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Metabolic profiling of synovial fluid in human temporomandibular joint osteoarthritis.
Zhang, Dahe; Zhang, Yuxin; Xia, Simo; Shen, Pei; Yang, Chi.
Affiliation
  • Zhang D; Department of Oral Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
  • Zhang Y; College of Stomatology, Shanghai Jiao Tong University, Shanghai, China.
  • Xia S; National Center for Stomatology, Shanghai, China.
  • Shen P; National Clinical Research Center for Oral Diseases, Shanghai, China.
  • Yang C; Shanghai Key Laboratory of Stomatology, Shanghai, China.
Front Immunol ; 15: 1335181, 2024.
Article in En | MEDLINE | ID: mdl-38529278
ABSTRACT

Introduction:

Temporomandibular joint (TMJ) osteoarthritis (OA) is a common TMJ degenerative disease with an unclear mechanism. Synovial fluid (SF), an important component of TMJ, contains various proteins and metabolites that may directly contribute to OA. The present study aimed to investigate the influence of SF in TMJOA at the metabolite level.

Methods:

Untargeted and widely targeted metabolic profiling were employed to identify metabolic changes in SF of 90 patients with different TMJOA grades according to TMJ magnetic resonance imaging.

Results:

A total 1498 metabolites were detected. Most of the metabolites were amino acids and associated metabolites, benzene and substituted derivatives, and lipids. Among patients with mild, moderate and severe TMJOA, 164 gradually increasing and 176 gradually decreasing metabolites were identified, indicating that biosynthesis of cofactors, choline metabolism, mineral absorption and selenocompound metabolism are closely related to TMJOA grade. Combined metabolomics and clinical examination revealed 37 upregulated metabolites and 16 downregulated metabolites in patients with pain, of which 19 and 26 metabolites were positively and negatively correlated, respectively, with maximum interincisal opening. A model was constructed to diagnose TMJOA grade and nine biomarkers were identified. The identified metabolites are key to exploring the mechanism of TMJOA.

Discussion:

In the present study, a metabolic profile was constructed and assessed using a much larger number of human SF samples from patients with TMJOA, and a model was established to contribute to the diagnosis of TMJOA grade. The findings expand our knowledge of metabolites in human SF of TMJOA patients, and provide an important basis for further research on the pathogenesis and treatment of TMJOA.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteoarthritis / Temporomandibular Joint Disorders Limits: Humans Language: En Journal: Front Immunol Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteoarthritis / Temporomandibular Joint Disorders Limits: Humans Language: En Journal: Front Immunol Year: 2024 Document type: Article Affiliation country: China
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