Serum antibodies to periodontal pathogens and markers of systemic inflammation

Bruce A. Dye, Khalid Choudhary, Steven Shea, Panos N. Papapanou

Research output: Contribution to journalArticlepeer-review

87 Citations (Scopus)

Abstract

Aim: We examined the relationship between serum antibodies against Porphyromonas gingivalis and Actinobacillus actinomycetemcomitans, and plasma fibrinogen and serum C-reactive protein (CRP) in a nationally representative sample. Methods: Data on 2973 participants aged 40 years and older from the third National Health and Nutrition Examination Survey, second phase (1991-1994) were used. Three logistic regression models adjusted for gender, race, educational attainment, diabetes, cigarette smoking, body mass index (BMI), and other inflammatory conditions were constructed, based on three different assumptions: (A) no access to dental/periodontal data; (B) knowledge of number of teeth present but not of clinical periodontal status; and (C) knowledge of both dental and clinical periodontal status. Results: High fibrinogen (> 400 mg/dl) was unrelated to P. gingivalis and A. actinomycetemcomitans antibodies in all models. High CRP (> 0.4 mg/dl) was related to high antibody levels to P. gingivalis in models A [odds ratios (OR) 1.63, 95% confidence intervals (CI) 1.15-2.32], B (OR 1.69, 95% CI 1.18-2.41), and C (OR 1.58, 95% CI 1.12-2.23). In model C, high CRP was related to >30% extent of attachment loss of ≥ 3 mm (OR 1.58, 95% CI 1.19-2.08). Antibodies to A. actinomycetemcomitans were not associated with high CRP levels in any model. Conclusions: High serum titre to P. gingivalis and the presence of periodontal disease are independently related to high CRP levels.

Original languageEnglish
Pages (from-to)1189-1199
Number of pages11
JournalJournal of Clinical Periodontology
Volume32
Issue number12
DOIs
Publication statusPublished - Dec 2005

ASJC Scopus Subject Areas

  • Periodontics

Fingerprint

Dive into the research topics of 'Serum antibodies to periodontal pathogens and markers of systemic inflammation'. Together they form a unique fingerprint.

Cite this