Metabolic phenotyping of saliva to identify possible biomarkers of periodontitis using proton nuclear magnetic resonance
Aim The aim of this study was to propose biomarker candidates for periodontitis via untargeted metabolomics analysis. Materials and methods Metabolic profiling was performed using saliva samples from 92 healthy controls (H) and 129 periodontitis patients (P) in the discovery cohort using proton nucl...
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Veröffentlicht in: | Journal of clinical periodontology 2021-09, Vol.48 (9), p.1240-1249 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Aim
The aim of this study was to propose biomarker candidates for periodontitis via untargeted metabolomics analysis.
Materials and methods
Metabolic profiling was performed using saliva samples from 92 healthy controls (H) and 129 periodontitis patients (P) in the discovery cohort using proton nuclear magnetic resonance spectroscopy. Random forest was applied to identify metabolites that significantly differentiated the control group from the periodontitis group. Candidate metabolites were then validated in an independent validation cohort.
Results
In the discovery set, the metabolic profiles of the P group were clearly separated from those of the H group. A total of 31 metabolites were identified in saliva, and 7 metabolites were selected as candidate biomarkers. These metabolites were further confirmed in the validation set. Ethanol, taurine, isovalerate, butyrate, and glucose were finally confirmed as biomarkers. Furthermore, the biomarker panel showed more than 0.9 of the area under curve value in both discovery and validation sets, indicating that panels were more effective than individual metabolites for diagnosing periodontitis.
Conclusions
We identified five metabolite biomarkers that discriminated patients with periodontitis from healthy controls in two independent cohorts. These biomarkers have the potential for periodontal screening, detection of periodontitis, and monitoring of the outcome of periodontal therapy. |
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ISSN: | 0303-6979 1600-051X |
DOI: | 10.1111/jcpe.13516 |