4.6 Article

Saliva Metabolomics in Dry Mouth Patients with Head and Neck Cancer or Sjogren's Syndrome

Journal

CELLS
Volume 11, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/cells11030323

Keywords

radiotherapy; head and neck cancer; Sjogren's syndrome; saliva; metabolomics; pyrimidine signaling; purinergic receptors; amino acid metabolism

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Funding

  1. Oslo University Hospital
  2. University of Oslo

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Through metabolomics analysis, we found different metabolic profiles in patients with dry mouth conditions caused by head and neck cancer and primary Sjogren's syndrome. The dysregulation of purinergic signaling and amino acid metabolism may play a role in the pathophysiology of dry mouth. This finding is important for diagnosis and understanding the underlying mechanisms of dry mouth.
The etiology of dry mouth conditions is multi-faceted. Patients radiated after head and neck cancer (HNC) and those with primary Sjogren's syndrome (pSS) share many of the same symptoms despite different causes. With the aim of better understanding the pathophysiology and biochemical processes behind dry mouth with different etiologies, we investigated the metabolic profile of 10 HNC patients, 9 pSS patients and 10 healthy controls using high-performance liquid chromatography-high resolution mass spectrometry (HPLC-MS) metabolomics. Principal component analysis (PCA) revealed different metabolic profiles when comparing all subjects included in the study. Both patient groups showed higher ratios of several pyrimidine nucleotides and nucleosides when compared to controls. This finding may indicate that purinergic signaling plays a role in dry mouth conditions. Moreover, significantly increased levels of DL-3-aminoisobutyric acid were found in HNC patients when compared to controls, and a similar tendency was observed in the pSS patients. Furthermore, a dysregulation in amino acid metabolism was observed in both patient groups. In conclusion, metabolomics analysis showed separate metabolic profiles for HNC and pSS patients as compared to controls that could be useful in diagnostics and for elucidating the different pathophysiologies. The demonstrated dysregulation of pyrimidine nucleotides and levels of metabolites derived from amino acids in the patient groups should be studied further.

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