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SAT0089 The impact of periodontal disease on early inflammatory arthritis persists even after all teeth are lost

Identifieur interne : 003D18 ( Istex/Corpus ); précédent : 003D17; suivant : 003D19

SAT0089 The impact of periodontal disease on early inflammatory arthritis persists even after all teeth are lost

Auteurs : G. Westhoff ; T. Dietrich ; G. Schett ; P. De Pablo ; A. Zink

Source :

RBID : ISTEX:7BBFC81BDFEA41D219F15515E41E1544E4A7CEA9

English descriptors

Abstract

Background Data suggests that individuals with periodontal disease (PD) may be more likely to develop rheumatoid arthritis (RA) and have worse disease activity. PD is a common inflammatory disease characterized by gingival accumulation of inflammatory cells with endothelial cell proliferation and matrix degradation that may worsen joint inflammation. Since PD is a major cause of tooth loss, tooth loss may be a surrogate marker for chronic PD, an inflammatory process that may possibly end when the last tooth is lost. We therefore hypothesized that partial vs. complete tooth loss (edentulism) may be differentially associated with disease activity in persons with early arthritis naive to DMARD-therapy. Objectives To determine whether tooth loss and arthritis activity are interrelated by comparing DMARD-naive patients with complete tooth loss to those with partial or no tooth loss with regards to disease activity at arthritis onset. Methods The study included 1,009 patients with early arthritis (<6 months) naive to DMARD-treatment, enrolled in a longitudinal study (CAPEA 2010-2013). Data collection included disease activity (DAS28 calculated by TJC28, SJC28, ESR and Patient Global (PG; NRS 0-10)), the 2010 ACR-EULAR RA classification criteria and self-reported number of teeth. Patients were categorized according to number of teeth at study entry (no teeth, 1-19, 21-27, all teeth). Analysis of covariance was done to determine baseline disease activity by number of teeth. Results Study participants (65% female) were 55±14 years old and had mean symptom duration of 12±7 weeks. 56% were RF or ACPA pos. and 66% fulfilled the 2010 criteria for RA. No patient had received any DMARDs at baseline. Sample characteristics by tooth loss categories are shown on Table. Significantly more patients with edentulism met ACR/EULAR classification compared with those with complete dentition (OR 1.9, 95% CI 1.01-3.35; adj. for age, sex, BMI, smoking, and DAS28). Edentulous patients had neither lower nor higher disease activity (DAS28) than patients with considerable tooth loss (1-19 teeth). However, compared with those with moderate tooth loss (20-27; P=0.046) or complete dentition (P=0.006), they had significantly worse disease activity. Number of teethNAge*Positive RF/ACPA %RA %ESR*SJC28*TJC28*PG*DAS28*# (95% CI) Edentulous7768.26575456.410.05.55.2 (4.8-5.5) 1-1928963.75470397.410.05.35.3 (5.1-5.4) 20-2740153.65565285.87.84.94.8 (4.7-4.9) All teeth24243.95660245.27.74.84.6 (4.4-4.8) Total1.00955.35666326.28.65.04.9 P 0 vs 1-190.0010.0550.2700.0800.2920.9550.5780.470 P 0 vs 28<0.0010.1010.011<0.0010.1060.0130.0550.006 *Mean values, #ANCOVA adjusted for age and sex. Conclusions Tooth loss was associated with disease activity at disease onset in a large cohort of patients with early inflammatory arthritis (IA) naïve to DMARD-therapy. Contrary to the assumption that exposure to PD ends once all affected teeth are lost, edentulism does not improve the interrelation of dental health and IA. The impact of PD on IA starts before IA onset, and obviously persists even after all teeth have been lost. The data also support the notion that there might be a common underlying pathobiology for both conditions. Disclosure of Interest None Declared

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DOI: 10.1136/annrheumdis-2012-eular.3036

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ISTEX:7BBFC81BDFEA41D219F15515E41E1544E4A7CEA9

