Please use this identifier to cite or link to this item: http://repositorio.unitau.br/jspui/handle/20.500.11874/2133
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dc.contributor.authorPereira, Alexandre Lustosapt_BR
dc.contributor.authorCortelli, Sheila Cavalcapt_BR
dc.contributor.authorAquino, Davi Romeropt_BR
dc.contributor.authorFranco, Gilson Cesar Nobrept_BR
dc.contributor.authorMüller, Karina Cogopt_BR
dc.contributor.authorRodrigues, Edsonpt_BR
dc.contributor.authorCosta, Fernando de Oliveirapt_BR
dc.contributor.authorHolzhausen, Marlenept_BR
dc.contributor.authorCortelli, José Robertopt_BR
dc.date.accessioned2019-09-12T16:32:54Z-
dc.date.available2019-09-12T16:32:54Z-
dc.date.issued2012-
dc.citation.volume43pt_BR
dc.citation.issue9pt_BR
dc.citation.spage777-
dc.citation.epage787-
dc.identifier.issn336572-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84891403249&partnerID=40&md5=e5b6b4dd65171bb02dcf079643583212-
dc.identifier.urihttp://repositorio.unitau.br/jspui/handle/20.500.11874/2133-
dc.description.abstractObjective: Salivary enzymes may be used to diagnose periodontal conditions. Salivary arginase activity (SAA) is related to susceptibility to bacterial infection. Therefore, the aim of this controlled interventional study was to determine the SAA before and after non- surgical periodontal therapy. Method and Materials: Eighty-nine subjects were selected: 31 periodontally healthy patients (controls), 27 gingivitis patients, and 31 chronic peri- odontitis patients. Plaque and Gingival Indices, probing depth, and clinical attachment level were monitored. The presence of Campylobacter rectus, Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Tannerella forsythia, Treponema denticola, and Prevotella intermedia was evaluated by polymerase chain reaction. Salivary total protein level and SAA were also established by spectrophotometry. Clinical and arginase data were analyzed using the Wilcoxon, Mann-Withney, and Kruskal-Wallis tests (P < .05). For microbial data, the chi-square test was used. The Pearson correla- tion test was also used between each parameter evaluated. Results: After therapy, due to a significant reduction in SAA, the values observed for the gingivitis and periodontitis groups were similar to those found in the healthy group. Interestingly, after therapy, SAA followed the same positive pattern showed by the overall improvement of clinical parameters (gingivitis and periodontitis groups mean values, pre- > posttherapy) and by the reduction of target pathogens (gingivitis group T forsythia, pre- > posttherapy; periodontitis group P gingivalis, T denticola, P intermedia, and T forsythia, pre- > post- therapy). Conclusion: Based on the reduction of SAA after therapy, in accordance with the expected reduction in clinical and microbiologic parameters, it was concluded that SAA has the potential to serve as a reliable method to access to the therapeutic response of chronic periodontitis subjects treated with nonsurgical periodontal therapy. © 2012 by Quintessence Publishing Co Inc.en
dc.description.provenanceMade available in DSpace on 2019-09-12T16:32:54Z (GMT). No. of bitstreams: 0 Previous issue date: 2012en
dc.languageInglêspt_BR
dc.relation.ispartofQuintessence International-
dc.rightsAcesso Restritopt_BR
dc.sourceScopuspt_BR
dc.subject.otherArginaseen
dc.subject.otherGingivitisen
dc.subject.otherPeriodontitisen
dc.subject.otherTherapyen
dc.subject.otherarginaseen
dc.subject.otherbiological markeren
dc.subject.othersaliva proteinen
dc.subject.otheradulten
dc.subject.otherAggregatibacter actinomycetemcomitansen
dc.subject.otherarticleen
dc.subject.otherBacteroidesen
dc.subject.otherCampylobacter rectusen
dc.subject.otherchronic periodontitisen
dc.subject.othercomparative studyen
dc.subject.otherenzymologyen
dc.subject.othergingivitisen
dc.subject.otherhumanen
dc.subject.otherisolation and purificationen
dc.subject.othermethodologyen
dc.subject.othermicrobiologyen
dc.subject.othermiddle ageden
dc.subject.otherperiodontal diseaseen
dc.subject.otherperiodontal pocketen
dc.subject.otherperiodonticsen
dc.subject.otherphysiologyen
dc.subject.otherPorphyromonas gingivalisen
dc.subject.otherpreventive dentistryen
dc.subject.otherPrevotella intermediaen
dc.subject.othersalivaen
dc.subject.othertooth plaqueen
dc.subject.otherTreponema denticolaen
dc.subject.otherAdulten
dc.subject.otherAggregatibacter actinomycetemcomitansen
dc.subject.otherArginaseen
dc.subject.otherBacteroidesen
dc.subject.otherBiological Markersen
dc.subject.otherCampylobacter rectusen
dc.subject.otherChronic Periodontitisen
dc.subject.otherDental Plaqueen
dc.subject.otherDental Plaque Indexen
dc.subject.otherDental Prophylaxisen
dc.subject.otherDental Scalingen
dc.subject.otherGingivitisen
dc.subject.otherHumansen
dc.subject.otherMiddle Ageden
dc.subject.otherPeriodontal Attachment Lossen
dc.subject.otherPeriodontal Diseasesen
dc.subject.otherPeriodontal Indexen
dc.subject.otherPeriodontal Pocketen
dc.subject.otherPorphyromonas gingivalisen
dc.subject.otherPrevotella intermediaen
dc.subject.otherRoot Planingen
dc.subject.otherSalivaen
dc.subject.otherSalivary Proteins and Peptidesen
dc.subject.otherTreponema denticolaen
dc.titleReduction of salivary arginine catabolic activity through periodontal therapyen
dc.typeArtigo de Periódicopt_BR
dc.description.affiliationPereira, A.L., Department of Periodontology, University of Taubaté, Taubaté, SP, Brazil-
dc.description.affiliationCortelli, S.C., Department of Periodontology, University of Taubaté, Taubaté, SP, Brazil-
dc.description.affiliationAquino, D.R., Department of Periodontology, University of Taubaté, Taubaté, SP, Brazil-
dc.description.affiliationFranco, G.C.N., Department of Periodontology, University of Taubaté, Taubaté, SP, Brazil-
dc.description.affiliationCogo, K., Department of Periodontology, University of Taubaté, Taubaté, SP, Brazil-
dc.description.affiliationRodrigues, E., Department of Biology, University of Taubaté, Taubaté, SP, Brazil-
dc.description.affiliationCosta, F.O., Department of Periodontology, Federal University of Minas Gerais, Belo Horizonte, MG, Brazil-
dc.description.affiliationHolzhausen, M., Division of Periodontics, Department of Stomatology, School of Dentistry, University of São Paulo, São Paulo, SP, Brazil-
dc.description.affiliationCortelli, J.R., Department of Periodontology, University of Taubaté, Taubaté, SP, Brazil-
dc.identifier.scopus2-s2.0-84891403249-
dc.contributor.scopus55226591400pt_BR
dc.contributor.scopus6506127868pt_BR
dc.contributor.scopus8573898400pt_BR
dc.contributor.scopus34769589500pt_BR
dc.contributor.scopus13104130100pt_BR
dc.contributor.scopus55418271700pt_BR
dc.contributor.scopus15057595100pt_BR
dc.contributor.scopus34770613500pt_BR
dc.contributor.scopus6603263818pt_BR
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