
| *-845T>C (rs2227532) | 5′-gaattcagtaacccaggcat-3′ | AseI | (T) 791 + 736 |
| 5′- aagcttgtgtgctctgctgtc-3′ | (C) 1527 | ||
| *-353T>A (rs4073) | 5′-gaattcagtaacccaggcat-3′ | MfeI | (A) 1230 + 297 |
| 5′- aagcttgtgtgctctgctgtc-3′ | (T) 1527 | ||
| **-738T>A (***) | 5′-aacccagcagctccagtg-3′ | XbaI | (T) 302 + 232 |
| 5′-agataagccagccaatcatt-3′ | (A) 534 |
bp: base pairs;
Cycling conditions: * 95°C, 3’; 35 cycles (95°C 45”; 56°C, 30”; 68°C, 2’) and 68°C, 8’
** 94°C, 5’; 35 cycles (94°C, 30”; 61°C, 1’; 72°C, 1’) and 72°C, 8’
(***) It was not found a rs (reference sequence) identification number related to this SNP;
Statistical analysis
Allele and genotype frequencies were obtained by direct counts. The data were tested for their fit to Hardy-Weinberg equilibrium by calculating the expected frequencies of the genotypes and comparing them with the observed values, to test the deviation of genotype distribution. The Arlequin software, version 3.1 [26] was used to investigate linkage disequilibrium and the estimated frequencies of the possible haplotypes of IL8. The association between genetic polymorphisms and chronic periodontitis was evaluated using the Chi-square test with Yates correction or the Fisher's exact test for sample sizes of less than five. The correlation was deemed present by an odds ratio with 95% confidence intervals only for significant p-values. For these analyses, OpenEpi program Version 2.3.1 was used [27]. All tests were carried out using a significance level of 5%.
Results
The study population consisted of 311 unrelated individuals: 124 patients with chronic periodontitis and 187 controls. Most participants were female (60.5%), nonsmokers (60.8%) and Caucasian (64.3% - Table 3). Diabetes was significantly more frequent in patients than in controls, confirming its association to chronic periodontitis (p-value < 0.001; OR = 3.313; 95% CI = 1.883 -5.882). Smoking was also an important risk factor: smokers and ex-smokers were between 2 and 3 times more likely to develop chronic periodontitis than nonsmokers (Table 3). To exclude smoking as a predisposing factor, statistical analyses were performed in the total sample (smokers and nonsmokers), as well as in nonsmokers. The periodontitis patients that had diabetes were included in total sample and nonsmokers groups. However, although they are present in small numbers, these subjects were excluded from the groups during statistical analysis to prevent diabetes as predisposing factor. The genotype distributions of each SNP studied were consistent with the assumption of the Hardy–Weinberg equilibrium in the control and periodontal disease groups (p-value >0.05).
Table 3. Characteristics of patients with chronic periodontitis and control population.
| Category | Subcategory | Control | Periodontitis | Total |
|---|---|---|---|---|
| N = 187 | N = 124 | (%) | ||
| n (%) | n (%) | n (%) | ||
| Gender | Female | 120 (64.2) | 68 (54.8) | 188 (60.5) |
| Male | 67 (35.8) | 56 (45.2) | 123 (39.5) | |
| Age | 18 - 33 years | 35 (18.7) | 16 (12.9) | 51 (16.4) |
| 34 - 49 years | 98 (52.4) | 65 (52.4) | 163 (52.4) | |
| 50 - 65 years | 50 (26.7) | 35 (28.2) | 85 (27.3) | |
| 66 - 81 years | 4 (2.1) | 8 (6.5) | 12 (3.9) | |
| Ethnic background | Caucasian | 128 (68.5) | 72 (58.1) | 200 (64.3) |
| Afro-Brazilian | 14 (7.5) | 15 (12.1) | 29 (9.3) | |
| Mulatto | 45 (24.1) | 37 (29.8) | 82 (26.3) | |
| Smoking | Nonsmoker * | 134 (71.7) | 55 (44.4) | 189 (60.8) |
| Smoker ** | 23 (12.3) | 28 (22.6) | 51 (16.4) | |
| Ex- smoker *** | 30 (16.0) | 41 (33.1) | 71 (22.8) | |
| Diabetes | No | 180 (96.3) | 109 (87.9) | 289 (92.9) |
| Yes**** | 7 (3.7) | 15 (12.1) | 22 (7.1) |
* p-value < 0.001; OR = 0.31; 95% CI = 0.19-0.50;
** p-value = 0.03; OR = 2.07; 95% CI = 1.12-3.84;
*** p-value < 0.001; OR = 2.95; 95% CI = 1.56-5.62;
p-value < 0.001; OR = 3.31; 95% CI = 1.88-5.88.
For the Duffy blood group system, the prevalent genotype in all the analyzed groups was FY*01/FY*02, with FY*02 being the most common allele (Table 4). Differences in the genotype and allele frequencies were not observed between all the groups analyzed.
Table 4. Distribution of genotypes and alleles of the Duffy blood group system in patients with chronic periodontitis and controls.