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<div type="abstract">Background Data suggests that individuals with periodontal disease (PD) may be more likely to develop rheumatoid arthritis (RA) and have worse disease activity. PD is a common inflammatory disease characterized by gingival accumulation of inflammatory cells with endothelial cell proliferation and matrix degradation that may worsen joint inflammation. Since PD is a major cause of tooth loss, tooth loss may be a surrogate marker for chronic PD, an inflammatory process that may possibly end when the last tooth is lost. We therefore hypothesized that partial vs. complete tooth loss (edentulism) may be differentially associated with disease activity in persons with early arthritis naive to DMARD-therapy. Objectives To determine whether tooth loss and arthritis activity are interrelated by comparing DMARD-naive patients with complete tooth loss to those with partial or no tooth loss with regards to disease activity at arthritis onset. Methods The study included 1,009 patients with early arthritis (<6 months) naive to DMARD-treatment, enrolled in a longitudinal study (CAPEA 2010-2013). Data collection included disease activity (DAS28 calculated by TJC28, SJC28, ESR and Patient Global (PG; NRS 0-10)), the 2010 ACR-EULAR RA classification criteria and self-reported number of teeth. Patients were categorized according to number of teeth at study entry (no teeth, 1-19, 21-27, all teeth). Analysis of covariance was done to determine baseline disease activity by number of teeth. Results Study participants (65% female) were 55±14 years old and had mean symptom duration of 12±7 weeks. 56% were RF or ACPA pos. and 66% fulfilled the 2010 criteria for RA. No patient had received any DMARDs at baseline. Sample characteristics by tooth loss categories are shown on Table. Significantly more patients with edentulism met ACR/EULAR classification compared with those with complete dentition (OR 1.9, 95% CI 1.01-3.35; adj. for age, sex, BMI, smoking, and DAS28). Edentulous patients had neither lower nor higher disease activity (DAS28) than patients with considerable tooth loss (1-19 teeth). However, compared with those with moderate tooth loss (20-27; P=0.046) or complete dentition (P=0.006), they had significantly worse disease activity. Number of teethNAge*Positive RF/ACPA %RA %ESR*SJC28*TJC28*PG*DAS28*# (95% CI) Edentulous7768.26575456.410.05.55.2 (4.8-5.5) 1-1928963.75470397.410.05.35.3 (5.1-5.4) 20-2740153.65565285.87.84.94.8 (4.7-4.9) All teeth24243.95660245.27.74.84.6 (4.4-4.8) Total1.00955.35666326.28.65.04.9 P 0 vs 1-190.0010.0550.2700.0800.2920.9550.5780.470 P 0 vs 28<0.0010.1010.011<0.0010.1060.0130.0550.006 *Mean values, #ANCOVA adjusted for age and sex. Conclusions Tooth loss was associated with disease activity at disease onset in a large cohort of patients with early inflammatory arthritis (IA) naïve to DMARD-therapy. Contrary to the assumption that exposure to PD ends once all affected teeth are lost, edentulism does not improve the interrelation of dental health and IA. The impact of PD on IA starts before IA onset, and obviously persists even after all teeth have been lost. The data also support the notion that there might be a common underlying pathobiology for both conditions. Disclosure of Interest None Declared</div>
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<abstract>Background Data suggests that individuals with periodontal disease (PD) may be more likely to develop rheumatoid arthritis (RA) and have worse disease activity. PD is a common inflammatory disease characterized by gingival accumulation of inflammatory cells with endothelial cell proliferation and matrix degradation that may worsen joint inflammation. Since PD is a major cause of tooth loss, tooth loss may be a surrogate marker for chronic PD, an inflammatory process that may possibly end when the last tooth is lost. We therefore hypothesized that partial vs. complete tooth loss (edentulism) may be differentially associated with disease activity in persons with early arthritis naive to DMARD-therapy. Objectives To determine whether tooth loss and arthritis activity are interrelated by comparing DMARD-naive patients with complete tooth loss to those with partial or no tooth loss with regards to disease activity at arthritis onset. Methods The study included 1,009 patients with early arthritis (>6 months) naive to DMARD-treatment, enrolled in a longitudinal study (CAPEA 2010-2013). Data collection included disease activity (DAS28 calculated by TJC28, SJC28, ESR and Patient Global (PG; NRS 0-10)), the 2010 ACR-EULAR RA classification criteria and self-reported number of teeth. Patients were categorized according to number of teeth at study entry (no teeth, 1-19, 21-27, all teeth). Analysis of covariance was done to determine baseline disease activity by number of teeth. Results Study participants (65% female) were 55±14 years old and had mean symptom duration of 12±7 weeks. 