| Literature DB >> 29719272 |
Eun Young Kim1, Jae Won Lee2, Min Young Lee3, Se Hyun Kim4, Hyuck Jun Mok2, Kyooseob Ha5, Yong Min Ahn6, Kwang Pyo Kim7.
Abstract
Lipidomic analysis can be used to efficiently identify hundreds of lipid molecular species in biological materials and has been recently established as an important tool for biomarker discovery in various neuropsychiatric disorders including major depressive disorder (MDD). In this study, quantitative targeted serum lipidomic profiling was performed on female subjects using liquid chromatography-mass spectrometry. Global lipid profiling of pooled serum samples from 10 patients currently with MDD (cMDD), 10 patients with remitted MDD (rMDD), and 10 healthy controls revealed 37 differentially regulated lipids (DRLs). DRLs were further verified using multiple-reaction monitoring (MRM) in each of the 25 samples from the three groups of independent cohorts. Using multivariate analysis and MRM data we identified serum biomarker panels of discriminatory lipids that differentiated between pairs of groups: lysophosphatidic acid (LPA)(16:1), triglycerides (TG)(44:0), and TG(54:8) distinguished cMDD from controls with 76% accuracy; lysophosphatidylcholines(16:1), TG(44:0), TG(46:0), and TG(50:1) distinguished between cMDD and rMDD at 65% accuracy; and LPA(16:1), TG(52:6), TG(54:8), and TG(58:10) distinguished between rMDD and controls with 60% accuracy. Our lipidomic analysis identified peripheral lipid signatures of MDD, which thereby provides providing important biomarker candidates for MDD.Entities:
Keywords: Biomarker; Lipidomics; Major depressive disorder; Peripheral lipid signature
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Year: 2018 PMID: 29719272 DOI: 10.1016/j.psychres.2018.04.029
Source DB: PubMed Journal: Psychiatry Res ISSN: 0165-1781 Impact factor: 3.222