| Duffy |
Total
|
Nonsmokers
|
||
|---|---|---|---|---|
| Periodontitis | Controls | Periodontitis | Control | |
| N = 124 | N = 187 | N = 55 | N = 134 | |
| n(%) | n (%) | n(%) | n (%) | |
| Genotypes | ||||
| FY*01/FY*01 | 10 (8.1) | 27 (14.4) | 10 (18.1) | 23 (17.2) |
| FY*01/FY*02 | 45 (36.3) | 62 (33.2) | 15 (27.3) | 41 (30.6) |
| FY*02/FY*02 | 33 (26.6) | 57 (30.5) | 13 (23.6) | 40 (29.9) |
| FY*02/FY*02N.01 | 10 (8.1) | 12 (6.4) | 4 (7.3) | 9 (6.7) |
| FY*02/FY*02M.01 | 2 (1.6) | 3 (1.6) | 1 (1.8) | 2 (1.5) |
| FY*01/FY*02N.01 | 12 (9.7) | 10 (5.3) | 6 (11) | 8 (6) |
| FY*02N.01/FY*02N.01 | 7 (5.6) | 11 (5.9) | 3 (5.5) | 9 (6.7) |
| FY*02M.01/FY*02N.01 | 2 (1.6) | 3 (1.6) | 1 (1.8) | 1 (0.7) |
| FY*01/FY*02M.01 | 3 (2.4) | 2 (1.1) | 2 (3.6) | 1 (0.7) |
| Alleles | ||||
| FY*01 | 80 (32.3) | 128 (34.2) | 43 (39.1) | 96 (35.8) |
| FY*02 | 123 (49.6) | 191 (51.1) | 46 (41.8) | 132 (49.3) |
| FY*02N. 01 | 38 (15.3) | 47 (12.6) | 17 (15.5) | 36 (13.4) |
| FY*02M.01 | 7 (2.8) | 8 (2.1) | 4 (3.6) | 4 (1.5) |
The genotype and allele frequencies of the -845T>C, -738T>A and -353T>A SNPs in the IL8 gene promoter region are listed in Table 5. The -845C allele was most common in non-smoking patients with chronic periodontitis compared to controls (3.6% vs 0.4%; p-value = 0.024; OR = 10.4; 95% CI = 1.1-91.2), as was the -845 TC genotype (7.3% vs 0.7%; p-value = 0.024; OR = 10.1; 95% CI = 1.1-95.5) and the CTA haplotype (3.6% vs 0.4%; p-value = 0.024; OR = 10.1; 95% CI = 1.1-91.2), indicating positive correlations. Moreover, the CTA/TTT genotype was present only in patients with periodontitis (5.5% vs 0%; p-value = 0.024).
Table 5. Allele, genotypic and haplotype frequencies of the -845T>C, -738T>A and -353T>A polymorphisms in the IL8 promoter region in patients with periodontitis and controls.
| IL8 SNPs |
Total
|
Nonsmokers
|
||
|---|---|---|---|---|
| Periodontitis | Controls | Periodontitis | Controls | |
| N = 124 | N = 187 | N = 55 | N = 134 | |
| n (%) | n (%) | n (%) | n (%) | |
| -845 | ||||
| T | 240 (96.8) | 370 (98.9) | 106 (96.4) a | 267 (99.6) a |
| C | 8 (3.2) | 4 (1.1) | 4 (3.6) b | 1 (0.4) b |
| TT | 117 (94.4) | 183 (97.9) | 51 (92.7) c | 133 (99.3) c |
| TC | 6 (4.8) | 4 (2.1) | 4 (7.3) d | 1 (0.7) d |
| CC | 1 (0.8) | 0 (0) | 0 (0) | 0 (0) |
| -738 | ||||
| T | 247 (99.6) | 373 (99.7) | 109 (99.1) | 267 (99.6) |
| A | 1 (0.4) | 1 (0.3) | 1 (0.9) | 1 (0.4) |
| TT | 123 (99.2) | 186 (99.5) | 54 (98.2) | 133 (99.3) |
| TA | 1 (0.8) | 1 (0.5) | 1 (1.8) | 1 (0.7) |
| -353 | ||||
| T | 130 (52.4) | 198 (52.9) | 63 (57.3) | 145 (54.1) |
| A | 118 (47.6) | 176 (47.1) | 47 (42.7) | 123 (45.9) |
| TT | 34 (27.4) | 53 (28.3) | 17 (30.9) | 38 (28.4) |
| TA | 62 (50) | 92 (49.2) | 29 (52.7) | 69 (51.5) |
| AA | 28 (22.6) | 42 (22.5) | 9 (16.4) | 27 (20.1) |
| -845-738-353 | ||||
| TTT | 131 (52.8) | 198 (53) | 63 (57.3) | 145 (54.1) |
| TTA | 108 (43.6) | 171 (45.7) | 42 (38.2) | 121 (45.1) |
| TAA | 1 (0.4) | 1 (0.3) | 1 (0.9) | 1 (0.4) |
| CTA | 8 (3.2) | 4 (1.0) | 4 (3.6) e | 1 (0.4) e |
| -845-738-353/845-738-353 | ||||
| TTT/TTA | 57 (46) | 89 (47.6) | 25 (45.5) | 68 (50.7) |
| TTT/TTT | 34 (27.4) | 53 (28.3) | 17 (30.9) | 38 (28.4) |
| TTA/TTA | 25 (20.2) | 40 (21.4) | 8 (14.5) | 26 (19.4) |
| TTT/TAA | 1 (0.8) | 1 (0.5) | 1 (1.8) | 1 (0.75) |
| TTA/CTA | 2 (1.6) | 2 (1.1) | 1 (1.8) | 1 (0.75) |
| CTA/TTT | 4 (3.2) | 2 (1.1) | 3 (5.5) f | 0 (0) f |
| CTA/CTA | 1 (0.8) | 0 (0) | 0 (0) | 0(0) |
a p-value= 0.027; OR=0.1; CI95%=0.01- 0.9;
b p-value=0.024; OR=10.4; CI95%=1.1-91.2;
c p-value=0.027; OR=0.1; CI95%=0.01- 0.9;
d p-value=0.024; OR=10.1; CI95%=1.1-95.5;
e p-value=0.024; OR=10.1; CI95%=1.1-91.2;
f p-value= 0.024; OR, IC undefined (because the presence of zero).
To evaluate DARC expression on the surface of RBCs, two new groups were formed: the first, without polymorphisms, was formed by grouping individuals with the FY*01 and FY*02 alleles encoding Fya and Fyb expression, respectively, and the other, with polymorphisms, was composed of individuals carrying the FY alleles with the -67T>C SNP, FY*02N.01 allele, and the 265T>C SNP, FY*02M.01 allele. As the frequencies of DARC polymorphisms vary in different ethnic groups, the analyses were performed separately for Afro-Brazilians and Admixed-Brazilians. Brazilians population is very mixed and, in the Parana State, the degree of the European ancestry is high (80.6%), with a small but significant contribution of African (12.5%) and Amerindian (7.0%) genes, according to Probst et al. [28]. Thus the studied populations were considered as Admixed-Brazilians (Mulattos or pardos plus whites individuals) and Afro-Brazilians (black individuals). The results are shown in Table 6.
