4.7 Article

Cerebrospinal Fluid Metabolome in Mood Disorders-Remission State has a Unique Metabolic Profile

Journal

SCIENTIFIC REPORTS
Volume 2, Issue -, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/srep00667

Keywords

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Funding

  1. NIH [R24 GM078233]
  2. Department of Veterans Affairs Senior Research Scientist Award
  3. Amgen
  4. Bristol-Myers Squibb
  5. CeNeRx
  6. Corcept
  7. GlaxoSmithKline
  8. Johnson Johnson
  9. Lundbeck
  10. Merck
  11. Organon
  12. Pfizer
  13. Sepracor
  14. Wyeth
  15. Rules Based Medicine
  16. Eisai
  17. Abbott

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Targeted metabolomics provides an approach to quantify metabolites involved in specific molecular pathways. We applied an electrochemistry-based, targeted metabolomics platform to define changes in tryptophan, tyrosine, purine and related pathways in the depressed and remitted phases of major depressive disorder (MDD). Biochemical profiles in the cerebrospinal fluid of unmedicated depressed (n=14; dMDD) or remitted MDD subjects (n=14; rMDD) were compared against those in healthy controls (n=18; HC). The rMDD group showed differences in tryptophan and tyrosine metabolism relative to the other groups. The rMDD group also had higher methionine levels and larger methionine-to-glutathione ratios than the other groups, implicating methylation and oxidative stress pathways. The dMDD sample showed nonsignificant differences in the same direction in several of the metabolic branches assessed. The reductions in metabolites associated with tryptophan and tyrosine pathways in rMDD may relate to the vulnerability this population shows for developing depressive symptoms under tryptophan or catecholamine depletion.

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