4.5 Review

The assessment of stress, depression, and inflammation as a collective risk factor for periodontal diseases: a systematic review

Journal

CLINICAL ORAL INVESTIGATIONS
Volume 24, Issue 1, Pages 1-12

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00784-019-03089-3

Keywords

Psychological stress; Periodontitis; Salivary cortisol; Serum cortisol; Interleukins; DHEA

Funding

  1. University of Michigan Periodontal Graduate Student Research Fund - Tissue Engineering and Regenerative Medicine fellowship [5T32DE007057-42]

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Objectives The purpose of this review was to provide a novel perspective utilizing an assessment of biomarkers to evaluate the impact of stress-related disorders on the progression of periodontal disease and evaluate the growing body of evidence of stress as a risk indicator for periodontal disease progression. Methods Cross-sectional, case-control, and biomarker studies associating psychological disorders and periodontal disease were included in the literature search. Computational studies, animal studies, reviews, and studies lacking healthy controls were excluded. Electronic and manual literature searches were conducted by two independent reviewers in several databases as well as a manual search for relevant articles published up to January 2018. Results Twenty-six articles fulfilled the inclusion criteria and were included in the qualitative synthesis. Relationships between stress-related disorders and serum and salivary biomarkers such as cortisol, dehydroepiandrosterone (DHEA), chromogranin A (CgA), and pro-inflammatory cytokines were identified. Conclusions The use of salivary pro-inflammatory cytokines alone is not sufficient for the identification of periodontal disease severity/progression with or without the presence of stress-associated diseases. Keeping in mind the limitations of this review, a positive qualitative correlation was observed in the literature among stress-related biomarkers and the severity of periodontal disease. This correlation may serve as an important reporter of patient susceptibility for periodontal breakdown in the future.

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