Table 6. Distribution of FY allele frequencies with and without the -67T>C (FY*02N.01) and -265T>C (FY*02M.01) SNPs in Afro-Brazilian and Admixed-Brazilian patients with chronic periodontitis and controls.
| Duffy | Periodontitis | Controls |
|---|---|---|
| n (%) | n (%) | |
| Afro-Brazilians | N = 15 | N = 14 |
| FY*01 and FY*02 | 20 (66.7) | 12 (42.8) |
| FY*02N.01 | 10 (33.3) | 16 (57.2) |
| Admixed Brazilians | N = 109 | N = 173 |
| FY*01 and FY*02 | 183 (83.9) | 307 (88.7) |
| FY*02N.01 and FY*02M.01 | 35 (16.1) | 39 (11.3) |
The distribution of frequencies of the FY alleles without and with polymorphisms was similar between patients and controls. However, differences, although statistically non-significant, were observed in Afro-Brazilians. Afro-Brazilian patients with chronic periodontitis displayed a lower frequency of FY alleles with polymorphism (33.3% vs 57.2%). The allele, genotype and haplotype frequencies of the -845T>C, -738T>A and -353T>A polymorphisms of IL8 were analyzed separately in patients with periodontitis and controls, and in Afro-Brazilians and Admixed-Brazilians (Table 7). The frequency of the -353A SNP (allele and genotype) was lower in Afro-Brazilian patients (40% vs 60.7%), although not significantly. Moreover, the TTA haplotype had a lower frequency in Afro-Brazilians (33.3% vs 60.7%; p-value = 0.067; OR = 0.3; 95%CI = 0.1-0.9).
Table 7. Allele, genotype and haplotype frequencies of the -845T>C, -738T>A and -353T>A polymorphisms in the IL8 promoter region in Afro-Brazilian and Admixed-Brazilians patients and controls.
| SNP |
Afro-Brazilians
|
Admixed Brazilians
|
||
|---|---|---|---|---|
| Periodontitis | Controls | Periodontitis | Controls | |
| N = 15 | N = 14 | N = 109 | N = 173 | |
| n (%) | n (%) | n (%) | n (%) | |
| -845 | ||||
| T | 28 (93.3) | 28 (100) | 212 (97.2) | 342 (98.8) |
| C | 2 (6.7) | 0 (0) | 6 (2.8) | 4 (1.2) |
| TT | 13 (86.7) | 14 (100) | 104 (95.4) | 169 (97.7) |
| TC | 2 (13.3) | 0 (0) | 4 (3.7) | 4 (2.3) |
| -738 | ||||
| T | 30 (100) | 28 (100) | 217 (99.5) | 345 (99.7) |
| A | 0 (0) | 0 (0) | 1 (0.5) | 1 (0.3) |
| TT | 15 (100) | 14 (100) | 108 (99.1) | 172 (99.4) |
| TA | 0 (0) | 0 (0) | 1 (0.9) | 1 (0.6) |
| -353 | ||||
| T | 18 (60.0) | 11 (39.3) | 112 (51.4) | 187 (54.0) |
| A | 12 (40.0) | 17 (60.7) | 106 (48.6) | 159(46.0) |
| TT | 5 (33.3) | 3 (21.4) | 29 (26.6) | 50 (28.9) |
| TA | 8 (53.3) | 5 (35.7) | 54 (49.5) | 87 (50.3) |
| AA | 2 (13.3) | 6 (42.9) | 26 (23.9) | 36 (20.8) |
| -845-738-353 | ||||
| TTT | 18 (60) | 11 (39.3) | 113 (51.8) | 187 (54.0) |
| TTA | 10 (33.3) * | 17 (60.7) * | 98 (45.0) | 154 (44.5) |
| TAA | 0 (0) | 0 (0) | 1 (0.5) | 1 (0.3) |
| CTA | 2 (6.7) | 0 (0) | 6 (2.8) | 4(1.2) |
| -845-738-353/-845-738-353 | ||||
| TTT/TTA | 6 (40.0) | 5 (35.7) | 51 (46.8) | 84 (48.6) |
| TTT/TTT | 5 (33.4) | 3 (21.4) | 29 (26.6) | 50 (28.9) |
| TTA/TTA | 2 (13.3) | 6 (42.9) | 23 (21.1) | 34 (19.7) |
| TTT/TAA | 0 (0) | 0 (0) | 1 (0.9) | 1 (0.6) |
| TTA/CTA | 0 (0) | 0 (0) | 2 (1.8) | 2 (1.2) |
| CTA/TTT | 2 (13.3) | 0 (0) | 2 (1.8) | 2 (1.2) |
* p-value = 0.067; OR = 0.3; 95% CI = 0.1- 0.9.
The genotypes -845CC, -738AA and TAT, CTT, CAT, CAA and CTA/CTA were not found in patients and controls.
An analysis of the FY genotypes both with and without polymorphism versus the -353T>A IL8 polymorphism was performed in patients and controls (Table 8). In Afro-Brazilians patients, the presence of the FY genotype with polymorphism and the -353A SNP was lower (20% vs 50%; p-value = 0.032; OR = 0.25; 95% CI = 0.078-0.79). The genotype -353AA was also lower in the same group, although not significant (6.7% vs 35.7%; p-value= 0.06). In Admixed-Brazilians, the simultaneous presence of the FY genotype the -353T>A IL8 polymorphism was not significant.
Table 8. Distribution of FY genotypes with the presence and absence of the -67T>C and 265T>C polymorphisms versus the -353T>A IL8 SNP in patients with chronic periodontitis and controls.
