Lipid-lowering agents use and systemic and oral inflammation in overweight or obese adult Puerto Ricans: the San Juan Overweight Adults Longitudinal Study (SOALS)

J Clin Periodontol. 2015 Dec;42(12):1090-6. doi: 10.1111/jcpe.12461. Epub 2015 Dec 11.

Abstract

The effects of lipid-lowering agents (LLA) on reducing systemic and oral inflammation have not been evaluated.

Objective: To assess the association of LLA use with high-sensitivity C-reactive protein (hs-CRP) and oral inflammation.

Design: Cross-sectional analysis using baseline data from 1300 overweight/obese participants aged 40-65 years, recruited for the ongoing San Juan Overweight Adults Longitudinal Study. Serum hs-CRP was measured by ELISA, gingival/periodontal inflammation was evaluated as bleeding upon probing (BOP), and LLA was self-reported. Separate logistic models were performed for systemic and oral inflammation.

Results: In all, 24% participants reported history of dyslipidaemia, of which, 50.3% self-reported LLA use. Sixty percent of the participants had elevated hs-CRP (>3 mg/dl) and 50% had high BOP (defined as at or above the median: 21%). After adjusting for age, gender, smoking, HDL-C, physical activity, diabetes, blood pressure medications, and percent body fat composition, LLA users had significantly lower odds of elevated hs-CRP compared to LLA non-users (OR = 0.58; 95% CI: 0.39-0.85). After adjusting for age, gender, smoking status, educational level, mean plaque index and percent body fat, LLA users had significantly lower odds of high BOP compared to LLA non-users (OR = 0.62; 95% CI: 0.42-0.91).

Conclusions: Lipid-lowering agents may reduce both systemic and oral inflammatory responses.

Keywords: hs-CRP; lipid-lowering agents; periodontitis; statins; systemic inflammation.

MeSH terms

  • Adult
  • Aged
  • C-Reactive Protein
  • Cross-Sectional Studies
  • Hispanic or Latino
  • Humans
  • Inflammation
  • Lipids
  • Longitudinal Studies
  • Middle Aged
  • Obesity*
  • Overweight*

Substances

  • Lipids
  • C-Reactive Protein