Biological Markers for Pulpal Inflammation: A Systematic Review

PLoS One. 2016 Nov 29;11(11):e0167289. doi: 10.1371/journal.pone.0167289. eCollection 2016.

Abstract

Background and objective: Pulpitis is mainly caused by an opportunistic infection of the pulp space with commensal oral microorganisms. Depending on the state of inflammation, different treatment regimes are currently advocated. Predictable vital pulp therapy depends on accurate determination of the pulpal status that will allow repair to occur. The role of several players of the host response in pulpitis is well documented: cytokines, proteases, inflammatory mediators, growth factors, antimicrobial peptides and others contribute to pulpal defense mechanisms; these factors may serve as biomarkers that indicate the status of the pulp. Therefore, the aim of this systematic review was to evaluate the presence of biomarkers in pulpitis.

Methods: The electronic databases of MEDLINE, EMBASE, Scopus and other sources were searched for English and non-English articles published through February 2015. Two independent reviewers extracted information regarding study design, tissue or analyte used, outcome measures, results and conclusions for each article. The quality of the included studies was assessed using a modification of the Newcastle-Ottawa-Scale.

Results and conclusions: From the initial 847 publications evaluated, a total of 57 articles were included in this review. In general, irreversible pulpitis was associated with different expression of various biomarkers compared to normal controls. These biomarkers were significantly expressed not only in pulp tissue, but also in gingival crevicular fluid that can be collected non-invasively, and in dentin fluid that can be analyzed without extirpating the entire pulpal tissue. Such data may then be used to accurately differentiate diseased from healthy pulp tissue. The interplay of pulpal biomarkers and their potential use for a more accurate and biologically based diagnostic tool in endodontics is envisaged.

Publication types

  • Review
  • Systematic Review

MeSH terms

  • Antimicrobial Cationic Peptides / metabolism
  • Biomarkers / metabolism*
  • Cytokines / metabolism
  • Databases, Factual
  • Dental Pulp / metabolism*
  • Dental Pulp / pathology
  • Enzymes / metabolism
  • Humans
  • Inflammation / metabolism*
  • Inflammation / pathology
  • Leukocytes / cytology
  • Leukocytes / immunology
  • Leukocytes / metabolism
  • Peptide Hydrolases / metabolism

Substances

  • Antimicrobial Cationic Peptides
  • Biomarkers
  • Cytokines
  • Enzymes
  • Peptide Hydrolases

Grants and funding

This research was supported by institutional funds of the Department of Preventive Dentistry, Periodontology, and Cariology, University of Zürich Center for Dental Medicine. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.