|
Periodontitis
|
Controls
|
|||||||||
|---|---|---|---|---|---|---|---|---|---|---|
| -353 IL-8 | -353 IL-8 | |||||||||
| Duffy genotypes | TT | TA | AA | A | T | TT | TA | AA | A | T |
| Total | N = 124 | N = 187 | ||||||||
| Without polymorphisma | 24 (19.4) | 42 (33.9) | 22 (17.7) | 86 (34.7) | 90 (36.3) | 43 (23) | 72 (38.5) | 31 (16.6) | 134 (35.8) | 158 (42.2) |
| With polymorphismb | 10 (8.1) | 20 (16.1) | 6 (4.8) | 32 (12.9) | 40 (16.1) | 10 (5.34) | 21 (11.22) | 10 (5.34) | 41 (11) | 41 (11) |
| Afro-Brazilians | N = 15 | N = 14 | ||||||||
| Without polymorphism | 3 (20) | 4 (26.7) | 1 (6.7) | 6 (20) | 10 (33.3) | 2 (14.3) | 1 (7.1) | 1 (7.1) | 3 (10.7) | 5 (17.9) |
| With polymorphism | 2 (13.3) | 4 (26.7) | 1 (6.7) | 6 (20)c | 8 (26.7) | 1 (7.1) | 4 (28.6) | 5 (35.7) | 14 (50)c | 6 (21.4) |
| Admixed- Brazilians | N = 109 | N = 173 | ||||||||
| Without polymorphism | 21 (19.3) | 38 (34.8) | 21 (19.3) | 80 (36.7) | 80 (36.7) | 41 (23.7) | 71 (41.0) | 30 (17.3) | 131 (37.9) | 153 (44.2) |
| With polymorphism | 8 (7.3) | 16 (14.7) | 5 (4.6) | 26 (11.9) | 32 (14.7) | 9 (5.2) | 16 (9.2) | 6 (3.5) | 28 (8.1) | 34 (9.8) |
a FY genotypes without -67T>C and/or 265T>C SNPs;
b FY genotypes with -67T>C and/or 265T>C SNPs in homozygosis or heterozygosis (without DARC expression or lower DARC expression);
cp-value = 0.03; OR = 0.25; 95% CI = 0.078- 0.79;
Discussion
The Duffy blood group system acts as a receptor for IL-8, an inflammatory chemokine involved in neutrophil activation and trafficking [10,29-31]. When IL-8 is bound to DARC on the surface of RBCs, it is effectively inactivated. RBCs of individuals with the Fy(a‑b-) phenotype do not bind IL-8 and therefore, do not have this function of sink as proposed for the DARC on RBCs [10,29]. As high levels of serum IL-8 and neutrophils are involved in the pathogenesis of chronic periodontitis [32], we decided to investigate the role of DARC in this disease.
Several periodontal disease risk factors have been previously identified [33,34], including diabetes, a strong causal risk factor for periodontal pathology [35-39]. In the present study, subjects with diabetes were three times more likely to develop chronic periodontitis than non-diabetic subjects (p-value <0.001; OR = 3.31; 95%CI = 1.88-5.88). The biological plausibility has been well documented. The potential influence of diabetes on periodontal disease is likely to be due to the hyperinflammatory response to infection, uncoupling of bone destruction and repair, and/or the effects of advanced glycation and the resulting products [38,39]. The proinflammatory cytokine profiles in the diabetes mellitus patients, including IL-8, were correlated with severity of the course of disease [40-43] and polymorphisms of pro-inflammatory cytokine genes (CCL2, TGFB1, IL8, CCR5, and MMP9) were found to be associated with the risk of diabetic nephropathy [44]. Although the diabetes patients were present in small numbers, these subjects were excluded from the groups during statistical analyses of IL8 SNPs (dates not shown) and no differences were observed.
Smoking is another important risk factor for the onset and progression of chronic periodontitis [45-47] and the present study confirmed these findings. Potential mechanisms for the effect of smoking on periodontal disease include immunosuppression and exacerbated inflammatory cell response [48]. The risk associated with smoking can often obscure genetic risk factors [49]; thus, the statistical analysis of the subgroup of nonsmokers was carried out to exclude any possible influence of smoking on the genetic factors.
The distribution of FY alleles and genotypes and most of the IL8 polymorphisms -845T>C, -738T>A and -353T>A were similar between patients with chronic periodontitis and controls (total population and nonsmokers). The exception was the -845T>C IL8 polymorphism in nonsmokers: the -845C allele and -845TC genotype were associated with susceptibility to chronic periodontitis (-845C allele: 3.6% vs 0.4%; OR = 10.4; -845TC genotype: 7.3% vs 0.7%; OR = 10.1). Thus, individuals who had the -845C allele or -845TC genotype were 10 times more likely to develop the disease than those who did not. As far as we know, the IL8 -845T>C and -738T>A SNPs are not associated with different levels of production of this cytokine. Moreover, these SNPs have been associated with disease in only a few studies [20,21,50], possibly due to low genetic diversity: C and A mutant alleles were observed in Afro-American populations (C: 8% and A: 5%) [20], but were absent in Europeans [20,21]. Kim et al. [21] studied the association of the -845T>C, -738T>A and -353T>A IL8 polymorphisms in chronic periodontitis in a Brazilian population and did not observe any association between alleles and genotypes in the total sample or in nonsmokers. However, in the haplotype analysis, significant differences were obtained for the CTA, TTA and TAT haplotypes, which were associated with susceptibility to periodontitis and TTT and TAA seemed to have the opposite effects, in the total sample and in nonsmokers. Nonsmokers carrying the TAT/CTA and TTA/CAT genotype seemed to be susceptible and those that carrying TTT/TAA seemed protected against the development of chronic periodontitis. In the current study, the CTA haplotype and CTA/TTT genotype were associated with susceptibility to the disease. However, TAT was not found because the frequency of the -738A allele in the study population was very low (<1%). CTA/TTT genotype was only found in patients with chronic periodontitis (5% vs 0%; p-value = 0.024).
The IL8 -353TγA SNP, also found in the literature as -251T>A and rs4073TA, was linked to high transcription levels of IL-8 after whole blood stimulation with lipopolysaccharides [19]. This polymorphism has been described in the literature as being associated with various diseases: respiratory syncytial virus bronchiolitis, prostate cancer, distal gastric cancer, breast cancer, oral squamous cell carcinoma, age-related macular degeneration and oral lichen planus [19,50-55]. In Brazil, studies correlating the IL8 -353TγA SNP with chronic periodontitis were carried out by Kim et al. in 2009 [56] and Andia et al. in 2011 [57]. Kim et al. evaluated the population as a whole, as well as nonsmokers, and found no association with periodontitis. Andia et al., who only studied nonsmokers, found a reduction in the frequency of the TT genotype (13.8% vs 35.2%) and a significant increase in the frequency of the TA genotype (74.6% vs 52.8%) associated with periodontitis; and susceptibility to periodontitis in individuals with the TA genotype was also observed when Caucasians were analyzed separately. High levels of IL-8 mRNA were also identified in individuals with the TA genotype. The differences of these results may be related to the selection of groups (smokers or nonsmokers) and the differences in the composition of the population, given that the Brazilian population is highly racially mixed. According to Ioannidis et al. [58], genetic associations may not be uniform across the population and the frequency of different polymorphisms may vary between ethnic groups.