56% were RF or ACPA pos. and 66% fulfilled the 2010 criteria for RA. No patient had received any DMARDs at baseline. Sample characteristics by tooth loss categories are shown on Table. Significantly more patients with edentulism met ACR/EULAR classification compared with those with complete dentition (OR 1.9, 95% CI 1.01-3.35; adj. for age, sex, BMI, smoking, and DAS28). Edentulous patients had neither lower nor higher disease activity (DAS28) than patients with considerable tooth loss (1-19 teeth). However, compared with those with moderate tooth loss (20-27; P=0.046) or complete dentition (P=0.006), they had significantly worse disease activity. Number of teethNAge*Positive RF/ACPA %RA %ESR*SJC28*TJC28*PG*DAS28*# (95% CI) Edentulous7768.26575456.410.05.55.2 (4.8-5.5) 1-1928963.75470397.410.05.35.3 (5.1-5.4) 20-2740153.65565285.87.84.94.8 (4.7-4.9) All teeth24243.95660245.27.74.84.6 (4.4-4.8) Total1.00955.35666326.28.65.04.9 P 0 vs 1-190.0010.0550.2700.0800.2920.9550.5780.470 P 0 vs 28>0.0010.1010.011>0.0010.1060.0130.0550.006 *Mean values, #ANCOVA adjusted for age and sex. Conclusions Tooth loss was associated with disease activity at disease onset in a large cohort of patients with early inflammatory arthritis (IA) naïve to DMARD-therapy. Contrary to the assumption that exposure to PD ends once all affected teeth are lost, edentulism does not improve the interrelation of dental health and IA. The impact of PD on IA starts before IA onset, and obviously persists even after all teeth have been lost. The data also support the notion that there might be a common underlying pathobiology for both conditions. Disclosure of Interest None Declared</abstract>
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<p>Background Data suggests that individuals with periodontal disease (PD) may be more likely to develop rheumatoid arthritis (RA) and have worse disease activity. PD is a common inflammatory disease characterized by gingival accumulation of inflammatory cells with endothelial cell proliferation and matrix degradation that may worsen joint inflammation. Since PD is a major cause of tooth loss, tooth loss may be a surrogate marker for chronic PD, an inflammatory process that may possibly end when the last tooth is lost. We therefore hypothesized that partial vs. complete tooth loss (edentulism) may be differentially associated with disease activity in persons with early arthritis naive to DMARD-therapy. Objectives To determine whether tooth loss and arthritis activity are interrelated by comparing DMARD-naive patients with complete tooth loss to those with partial or no tooth loss with regards to disease activity at arthritis onset. Methods The study included 1,009 patients with early arthritis (<6 months) naive to DMARD-treatment, enrolled in a longitudinal study (CAPEA 2010-2013). Data collection included disease activity (DAS28 calculated by TJC28, SJC28, ESR and Patient Global (PG; NRS 0-10)), the 2010 ACR-EULAR RA classification criteria and self-reported number of teeth. Patients were categorized according to number of teeth at study entry (no teeth, 1-19, 21-27, all teeth). Analysis of covariance was done to determine baseline disease activity by number of teeth. Results Study participants (65% female) were 55±14 years old and had mean symptom duration of 12±7 weeks. 56% were RF or ACPA pos. and 66% fulfilled the 2010 criteria for RA. No patient had received any DMARDs at baseline. Sample characteristics by tooth loss categories are shown on Table. Significantly more patients with edentulism met ACR/EULAR classification compared with those with complete dentition (OR 1.9, 95% CI 1.01-3.35; adj. for age, sex, BMI, smoking, and DAS28). Edentulous patients had neither lower nor higher disease activity (DAS28) than patients with considerable tooth loss (1-19 teeth). However, compared with those with moderate tooth loss (20-27; P=0.046) or complete dentition (P=0.006), they had significantly worse disease activity. Number of teethNAge*Positive RF/ACPA %RA %ESR*SJC28*TJC28*PG*DAS28*# (95% CI) Edentulous7768.26575456.410.05.55.2 (4.8-5.5) 1-1928963.75470397.410.05.35.3 (5.1-5.4) 20-2740153.65565285.87.84.94.8 (4.7-4.9) All teeth24243.95660245.27.74.84.6 (4.4-4.8) Total1.00955.35666326.28.65.04.9 P 0 vs 1-190.0010.0550.2700.0800.2920.9550.5780.470 P 0 vs 28<0.0010.1010.011<0.0010.1060.0130.0550.006 *Mean values, #ANCOVA adjusted for age and sex. Conclusions Tooth loss was associated with disease activity at disease onset in a large cohort of patients with early inflammatory arthritis (IA) naïve to DMARD-therapy. Contrary to the assumption that exposure to PD ends once all affected teeth are lost, edentulism does not improve the interrelation of dental health and IA. The impact of PD on IA starts before IA onset, and obviously persists even after all teeth have been lost. The data also support the notion that there might be a common underlying pathobiology for both conditions. Disclosure of Interest None Declared</p>
