Saliva/Pathogen Biomarker Signatures and Periodontal Disease Progression

被引:154
作者
Kinney, J. S. [1 ]
Morelli, T. [1 ]
Braun, T. [2 ]
Ramseier, C. A. [1 ,3 ]
Herr, A. E. [4 ]
Sugai, J. V. [1 ]
Shelburne, C. E. [6 ]
Rayburn, L. A. [1 ]
Singh, A. K. [5 ]
Giannobile, W. V. [1 ,7 ]
机构
[1] Univ Michigan, Sch Dent, Michigan Ctr Oral Hlth Res, Dept Periodont & Oral Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Publ Hlth, Dept Biostat, Ann Arbor, MI 48109 USA
[3] Univ Bern, Sch Dent Med, Dept Periodontol, CH-3012 Bern, Switzerland
[4] Univ Calif Berkeley, Dept Bioengn, Berkeley, CA 94720 USA
[5] Sandia Natl Labs, Biosyst Res Dept, Livermore, CA 94551 USA
[6] Univ Michigan, Sch Dent, Dept Biol & Mat Sci, Ann Arbor, MI 48108 USA
[7] Univ Michigan, Coll Engn, Dept Biomed Engn, Ann Arbor, MI 48109 USA
关键词
periodontal disease; pro-inflammatory biomarkers; saliva; periodontal pathogens; diagnosis; salivary diagnostics; GINGIVAL CREVICULAR FLUID; CLINICAL-PARAMETERS; SALIVARY; PATHOGENS; RISK;
D O I
10.1177/0022034511399908
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
The purpose of this study was to determine the role of saliva-derived biomarkers and periodontal pathogens during periodontal disease progression (PDP). One hundred human participants were recruited into a 12-month investigation. They were seen bi-monthly for saliva and clinical measures and bi-annually for subtraction radiography, serum and plaque biofilm assessments. Saliva and serum were analyzed with protein arrays for 14 proinflammatory and bone turnover markers, while qPCR was used for detection of biofilm. A hierarchical clustering algorithm was used to group study participants based on clinical, microbiological, salivary/serum biomarkers, and PDP. Eighty-three individuals completed the six-month monitoring phase, with 44 exhibiting PDP, while 39 demonstrated stability. Participants assembled into three clusters based on periodontal pathogens, serum and salivary biomarkers. Cluster 1 members displayed high salivary biomarkers and biofilm; 82% of these individuals were undergoing PDP. Cluster 2 members displayed low biofilm and biomarker levels; 78% of these individuals were stable. Cluster 3 members were not discriminated by PDP status; however, cluster stratification followed groups 1 and 2 based on thresholds of salivary biomarkers and biofilm pathogens. The association of cluster membership to PDP was highly significant (p < 0.0002). The use of salivary and biofilm biomarkers offers potential for the identification of PDP or stability (ClinicalTrials.gov number, CT00277745).
引用
收藏
页码:752 / 758
页数:7
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