As ethnic background is an important factor to be considered and many studies have reported contradictory results when comparing distinct populations [59-61], we subdivided the study population by two ethnic groups.
When DARC expression on the surface of RBCs was compared between the without and with polymorphism groups of different ethnicities (Afro-Brazilians and Admixed-Brazilians), there were no statistically significant differences, although there was a decrease in the frequency of the -67T>C SNP (FY*02N.01 allele) in Afro-Brazilian patients (33% vs 57.2%). This decrease may suggest protection from the disease. The -67T>C SNP in the 5´ untranslated region of the FY gene, resulting in the absence of Fyb from RBCs and eliciting the Fy(b-) phenotype, does not change the expression of this protein in other tissues [13]. This polymorphism is very common in African descents; approximately 67% of Afro-Brazilians have the Fy(a‑b-) phenotype [62]. In this study, we observed that the frequency of the FY*02N.01 allele was lower than expected for this ethnic group in patients with periodontitis, albeit not significant. An analysis of a larger number of Afro-Brazilians may provide clearer conclusions with respect to the -67T>C SNP and chronic periodontitis in this ethnic group.
The analysis of the IL8 -845T>C, -738T>A and -353T>A SNPs in the Afro-Brazilian ethnic group and Admixed-Brazilians identified no significant differences in genotype and allele frequencies between controls and patients. The C allele of the -845 SNP was rarely found and the A allele of the -738 SNP was not found in Afro-Brazilians. Thus, the TTA haplotype may protect against periodontitis in Afro-Brazilians, with a p-value tending toward statistical significance (p-value = 0.067; OR = 0.3; 95% CI 0.1-0.9). Oppositely, Kim et al. [21] found that individuals with the TTA haplotype were susceptible to periodontitis; however, the population analyzed in their work was mixed and not categorized according to ethnic group.
Differences were not observed when the FY genotypes with and without polymorphism were analyzed together versus the IL8 -353T>A polymorphism in total of patients. However, Afro-Brazilians who were homozygous or heterozygous for the -67T>C SNP in the 5´ untranslated region of the FY gene and also had the IL8 -353A SNP (high producer of IL-8) were resistant to chronic periodontitis (p-value = 0.032; OR = 0.25; 95% CI = 0.078-0.79). In Admixed Brazilians, the Duffy genotype with the -67T>C (absence of DARC) and/or 265T>C (low expression of DARC) SNPs, together with the IL8 -353T SNP (low production of IL-8), was not related to periodontitis.
Usually, a specific combination of polymorphisms in different genes, or a gene polymorphism interacting with environmental factors, can significantly affect the risk of an individual developing a phenotype for certain diseases [63,64]. In Afro-Brazilians the IL8 -353A SNP (high producer of IL-8) was associated with higher DARC expression, different than expected to this ethnic group (the FY -67C allele frequency was 33%, lower than expected). Possibly, this fact is related a compensatory effect. According Hansell et al. [65] inflammation appears to substantially up-regulate DARC expression; and DARC-bound chemokines are incapable of activating chemokine receptor on leukocytes, whilst those in plasma will be free to interact with blood leukocytes (leading to desensitisation) or become immobilized on endothelial surfaces [18]. Thus, based on the results our hypothesis is that for Afro-Brazilians, the over expression of DARC on the surface of RBCs together with a large production of IL-8 are important in protecting against tissue lesions.
To confirm these findings, and to contribute to a better understanding of the etiology and pathogenesis of chronic periodontal disease, the expression of IL-8 has to be assessed and the largest number of African-Brazilian patients should be analyzed.
Conclusion
For the first time to our knowledge, the polymorphisms of erythroid DARC plus IL8 -353T>A SNPs were associated with chronic periodontitis in Brazilian individuals. In Afro-Brazilians patients, the FY*02N.01 with IL8 -353A SNP was associated with protection to chronic periodontitis.
Acknowledgments
The authors wish to thank CAPES, Fundação Araucária, and Laboratory of Immunogenetics LIG-UEM.
Funding Statement
The authors wish to thank CAPES, Fundação Araucária, and Laboratory of Immunogenetics LIG-UEM. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
References
- 1. Neote K, Mak JY, Kolakowski LF Jr, Schall TJ (1994) Functional and biochemical analysis of the cloned Duffy antigen: identity with the red blood cell chemokine receptor. Blood 84: 44-52. PubMed: 7517217. [PubMed] [Google Scholar]
- 2. Chaudhuri A, Zbrzezna V, Polyakova J, Pogo AO, Hesselgesser J et al. (1994) Expression of the Duffy antigen in K562 cells. Evidence that it is the human erythrocyte chemokine receptor. J Biol Chem 269: 7835-7838. PubMed: 8132497. [PubMed] [Google Scholar]
- 3. Murphy PM (1994) The molecular biology of leukocyte chemoattractant receptors. Annu Rev Immunol 12: 593-633. doi: 10.1146/annurev.iy.12.040194.003113. PubMed: 8011292. [DOI] [PubMed] [Google Scholar]
- 4. Chaudhuri A, Polyakova J, Zbrzezna V, Pogo AO (1995) The coding sequence of Duffy blood group gene in humans and simians: restriction fragment length polymorphism, antibody and malarial parasite specificities, and expression in nonerythroid tissues in Duffy-negative individuals. Blood 85: 615-621. PubMed: 7833466. [PubMed] [Google Scholar]
