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Local and Plasma Biomarker Profiles in Localized Aggressive Periodontitis
L S Branco-de-Almeida1,2, Y Cruz-Almeida3, Y Gonzalez-Marrero1
1Department of Periodontology, College of Dentistry, University of Florida, Gainesville, FL, USA.
JDR Clinical and Translational Research
|September 8, 2017
Summary
Localized aggressive periodontitis (LAP) involves distinct inflammatory profiles in gingival crevicular fluid (GCF) and plasma. Specific GCF and plasma biomarkers can differentiate LAP patients from healthy individuals, aiding future diagnostics.
Area of Science:
- Periodontology
- Immunology
- Biomarker Discovery
Background:
- Localized aggressive periodontitis (LAP) is associated with a systemic hyperinflammatory response to lipopolysaccharide.
- Biomarker profiles in plasma and gingival crevicular fluid (GCF) and their interrelations in LAP remain largely uncharacterized.
Purpose of the Study:
- To characterize GCF and plasma inflammatory and bone biomarker profiles in LAP patients, healthy siblings (HS), and healthy unrelated controls (HC).
- To investigate associations between local and systemic biomarkers in LAP.
- To identify biomarker groups that discriminate LAP from healthy controls.
Main Methods:
- Cross-sectional study including 58 LAP patients, 33 HS, and 49 HC (African Americans, 5-25 years).
- Collection of clinical parameters, GCF, and plasma samples.
- Quantification of 16 inflammatory and bone resorption biomarkers using Milliplex; statistical analyses including univariate, correlation, and discriminant analyses.
Main Results:
- LAP patients exhibited higher GCF levels of cytokines, chemokines, and RANKL:OPG ratio, correlating with clinical periodontal parameters.
- Specific GCF biomarkers (IL-12p40, IL-6, IL-12p70, IL-2, MIP-1α) distinguished LAP sites from healthy sites and controls.
- Plasma RANKL levels were elevated in LAP and correlated with disease extent; a distinct plasma inflammatory profile (MIP-1α, IL-8, IL-10, INF-γ) differentiated LAP patients from controls. No GCF-plasma biomarker correlations were observed.
Conclusions:
- Distinct GCF and plasma inflammatory biomarker profiles can significantly discriminate LAP patients from healthy individuals.
- The hyperinflammatory response in LAP is largely localized, with minimal systemic influence beyond lipopolysaccharide stimulation.
- These findings suggest potential for GCF and plasma biomarkers as future diagnostic tools for LAP.

