9
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Periodontal Health and Oral Microbiota in Patients with Rheumatoid Arthritis

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          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.

          Related collections

          Most cited references54

          • Record: found
          • Abstract: found
          • Article: not found

          Case definitions for use in population-based surveillance of periodontitis.

          Many definitions of periodontitis have been used in the literature for population-based studies, but there is no accepted standard. In early epidemiologic studies, the two major periodontal diseases, gingivitis and periodontitis, were combined and considered to be a continuum. National United States surveys were conducted in 1960 to 1962, 1971 to 1974, 1981, 1985 to 1986, 1988 to 1994, and 1999 to 2000. The case definitions and protocols used in the six national surveys reflect a continuing evolution and improvement over time. Generally, the clinical diagnosis of periodontitis is based on measures of probing depth (PD), clinical attachment level (CAL), the radiographic pattern and extent of alveolar bone loss, gingival inflammation measured as bleeding on probing, or a combination of these measures. Several other patient characteristics are considered, and several factors, such as age, can affect measurements of PD and CAL. Accuracy and reproducibility of measurements of PD and CAL are important because case definitions for periodontitis are based largely on either or both measurements, and relatively small changes in these values can result in large changes in disease prevalence. The classification currently accepted by the American Academy of Periodontology (AAP) was devised by the 1999 International Workshop for a Classification of Periodontal Diseases and Conditions. However, in 2003 the Centers for Disease Control and Prevention and the AAP appointed a working group to develop further standardized clinical case definitions for population-based studies of periodontitis. This classification defines severe periodontitis and moderate periodontitis in terms of PD and CAL to enhance case definitions and further demonstrates the importance of thresholds of PD and CAL and the number of affected sites when determining prevalence.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Periodontal disease and the oral microbiota in new-onset rheumatoid arthritis.

            To profile the abundance and diversity of subgingival oral microbiota in patients with never-treated, new-onset rheumatoid arthritis (RA). Periodontal disease (PD) status, clinical activity, and sociodemographic factors were determined in patients with new-onset RA, patients with chronic RA, and healthy subjects. Multiplexed-454 pyrosequencing was used to compare the composition of subgingival microbiota and establish correlations between the presence/abundance of bacteria and disease phenotypes. Anti-Porphyromonas gingivalis antibody testing was performed to assess prior exposure to the bacterial pathogen P gingivalis. The more advanced forms of periodontitis were already present at disease onset in patients with new-onset RA. The subgingival microbiota observed in patients with new-onset RA was distinct from that found in healthy controls. In most cases, however, these microbial differences could be attributed to the severity of PD and were not inherent to RA. The presence and abundance of P gingivalis were also directly associated with the severity of PD and were not unique to RA. The presence of P gingivalis was not correlated with anti-citrullinated protein antibody (ACPA) titers. Overall exposure to P gingivalis was similar between patients with new-onset RA and controls, observed in 78% of patients and 83% of controls. The presence and abundance of Anaeroglobus geminatus correlated with the presence of ACPAs/rheumatoid factor. Prevotella and Leptotrichia species were the only characteristic taxa observed in patients with new-onset RA irrespective of PD status. Patients with new-onset RA exhibited a high prevalence of PD at disease onset, despite their young age and paucity of smoking history. The subgingival microbiota profile in patients with new-onset RA was similar to that in patients with chronic RA and healthy subjects whose PD was of comparable severity. Although colonization with P gingivalis correlated with the severity of PD, overall exposure to P gingivalis was similar among the groups. The role of A geminatus and Prevotella/Leptotrichia species in this process merits further study. Copyright © 2012 by the American College of Rheumatology.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              DegePrime, a program for degenerate primer design for broad-taxonomic-range PCR in microbial ecology studies.

