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1.
J Clin Periodontol ; 34(2): 111-7, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17309585

ABSTRACT

OBJECTIVE: To study whether there is an association between the frequency of functional polymorphisms in the toll-like receptor 4 (TLR4) and cluster differentiation 14 (CD14) genes and periodontitis. METHODOLOGY: Genotyping for the TLR4 single-nucleotide polymorphisms (SNPs) Asp299Gly, Thr399Ile and the CD14 SNPs -159 and -1359 was completed for subjects with periodontal disease compared with control subjects. Two disease populations were investigated: 73 subjects with aggressive periodontitis (AgP; 28 males, 45 females) and 95 males with chronic periodontitis (CP). The TLR4 and CD14 polymorphisms were determined using SNaPshot primer extension with capillary electrophoresis. Comparison of allele and genotype frequencies for each polymorphism was by Fisher's exact test or chi2 analysis. RESULTS: The TLR4 Asp299Gly genotype was present in a significantly (p=0.026) lower proportion of AgP subjects (5.5%) compared with control subjects (16.3%). The unadjusted odds ratio for the Asp299Gly genotype to be associated with AgP was 0.30, 95% confidence interval 0.10-0.91. No differences were found in the prevalence of the TLR4 Asp299Gly genotype in men with CP (18.9%) compared with an age-matched control group with no evidence of periodontitis (17%). In addition, there was no difference in the distribution of the CD14 polymorphisms in either the AgP or CP populations studied compared with controls. CONCLUSION: It is concluded that in West European Caucasians, the Asp299Gly TLR4 gene polymorphism is associated with a decreased risk of AgP but not CP. Promoter polymorphisms of the CD14 gene, however, did not influence susceptibility to inflammatory periodontitis in the population cohorts studied.


Subject(s)
Genetic Predisposition to Disease/genetics , Lipopolysaccharide Receptors/genetics , Periodontitis/genetics , Toll-Like Receptor 4/genetics , Adult , Aged , Case-Control Studies , Chi-Square Distribution , Chronic Disease , Cluster Analysis , Comorbidity , Female , Humans , Male , Periodontitis/epidemiology , Polymorphism, Single Nucleotide , Severity of Illness Index , Smoking/epidemiology , United Kingdom/epidemiology
2.
J Clin Periodontol ; 33(11): 771-8, 2006 Nov.
Article in English | MEDLINE | ID: mdl-16965524

ABSTRACT

AIM: Levels of interleukin-1alpha (IL-1alpha) are elevated in periodontal inflammation. IL-1A gene polymorphisms are associated with inflammatory diseases. This study aimed to investigate IL-1A gene polymorphism in Cyclosporin A (CsA)-treated renal transplant patients and investigate the association between this polymorphism and gingival crevicular fluid (GCF) levels of several cytokines. MATERIALS AND METHODS: Fifty-one renal transplant patients on CsA treatment (25 with and 26 without gingival overgrowth) and 29 healthy controls were recruited for the study. Demographic, pharmacological and periodontal parameters were recorded and gingival overgrowth was assessed. RESULTS: Multiple regression analysis showed that genotype was significantly associated with gingival overgrowth (p=0.02). Carriage of the IL-1A (-889) T allele was strongly protective [95% confidence interval (CI): 0.046-0.77], although not significantly associated with IL-1alpha protein levels in GCF. IL-1alpha, IL-1beta and IL-8, but not IL-6, were detected in GCF of CsA-treated patients, but none of them was significantly associated with gingival overgrowth. CONCLUSIONS: This study is the first to associate a gene polymorphism as a risk factor for CsA-induced gingival overgrowth in renal transplant patients, demonstrating that IL-1A polymorphism might alter individual susceptibility to CsA. However, there was no association between GCF cytokine levels and the presence of gingival overgrowth or patient IL-1A genotype.


Subject(s)
Cyclosporine/adverse effects , Gingival Hyperplasia/chemically induced , Immunosuppressive Agents/adverse effects , Interleukin-1alpha/genetics , Kidney Transplantation , Polymorphism, Genetic/genetics , Adult , Age Factors , Alleles , Cytosine , Female , Genetic Predisposition to Disease , Genotype , Gingival Crevicular Fluid/chemistry , Gingival Hyperplasia/genetics , Humans , Interleukin-1alpha/analysis , Interleukin-1beta/analysis , Interleukin-6/analysis , Interleukin-8/analysis , Male , Risk Factors , Thymine
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