期刊
JOURNAL OF INVESTIGATIVE AND CLINICAL DENTISTRY
卷 7, 期 4, 页码 401-409出版社
WILEY
DOI: 10.1111/jicd.12176
关键词
cytokine; dental implant; periodontal pathogen; smoking; tobacco
Aim: The aim of the present study was to investigate how heavy smoking influences the clinical, microbiological, and host-response characteristics in peri-implant sulcus fluid of patients with healthy dental implants. Methods: A total of 29 individuals with 74 dental implants were included in the present study; 20 implants were in heavy smokers and 54 were in nonsmokers. The modified gingival index, modified plaque index, and probing pocket depth were evaluated. Periodontopathogenic bacteria Tannerella forsythia, Treponema denticola, and Porphyromonas gingivalis were evaluated, together with the total bacterial load. Peri-implant sulcus fluid samples were analyzed for the quantification of interleukin-8, interleukin-1 beta, interleukin-6, interleukin-10, and tumor necrosis factor-alpha. Results: No significant differences in the clinical parameters evaluated were found between the groups, although smokers had poorer peri-implant parameters. Among the smokers, subgingival microbiota was composed of a greater number of periodontal pathogens; these differences were not statistically significant. Smokers showed a greater expression of interleukin-1 beta, interleukin-6, interleukin-10, and tumor necrosis factor-alpha, but interleukin-8 was slightly higher among non-smokers, but not significantly. Conclusions: Although smokers presented deeper probing depths, bleeding on probing, and peri-implant microbiota composed of a greater number of periodontal pathogens than in non-smoking patients, these data did not show significant differences. In the present study, and in relation to the samples analyzed, smoking alone did not influence the immunological and microbiological parameters in dental implants with healthy peri-implant tissues. Further studies with larger samples are required to better evaluate the influence of smoking on dental implants.
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