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
相关论文
共 22 条
[1]  
Andriankaja OM, 2009, J PERIODONTOL, V80, P307, DOI [10.1902/jop.2009.080385, 10.1902/jop.2009.080385 ]
[2]  
Burrell RC, 2008, J PERIODONTOL, V79, P1712, DOI [10.1902/jop.2008.080013, 10.1902/jop.2008.080013 ]
[3]   Local chemokine paralysis, a novel pathogenic mechanism for Porphyromonas gingivalis [J].
Darveau, RP ;
Belton, CM ;
Reife, RA ;
Lamont, RJ .
INFECTION AND IMMUNITY, 1998, 66 (04) :1660-1665
[4]   GENERAL-CLASS OF COVARIANCE-STRUCTURES FOR 2 OR MORE REPEATED FACTORS IN LONGITUDINAL DATA-ANALYSIS [J].
GALECKI, AT .
COMMUNICATIONS IN STATISTICS-THEORY AND METHODS, 1994, 23 (11) :3105-3119
[5]   CHANGES IN CREVICULAR FLUID LEVELS OF INTERLEUKIN-1-BETA, LEUKOTRIENE-B4, PROSTAGLANDIN-E2, THROMBOXANE-B2 AND TUMOR-NECROSIS-FACTOR-ALPHA IN EXPERIMENTAL GINGIVITIS IN HUMANS [J].
HEASMAN, PA ;
COLLINS, JG ;
OFFENBACHER, S .
JOURNAL OF PERIODONTAL RESEARCH, 1993, 28 (04) :241-247
[6]   Modulation of the expression of matrix metalloproteinase and tissue inhibitors of metalloproteinases by TGF-β1 and IGF-1 in primary human articular and bovine nasal chondrocytes stimulated with TNF-α [J].
Hui, W ;
Rowan, AD ;
Cawston, T .
CYTOKINE, 2001, 16 (01) :31-35
[7]   Chemokines as Mediators of Neovascularization [J].
Keeley, Ellen C. ;
Mehrad, Borna ;
Strieter, Robert M. .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2008, 28 (11) :1928-1936
[8]   Small sample inference for fixed effects from restricted maximum likelihood [J].
Kenward, MG ;
Roger, JH .
BIOMETRICS, 1997, 53 (03) :983-997
[9]  
LAMSTER IB, 1994, J CLIN PERIODONTOL, V21, P118
[10]   An overview of the serpin superfamily [J].
Law, Ruby H. P. ;
Zhang, Qingwei ;
McGowan, Sheena ;
Buckle, Ashley M. ;
Silverman, Gary A. ;
Wong, Wilson ;
Rosado, Carlos J. ;
Langendorf, Chris G. ;
Pike, Rob N. ;
Bird, Philip I. ;
Whisstock, James C. .
GENOME BIOLOGY, 2006, 7 (05)