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Conference Paper: Periodontal and peri-implant microbiota in patients with both healthy and inflamed peri-implant tissues

TitlePeriodontal and peri-implant microbiota in patients with both healthy and inflamed peri-implant tissues
Authors
Issue Date2013
PublisherFaculty of Dentistry.
Citation
Annual Scientific Meeting, Faculty of Dentistry, University of Hong Kong, 12 December, 2013 How to Cite?
AbstractAim: To compare the prevalence and levels of putative ‘periodontal pathogens’ present in the subgingival/submucosal microbiota surrounding teeth or implants in subjects with differing periodontal/peri-implant health statuses. Materials and Methods: 22 subjects were included in the study. Within each subject, 4 sites were selected for sampling: (1) healthy implant, (2) diseased implant [PPD≥5mm, presence of bleeding on probing (BOP) and radiographic bone loss], (3) healthy tooth and (4) periodontally-diseased tooth (presence of BOP, PPD≥4mm). Subgingival/submucosal plaque was sampled using paper points. After DNA extraction, quantitative real-time PCR (q-PCR) was used to detect and quantify six bacterial species: Treponema denticola, Fusobacterium nucleatum, Aggregatibacter actinomycetemcomitans, Prevotella intermedia, Porphyromonas gingivalis and Staphylococcus. aureus. The absolute counts were log10-transformed before statistical analysis. Results: The most commonly-detected species were F. nucleatum (n=85), T. denticola (n=84) and S. aureus (n=82); while P. gingivalis had the lowest detection frequency (n=61). The overall detection frequencies of target species was generally higher in diseased compared to healthy sites with no statistically significant differences for any particular species (p>0.05, Cochran Q test). Regarding bacterial loads, no significant differences were found among groups except for F. nucleatum (p=0.023, Friedman’s 2-way ANOVA). Submucosal/subgingival plaque from diseased teeth (3.95) and implants (3.54) harbored significantly more F. nucleatum than healthy implants (3.06) and teeth (2.93). Both periodontal and peri-implant sites, independent of health status, were found to harbor S.aureus. The loads (log10) of S.aureus were ca. 3.5 for all the 4 groups (p=0.232), which was the highest of all the species detected. Conclusions: Our results indicate that putative periodontal pathogens are common to both periodontal and peri-implant sites independent of the health status, which may explain the high risk of peri-implantitis in patients with untreated periodontal diseases. S. aureus is commonly present in the subgingival/submucosal microbiota surrounding both teeth and implants. close . . 2013 Annual Scientific Meeting Logo . . Home Programme Oral Presentation Sessions Poster Assessment Sessions Contact . . . . Oral Presentation Sessions : * If you see any discrepancies of the content, please contact Mr. Alvin Kong for assistance. Venue: Please refer to different oral presentation sessions in the table below. Oral Presentation Session A Oral Presentation Session B Oral Presentation Session C Oral Presentation Session D Oral Presentation Session B : Infection and Immunity - Junior and Senior category December 12, 2013 11:00am - 1:00pm Lecture Theatre 2, G/F., The Prince Philip Dental Hiospital. Presentation Session & Time Presenter Oral Presentation Title Category 1 Sess. B LT 2 11:00am-11:15am Li, Xuan Baicalin loading efficiencies in spherical and rod-like mesoporous silica nanoparticles synthesized by lipid crystal mechanism Abstract Oral presentation - junior 2 Sess. B LT 2 11:15am-11:30am Zhuang, Long-fei Periodontal and peri-implant microbiota in patients with both healthy and inflamed peri-implant tissues Abstract Oral presentation - junior 3 Sess. B LT 2 11:30am-11:45am Li, Peng Inability to Eradicate Candida Biofilm Persisters by Consecutive Antifungal Treatments Abstract Oral presentation - junior 4 Sess. B LT 2 11:45am-12:00pm
DescriptionOral Presentation Session B
Persistent Identifierhttp://hdl.handle.net/10722/193627

 

