Salivary metabolites associated with a 5-year tooth loss identified in a population-based setting

• Main Authors: Leonie Andörfer, Birte Holtfreter, Stefan Weiss, Rutger Matthes, Vinay Pitchika, Carsten Oliver Schmidt, Stefanie Samietz, Gabi Kastenmüller, Matthias Nauck, Uwe Völker, Henry Völzke, Laszlo N. Csonka, Karsten Suhre, Maik Pietzner, Thomas Kocher
• Format: Article
• Language: English
• Published: BMC 2021-07-01
• Series: BMC Medicine
• Subjects: Metabolomics; Periodontitis; Progression; Tooth loss; 2-Pyrrolidineacetic acid; Butyrylputrescine
• Online Access: https://doi.org/10.1186/s12916-021-02035-z

Abstract Background Periodontitis is among the most common chronic diseases worldwide, and it is one of the main reasons for tooth loss. Comprehensive profiling of the metabolite content of the saliva can enable the identification of novel pathways associated with periodontitis and highlight non-invasive markers to facilitate time and cost-effective screening efforts for the presence of periodontitis and the prediction of tooth loss. Methods We first investigated cross-sectional associations of 13 oral health variables with saliva levels of 562 metabolites, measured by untargeted mass spectrometry among a sub-sample (n = 938) of the Study of Health in Pomerania (SHIP-2) using linear regression models adjusting for common confounders. We took forward any candidate metabolite associated with at least two oral variables, to test for an association with a 5-year tooth loss over and above baseline oral health status using negative binomial regression models. Results We identified 84 saliva metabolites that were associated with at least one oral variable cross-sectionally, for a subset of which we observed robust replication in an independent study. Out of 34 metabolites associated with more than two oral variables, baseline saliva levels of nine metabolites were positively associated with a 5-year tooth loss. Across all analyses, the metabolites 2-pyrrolidineacetic acid and butyrylputrescine were the most consistent candidate metabolites, likely reflecting oral dysbiosis. Other candidate metabolites likely reflected tissue destruction and cell proliferation. Conclusions Untargeted metabolic profiling of saliva replicated metabolic signatures of periodontal status and revealed novel metabolites associated with periodontitis and future tooth loss.