Changes in gingival crevicular fluid inflammatory mediator levels during the induction and resolution of experimental gingivitis in humans

被引:84
作者
Offenbacher, Steven [1 ]
Barros, Silvana [1 ]
Mendoza, L.
Mauriello, S.
Preisser, J.
Moss, K.
de Jager, Marko [2 ]
Aspiras, Marcelo [2 ]
机构
[1] UNC Ctr Oral & Syst Dis, N Carolina Oral Hlth Inst, UNC Sch Dent, Durham, NC 27709 USA
[2] Philips Oral Healthcare, Snoqualmie, WA USA
关键词
biofilm; crevicular fluid; gingivitis; inflammation; periodontal disease; PERIODONTAL-DISEASE; PROSTAGLANDIN E-2; INTERLEUKIN-1-BETA; EXPRESSION;
D O I
10.1111/j.1600-051X.2010.01543.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
P>Aim The goal of this study is to characterize the changes in 33 biomarkers within the gingival crevicular fluid during the 3-week induction and 4-week resolution of stent-induced, biofilm overgrowth mediated, experimental gingivitis in humans. Methods Experimental gingivitis was induced in 25 subjects for 21 days followed by treatment with a sonic powered toothbrush for 28 days. Clinical indices and gingival crevicular fluids were collected weekly during induction and biweekly during resolution. Samples were analysed using a bead-based multiplexing analysis for the simultaneous measurements of 33 biomarkers within each sample including cytokines, matrix-metalloproteinases (MMPs) and adipokines. Prostaglandin-E-2 was measured by enzyme-linked immunoadsorbant assay. Statistical testing using general linear models with structured covariance matrices were performed to compare stent to contralateral (non-stent) changes in clinical signs and in biomarker levels over time. Results Gingivitis induction was associated with a significant 2.6-fold increase in interleukin 1-beta (IL-beta), a 3.1-fold increase in IL-1 alpha and a significant decrease in multiple chemokines as well as MMPs-1, -3 and 13. All changes in clinical signs and mediators rebounded to baseline in response to treatment in the resolution phase. Conclusions Stent-induced gingivitis is associated with marked, but reversible increases in IL-alpha a and IL-1 beta with suppression of multiple chemokines as well as selected MMPs.
引用
收藏
页码:324 / 333
页数:10
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