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1.
Clin Oral Investig ; 21(2): 665-674, 2017 Mar.
Article in English | MEDLINE | ID: mdl-27558382

ABSTRACT

OBJECTIVES: The aim of this study was to evaluate the quality of prediction for stable results after nonsurgical periodontal therapy by several microbiological variables of the subgingival biofilm and biomarkers of gingival crevicular fluid or oral lavage. MATERIAL AND METHODS: Forty-six individuals with moderate or severe chronic periodontitis receiving nonsurgical periodontal therapy were monitored for clinical variables, selected microorganisms, and biomarkers at baseline and 3 and 6 months thereafter. Logistic regression analysis and general linear model (GLM) were applied for analysis of variance and covariance. RESULTS: At 6 months, 20 patients showed a high response (HR) to treatment (at least 60 % of reduction of numbers of sites with PD >4 mm), whereas 26 did not (low response, LR). All clinical variables were significantly improved at 3 and 6 months within each group (p < 0.001, each compared with baseline). Modeling the impact of Porphyromonas gingivalis, Treponema denticola, and median of MMP-8 on to the response to treatment as continuous variables by GLM showed a significant influence of these variables (p = 0.045) with the strongest influence of P. gingivalis (p = 0.012) followed by T. denticola (p = 0.045) and no association with MMP-8 (p = 0.982). Samples tested positively for P. gingivalis decreased only in HR (3 months: p = 0.003; 6 months: p = 0.002). Calprotectin levels in GCF were lower in the HR group compared with the LR group at 3 months (p = 0.008) and at 6 months (p = 0.018). CONCLUSION: Persistence of P. gingivalis combined with a high GCF level of calprotectin may have a negative predictive value on response to periodontal therapy. CLINICAL RELEVANCE: Microbiological diagnostics for P. gingivalis before and 3 months after SRP may have a predictive value on response to periodontal therapy. The combination with MMP-8 in oral lavage or preferably calprotectin in GCF might give additional information.


Subject(s)
Gingival Crevicular Fluid/microbiology , Periodontitis/microbiology , Periodontitis/therapy , Porphyromonas gingivalis/isolation & purification , Adult , Aged , Biofilms , Biomarkers/analysis , Female , Humans , Male , Middle Aged
2.
J Periodontol ; 82(7): 1051-60, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21235330

ABSTRACT

BACKGROUND: The analysis of samplings from periodontal pockets is important in the diagnosis and therapy of periodontitis. In this study, three different sampling techniques were compared to determine whether one method yielded samples suitable for the reproducible and simultaneous determination of bacterial load, cytokines, neutrophil elastase, and arginine-specific gingipains (Rgps). Rgps are an important virulence factor of Porphyromonas gingivalis, the exact concentration of which in gingival crevicular fluid (GCF) has not been quantified. METHODS: GCF was sampled from four sites per patient (one sample per quadrant using two samples per method) in 36 patients with chronic periodontitis. One week later, the procedure was repeated with alternative methods. Variables determined were loads of Aggregatibacter actinomycetemcomitans (previously Actinobacillus actinomycetemcomitans) and P. gingivalis, levels of interleukin-6 and -8, activity of neutrophil elastase, and level of Rgps. RESULTS: The detected cytokine levels were higher using paper strips compared to paper points. Bacteria were found in similar loads from paper strips and paper points. Rgps were only detectable in high quantities by washing the periodontal pocket. The level of Rgps correlated with the load of P. gingivalis. CONCLUSIONS: The use of paper strips was suitable for the simultaneous determination of microbial and immunologic parameters. Obtaining GCF by washing can be useful for special purposes. The gingipain concentration in periodontal pockets was directly determined to be ≤1.5 µM. This value indicated that most of the substrates of these proteases by in vitro assays identified until now can be easily degraded in P. gingivalis-infected sites.


Subject(s)
Chronic Periodontitis/metabolism , Gingival Crevicular Fluid/chemistry , Specimen Handling/methods , Adhesins, Bacterial/analysis , Adult , Aggregatibacter actinomycetemcomitans/isolation & purification , Bacterial Load , Cysteine Endopeptidases/analysis , Female , Gingipain Cysteine Endopeptidases , Gingival Hemorrhage/metabolism , Hemagglutinins/analysis , Humans , Interleukin-6/analysis , Interleukin-8/analysis , Leukocyte Elastase/analysis , Male , Middle Aged , Paper , Periodontal Attachment Loss/metabolism , Periodontal Pocket/metabolism , Porphyromonas gingivalis/isolation & purification , Porphyromonas gingivalis/pathogenicity , Specimen Handling/instrumentation , Therapeutic Irrigation/methods , Virulence Factors/analysis
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