DC FieldValueLanguage
dc.contributor.authorZhuang, Len_US
dc.contributor.authorLang, NPen_US
dc.contributor.authorMattheos, Nen_US
dc.contributor.authorSi, Men_US
dc.contributor.authorLai, HCen_US
dc.contributor.authorWatt, RMen_US
dc.date.accessioned2014-01-20T05:11:08Z-
dc.date.available2014-01-20T05:11:08Z-
dc.date.issued2013en_US
dc.identifier.citationAnnual Scientific Meeting, Faculty of Dentistry, University of Hong Kong, 12 December, 2013en_US
dc.identifier.urihttp://hdl.handle.net/10722/193627-
dc.descriptionOral Presentation Session B-
dc.description.abstractAim: To compare the prevalence and levels of putative ‘periodontal pathogens’ present in the subgingival/submucosal microbiota surrounding teeth or implants in subjects with differing periodontal/peri-implant health statuses. Materials and Methods: 22 subjects were included in the study. Within each subject, 4 sites were selected for sampling: (1) healthy implant, (2) diseased implant [PPD≥5mm, presence of bleeding on probing (BOP) and radiographic bone loss], (3) healthy tooth and (4) periodontally-diseased tooth (presence of BOP, PPD≥4mm). Subgingival/submucosal plaque was sampled using paper points. After DNA extraction, quantitative real-time PCR (q-PCR) was used to detect and quantify six bacterial species: Treponema denticola, Fusobacterium nucleatum, Aggregatibacter actinomycetemcomitans, Prevotella intermedia, Porphyromonas gingivalis and Staphylococcus. aureus. The absolute counts were log10-transformed before statistical analysis. Results: The most commonly-detected species were F. nucleatum (n=85), T. denticola (n=84) and S. aureus (n=82); while P. gingivalis had the lowest detection frequency (n=61). The overall detection frequencies of target species was generally higher in diseased compared to healthy sites with no statistically significant differences for any particular species (p>0.05, Cochran Q test). Regarding bacterial loads, no significant differences were found among groups except for F. nucleatum (p=0.023, Friedman’s 2-way ANOVA). Submucosal/subgingival plaque from diseased teeth (3.95) and implants (3.54) harbored significantly more F. nucleatum than healthy implants (3.06) and teeth (2.93). Both periodontal and peri-implant sites, independent of health status, were found to harbor S.aureus. The loads (log10) of S.aureus were ca. 3.5 for all the 4 groups (p=0.232), which was the highest of all the species detected. Conclusions: Our results indicate that putative periodontal pathogens are common to both periodontal and peri-implant sites independent of the health status, which may explain the high risk of peri-implantitis in patients with untreated periodontal diseases. S. aureus is commonly present in the subgingival/submucosal microbiota surrounding both teeth and implants. close . . 2013 Annual Scientific Meeting Logo . . Home Programme Oral Presentation Sessions Poster Assessment Sessions Contact . . . . Oral Presentation Sessions : * If you see any discrepancies of the content, please contact Mr. Alvin Kong for assistance. Venue: Please refer to different oral presentation sessions in the table below. Oral Presentation Session A Oral Presentation Session B Oral Presentation Session C Oral Presentation Session D Oral Presentation Session B : Infection and Immunity - Junior and Senior category December 12, 2013 11:00am - 1:00pm Lecture Theatre 2, G/F., The Prince Philip Dental Hiospital. Presentation Session & Time Presenter Oral Presentation Title Category 1 Sess. B LT 2 11:00am-11:15am Li, Xuan Baicalin loading efficiencies in spherical and rod-like mesoporous silica nanoparticles synthesized by lipid crystal mechanism Abstract Oral presentation - junior 2 Sess. B LT 2 11:15am-11:30am Zhuang, Long-fei Periodontal and peri-implant microbiota in patients with both healthy and inflamed peri-implant tissues Abstract Oral presentation - junior 3 Sess. B LT 2 11:30am-11:45am Li, Peng Inability to Eradicate Candida Biofilm Persisters by Consecutive Antifungal Treatments Abstract Oral presentation - junior 4 Sess. B LT 2 11:45am-12:00pm-
dc.languageengen_US
dc.publisherFaculty of Dentistry.-
dc.titlePeriodontal and peri-implant microbiota in patients with both healthy and inflamed peri-implant tissuesen_US
dc.typeConference_Paperen_US
dc.identifier.emailLang, NP: nplang@hkucc.hku.hken_US
dc.identifier.emailMattheos, N: mattheos@hku.hken_US
dc.identifier.emailWatt, RM: rmwatt@hku.hken_US
dc.identifier.authorityLang, NP=rp00031en_US
dc.identifier.authorityMattheos, N=rp01662en_US
dc.identifier.authorityWatt, RM=rp00043en_US
dc.identifier.hkuros227281en_US
dc.publisher.placeHong Kong-
dc.customcontrol.immutableyiu 140624-

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