Gene expression signatures in chronic and aggressive periodontitis: a pilot study

• Published in: European journal of oral sciences Vol. 112; no. 3; pp. 216 - 223
• Main Authors: Papapanou, Panos N., Abron, Armin, Verbitsky, Miguel, Picolos, Doros, Yang, Jun, Qin, Jie, Fine, James B., Pavlidis, Paul
• Format: Journal Article
• Language: English
• Published: Oxford, UK Munksgaard International Publishers 01.06.2004
• Subjects: Acute Disease; Adolescent; Adult; Aggregatibacter actinomycetemcomitans - genetics; Aggressive Periodontitis - genetics; Aggressive Periodontitis - immunology; Aggressive Periodontitis - microbiology; Antibodies, Bacterial - genetics; Bacteroides - genetics; Campylobacter rectus - genetics; Chronic Disease; classification; Dental Plaque - microbiology; Dentistry; DNA, Bacterial - analysis; Female; gene expression; Gene Expression Profiling; Humans; Immunoglobulin G - blood; Immunoglobulin G - genetics; Male; microarray; Oligonucleotide Array Sequence Analysis; periodontitis; Periodontitis - genetics; Periodontitis - immunology; Periodontitis - microbiology; Pilot Projects; Porphyromonas gingivalis - genetics
• DOI: 10.1111/j.1600-0722.2004.00124.x
• ISSN: 0909-8836

This pilot study examined gene expression signatures in pathological gingival tissues of subjects with chronic or aggressive periodontitis, and explored whether new subclasses of periodontitis can be identified based on gene expression profiles. A total of 14 patients, seven with chronic and seven with aggressive periodontitis, were examined with respect to clinical periodontal status, composition of subgingival bacterial plaque assessed by checkerboard hybridizations, and levels of serum IgG antibodies to periodontal bacteria assayed by checkerboard immunoblotting. In addition, at least two pathological pockets/patient were biopsied, processed for RNA extraction, amplification and labeling, and used to study gene expression using Affymetrix U‐133 A arrays. Based on a total of 35 microarrays, no significantly different gene expression profiles appeared to emerge between chronic and aggressive periodontitis. However, a de novo grouping of the 14 subjects into two fairly robust clusters was possible based on similarities in gene expression. These two groups had similar clinical periodontal status and subgingival bacterial profiles, but differed significantly with respect to serum IgG levels against the important periodontal pathogens Porphyromonas gingivalis, Tannerella forsythensis and Campylobacter rectus. These early data point to the usefulness of gene expression profiling techniques in the identification of subclasses of periodontitis with common pathobiology.