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Patterns of subgingival microbiota in different periodontal phenotypes.
Nibali, L; Sousa, V; Davrandi, M; Liu, L S; Spratt, D; Donos, N.
Afiliação
  • Nibali L; Periodontology Unit, Centre for Host Microbiome Interactions, Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, Centre for Oral, London, United Kingdom; Centre for Immunobiology & Regenerative Medicine and Centre for Oral Clinical Research, Institute of Dentistry, Ba
  • Sousa V; Periodontology Unit, Centre for Host Microbiome Interactions, Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, Centre for Oral, London, United Kingdom; Centre for Immunobiology & Regenerative Medicine and Centre for Oral Clinical Research, Institute of Dentistry, Ba
  • Davrandi M; Microbiology Department, University College London Eastman Dental Institute, London, UK.
  • Liu LS; Periodontology Unit, University College London Eastman Dental Institute, London, UK.
  • Spratt D; Microbiology Department, University College London Eastman Dental Institute, London, UK.
  • Donos N; Centre for Immunobiology & Regenerative Medicine and Centre for Oral Clinical Research, Institute of Dentistry, Barts and The London School of Medicine and Dentistry, Queen Mary University London (QMUL), London, United Kingdom.
J Dent ; 117: 103912, 2022 02.
Article em En | MEDLINE | ID: mdl-34890714
ABSTRACT

OBJECTIVES:

To compare the subgingival microbiota of patients with aggressive (AgP) or chronic periodontitis (CP) to healthy (H), non-periodontitis patients as well as to explore their relevant associations to different host genetic variants.

METHODS:

Following clinical examination, blood and subgingival plaque sampling of 471 study participants (125 AgP, 121 CP, 225 H), subgingival community analysis was performed by next generation sequencing of the 16S rRNA. Microbial data from 266 participants (75 AgP, 95 CP, 98 H) were available for analysis. SNPs in the IL6, IL6R and FTO gene were selected for genetic marker analyses.

RESULTS:

Combined periodontitis patients (AgP + CP), particularly those classified with AgP, exhibited lower alpha- and beta- diversity. Several genera (including Peptostreptococcaceae, Filifactor, Desulfobulbus, Tannerella and Lachnospiracee) and species were over-abundant in combined periodontitis vs. healthy individuals, while other genera such as Prevotella or Dialister were found to be more abundant in healthy cases. The only genus with difference in abundance between AgP and CP was Granulicatella. No associations between IL6, IL6RA and FTO genetic variants and microbial findings were detected.

CONCLUSION:

This study suggests that limited microbial differences existed between AgP and CP and challenges the current notion that periodontitis is associated with increased subgingival microbial diversity compared with periodontal health. CLINICAL

SIGNIFICANCE:

The findings of this study cast some doubts on the notion that the dysbiosis characteristic of periodontal disease is expressed as increased microbial diversity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Periodontite Agressiva / Periodontite Crônica / Microbiota Limite: Humans Idioma: En Revista: J Dent Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Bósnia-Herzegóvina

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Periodontite Agressiva / Periodontite Crônica / Microbiota Limite: Humans Idioma: En Revista: J Dent Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Bósnia-Herzegóvina