Periodontal Health and Oral Microbiota in Patients with Rheumatoid Arthritis

This study aimed to investigate the periodontal health of patients with established rheumatoid arthritis (RA) in relation to oral microbiota, systemic and oral inflammatory mediators, and RA disease activity. Forty patients underwent full-mouth dental/periodontal and rheumatological examination, inc...

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Published inJournal of clinical medicine Vol. 8; no. 5; p. 630
Main Authors Eriksson, Kaja, Fei, Guozhong, Lundmark, Anna, Benchimol, Daniel, Lee, Linkiat, Hu, Yue O. O., Kats, Anna, Saevarsdottir, Saedis, Catrina, Anca Irinel, Klinge, Björn, Andersson, Anders F., Klareskog, Lars, Lundberg, Karin, Jansson, Leif, Yucel-Lindberg, Tülay
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Published Switzerland MDPI 08.05.2019
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Abstract This study aimed to investigate the periodontal health of patients with established rheumatoid arthritis (RA) in relation to oral microbiota, systemic and oral inflammatory mediators, and RA disease activity. Forty patients underwent full-mouth dental/periodontal and rheumatological examination, including collection of blood, saliva, gingival crevicular fluid (GCF) and subgingival plaque. Composition of plaque and saliva microbiota were analysed using 16S rRNA sequencing and levels of inflammatory mediators by multiplex-immunoassay. The majority of the patients (75%) had moderate or severe periodontitis and the rest had no/mild periodontitis. Anti-citrullinated protein antibody (ACPA) positivity was significantly more frequent in the moderate/severe periodontitis (86%) compared to the no/mild group (50%). No significance between groups was observed for RA disease duration or activity, or type of medication. Levels of sCD30/TNFRSF8, IFN-α2, IL-19, IL-26, MMP-1, gp130/sIL-6Rß, and sTNF-R1 were significantly higher in serum or GCF, and April/TNFSF13 was significantly higher in serum and saliva samples in moderate/severe periodontitis. The microbial composition in plaque also differed significantly between the two groups. In conclusion, the majority of RA patients had moderate/severe periodontitis and that this severe form of the disease was significantly associated with ACPA positivity, an altered subgingival microbial profile, and increased levels of systemic and oral inflammatory mediators.
AbstractList This study aimed to investigate the periodontal health of patients with established rheumatoid arthritis (RA) in relation to oral microbiota, systemic and oral inflammatory mediators, and RA disease activity. Forty patients underwent full-mouth dental/periodontal and rheumatological examination, including collection of blood, saliva, gingival crevicular fluid (GCF) and subgingival plaque. Composition of plaque and saliva microbiota were analysed using 16S rRNA sequencing and levels of inflammatory mediators by multiplex-immunoassay. The majority of the patients (75%) had moderate or severe periodontitis and the rest had no/mild periodontitis. Anti-citrullinated protein antibody (ACPA) positivity was significantly more frequent in the moderate/severe periodontitis (86%) compared to the no/mild group (50%). No significance between groups was observed for RA disease duration or activity, or type of medication. Levels of sCD30/TNFRSF8, IFN-α2, IL-19, IL-26, MMP-1, gp130/sIL-6Rß, and sTNF-R1 were significantly higher in serum or GCF, and April/TNFSF13 was significantly higher in serum and saliva samples in moderate/severe periodontitis. The microbial composition in plaque also differed significantly between the two groups. In conclusion, the majority of RA patients had moderate/severe periodontitis and that this severe form of the disease was significantly associated with ACPA positivity, an altered subgingival microbial profile, and increased levels of systemic and oral inflammatory mediators.
