TY - JOUR
T1 - Rheumatoid arthritis and salivary biomarkers of periodontal disease
AU - Mirrielees, Jeffrey
AU - Crofford, Leslie J.
AU - Lin, Yushun
AU - Kryscio, Richard J.
AU - Dawson, Dolphus R.
AU - Ebersole, Jeffrey L.
AU - Miller, Craig S.
PY - 2010/12
Y1 - 2010/12
N2 - Aim: To test the hypothesis that rheumatoid arthritis (RA) influenced levels of salivary biomarkers of periodontal disease. Methods: Medical assessments, periodontal examinations and pain ratings were obtained from 35 RA, 35 chronic periodontitis and 35 age- and gender-matched healthy controls in a cross-sectional, case-controlled study. Unstimulated whole saliva samples were analysed for interleukin-1 (IL-1), matrix metalloproteinase-8 (MMP-8) and tumour necrosis factor-± (TNF-±) concentrations. Results: The arthritis and healthy groups had significantly less oral disease than the periodontitis group (P<0.0001), with the arthritis group having significantly more sites bleeding on probing (BOP) than matched controls (P=0.012). Salivary levels of MMP-8 and IL-1 were significantly elevated in the periodontal disease group (P<0.002), and IL-1 was the only biomarker with significantly higher levels in the arthritis group compared with controls (P=0.002). Arthritis patients receiving anti-TNF-± antibody therapy had significantly lower IL-1 and TNF-± levels compared with arthritis patients not on anti-TNF-± therapy (P=0.016, 0.024) and healthy controls (P<0.001, P=0.011), respectively. Conclusion: RA patients have higher levels of periodontal inflammation than healthy controls, i.e., an increased BOP. Systemic inflammation appears to influence levels of select salivary biomarkers of periodontal disease, and anti-TNF-± antibody-based disease-modifying therapy significantly lowers salivary IL-1 and TNF-± levels in RA.
AB - Aim: To test the hypothesis that rheumatoid arthritis (RA) influenced levels of salivary biomarkers of periodontal disease. Methods: Medical assessments, periodontal examinations and pain ratings were obtained from 35 RA, 35 chronic periodontitis and 35 age- and gender-matched healthy controls in a cross-sectional, case-controlled study. Unstimulated whole saliva samples were analysed for interleukin-1 (IL-1), matrix metalloproteinase-8 (MMP-8) and tumour necrosis factor-± (TNF-±) concentrations. Results: The arthritis and healthy groups had significantly less oral disease than the periodontitis group (P<0.0001), with the arthritis group having significantly more sites bleeding on probing (BOP) than matched controls (P=0.012). Salivary levels of MMP-8 and IL-1 were significantly elevated in the periodontal disease group (P<0.002), and IL-1 was the only biomarker with significantly higher levels in the arthritis group compared with controls (P=0.002). Arthritis patients receiving anti-TNF-± antibody therapy had significantly lower IL-1 and TNF-± levels compared with arthritis patients not on anti-TNF-± therapy (P=0.016, 0.024) and healthy controls (P<0.001, P=0.011), respectively. Conclusion: RA patients have higher levels of periodontal inflammation than healthy controls, i.e., an increased BOP. Systemic inflammation appears to influence levels of select salivary biomarkers of periodontal disease, and anti-TNF-± antibody-based disease-modifying therapy significantly lowers salivary IL-1 and TNF-± levels in RA.
KW - biological markers
KW - inflammation
KW - interleukin-1
KW - matrix metalloproteinase (MMP)
KW - periodontal disease
KW - rheumatoid arthritis
KW - saliva
KW - salivary biomarkers
KW - tumour necrosis factor (TNF)-±
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U2 - 10.1111/j.1600-051X.2010.01625.x
DO - 10.1111/j.1600-051X.2010.01625.x
M3 - Article
C2 - 20880053
AN - SCOPUS:78649242153
SN - 0303-6979
VL - 37
SP - 1068
EP - 1074
JO - Journal of Clinical Periodontology
JF - Journal of Clinical Periodontology
IS - 12
ER -