- 5. Horuk R, Colby TJ, Darbonne WC, Schall TJ, Neote K (1993) The human erythrocyte inflammatory peptide (chemokine) receptor. Biochemical characterization, solubilization, and development of a binding assay for the soluble receptor. Biochemistry 32: 5733-5738. doi: 10.1021/bi00073a002. PubMed: 8389192. [DOI] [PubMed] [Google Scholar]
- 6. He W, Neil S, Kulkarni H, Wright E, Agan BK et al. (2008) Duffy antigen receptor for chemokines mediates transinfection of HIV-1 from red blood cells to target cells and affects HIV-AIDS susceptibility. Cell Host Microbe 4: 52–62. doi: 10.1016/j.chom.2008.06.002. PubMed: 18621010. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. Bandyopadhyay S, Zhan R, Chaudhuri A, Watabe M, Pai SK et al. (2006) Interaction of KAI1 on tumor cells with DARC on vascular endothelium leads to metastasis suppression. Nat Med 12: 933–938. doi: 10.1038/nm1444. PubMed: 16862154. [DOI] [PubMed] [Google Scholar]
- 8. Neote K, Darbonne W, Ogez J, Horuk R, Schall TJ et al. (1993) Identification of a promiscuous inflammatory peptide receptor on the surface of red blood cells. J Biol Chem 268: 12247–12249. PubMed: 8389755. [PubMed] [Google Scholar]
- 9. Römpler H, Yu HT, Arnold A, Orth A, Schöneberg T et al. (2006) Functional consequences of naturally occurring DRY motif variants in the mammalian chemoattractant receptor GPR33. Genomics 87: 724–732. doi: 10.1016/j.ygeno.2006.02.009. PubMed: 16595170. [DOI] [PubMed] [Google Scholar]
- 10. Hadley TJ, Peiper SC (1997) From malaria to chemokine receptor: the emerging physiologic role of the Duffy blood group antigen. Blood 89: 3077–3091. PubMed: 9129009. [PubMed] [Google Scholar]
- 11. ISBT, International Society of Blood Transfusion. Available: http://www.isbtweb.org/fileadmin/user_upload/WP_on_Red_Cell_Immunogenetics_and/008_FY_Alleles_v2.0_110914.pdf. Accessed 16 January 2013
- 12. Tournamille C, Le Van Kim C, Gane P, Cartron JP, Colin Y et al. (1995) Molecular basis and PCR-DNA typing of the Fya/Fyb blood group polymorphism. Hum Genet 95: 407-410. PubMed: 7705836. [DOI] [PubMed] [Google Scholar]
- 13. Tournamille C, Colin Y, Cartron JP, Le Van Kim C (1995) Disruption of a GATA motif in the Duffy gene promoter abolishes erythroid gene expression in Duffy-negative individuals. Nat Genet 10: 224-228. doi: 10.1038/ng0695-224. PubMed: 7663520. [DOI] [PubMed] [Google Scholar]
- 14. Howes RE , Patil AP , Piel FB , Nyangiri OA, Kabaria CW et al. (2011) The global distribution of the Duffy blood group. Nat Commun 2: 266. doi: 10.1038/ncomms1265. PubMed: 21468018. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15. Parasol N, Reid M, Rios M, Castilho L, Harari I et al. (1998) A novel mutation in the coding sequence of the FY*B allele of the Duffy chemokine receptor gene is associated with an altered erythrocyte phenotype. Blood 92: 2237–2243. PubMed: 9746760. [PubMed] [Google Scholar]
- 16. Tournamille C, Le Van Kim C, Gane P, Le Pennec PY, Roubinet F et al. (1998) Arg89Cyssubstitution results in very low membrane expression of the Duffy antigen/receptor for chemokines in Fy(x) individuals. Blood 92: 2147-2156. PubMed: 9731074. [PubMed] [Google Scholar]
- 17. Estalote AC, Proto-Siqueira R, Silva WA Jr, Zago MA, Palatnik M et al. (2005) The mutation G298A--Ala100Thr on the coding sequence of the Duffy antigen/chemokine receptor gene in non-caucasian Brazilians. Genet Mol Res 4: 166-173. PubMed: 16110438. [PubMed] [Google Scholar]
- 18. Rot A (2005) Contribution of Duffy antigen to chemokine function. Cytokine Growth Factor Rev 16: 687-694. doi: 10.1016/j.cytogfr.2005.05.011. PubMed: 16054417. [DOI] [PubMed] [Google Scholar]
- 19. Hull J, Thomson A, Kwiatkowski D (2000) Association of respiratory syncytial virus bronchiolitis with the interleukin 8 gene region in UK families. Thorax 55: 1023-1027. doi: 10.1136/thorax.55.12.1023. PubMed: 11083887. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20. Rovin BH, Lu L, Zhang X (2002) A novel interleukin-8 polymorphism is associated with severe systemic lupus erythematosus nephritis. Kidney Int 62: 261–265. doi: 10.1046/j.1523-1755.2002.00438.x. PubMed: 12081586. [DOI] [PubMed] [Google Scholar]
- 21. Kim YJ, Viana AC, Curtis KM, Orrico SR, Cirelli JA et al. (2010) Association of haplotypes in the IL-8 gene with susceptibility to chronic periodontitis in a Brazilian population. Clin Chim Acta 411: 1264–1268. doi: 10.1016/j.cca.2010.05.014. PubMed: 20488171. [DOI] [PubMed] [Google Scholar]
- 22. Gainet J, Chollet-Martin S, Brion M, Hakim J, Gougerot-Pocidalo MA et al. (1998) Interleukin-8 production by polymorphonuclear neutrophils in patients with rapidly progressive periodontitis: an amplifying loop of polymorphonuclear neutrophil activation. Lab Invest 78: 755-762. PubMed: 9645766. [PubMed] [Google Scholar]
- 23. Castilho L, Rios M, Pellegrino J Jr, Saad ST, Costa FF et al. (2004) A novel FY allele in Brazilians. Vox Sang 87: 190-195. doi: 10.1111/j.1423-0410.2004.00554.x. PubMed: 15569072. [DOI] [PubMed] [Google Scholar]
- 24. Heinzmann A, Ahlert I, Kurz T, Berner R, KAl Deichmann (2004) Association study suggests opposite effects of polymorphisms within IL-8 on bronchial asthma and respiratory syncytial virus bronchiolitis. J Allergy Clin Immunol 114: 671–676. doi: 10.1016/j.jaci.2004.06.038. PubMed: 15356575. [DOI] [PubMed] [Google Scholar]
- 25. Lee EB, Kim JY, Zhao J, Park MH, Song YW (2006) Haplotype association of IL-8 gene with Behcet’s disease. Tissue Antigens 69: 128–132. [DOI] [PubMed] [Google Scholar]
- 26. ARLEQUIN. Available: http://cmpg.unibe.ch/software/arlequin3. Accessed 16 January 2013
- 27.http://www.openepi.com/OE2.3/Menu/OpenEpiMenu.htm Open Source Epidemiologic Statistics for Public Health Available: . Accessed 16 january 2013.