This study aimed to investigate the periodontal health of patients with established rheumatoid arthritis (RA) in relation to oral microbiota, systemic and oral inflammatory mediators, and RA disease activity. Forty patients underwent full-mouth dental/periodontal and rheumatological examination, including collection of blood, saliva, gingival crevicular fluid (GCF) and subgingival plaque. Composition of plaque and saliva microbiota were analysed using 16S rRNA sequencing and levels of inflammatory mediators by multiplex-immunoassay. The majority of the patients (75%) had moderate or severe periodontitis and the rest had no/mild periodontitis. Anti-citrullinated protein antibody (ACPA) positivity was significantly more frequent in the moderate/severe periodontitis (86%) compared to the no/mild group (50%). No significance between groups was observed for RA disease duration or activity, or type of medication. Levels of sCD30/TNFRSF8, IFN-2, IL-19, IL-26, MMP-1, gp130/sIL-6R ss, and sTNF-R1 were significantly higher in serum or GCF, and April/TNFSF13 was significantly higher in serum and saliva samples in moderate/severe periodontitis. The microbial composition in plaque also differed significantly between the two groups. In conclusion, the majority of RA patients had moderate/severe periodontitis and that this severe form of the disease was significantly associated with ACPA positivity, an altered subgingival microbial profile, and increased levels of systemic and oral inflammatory mediators.
This study aimed to investigate the periodontal health of patients with established rheumatoid arthritis (RA) in relation to oral microbiota, systemic and oral inflammatory mediators, and RA disease activity. Forty patients underwent full-mouth dental/periodontal and rheumatological examination, including collection of blood, saliva, gingival crevicular fluid (GCF) and subgingival plaque. Composition of plaque and saliva microbiota were analysed using 16S rRNA sequencing and levels of inflammatory mediators by multiplex-immunoassay. The majority of the patients (75%) had moderate or severe periodontitis and the rest had no/mild periodontitis. Anti-citrullinated protein antibody (ACPA) positivity was significantly more frequent in the moderate/severe periodontitis (86%) compared to the no/mild group (50%). No significance between groups was observed for RA disease duration or activity, or type of medication. Levels of sCD30/TNFRSF8, IFN-α2, IL-19, IL-26, MMP-1, gp130/sIL-6Rß, and sTNF-R1 were significantly higher in serum or GCF, and April/TNFSF13 was significantly higher in serum and saliva samples in moderate/severe periodontitis. The microbial composition in plaque also differed significantly between the two groups. In conclusion, the majority of RA patients had moderate/severe periodontitis and that this severe form of the disease was significantly associated with ACPA positivity, an altered subgingival microbial profile, and increased levels of systemic and oral inflammatory mediators.This study aimed to investigate the periodontal health of patients with established rheumatoid arthritis (RA) in relation to oral microbiota, systemic and oral inflammatory mediators, and RA disease activity. Forty patients underwent full-mouth dental/periodontal and rheumatological examination, including collection of blood, saliva, gingival crevicular fluid (GCF) and subgingival plaque. Composition of plaque and saliva microbiota were analysed using 16S rRNA sequencing and levels of inflammatory mediators by multiplex-immunoassay. The majority of the patients (75%) had moderate or severe periodontitis and the rest had no/mild periodontitis. Anti-citrullinated protein antibody (ACPA) positivity was significantly more frequent in the moderate/severe periodontitis (86%) compared to the no/mild group (50%). No significance between groups was observed for RA disease duration or activity, or type of medication. Levels of sCD30/TNFRSF8, IFN-α2, IL-19, IL-26, MMP-1, gp130/sIL-6Rß, and sTNF-R1 were significantly higher in serum or GCF, and April/TNFSF13 was significantly higher in serum and saliva samples in moderate/severe periodontitis. The microbial composition in plaque also differed significantly between the two groups. In conclusion, the majority of RA patients had moderate/severe periodontitis and that this severe form of the disease was significantly associated with ACPA positivity, an altered subgingival microbial profile, and increased levels of systemic and oral inflammatory mediators.
Author Klareskog, Lars
Klinge, Björn
Lee, Linkiat
Benchimol, Daniel
Lundmark, Anna
Saevarsdottir, Saedis
Lundberg, Karin
Hu, Yue O. O.
Eriksson, Kaja
Fei, Guozhong
Catrina, Anca Irinel
Yucel-Lindberg, Tülay
Kats, Anna
Jansson, Leif
Andersson, Anders F.