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<name name-style="western">
<surname>Westhoff</surname>
<given-names>G.</given-names>
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<xref ref-type="aff" rid="AFF_1">
<sup>1</sup>
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<name name-style="western">
<surname>Dietrich</surname>
<given-names>T.</given-names>
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<sup>2</sup>
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<sup>3</sup>
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<name name-style="western">
<surname>de Pablo</surname>
<given-names>P.</given-names>
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<sup>4</sup>
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<sup>1</sup>
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<aff id="AFF_1">
<sup>1</sup>
Epidemiology Unit, German Rheumatism Research Centre, Berlin, Germany</aff>
<aff id="AFF_2">
<sup>2</sup>
The School of Dentistry, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom</aff>
<aff id="AFF_3">
<sup>3</sup>
Department of Internal Medicine, University of Erlangen-Nuremberg, Erlangen, Erlangen, Germany</aff>
<aff id="AFF_4">
<sup>4</sup>
2Rheumatology Research Group, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom</aff>
<pub-date pub-type="ppub">
<month>6</month>
<year>2013</year>
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<volume>71</volume>
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<volume-id pub-id-type="other">71</volume-id>
<issue>Suppl 3</issue>
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<issue-title>Annual European Congress of Rheumatology EULAR abstracts 2012, 6 – 9 June 2012, Berlin, Germany</issue-title>
<fpage seq="1">500</fpage>
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<copyright-statement>© 2013, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</copyright-statement>
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<sec>
<title>Background</title>
<p>Data suggests that individuals with periodontal disease (PD) may be more likely to develop rheumatoid arthritis (RA) and have worse disease activity. PD is a common inflammatory disease characterized by gingival accumulation of inflammatory cells with endothelial cell proliferation and matrix degradation that may worsen joint inflammation. Since PD is a major cause of tooth loss, tooth loss may be a surrogate marker for chronic PD, an inflammatory process that may possibly end when the last tooth is lost. We therefore hypothesized that partial vs. complete tooth loss (edentulism) may be differentially associated with disease activity in persons with early arthritis naive to DMARD-therapy.</p>
</sec>
<sec>
<title>Objectives</title>
<p>To determine whether tooth loss and arthritis activity are interrelated by comparing DMARD-naive patients with complete tooth loss to those with partial or no tooth loss with regards to disease activity at arthritis onset.</p>
</sec>
<sec>
<title>Methods</title>
<p>The study included 1,009 patients with early arthritis (<6 months) naive to DMARD-treatment, enrolled in a longitudinal study (CAPEA 2010-2013). Data collection included disease activity (DAS28 calculated by TJC28, SJC28, ESR and Patient Global (PG; NRS 0-10)), the 2010 ACR-EULAR RA classification criteria and self-reported number of teeth. Patients were categorized according to number of teeth at study entry (no teeth, 1-19, 21-27, all teeth). Analysis of covariance was done to determine baseline disease activity by number of teeth.</p>
</sec>
<sec>
<title>Results</title>
<p>Study participants (65% female) were 55±14 years old and had mean symptom duration of 12±7 weeks. 56% were RF or ACPA pos. and 66% fulfilled the 2010 criteria for RA. No patient had received any DMARDs at baseline. Sample characteristics by tooth loss categories are shown on