- 28. Probst CM, Bompeixe EP, Pereira NF, de O Dalalio MM, Visentainer JE et al. (2000) HLA polymorphism and evaluation of European, African, and Amerindian contribution to the white and mulatto populations from Paraná, Brazil. Hum Biol 72: 597-617. PubMed: 11048789. [PubMed] [Google Scholar]
- 29. Darbonne WC, Rice GC, Mohler MA, Apple T, Hébert CA et al. (1991) Red blood cells are a sink for interleukin 8, a leukocyte chemotaxin. J Clin Invest 88: 1362-1369. doi: 10.1172/JCI115442. PubMed: 1918386. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30. Cartron JP, Bailly P, Le Van Kim C, Cherif-Zahar B, Matassi G et al. (1998) Insights into the structure and function of membrane polypeptides carrying blood group antigens. Vox Sang 74: 29-64. doi: 10.1111/j.1423-0410.1998.tb05397.x. PubMed: 9704424. [DOI] [PubMed] [Google Scholar]
- 31. Adams DH, Lloyd AR (1997) Chemokines: Leukocyte recruitment and activation cytokines. Lancet 349: 490–495. doi: 10.1016/S0140-6736(96)07524-1. PubMed: 9040590. [DOI] [PubMed] [Google Scholar]
- 32. Okada H, Murakami S (1998) Cytokine expression in periodontal health and disease. Crit Rev Oral Biol Med 9: 248–266. doi: 10.1177/10454411980090030101. PubMed: 9715365. [DOI] [PubMed] [Google Scholar]
- 33. Grossi SG, Zambon JJ, Ho AW, Koch G, Dunford RG et al. (1994) Assessment of risk for periodontal disease. I. Risk indicators for attachment loss. J Periodontol 65: 260–267. doi: 10.1902/jop.1994.65.3.260. PubMed: 8164120. [DOI] [PubMed] [Google Scholar]
- 34. Grossi SG, Genco RJ, Machtei EE, Ho AW, Koch G et al. (1995) Assessment of risk for periodontal disease. II. Risk indicators for alveolar bone loss. J Periodontol 66: 23–29. doi: 10.1902/jop.1995.66.1.23. PubMed: 7891246. [DOI] [PubMed] [Google Scholar]
- 35. Nelson RG, Shlossman M, Budding LM, Pettitt DJ, Saad MF et al. (1990) Periodontal disease and NIDDM in Pima Indians. Diabetes Care 13: 836–840. PubMed: 2209317. [DOI] [PubMed] [Google Scholar]
- 36. Taylor GW (2001) Bidirectional interrelationships between diabetes and periodontal diseases: an epidemiologic perspective. Ann Periodontol 6: 99–112. doi: 10.1902/annals.2001.6.1.99. PubMed: 11887478. [DOI] [PubMed] [Google Scholar]
- 37. Tsai C, Hayes C, Taylor GW (2002) Glycemic control of type 2 diabetes and severe periodontal disease in the US adult population. Community Dent Oral Epidemiol 30: 182–192. doi: 10.1034/j.1600-0528.2002.300304.x. PubMed: 12000341. [DOI] [PubMed] [Google Scholar]
- 38. Lalla E, Papapanou PN (2011) Diabetes mellitus and periodontitis: a tale of two common interrelated diseases. Nat Rev Endocrinol 7: 738–748. doi: 10.1038/nrendo.2011.106. PubMed: 21709707. [DOI] [PubMed] [Google Scholar]
- 39. Mealey BL (2006) Periodontal disease and diabetes. A two-way street. J Am Dent Assoc 137: 26S–31S. PubMed: 17012733. [DOI] [PubMed] [Google Scholar]
- 40. Voisine P, Ruel M, Khan TA, Bianchi C, Xu SH, et al. (2004) Differences in gene expression profiles of diabetic and nondiabetic patients undergoing cardiopulmonary bypass and cardioplegic arrest. Circulation 14(11 Suppl 1);110: II280-286 [DOI] [PubMed] [Google Scholar]
- 41. Kawashima M, Shoji J, Kamura Y, Sato Y (2005) Role of chemokines in the vitreous of proliferative diabetic retinopathy. Nihon Ganka Gakkai Zasshi 109(9): 596-602. PubMed: 16218438. [PubMed] [Google Scholar]
- 42. Kyiak IuH, Fartushok NV, Onyshchuk IuI, Fedevych IuM, Bashta HV (2012) Profile of proinflammatory cytokines in type 1 diabetes mellitus. Fiziol Zh 58(5): 65-69. PubMed: 23233948. [PubMed] [Google Scholar]
- 43. Tuller T, Atar S, Ruppin E, Gurevich M, Achiron A (2013) Common and specific signatures of gene expression and protein-protein interactions in autoimmune diseases. Genes Immun 14(2): 67-82. doi: 10.1038/gene.2012.55. PubMed: 23190644. [DOI] [PubMed] [Google Scholar]
- 44. Ahluwalia TS, Khullar M, Ahuja M, Kohli HS, Bhansali A et al. (2009) Common variants of inflammatory cytokine genes are associated with risk of nephropathy in type 2 diabetes among Asian Indians. PLOS ONE 4(4): e5168. doi: 10.1371/journal.pone.0005168. PubMed: 19357773. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 45. Kornman KS (2005) Diagnostic and prognostic tests for oral diseases: practical applications. J Dent Educ 69: 498–508. PubMed: 15897332. [PubMed] [Google Scholar]
- 46. Genco RJ (1996) Current view of risk factors for periodontal diseases. J Periodontol 67: 1041–1049. doi: 10.1902/jop.1996.67.10s.1041. PubMed: 8910821. [DOI] [PubMed] [Google Scholar]
- 47. Bergström J (2004) Tobacco smoking and chronic destructive periodontal disease. Odontology 92: 1–8. doi: 10.1007/s10266-004-0043-4. PubMed: 15490298. [DOI] [PubMed] [Google Scholar]
- 48. Salvi GE, Lawrence HP, Offenbacher S, Beck JD (1997) Influence of risk factors on the pathogenesis of periodontitis. Periodontol 2000 14: 173-201. doi: 10.1111/j.1600-0757.1997.tb00197.x. PubMed: 9567971. [DOI] [PubMed] [Google Scholar]
