Oral microbial dysbiosis linked to worsened periodontal condition in rheumatoid arthritis patients
Autor(a) principal: | |
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Data de Publicação: | 2019 |
Outros Autores: | , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFMG |
Texto Completo: | http://hdl.handle.net/1843/56823 |
Resumo: | Rheumatoid arthritis (RA) is an autoimmune disease characterized by joint inflammation. Individuals with RA have a higher risk of periodontitis and periodontitis has been linked to RA through the production of enzymes by periodontal pathogens that citrullinate proteins. This linkage is supported by findings that periodontitis is associated with increased RA severity and treatment of periodontitis can improve the symptoms of RA. The possible mechanism for this association is through dysbiosis of the oral microbiota triggered by RA-induced systemic inflammation. We examined the RA status of subjects by measuring the number of tender and swollen joints, anti-citrullinated protein antibody and rheumatoid factor. Periodontal disease status and salivary cytokine levels were measured, and dental plaque analyzed by 16S rRNA high throughput sequencing. RA patients had a higher bacterial load, a more diverse microbiota, an increase in bacterial species associated with periodontal disease, more clinical attachment loss, and increased production of inflammatory mediators including IL17, IL-2, TNF, and IFN-γ. Furthermore, changes in the oral microbiota were linked to worse RA conditions. Our study provides new insights into the bi-directional relationship between periodontitis and RA and suggest that monitoring the periodontal health of RA patients is particularly important. |
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Oral microbial dysbiosis linked to worsened periodontal condition in rheumatoid arthritis patientsDysbiosisArthritis, RheumatoidPeriodontitisCytokineDisbioseArtrite reumatóidePeriodontiteCitocinaRheumatoid arthritis (RA) is an autoimmune disease characterized by joint inflammation. Individuals with RA have a higher risk of periodontitis and periodontitis has been linked to RA through the production of enzymes by periodontal pathogens that citrullinate proteins. This linkage is supported by findings that periodontitis is associated with increased RA severity and treatment of periodontitis can improve the symptoms of RA. The possible mechanism for this association is through dysbiosis of the oral microbiota triggered by RA-induced systemic inflammation. We examined the RA status of subjects by measuring the number of tender and swollen joints, anti-citrullinated protein antibody and rheumatoid factor. Periodontal disease status and salivary cytokine levels were measured, and dental plaque analyzed by 16S rRNA high throughput sequencing. RA patients had a higher bacterial load, a more diverse microbiota, an increase in bacterial species associated with periodontal disease, more clinical attachment loss, and increased production of inflammatory mediators including IL17, IL-2, TNF, and IFN-γ. Furthermore, changes in the oral microbiota were linked to worse RA conditions. Our study provides new insights into the bi-directional relationship between periodontitis and RA and suggest that monitoring the periodontal health of RA patients is particularly important.Universidade Federal de Minas GeraisBrasilICB - DEPARTAMENTO DE MORFOLOGIAMED - DEPARTAMENTO DE APARELHO LOCOMOTORMED - DEPARTAMENTO DE CLÍNICA MÉDICAUFMG2023-07-20T22:12:07Z2023-07-20T22:12:07Z2019-06-10info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlepdfapplication/pdf10.1038/s41598-019-44674-620452322http://hdl.handle.net/1843/56823engscientific reportsJôice DiascorrêaAntônio Lúcio TeixeiraChiranjit MukherjeeEugene j. LeysTarcília Aparecida da SilvaDana t. GravesGabriel r. FernandesDébora Cerqueira CalderaroSantuza Maria Souza MendonçaJanine Mayra SilvaMayra Laino AlbieroFernando q. Cunhae. XiaoGilda Aparecida Ferreirainfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFMGinstname:Universidade Federal de Minas Gerais (UFMG)instacron:UFMG2023-07-21T16:36:15Zoai:repositorio.ufmg.br:1843/56823Repositório InstitucionalPUBhttps://repositorio.ufmg.br/oairepositorio@ufmg.bropendoar:2023-07-21T16:36:15Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG)false |
dc.title.none.fl_str_mv |
Oral microbial dysbiosis linked to worsened periodontal condition in rheumatoid arthritis patients |
title |
Oral microbial dysbiosis linked to worsened periodontal condition in rheumatoid arthritis patients |
spellingShingle |
Oral microbial dysbiosis linked to worsened periodontal condition in rheumatoid arthritis patients Jôice Diascorrêa Dysbiosis Arthritis, Rheumatoid Periodontitis Cytokine Disbiose Artrite reumatóide Periodontite Citocina |