<xref ref-type="table" rid="T1">Table</xref>
. Significantly more patients with edentulism met ACR/EULAR classification compared with those with complete dentition (OR 1.9, 95% CI 1.01-3.35; adj. for age, sex, BMI, smoking, and DAS28). Edentulous patients had neither lower nor higher disease activity (DAS28) than patients with considerable tooth loss (1-19 teeth). However, compared with those with moderate tooth loss (20-27; P=0.046) or complete dentition (P=0.006), they had significantly worse disease activity.</p>
<p>
<table-wrap id="T1" position="float">
<table frame="hsides">
<thead>
<tr>
<th align="left" rowspan="1" colspan="1">Number of teeth</th>
<th align="center" rowspan="1" colspan="1">N</th>
<th align="center" rowspan="1" colspan="1">Age*</th>
<th align="center" rowspan="1" colspan="1">Positive RF/ACPA %</th>
<th align="center" rowspan="1" colspan="1">RA %</th>
<th align="center" rowspan="1" colspan="1">ESR*</th>
<th align="center" rowspan="1" colspan="1">SJC28*</th>
<th align="center" rowspan="1" colspan="1">TJC28*</th>
<th align="center" rowspan="1" colspan="1">PG*</th>
<th align="center" rowspan="1" colspan="1">DAS28*
<sup>#</sup>
(95% CI)</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" rowspan="1" colspan="1">Edentulous</td>
<td align="center" rowspan="1" colspan="1">77</td>
<td align="center" rowspan="1" colspan="1">68.2</td>
<td align="center" rowspan="1" colspan="1">65</td>
<td align="center" rowspan="1" colspan="1">75</td>
<td align="center" rowspan="1" colspan="1">45</td>
<td align="center" rowspan="1" colspan="1">6.4</td>
<td align="center" rowspan="1" colspan="1">10.0</td>
<td align="center" rowspan="1" colspan="1">5.5</td>
<td align="center" rowspan="1" colspan="1">5.2 (4.8-5.5)</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">1-19</td>
<td align="center" rowspan="1" colspan="1">289</td>
<td align="center" rowspan="1" colspan="1">63.7</td>
<td align="center" rowspan="1" colspan="1">54</td>
<td align="center" rowspan="1" colspan="1">70</td>
<td align="center" rowspan="1" colspan="1">39</td>
<td align="center" rowspan="1" colspan="1">7.4</td>
<td align="center" rowspan="1" colspan="1">10.0</td>
<td align="center" rowspan="1" colspan="1">5.3</td>
<td align="center" rowspan="1" colspan="1">5.3 (5.1-5.4)</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">20-27</td>
<td align="center" rowspan="1" colspan="1">401</td>
<td align="center" rowspan="1" colspan="1">53.6</td>
<td align="center" rowspan="1" colspan="1">55</td>
<td align="center" rowspan="1" colspan="1">65</td>
<td align="center" rowspan="1" colspan="1">28</td>
<td align="center" rowspan="1" colspan="1">5.8</td>
<td align="center" rowspan="1" colspan="1">7.8</td>
<td align="center" rowspan="1" colspan="1">4.9</td>
<td align="center" rowspan="1" colspan="1">4.8 (4.7-4.9)</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">All teeth</td>
<td align="center" rowspan="1" colspan="1">242</td>
<td align="center" rowspan="1" colspan="1">43.9</td>
<td align="center" rowspan="1" colspan="1">56</td>
<td align="center" rowspan="1" colspan="1">60</td>
<td align="center" rowspan="1" colspan="1">24</td>
<td align="center" rowspan="1" colspan="1">5.2</td>
<td align="center" rowspan="1" colspan="1">7.7</td>
<td align="center" rowspan="1" colspan="1">4.8</td>
<td align="center" rowspan="1" colspan="1">4.6 (4.4-4.8)</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">Total</td>
<td align="center" rowspan="1" colspan="1">1.009</td>
<td align="center" rowspan="1" colspan="1">55.3</td>
<td align="center" rowspan="1" colspan="1">56</td>
<td align="center" rowspan="1" colspan="1">66</td>
<td align="center" rowspan="1" colspan="1">32</td>
<td align="center" rowspan="1" colspan="1">6.2</td>
<td align="center" rowspan="1" colspan="1">8.6</td>
<td align="center" rowspan="1" colspan="1">5.0</td>
<td align="center" rowspan="1" colspan="1">4.9</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">P 0 vs 1-19</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1">0.001</td>
<td align="center" rowspan="1" colspan="1">0.055</td>
<td align="center" rowspan="1" colspan="1">0.270</td>
<td align="center" rowspan="1" colspan="1">0.080</td>
<td align="center" rowspan="1" colspan="1">0.292</td>
<td align="center" rowspan="1" colspan="1">0.955</td>
<td align="center" rowspan="1" colspan="1">0.578</td>