AuthorAffiliation 6 Department of Medicine, Rheumatology Unit, Karolinska University Hospital, Solna, 17176 Stockholm, Sweden; Saedis.Saevarsdottir@ki.se (S.S.); anca.catrina@ki.se (A.I.C.); Lars.Klareskog@ki.se (L.K.); Karin.Lundberg@ki.se (K.L.)
5 Department of Microbiology, Tumor and Cell Biology, Centre for Translational Microbiome Research (CTMR), Karolinska Institutet, 17164 Stockholm, Sweden
8 Department of Periodontology at Eastmaninstitutet, Stockholm County Council, 11382 Stockholm, Sweden
1 Department of Dental Medicine, Division of Periodontology, Karolinska Institutet, 14104 Huddinge, Sweden; anna.m.l.lundmark@gmail.com (A.L.); linkiatlee@gmail.com (L.L.); anna.kats@hotmail.com (A.K.); bjorn.klinge@ki.se (B.K.); leif.jansson@sll.se (L.J.)
4 Science for Life Laboratory School of Biotechnology, KTH Royal Institute of Technology, 17121 Stockholm, Sweden; yue.hu@ki.se (Y.O.O.H.); anders.andersson@scilifelab.se (A.F.A.)
2 Center for Rheumatology, Academic Specialist Center, Stockholm Health Services,
AuthorAffiliation_xml – name: 7 Department of Periodontology, Faculty of Odontology, Malmö University, 20506 Malmö, Sweden
– name: 3 Department of Dental Medicine, Division of Orofacial Diagnostics and Surgery—Image and Functional Odontology, Karolinska Institutet, Huddinge 14104, Sweden; daniel.benchimol@ki.se
– name: 4 Science for Life Laboratory School of Biotechnology, KTH Royal Institute of Technology, 17121 Stockholm, Sweden; yue.hu@ki.se (Y.O.O.H.); anders.andersson@scilifelab.se (A.F.A.)
– name: 1 Department of Dental Medicine, Division of Periodontology, Karolinska Institutet, 14104 Huddinge, Sweden; anna.m.l.lundmark@gmail.com (A.L.); linkiatlee@gmail.com (L.L.); anna.kats@hotmail.com (A.K.); bjorn.klinge@ki.se (B.K.); leif.jansson@sll.se (L.J.)
– name: 2 Center for Rheumatology, Academic Specialist Center, Stockholm Health Services, 10235 Stockholm, Sweden; guozhong.fei@sll.se
– name: 6 Department of Medicine, Rheumatology Unit, Karolinska University Hospital, Solna, 17176 Stockholm, Sweden; Saedis.Saevarsdottir@ki.se (S.S.); anca.catrina@ki.se (A.I.C.); Lars.Klareskog@ki.se (L.K.); Karin.Lundberg@ki.se (K.L.)
– name: 5 Department of Microbiology, Tumor and Cell Biology, Centre for Translational Microbiome Research (CTMR), Karolinska Institutet, 17164 Stockholm, Sweden
– name: 8 Department of Periodontology at Eastmaninstitutet, Stockholm County Council, 11382 Stockholm, Sweden
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Issue 5
Keywords Porphyromonas gingivalis
rheumatoid factor
periodontitis
smoking
medication
rheumatoid arthritis
periodontal disease
anti-citrullinated protein autoantibodies
Language English
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Snippet This study aimed to investigate the periodontal health of patients with established rheumatoid arthritis (RA) in relation to oral microbiota, systemic and oral...
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SubjectTerms anti-citrullinated protein autoantibodies
medication
periodontal disease
periodontitis
Porphyromonas gingivalis
rheumatoid arthritis
rheumatoid factor
smoking
Title Periodontal Health and Oral Microbiota in Patients with Rheumatoid Arthritis
URI https://www.ncbi.nlm.nih.gov/pubmed/31072030
https://www.proquest.com/docview/2231901827
https://pubmed.ncbi.nlm.nih.gov/PMC6572048
https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-270845
https://urn.kb.se/resolve?urn=urn:nbn:se:mau:diva-6635
Volume 8
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