An interleukin-1 beta (IL-1 beta) single-nucleotide polymorphism at position 3954 and red complex periodontopathogens independently and additively modulate the levels of IL-1 beta in diseased periodontal tissues
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
20/10/2012
20/10/2012
2008
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Resumo |
Inflammatory cytokines such as interieukin-1 beta (IL-1 beta) are involved in the pathogenesis of periodontal diseases. A high individual variation in the levels of IL-10 mRNA has been verified, which is possibly determined by genetic polymorphisms and/or by the presence of periodontopathogens such as Porphyromonas gingivalis, Tannerella forsythia, Treponema denticola, and Aggregatibacter actinomycetemcomitans. In this study, we investigated the role of an IL-10 promoter single-nucleotide polymorphism at position 3954 [IL-1 beta(3954) SNP] and the presence of the periodontopathogens in the determination of the IL-1 beta levels in the periodontal tissues of nonsmoking chronic periodontitis (CP) patients (n = 117) and control (C) subjects in = 175) and the possible correlations with the clinical parameters of the disease. IL-1 beta(3954) SNP was investigated by restriction fragment length polymorphism, while the IL-1 beta levels and the presence of the periodontopathogens were determined by real-time PCR. Similar frequencies of IL-1 beta(3954) SNP were found in the C and CP groups, in spite of a trend toward a higher incidence of T alleles in the CP group. The IL-1 beta (3954) SNP CT and TT genotypes, as well as P. gingivalis, T. forsythia, and T. denticola, were associated with higher IL-1 beta levels and with higher values of the clinical parameters of disease severity. Concomitant analyses demonstrate that IL-1 beta(3954) and the red complex periodontopathogens were found to independently and additively modulate the levels of IL-1 beta in periodontal tissues. Similarly, the concurrent presence of both factors was associated with increased scores of disease severity. IL-1 beta(3954) genotypes and red complex periodontopathogens, individually and additively, modulate the levels of IL-1 beta in the diseased tissues of nonsmoking CP patients and, consequently, are potentially involved in the determination of the disease outcome. Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) Fundacao de Amparo a Pesquisa do Estado de Sao Paulo-FAPESP Conselho Nacional de Desenvolvimento Cientffico e Tecnologico-CNPq Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) |
Identificador |
INFECTION AND IMMUNITY, v.76, n.8, p.3725-3734, 2008 0019-9567 http://producao.usp.br/handle/BDPI/28361 10.1128/IAI.00546-08 |
Idioma(s) |
eng |
Publicador |
AMER SOC MICROBIOLOGY |
Relação |
Infection and Immunity |
Direitos |
restrictedAccess Copyright AMER SOC MICROBIOLOGY |
Palavras-Chave | #TUMOR-NECROSIS-FACTOR #GENE-CLUSTER POLYMORPHISMS #5TH EUROPEAN WORKSHOP #PORPHYROMONAS-GINGIVALIS #TANNERELLA-FORSYTHIA #TREPONEMA-DENTICOLA #AGGREGATIBACTER-ACTINOMYCETEMCOMITANS #BIOFILM FORMATION #CONSENSUS REPORT #FACTOR-ALPHA #Immunology #Infectious Diseases |
Tipo |
article original article publishedVersion |