<td align="center" rowspan="1" colspan="1">0.470</td>
</tr>
<tr>
<td align="left" rowspan="1" colspan="1">P 0 vs 28</td>
<td align="center" rowspan="1" colspan="1"></td>
<td align="center" rowspan="1" colspan="1"><0.001</td>
<td align="center" rowspan="1" colspan="1">0.101</td>
<td align="center" rowspan="1" colspan="1">0.011</td>
<td align="center" rowspan="1" colspan="1"><0.001</td>
<td align="center" rowspan="1" colspan="1">0.106</td>
<td align="center" rowspan="1" colspan="1">0.013</td>
<td align="center" rowspan="1" colspan="1">0.055</td>
<td align="center" rowspan="1" colspan="1">0.006</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>*Mean values,
<sup>#</sup>
ANCOVA adjusted for age and sex.</p>
</fn>
</table-wrap-foot>
</table-wrap>
</p>
</sec>
<sec>
<title>Conclusions</title>
<p>Tooth loss was associated with disease activity at disease onset in a large cohort of patients with early inflammatory arthritis (IA) naïve to DMARD-therapy. Contrary to the assumption that exposure to PD ends once all affected teeth are lost, edentulism does not improve the interrelation of dental health and IA. The impact of PD on IA starts before IA onset, and obviously persists even after all teeth have been lost. The data also support the notion that there might be a common underlying pathobiology for both conditions.</p>
</sec>
<sec>
<title>Disclosure of Interest</title>
<p>None Declared</p>
</sec>
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<title>SAT0089 The impact of periodontal disease on early inflammatory arthritis persists even after all teeth are lost</title>
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<title>SAT0089 The impact of periodontal disease on early inflammatory arthritis persists even after all teeth are lost</title>
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<name type="personal">
<namePart type="given">G.</namePart>
<namePart type="family">Westhoff</namePart>
<affiliation>Epidemiology Unit, German Rheumatism Research Centre, Berlin, Germany</affiliation>
<affiliation>Epidemiology Unit, German Rheumatism Research Centre, Berlin, Germany</affiliation>
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<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">T.</namePart>
<namePart type="family">Dietrich</namePart>
<affiliation>The School of Dentistry, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom</affiliation>
<affiliation>The School of Dentistry, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
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<name type="personal">
<namePart type="given">G.</namePart>
<namePart type="family">Schett</namePart>
<affiliation>Department of Internal Medicine, University of Erlangen-Nuremberg, Erlangen, Erlangen, Germany</affiliation>
<affiliation>Department of Internal Medicine, University of Erlangen-Nuremberg, Erlangen, Erlangen, Germany</affiliation>
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<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">P.</namePart>
<namePart type="family">de Pablo</namePart>
<affiliation>2Rheumatology Research Group, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom</affiliation>
<affiliation>2Rheumatology Research Group, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">A.</namePart>
<namePart type="family">Zink</namePart>
<affiliation>Epidemiology Unit, German Rheumatism Research Centre, Berlin, Germany</affiliation>
<affiliation>Epidemiology Unit, German Rheumatism Research Centre, Berlin, Germany</affiliation>
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<publisher>BMJ Publishing Group Ltd and European League Against Rheumatism</publisher>
<dateIssued encoding="w3cdtf">2013-06</dateIssued>
<copyrightDate encoding="w3cdtf">2013</copyrightDate>
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<languageTerm type="code" authority="iso639-2b">eng</languageTerm>
