Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/121796
Citations
Scopus Web of Science® Altmetric
?
?
Type: Journal article
Title: Targeted proteomic analysis of cognitive dysfunction in remitted major depressive disorder: Opportunities of multi-omics approaches towards predictive, preventive, and personalized psychiatry
Author: Schubert, K.
Stacey, D.
Arentz, G.
Clark, S.
Air, T.
Hoffmann, P.
Baune, B.
Citation: Journal of Proteomics, 2018; 188:63-70
Publisher: Elsevier
Issue Date: 2018
ISSN: 1874-3919
1876-7737
Statement of
Responsibility: 
K. Oliver Schubert, David Stacey, Georgia Arentz, Scott R. Clark, Tracy Air, Peter Hoffmann, Bernhard T. Baune
Abstract: In order to accelerate the understanding of pathophysiological mechanisms and clinical biomarker discovery and in psychiatry, approaches that integrate multiple -omics platforms are needed. We introduce a workflow that investigates a narrowly defined psychiatric phenotype, makes use of the potent and cost-effective discovery technology of gene expression microarrays, applies Weighted Gene Co-Expression Network Analysis (WGCNA) to better capture complex and polygenic traits, and finally explores gene expression findings on the proteomic level using targeted mass-spectrometry (MS) technologies. To illustrate the effectiveness of the workflow, we present a proteomic analysis of peripheral blood plasma from patient's remitted major depressive disorder (MDD) who experience ongoing cognitive deficits. We show that co-expression patterns previous detected on the transcript level could be replicated for plasma proteins, as could the module eigengene correlation with cognitive performance. Further, we demonstrate that functional analysis of multi-omics data has the potential to point to cellular mechanisms and candidate biomarkers for cognitive dysfunction in MDD, implicating cell cycle regulation by cyclin D3 (CCND3), regulation of protein processing in the endoplasmatic reticulum by Thioredoxin domain-containing protein 5 (TXND5), and modulation of inflammatory cytokines by Tripartite Motif Containing 26 (TRI26).This paper discusses how data from multiple -omics platforms can be integrated to accelerate biomarker discovery in psychiatry. Using the phenotype of cognitive impairment in remitted major depressive disorder (MDD) as an example, we show that the application of a systems biology approach - weighted gene co-expression network analysis (WGCNA) - in the discovery phase, and targeted proteomic follow-up of results, provides a structured avenue towards uncovering novel candidate markers and pathways for personalized clinical psychiatry.
Keywords: Cognitive deficits
Gene expression
Major depression
Proteomics
WGCNA
Rights: © 2018 Elsevier B.V. All rights reserved.
DOI: 10.1016/j.jprot.2018.02.023
Appears in Collections:Aurora harvest 8
Chemistry publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.