Ability of matrix metalloproteinase-8 biosensor, IFMA, and ELISA immunoassays to differentiate between periodontal health, gingivitis, and periodontitis

被引:17
|
作者
Umeizudike, Kehinde Adesola [1 ,2 ]
Lahteenmaki, Hanna [2 ]
Raisanen, Ismo T. [2 ]
Taylor, John J. [3 ,4 ]
Preshaw, Philip M. [5 ]
Bissett, Susan M. [3 ,4 ]
Tervahartiala, Taina [2 ]
Nwhator, Solomon [6 ]
Parnanen, Pirjo [2 ]
Sorsa, Timo [2 ,7 ]
机构
[1] Univ Lagos, Fac Dent Sci, Dept Prevent Dent, Coll Med, PMB 12003, Lagos, Nigeria
[2] Univ Helsinki, Helsinki Univ Hosp, Dept Oral & Maxillofacial Dis, Helsinki, Finland
[3] Newcastle Univ, Sch Dent Sci & Translat, Newcastle Upon Tyne, Tyne & Wear, England
[4] Newcastle Univ, Clin Res Inst, Newcastle Upon Tyne, Tyne & Wear, England
[5] Univ Dundee, Sch Dent, Dundee, Scotland
[6] Obafemi Awolowo Univ, Dept Prevent & Community Dent, Coll Hlth Sci, Fac Dent, Ife, Nigeria
[7] Karolinska Inst, Div Periodontol, Dept Dent Med, Stockholm, Sweden
关键词
active; total matrix metalloproteinase-8; saliva; biosensor; periodontal disease; NEUTROPHIL COLLAGENASE ACTIVITY; CREVICULAR FLUID; INTERSTITIAL COLLAGENASES; ADULT PERIODONTITIS; TISSUE DESTRUCTION; GLOBAL BURDEN; MMP-8; CLASSIFICATION; MOUTHRINSE; DIAGNOSIS;
D O I
10.1111/jre.12985
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective: The aim of this study was to determine the diagnostic utility of an MMP-8 biosensor assay in differentiating periodontal health from gingivitis and periodontitis and compare it with an established time-resolved immunofluorescence assay (IFMA) and enzyme-linked immunosorbent assay (ELISA). Background: Currently available antibody-based assays display a wide variability in their ability to accurately measure matrix metalloproteinase-8 (MMP-8) levels in saliva. Methods: Salivary MMP-8 levels were analyzed in 189 systemically healthy participants using an antibody-based biosensor prototype that operates using a surface acoustic wave technology and compared with IFMA and ELISA antibody assays. Participants were categorized into 3 groups: periodontal health (59), gingivitis (63), and periodontitis (67). A sub-population of participants (n = 20) with periodontitis received periodontal treatment and were monitored for 6 months. Results: All the assays demonstrated significantly higher salivary MMP-8 concentrations in participants with periodontitis versus gingivitis, periodontitis versus health, and gingivitis versus health (all p < .05). The biosensor data demonstrated significant correlations with IFMA (r = .354, p < .001) and ELISA (r = .681, p < .001). Significant reductions in salivary MMP-8 concentrations were detected by the biosensor (p = .030) and IFMA (p = .002) in participants with periodontitis 6 months after non-surgical periodontal treatment. IFMA had the best sensitivity (89.2%) for detecting periodontitis and gingivitis versus health and 96.6% for detecting periodontitis versus health and gingivitis. The biosensor had an AUC value of 0.81 and diagnostic accuracy of 74.2% for differentiating periodontitis and gingivitis from health; an AUC value of 0.86 and diagnostic accuracy of 82.8% for periodontitis versus health and gingivitis. Conclusions: The biosensor, IFMA, and ELISA assays differentiated between periodontal health, gingivitis, and periodontitis based on salivary MMP-8 levels. Only the biosensor and, particularly, IFMA identified an effect of periodontal treatment in the participants with periodontitis. Our findings support the potential utility of salivary oral fluid aMMP-8-based point-of-care technology in the future of periodontal diagnostics.
引用
收藏
页码:558 / 567
页数:10
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