Literature DB >> 8832482

Correlation between gingivain/gingipain and bacterial dipeptidyl peptidase activity in gingival crevicular fluid and periodontal attachment loss in chronic periodontitis patients. A 2-year longitudinal study.

B M Eley1, S W Cox.   

Abstract

The aim of this study is to determine whether either gingival crevicular fluid (GCF) bacterial gingivain/gingipain or dipeptidyl peptidase (DPP) levels, total activity (TA) and concentration (EC), predict progressive attachment loss (AL) in 75 patients with moderate periodontitis. GCF was collected from 16 molar and premolar mesiobuccal sites and then clinical attachment level (CAL) and probing depth (PD) were measured with an electronic constant pressure probe. Lastly, gingival, gingival bleeding, and plaque indices were scored. Prior to the baseline visit, patients were given basic periodontal treatment after which the above procedures were repeated. In addition, carefully localized radiographs were taken of the test teeth and repeated annually. Patients were then seen every 3 months for 2 years and the clinical measurements repeated at each visit. In 48 patients, 124 AL sites, 91 rapid AL (RAL), and 33 gradual AL (GAL) were detected. Gingivain/gingipain and bacterial DPP levels (TA and EC) at RAL sites were significantly higher (P < or = 0.0001) than at paired control sites at the attachment loss time (ALT) and prediction time (PT). Mean levels over the study period of both proteases (TA and EC) at GAL sites were significantly higher (P < or = 0.0001) than those at paired control sites. The GCF levels of gingivain/gingipain were always higher than those of DPP. Critical values (CV) of 5 microU/30 seconds (TA) and 30 microU/microL (EC) for both proteases showed high sensitivity and specificity values for TA and EC, which were the same at both ALT and PT. The positive predictive values were higher for gingivain/ gingipain. Mean site levels, over the course of the study, of both proteases (TA and EC) were significantly higher (P < or = 0.0001) at AL, RAL, and GAL sites than non-attachment loss (NAL) sites in AL patients and mean patient levels were significantly higher (P < or = 0.0001) in AL, RAL, and GAL patients than NAL patients. These results indicate that both of these bacterial proteases in GCF may be predictors of periodontal attachment loss.

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Year:  1996        PMID: 8832482     DOI: 10.1902/jop.1996.67.7.703

Source DB:  PubMed          Journal:  J Periodontol        ISSN: 0022-3492            Impact factor:   6.993


  9 in total

1.  Functional implication of the hydrolysis of platelet endothelial cell adhesion molecule 1 (CD31) by gingipains of Porphyromonas gingivalis for the pathology of periodontal disease.

Authors:  Peter L W Yun; Arthur A Decarlo; Cheryl C Chapple; Neil Hunter
Journal:  Infect Immun       Date:  2005-03       Impact factor: 3.441

2.  Gingipains from Porphyromonas gingivalis W83 synergistically disrupt endothelial cell adhesion and can induce caspase-independent apoptosis.

Authors:  Shaun M Sheets; Jan Potempa; James Travis; Hansel M Fletcher; Carlos A Casiano
Journal:  Infect Immun       Date:  2006-10       Impact factor: 3.441

3.  Blockade of protease-activated receptors on T cells correlates with altered proteolysis of CD27 by gingipains of Porphyromonas gingivalis.

Authors:  L W P Yun; A A Decarlo; N Hunter
Journal:  Clin Exp Immunol       Date:  2007-11       Impact factor: 4.330

4.  Comparison of gingival crevicular fluid sampling methods in patients with severe chronic periodontitis.

Authors:  Arndt Guentsch; Martin Kramesberger; Aneta Sroka; Wolfgang Pfister; Jan Potempa; Sigrun Eick
Journal:  J Periodontol       Date:  2011-01-14       Impact factor: 6.993

5.  Porphyrin-mediated binding to hemoglobin by the HA2 domain of cysteine proteinases (gingipains) and hemagglutinins from the periodontal pathogen Porphyromonas gingivalis.

Authors:  A A DeCarlo; M Paramaesvaran; P L Yun; C Collyer; N Hunter
Journal:  J Bacteriol       Date:  1999-06       Impact factor: 3.490

6.  Gingipains from Porphyromonas gingivalis W83 induce cell adhesion molecule cleavage and apoptosis in endothelial cells.

Authors:  Shaun M Sheets; Jan Potempa; James Travis; Carlos A Casiano; Hansel M Fletcher
Journal:  Infect Immun       Date:  2005-03       Impact factor: 3.441

7.  Saliva/pathogen biomarker signatures and periodontal disease progression.

Authors:  J S Kinney; T Morelli; T Braun; C A Ramseier; A E Herr; J V Sugai; C E Shelburne; L A Rayburn; A K Singh; W V Giannobile
Journal:  J Dent Res       Date:  2011-03-15       Impact factor: 6.116

8.  Purification, characterization, and sequence analysis of a potential virulence factor from Porphyromonas gingivalis, peptidylarginine deiminase.

Authors:  W T McGraw; J Potempa; D Farley; J Travis
Journal:  Infect Immun       Date:  1999-07       Impact factor: 3.441

9.  Periodontal disease and spontaneous preterm birth: a case control study.

Authors:  Stephen Wood; Albert Frydman; Stephen Cox; Rollin Brant; Sheilia Needoba; Barry Eley; Reg Sauve
Journal:  BMC Pregnancy Childbirth       Date:  2006-07-19       Impact factor: 3.007

  9 in total

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