              The taxonomic composition of a microbial community can be deduced by analyzing its rRNA gene content by, e.g., high-throughput DNA sequencing or DNA chips. Such methods typically are based on PCR amplification of rRNA gene sequences using broad-taxonomic-range PCR primers. In these analyses, the use of optimal primers is crucial for achieving an unbiased representation of community composition. Here, we present the computer program DegePrime that, for each position of a multiple sequence alignment, finds a degenerate oligomer of as high coverage as possible and outputs its coverage among taxonomic divisions. We show that our novel heuristic, which we call weighted randomized combination, performs better than previously described algorithms for solving the maximum coverage degenerate primer design problem. We previously used DegePrime to design a broad-taxonomic-range primer pair that targets the bacterial V3-V4 region (341F-805R) (D. P. Herlemann, M. Labrenz, K. Jurgens, S. Bertilsson, J. J. Waniek, and A. F. Andersson, ISME J. 5:1571-1579, 2011, http://dx.doi.org/10.1038/ismej.2011.41), and here we use the program to significantly increase the coverage of a primer pair (515F-806R) widely used for Illumina-based surveys of bacterial and archaeal diversity. By comparison with shotgun metagenomics, we show that the primers give an accurate representation of microbial diversity in natural samples.
                Bookmark

                Author and article information

                Journal
                J Clin Med
                J Clin Med
                jcm
                Journal of Clinical Medicine
                MDPI
                2077-0383
                08 May 2019
                May 2019
                : 8
                : 5
                : 630
                Affiliations
                [1 ]Department of Dental Medicine, Division of Periodontology, Karolinska Institutet, 14104 Huddinge, Sweden; anna.m.l.lundmark@ 123456gmail.com (A.L.); linkiatlee@ 123456gmail.com (L.L.); anna.kats@ 123456hotmail.com (A.K.); bjorn.klinge@ 123456ki.se (B.K.); leif.jansson@ 123456sll.se (L.J.)
                [2 ]Center for Rheumatology, Academic Specialist Center, Stockholm Health Services, 10235 Stockholm, Sweden; guozhong.fei@ 123456sll.se
                [3 ]Department of Dental Medicine, Division of Orofacial Diagnostics and Surgery—Image and Functional Odontology, Karolinska Institutet, Huddinge 14104, Sweden; daniel.benchimol@ 123456ki.se
                [4 ]Science for Life Laboratory School of Biotechnology, KTH Royal Institute of Technology, 17121 Stockholm, Sweden; yue.hu@ 123456ki.se (Y.O.O.H.); anders.andersson@ 123456scilifelab.se (A.F.A.)
                [5 ]Department of Microbiology, Tumor and Cell Biology, Centre for Translational Microbiome Research (CTMR), Karolinska Institutet, 17164 Stockholm, Sweden
                [6 ]Department of Medicine, Rheumatology Unit, Karolinska University Hospital, Solna, 17176 Stockholm, Sweden; Saedis.Saevarsdottir@ 123456ki.se (S.S.); anca.catrina@ 123456ki.se (A.I.C.); Lars.Klareskog@ 123456ki.se (L.K.); Karin.Lundberg@ 123456ki.se (K.L.)
                [7 ]Department of Periodontology, Faculty of Odontology, Malmö University, 20506 Malmö, Sweden
                [8 ]Department of Periodontology at Eastmaninstitutet, Stockholm County Council, 11382 Stockholm, Sweden
                Author notes
                [* ]Correspondence: Kaja.Eriksson@ 123456ki.se (K.E.); Tulay.Lindberg@ 123456ki.se (T.Y.-L.); Tel.: +46-73-522 4998 (K.E.); +46-70-508 8126 (T.Y.-L.)
                Author information
                https://orcid.org/0000-0003-2100-2446
                https://orcid.org/0000-0003-0129-8809
                Article
                jcm-08-00630
                10.3390/jcm8050630
                6572048
                31072030
                e6d1edeb-23bb-4692-ad43-ca5791f8b42d
                © 2019 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 31 March 2019
                : 01 May 2019
                Categories
                Article

                rheumatoid arthritis,periodontitis,periodontal disease,anti-citrullinated protein autoantibodies,rheumatoid factor,smoking,medication,porphyromonas gingivalis

                Comments

                Comment on this article