Gas Chromatography-Mass Spectrometry Reveals Stage-Specific Metabolic Signatures of Ankylosing Spondylitis.
Yixuan GuoShuangshuang WeiMengdi YinDandan CaoYiling LiChengping WenJia ZhouPublished in: Metabolites (2023)
Ankylosing spondylitis (AS) is a type of chronic rheumatic immune disease, and the crucial point of AS treatment is identifying the correct stage of the disease. However, there is a lack of effective diagnostic methods for AS staging. The primary objective of this study was to perform an untargeted metabolomic approach in AS patients in an effort to reveal metabolic differences between patients in remission and acute stages. Serum samples from 40 controls and 57 AS patients were analyzed via gas chromatography-mass spectrometry (GC-MS). Twenty-four kinds of differential metabolites were identified between the healthy controls and AS patients, mainly involving valine/leucine/isoleucine biosynthesis and degradation, phenylalanine/tyrosine/tryptophan biosynthesis, glutathione metabolism, etc. Furthermore, the levels of fatty acids (linoleate, dodecanoate, hexadecanoate, and octadecanoate), amino acids (serine and pyroglutamate), 2-hydroxybutanoate, glucose, etc., were lower in patients in the acute stage than those in the remission stage, which may be associated with the aggravated inflammatory response and elevated oxidative stress in the acute stage. Multiple stage-specific metabolites were significantly correlated with inflammatory indicators (CRP and ESR). In addition, the combination of serum 2-hydroxybutanoate and hexadecanoate plays a significant role in the diagnosis of AS stages. These metabolomics-based findings provide new perspectives for AS staging, treatment, and pathogenesis studies.
Keyphrases
- end stage renal disease
- ankylosing spondylitis
- ejection fraction
- oxidative stress
- newly diagnosed
- chronic kidney disease
- gas chromatography mass spectrometry
- inflammatory response
- prognostic factors
- lymph node
- rheumatoid arthritis
- fatty acid
- blood pressure
- gene expression
- mass spectrometry
- type diabetes
- dna damage
- amino acid
- insulin resistance
- intensive care unit
- single cell
- genome wide
- heat shock protein
- cell wall
- diabetic rats
- estrogen receptor
- mechanical ventilation