Tumor necrosis factor-alpha-308G/A single nucleotide polymorphism and red-complex periodontopathogens are independently associated with increased levels of tumor necrosis factor-alpha in diseased periodontal tissues


Autoria(s): TROMBONE, A. P. F.; CARDOSO, C. R.; REPEKE, C. E.; FERREIRA JR., S. B.; MARTINS JR., W.; CAMPANELLI, A. P.; AVILA-CAMPOS, M. J.; TREVILATTO, P. C.; SILVA, J. S.; GARLET, G. P.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

Resumo

Background and Objective: Inflammatory cytokines such as tumor necrosis factor-alpha are involved in the pathogenesis of periodontal diseases. A high between-subject variation in the level of tumor necrosis factor-alpha mRNA has been verified, which may be a result of genetic polymorphisms and/or the presence of periodontopathogens such as Porphyromonas gingivalis, Tannerella forsythia, Treponema denticola (called the red complex) and Aggregatibacter actinomycetemcomitans. In this study, we investigated the effect of the tumor necrosis factor-alpha (TNFA) -308G/A gene polymorphism and of periodontopathogens on the tumor necrosis factor-alpha levels in the periodontal tissues of nonsmoking patients with chronic periodontitis (n = 127) and in control subjects (n = 177). Material and Methods: The TNFA-308G/A single nucleotide polymorphism was investigated using polymerase chain reaction-restriction fragment length polymorphism analysis, whereas the tumor necrosis factor-alpha levels and the periodontopathogen load were determined using real-time polymerase chain reaction. Results: No statistically significant differences were found in the frequency of the TNFA-308 single nucleotide polymorphism in control and chronic periodontitis groups, in spite of the higher frequency of the A allele in the chronic periodontitis group. The concomitant analyses of genotypes and periodontopathogens demonstrated that TNFA-308 GA/AA genotypes and the red-complex periodontopathogens were independently associated with increased levels of tumor necrosis factor-alpha in periodontal tissues, and no additive effect was seen when both factors were present. P. gingivalis, T. forsythia and T. denticola counts were positively correlated with the level of tumor necrosis factor-alpha. TNFA-308 genotypes were not associated with the periodontopathogen detection odds or with the bacterial load. Conclusion: Our results demonstrate that the TNFA-308 A allele and red-complex periodontopathogens are independently associated with increased levels of tumor necrosis factor-alpha in diseased tissues of nonsmoking chronic periodontitis patients and consequently are potentially involved in determining the disease outcome.

Fundacao de Amparo Pesquisa do Estado de Sao Paulo, FAPESP

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Identificador

JOURNAL OF PERIODONTAL RESEARCH, v.44, n.5, p.598-608, 2009

0022-3484

http://producao.usp.br/handle/BDPI/28443

10.1111/j.1600-0765.2008.01166.x

http://dx.doi.org/10.1111/j.1600-0765.2008.01166.x

Idioma(s)

eng

Publicador

WILEY-BLACKWELL PUBLISHING, INC

Relação

Journal of Periodontal Research

Direitos

restrictedAccess

Copyright WILEY-BLACKWELL PUBLISHING, INC

Palavras-Chave #tumor necrosis factor-alpha #genetic polymorphism #cytokines #periodontal disease #periodontopathogens #Porphyromonas gingivalis #PORPHYROMONAS-GINGIVALIS INFECTION #5TH EUROPEAN WORKSHOP #RHEUMATOID-ARTHRITIS #TNF-ALPHA #ACTINOBACILLUS-ACTINOMYCETEMCOMITANS #PROMOTER POLYMORPHISM #TANNERELLA-FORSYTHIA #TREPONEMA-DENTICOLA #GENE POLYMORPHISMS #BRAZILIAN PATIENTS #Dentistry, Oral Surgery & Medicine
Tipo

article

original article

publishedVersion