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1.
J Periodontol ; 80(2): 234-43, 2009 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-19186963

RESUMO

BACKGROUND: The objectives of this study were to clinically and immunologically assess the effects of mechanical anti-infective therapies for mucositis and peri-implantitis and to compare the levels of cytokines in untreated and treated peri-implant diseased sites to healthy ones. METHODS: Titanium dental implants were assigned to one of the following groups: healthy (n = 10) = control; mucositis (n = 10) = mechanical debridement using abrasive sodium carbonate air-powder and resin curets; and peri-implantitis (n = 20) = open surgical debridement using abrasive sodium carbonate air-powder and resin curets. Visible plaque accumulation, marginal bleeding, bleeding on probing, suppuration, and probing depth were assessed at baseline for all groups and at 3 months after therapies for diseased groups. At these times, the total amounts of interleukin (IL)-4, -10, and -12, tumor necrosis factor-alpha (TNF-alpha), receptor activator of nuclear factor-kappa B ligand (RANKL), and osteoprotegerin (OPG) in the peri-implant crevicular fluid (PICF) were measured by enzyme-linked immunosorbent assay. RESULTS: At 3 months, the anti-infective treatments resulted in a significant improvement in all clinical parameters for mucositis and peri-implantitis (P <0.05). Moreover, the total amounts of TNF-alpha in PICF were significantly higher in untreated diseased implants compared to healthy ones, and the OPG/RANKL ratio was higher for healthy implants than for untreated peri-implantitis (P <0.05). TNF-alpha levels were significantly reduced for both diseased groups (P <0.05), achieving the same level as the healthy group at 3 months after therapies (P >0.05). CONCLUSION: The proposed anti-infective therapies may locally modulate the levels of TNF-alpha and the OPG/RANKL ratio and improve clinical parameters around peri-implant tissues.


Assuntos
Citocinas/análise , Implantes Dentários/efeitos adversos , Líquido do Sulco Gengival/química , Periodontite/imunologia , Periodontite/terapia , Estomatite/imunologia , Estomatite/terapia , Adulto , Idoso , Anti-Infecciosos Locais/uso terapêutico , Estudos de Casos e Controles , Clorexidina/uso terapêutico , Implantação Dentária Endóssea/efeitos adversos , Índice de Placa Dentária , Raspagem Dentária , Feminino , Humanos , Interleucinas/análise , Masculino , Pessoa de Meia-Idade , Antissépticos Bucais/uso terapêutico , Mucosite/etiologia , Mucosite/imunologia , Mucosite/terapia , Osteoprotegerina/análise , Índice Periodontal , Periodontite/etiologia , Ligante RANK/análise , Estomatite/etiologia , Fator de Necrose Tumoral alfa/análise
2.
Clin Oral Implants Res ; 20(5): 514-20, 2009 May.
Artigo em Inglês | MEDLINE | ID: mdl-19302394

RESUMO

OBJECTIVE: This study assessed gene expression by quantitative polymerase chain reaction of inflammatory- [interleukin (IL)-12, tumor necrosis factor-alpha (TNF-alpha), IL-4, and IL-10] and osteoclastogenesis-related factors [receptor activator of NF-kappaB ligand (RANKL) and osteoprotegerin (OPG)] in sites exhibiting different severities of peri-implant disease. MATERIAL AND METHODS: Peri-implant soft tissue biopsies (n=48) were harvested from healthy implant (HI), mucositis (MC), initial peri-implantitis (IP) and severe peri-implantitis (SP) sites. RESULTS: IL-12 and TNF-alpha mRNA levels were higher in SP, followed by IP and MC (P <0.05). IL-4 was higher in HI, followed by MC, SP and IP (P <0.05). IL-10 was the lowest in HI, while no differences were detected among the diseased groups (P>0.05). OPG mRNA levels were higher in HI, followed by IP, SP and MC, whereas RANKL was increased as the peri-implantitis severity increased (P<0.05). The highest OPG/RANKL ratio was observed in HI and the lowest in SP (P<0.01). CONCLUSION: These findings suggest that expressions of inflammatory- and osteoclastogenesis-related factors may play an important role in the onset and severity of the peri-implant diseases.


Assuntos
Citocinas/metabolismo , Implantes Dentários/efeitos adversos , Mucosite/metabolismo , Osteoclastos/imunologia , Periodontite/metabolismo , Adulto , Análise de Variância , Diferenciação Celular/imunologia , Citocinas/imunologia , Feminino , Regulação da Expressão Gênica/imunologia , Regulação da Expressão Gênica/fisiologia , Humanos , Interleucina-10/genética , Interleucina-10/metabolismo , Interleucina-12/genética , Interleucina-12/metabolismo , Interleucina-4/genética , Interleucina-4/metabolismo , Arcada Edêntula/imunologia , Arcada Edêntula/reabilitação , Masculino , Pessoa de Meia-Idade , Mucosite/etiologia , Mucosite/imunologia , Osteoclastos/metabolismo , Osteoprotegerina/genética , Osteoprotegerina/metabolismo , Periodontite/etiologia , Periodontite/imunologia , Ligante RANK/genética , Ligante RANK/metabolismo , RNA Mensageiro/análise , Valores de Referência , Índice de Gravidade de Doença , Fator de Necrose Tumoral alfa/genética , Fator de Necrose Tumoral alfa/metabolismo
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