- 49. Kornman KS, Crane A, Wang HY, di Giovine FS, Newman MG et al. (1997) The interleukin-1 genotype as a severity factor in adult periodontal disease. J Clin Periodontol 24: 72–77. doi: 10.1111/j.1600-051X.1997.tb01187.x. PubMed: 9049801. [DOI] [PubMed] [Google Scholar]
- 50. Dan H, Liu W, Zhou Y, Wang J, Chen Q et al. (2010) Association of Interleukin-8 gene polymorphisms and haplotypes with oral lichen planus in a Chinese population. Inflammation 33: 76–81. doi: 10.1007/s10753-009-9160-0. PubMed: 19842025. [DOI] [PubMed] [Google Scholar]
- 51. McCarron SL, Edwards S, Evans PR, Gibbs R, Dearnaley DP et al. (2002) Influence of cytokine gene polymorphisms on the development of prostate cancer. Cancer Res 62: 3369-3372. PubMed: 12067976. [PubMed] [Google Scholar]
- 52. Garza-Gonzalez E, Bosques-Padilla FJ, Mendoza-Ibarra SI, Flores-Gutierrez JP, Maldonado-Garza HJ et al. (2007) Assessment of the toll-like receptor 4Asp299Gly, Thr399Ile and interleukin-8 -251 polymorphisms in the risk for the development of distal gastric cancer. BMC Cancer 7: 70. doi: 10.1186/1471-2407-7-70. PubMed: 17462092. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 53. Kamali-Sarvestani E, Aliparasti MR, Atefi S (2007) Association of interleukin-8 (IL-8 or CXCL8) -251T/A and CXCR2 +1208C/T gene polymorphisms with breast cancer. Neoplasma 54: 484-489. PubMed: 17949231. [PubMed] [Google Scholar]
- 54. Vairaktaris E, Yapijakis C, Serefoglou Z, Derka S, Vassiliou S et al. (2007) The interleukin-8 (-251A/T) polymorphism is associated with increased risk for oral squamous cell carcinoma. Eur J Surg Oncol 33: 504-507. doi: 10.1016/j.ejso.2006.11.002. PubMed: 17174061. [DOI] [PubMed] [Google Scholar]
- 55. Goverdhan V, Ennis S, Hannan SR, Madhusudhana KC, Cree AJ et al. (2008) Interleukin-8 promoter polymorphism -251A/T is a risk factor for age-related macular degeneration. Br J Ophthalmol 92: 537-540. doi: 10.1136/bjo.2007.123190. PubMed: 18310311. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 56. Kim YJ, Viana AC, Curtis KM, Orrico SR, Cirelli JA et al. (2009) Lack of association of a functional polymorphism in the interleukin 8 gene with susceptibility to periodontitis. DNA Cell Biol 28: 185–190. doi: 10.1089/dna.2008.0816. PubMed: 19364277. [DOI] [PubMed] [Google Scholar]
- 57. Andia DC, de Oliveira NF, Letra AM, Nociti FH Jr, Line SR et al. (2011) Interleukin-8 gene promoter polymorphism (rs4073) may contribute to chronic periodontitis. J Periodontol 82: 893-899. doi: 10.1902/jop.2010.100513. PubMed: 21091348. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58. Ioannidis JP, Ntzani EE, Trikalinos TA, Contopoulos-Ioannidis DG (2001) Replication validity of genetic association studies. Nat Genet 29: 306–309. doi: 10.1038/ng749. PubMed: 11600885. [DOI] [PubMed] [Google Scholar]
- 59. Papapanou PN, Neiderud AM, Sandros J, Dahlén G (2001) Interleukin-1 gene polymorphism and periodontal status: a case-control study. J Clin Periodontol 28: 389-396. doi: 10.1034/j.1600-051x.2001.028005389.x. PubMed: 11350500. [DOI] [PubMed] [Google Scholar]
- 60. Soga Y, Nishimura F, Ohyama H, Maeda H, Takashiba S et al. (2003) Tumor necrosis factor-alpha gene (TNF-alpha) -1031/-863, -857 single-nucleotide polymorphisms (SNPs) are associated with severe adult periodontitis in Japanese. J Clin Periodontol 30: 524-531. doi: 10.1034/j.1600-051X.2003.00287.x. PubMed: 12795791. [DOI] [PubMed] [Google Scholar]
- 61. Moreira PR, De Sá AR, Xavier GM, Costa JE, Gomez RS et al. (2005) A functional interleukin-1 beta gene polymorphism is associated with chronic periodontitis in a sample of Brazilian individuals. J Periodontal Res 40: 306-311. doi: 10.1111/j.1600-0765.2005.00801.x. PubMed: 15966908. [DOI] [PubMed] [Google Scholar]
- 62. Novaretti MCZ, Dorlhiac-Llacer PE, Chamone DAF (2000) Estudo de grupos sangüíneos em doadores de sangue caucasóides e negróides na cidade de São Paulo. Rev Bras Hematol Hemoter 22: 23-32. [Google Scholar]
- 63. Guzman S, Karima M, Wang HY, Van Dyke TE (2003) Association between interleukin-1 genotype and periodontal disease in a diabetic population. J Periodontol 74: 1183-1190. doi: 10.1902/jop.2003.74.8.1183. PubMed: 14514232. [DOI] [PubMed] [Google Scholar]
- 64. Gonzales JR, Kobayashi T, Michel J, Mann M, Yoshie H et al. (2004) Interleukin-4 gene polymorphisms in Japanese and Caucasian patients with aggressive periodontitis. J Clin Periodontol 31: 384-389. doi: 10.1111/j.1600-051X.2004.00492.x. PubMed: 15086621. [DOI] [PubMed] [Google Scholar]
- 65. Hansell CA, Hurson CE, Nibbs RJ (2011) DARC and D6: silent partners in chemokine regulation? Immunol Cell Biol 89(2): 197-206. doi: 10.1038/icb.2010.147. PubMed: 21151196. [DOI] [PMC free article] [PubMed] [Google Scholar]