Burning mouth syndrome (BMS) is defined by a chronic oral pain affecting especially postmenopausal women. Its physiopathology is still unknown and several hypotheses have been put forward to explain this syndrome, such as neurological, hormonal or inflammatory process. The recent development of salivary metabolomic profiling in oral diseases has led to the identification of potential pathways in such disorders. The aim of this study is to analyze the salivary metabolomic in BMS patients compared to healthy controls.
Burning mouth syndrome (BMS) is defined by a chronic oral pain affecting especially postmenopausal women. Its physiopathology is still unknown and several hypotheses have been put forward to explain this syndrome, such as neurological, hormonal or inflammatory process. The recent development of salivary metabolomic profiling in oral diseases has led to the identification of potential pathways in such disorders. The aim of this study is to analyze the salivary metabolomic in BMS patients compared to healthy controls.
Study Type
OBSERVATIONAL
Enrollment
53
Collection of total saliva not stimulated
Department of Dermatology, Hospital University of Tours
Tours, France
Comparative analysis of salivary metabolomic profiles between cases (primary BMS) and controls
metabolites will be measured in saliva by chromatography-mass spectrometry
Time frame: at inclusion
Comparative analysis of salivary neuropeptides between cases (primary BMS) and controls
quantitative assessment of levels of neuropeptides (NGF, histamine, tryptase, kallicrein) will be assessed in saliva in cases and controls
Time frame: at inclusion
Comparative analysis of salivary hormones between cases (primary BMS) and controls
quantitative assessment of levels of steroid hormones (cortisol, 11-desoxycortisol, DHEA, SDHEA, progesterone, 17-hydroxyprogesterone, testosterone, androstenedione) will be assessed in saliva in cases and controls
Time frame: at inclusion
Comparative analysis of salivary inflammatory cytokines between cases (primary BMS) and controls
quantitative assessment of levels of cytokines (IL-2, IL-6, IL-18, TNFα) will be assessed in saliva in cases and controls
Time frame: at inclusion
Correlation between salivary biomarkers and pain characteristics
metabolites profile, salivary neuropeptides, hormones and cytokines will be compared according to the category of pain (type I-II-III, neuropathic pain score DN4\>4)
Time frame: at inclusion
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