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<abstract>Background Data suggests that individuals with periodontal disease (PD) may be more likely to develop rheumatoid arthritis (RA) and have worse disease activity. PD is a common inflammatory disease characterized by gingival accumulation of inflammatory cells with endothelial cell proliferation and matrix degradation that may worsen joint inflammation. Since PD is a major cause of tooth loss, tooth loss may be a surrogate marker for chronic PD, an inflammatory process that may possibly end when the last tooth is lost. We therefore hypothesized that partial vs. complete tooth loss (edentulism) may be differentially associated with disease activity in persons with early arthritis naive to DMARD-therapy. Objectives To determine whether tooth loss and arthritis activity are interrelated by comparing DMARD-naive patients with complete tooth loss to those with partial or no tooth loss with regards to disease activity at arthritis onset. Methods The study included 1,009 patients with early arthritis (<6 months) naive to DMARD-treatment, enrolled in a longitudinal study (CAPEA 2010-2013). Data collection included disease activity (DAS28 calculated by TJC28, SJC28, ESR and Patient Global (PG; NRS 0-10)), the 2010 ACR-EULAR RA classification criteria and self-reported number of teeth. Patients were categorized according to number of teeth at study entry (no teeth, 1-19, 21-27, all teeth). Analysis of covariance was done to determine baseline disease activity by number of teeth. Results Study participants (65% female) were 55±14 years old and had mean symptom duration of 12±7 weeks. 56% were RF or ACPA pos. and 66% fulfilled the 2010 criteria for RA. No patient had received any DMARDs at baseline. Sample characteristics by tooth loss categories are shown on Table. Significantly more patients with edentulism met ACR/EULAR classification compared with those with complete dentition (OR 1.9, 95% CI 1.01-3.35; adj. for age, sex, BMI, smoking, and DAS28). Edentulous patients had neither lower nor higher disease activity (DAS28) than patients with considerable tooth loss (1-19 teeth). However, compared with those with moderate tooth loss (20-27; P=0.046) or complete dentition (P=0.006), they had significantly worse disease activity. Number of teethNAge*Positive RF/ACPA %RA %ESR*SJC28*TJC28*PG*DAS28*# (95% CI) Edentulous7768.26575456.410.05.55.2 (4.8-5.5) 1-1928963.75470397.410.05.35.3 (5.1-5.4) 20-2740153.65565285.87.84.94.8 (4.7-4.9) All teeth24243.95660245.27.74.84.6 (4.4-4.8) Total1.00955.35666326.28.65.04.9 P 0 vs 1-190.0010.0550.2700.0800.2920.9550.5780.470 P 0 vs 28<0.0010.1010.011<0.0010.1060.0130.0550.006 *Mean values, #ANCOVA adjusted for age and sex. Conclusions Tooth loss was associated with disease activity at disease onset in a large cohort of patients with early inflammatory arthritis (IA) naïve to DMARD-therapy. Contrary to the assumption that exposure to PD ends once all affected teeth are lost, edentulism does not improve the interrelation of dental health and IA. The impact of PD on IA starts before IA onset, and obviously persists even after all teeth have been lost. The data also support the notion that there might be a common underlying pathobiology for both conditions. Disclosure of Interest None Declared</abstract>
<relatedItem type="host">
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<title>Annals of the Rheumatic Diseases</title>
</titleInfo>
<titleInfo type="abbreviated">
<title>Ann Rheum Dis</title>
</titleInfo>
<genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre>
<subject>
<topic>Poster Presentations</topic>
</subject>
<subject>
<topic>Posters</topic>
</subject>
<subject>
<topic>Rheumatoid arthritis – prognosis, predictors and outcome</topic>
</subject>
<identifier type="ISSN">0003-4967</identifier>
<identifier type="eISSN">1468-2060</identifier>
<identifier type="PublisherID">ard</identifier>
<identifier type="PublisherID-hwp">annrheumdis</identifier>
<identifier type="PublisherID-nlm-ta">Ann Rheum Dis</identifier>
<part>
<date>2013</date>
<detail type="title">
<title>Annual European Congress of Rheumatology EULAR abstracts 2012, 6 – 9 June 2012, Berlin, Germany</title>
</detail>
<detail type="volume">
<caption>vol.</caption>
<number>71</number>
</detail>
<detail type="issue">
<caption>no.</caption>
<number>Suppl 3</number>
</detail>
<extent unit="pages">
<start>500</start>
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<identifier type="ark">ark:/67375/NVC-VLL58RR0-T</identifier>
<identifier type="DOI">10.1136/annrheumdis-2012-eular.3036</identifier>
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<identifier type="ArticleID">annrheumdis-2012-eular.3036</identifier>
<identifier type="local">annrheumdis;71/Suppl_3/500-a</identifier>
<accessCondition type="use and reproduction" contentType="copyright">© 2013, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</accessCondition>
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