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Comprehensive analysis of the oral microbiota and metabolome change in patients of burning mouth syndrome with psychiatric symptoms.
Luo, Shihong; Lou, Fangzhi; Yan, Li; Dong, Yunmei; Zhang, Yingying; Liu, Yang; Ji, Ping; Jin, Xin.
Afiliación
  • Luo S; College of Stomatology, Chongqing Medical University, Chongqing, China.
  • Lou F; Department of Oral Implantology, The Affiliated Stomatology Hospital of Southwest Medical University, Luzhou, China.
  • Yan L; College of Stomatology, Chongqing Medical University, Chongqing, China.
  • Dong Y; College of Stomatology, Chongqing Medical University, Chongqing, China.
  • Zhang Y; College of Stomatology, Chongqing Medical University, Chongqing, China.
  • Liu Y; College of Stomatology, Chongqing Medical University, Chongqing, China.
  • Ji P; College of Stomatology, Chongqing Medical University, Chongqing, China.
  • Jin X; College of Stomatology, Chongqing Medical University, Chongqing, China.
J Oral Microbiol ; 16(1): 2362313, 2024.
Article en En | MEDLINE | ID: mdl-38835338
ABSTRACT

Background:

Burning mouth syndrome (BMS) is a chronic idiopathic facial pain with intraoral burning or dysesthesia. BMS patients regularly suffer from anxiety/depression, and the association of psychiatric symptoms with BMS has received considerable attention in recent years. The aims of this study were to investigate the potential interplay between psychiatric symptoms and BMS.

Methods:

Using 16S rRNA sequencing and liquid chromatography-mass spectrometry (LC/MS) to evaluate the oral microbiota and saliva metabolism of 40 BMS patients [including 29 BMS patients with depression or anxiety symptoms (DBMS)] and 40 age matched healthy control (HC).

Results:

The oral microbiota composition in BMS exhibited no significant differences from HC, although DBMS manifested decreased α-diversity relative to HC. Noteworthy was the discernible elevation in the abundance of proinflammatory microorganisms within the oral microbiome of individuals with DBMS. Parallel findings in LC/MS analyses revealed discernible disparities in metabolites between DBMS and HC groups. Principal differential metabolites were notably enriched in amino acid metabolism and lipid metabolism, exhibiting associations with infectious and immunological diseases. Furthermore, the integrated analysis underscores a definitive association between the oral microbiome and metabolism in DBMS.

Conclusions:

This study suggests possible future modalities for better understanding the pathogenesis and personalized treatment plans of BMS.
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Oral Microbiol Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: J Oral Microbiol Año: 2024 Tipo del documento: Article