title_short |
Oral microbial dysbiosis linked to worsened periodontal condition in rheumatoid arthritis patients |
title_full |
Oral microbial dysbiosis linked to worsened periodontal condition in rheumatoid arthritis patients |
title_fullStr |
Oral microbial dysbiosis linked to worsened periodontal condition in rheumatoid arthritis patients |
title_full_unstemmed |
Oral microbial dysbiosis linked to worsened periodontal condition in rheumatoid arthritis patients |
title_sort |
Oral microbial dysbiosis linked to worsened periodontal condition in rheumatoid arthritis patients |
author |
Jôice Diascorrêa |
author_facet |
Jôice Diascorrêa Antônio Lúcio Teixeira Chiranjit Mukherjee Eugene j. Leys Tarcília Aparecida da Silva Dana t. Graves Gabriel r. Fernandes Débora Cerqueira Calderaro Santuza Maria Souza Mendonça Janine Mayra Silva Mayra Laino Albiero Fernando q. Cunha e. Xiao Gilda Aparecida Ferreira |
author_role |
author |
author2 |
Antônio Lúcio Teixeira Chiranjit Mukherjee Eugene j. Leys Tarcília Aparecida da Silva Dana t. Graves Gabriel r. Fernandes Débora Cerqueira Calderaro Santuza Maria Souza Mendonça Janine Mayra Silva Mayra Laino Albiero Fernando q. Cunha e. Xiao Gilda Aparecida Ferreira |
author2_role |
author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Jôice Diascorrêa Antônio Lúcio Teixeira Chiranjit Mukherjee Eugene j. Leys Tarcília Aparecida da Silva Dana t. Graves Gabriel r. Fernandes Débora Cerqueira Calderaro Santuza Maria Souza Mendonça Janine Mayra Silva Mayra Laino Albiero Fernando q. Cunha e. Xiao Gilda Aparecida Ferreira |
dc.subject.por.fl_str_mv |
Dysbiosis Arthritis, Rheumatoid Periodontitis Cytokine Disbiose Artrite reumatóide Periodontite Citocina |
topic |
Dysbiosis Arthritis, Rheumatoid Periodontitis Cytokine Disbiose Artrite reumatóide Periodontite Citocina |
description |
Rheumatoid arthritis (RA) is an autoimmune disease characterized by joint inflammation. Individuals with RA have a higher risk of periodontitis and periodontitis has been linked to RA through the production of enzymes by periodontal pathogens that citrullinate proteins. This linkage is supported by findings that periodontitis is associated with increased RA severity and treatment of periodontitis can improve the symptoms of RA. The possible mechanism for this association is through dysbiosis of the oral microbiota triggered by RA-induced systemic inflammation. We examined the RA status of subjects by measuring the number of tender and swollen joints, anti-citrullinated protein antibody and rheumatoid factor. Periodontal disease status and salivary cytokine levels were measured, and dental plaque analyzed by 16S rRNA high throughput sequencing. RA patients had a higher bacterial load, a more diverse microbiota, an increase in bacterial species associated with periodontal disease, more clinical attachment loss, and increased production of inflammatory mediators including IL17, IL-2, TNF, and IFN-γ. Furthermore, changes in the oral microbiota were linked to worse RA conditions. Our study provides new insights into the bi-directional relationship between periodontitis and RA and suggest that monitoring the periodontal health of RA patients is particularly important. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-06-10 2023-07-20T22:12:07Z 2023-07-20T22:12:07Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
10.1038/s41598-019-44674-6 20452322 http://hdl.handle.net/1843/56823 |
identifier_str_mv |
10.1038/s41598-019-44674-6 20452322 |
url |
http://hdl.handle.net/1843/56823 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
scientific reports |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
pdf application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Federal de Minas Gerais Brasil ICB - DEPARTAMENTO DE MORFOLOGIA MED - DEPARTAMENTO DE APARELHO LOCOMOTOR MED - DEPARTAMENTO DE CLÍNICA MÉDICA UFMG |
publisher.none.fl_str_mv |
Universidade Federal de Minas Gerais Brasil ICB - DEPARTAMENTO DE MORFOLOGIA MED - DEPARTAMENTO DE APARELHO LOCOMOTOR MED - DEPARTAMENTO DE CLÍNICA MÉDICA UFMG |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFMG instname:Universidade Federal de Minas Gerais (UFMG) instacron:UFMG |
instname_str |
Universidade Federal de Minas Gerais (UFMG) |
instacron_str |
UFMG |
institution |
UFMG |
reponame_str |
Repositório Institucional da UFMG |
collection |
Repositório Institucional da UFMG |
repository.name.fl_str_mv |
Repositório Institucional da UFMG - Universidade Federal de Minas Gerais (UFMG) |
repository.mail.fl_str_mv |
repositorio@ufmg.br |
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1816829563545583616 |