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Blood biomarker discovery in drug-free schizophrenia: the contributionof proteomics and multiplex immunoassays.

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Version 2 2022-03-08, 15:21
Version 1 2019-11-22, 17:08
journal contribution
posted on 2019-11-22, 17:08 authored by Sophie Sabherwal, Jane A. English, Melanie Föcking, Gerard Cagney, David R. Cotter

INTRODUCTION: Recent evidence supports an association between systemic abnormalities and the pathology of psychotic disorders which has led to the search for peripheral blood-based biomarkers. Areas covered: Here, we summarize blood biomarker findings in schizophrenia from the literature identified by two methods currently driving biomarker discovery in the human proteome; mass spectrometry and multiplex immunoassay. From a total of 14 studies in the serum or plasma of drug-free schizophrenia patients; 47 proteins were found to be significantly altered twice or more, in the same direction. Pathway analysis was performed on these proteins, and the resulting pathways discussed in relation to schizophrenia pathology. Future directions are also discussed, with particular emphasis on the potential for high-throughput validation techniques such as data-independent analysis for confirmation of biomarker candidates. Expert commentary: We present promising findings that point to a convergence of pathophysiological mechanisms in schizophrenia that involve the acute-phase response, glucocorticoid receptor signalling, coagulation, and lipid and glucose metabolism.

Funding

This project was funded by the Health Research Board, Clinical Scientist Award to Prof. David R. Cotter.

History

Comments

The Version of Scholarly Record of this Article is published in Expert Review of Proteomics 2016, available online at http://www.tandfonline.com/ http://dx.doi.org/10.1080/14789450.2016.1252262

Published Citation

Sabherwal S, English JA, Föcking M, Cagney G, Cotter DR. Blood biomarker discovery in drug-free schizophrenia: the contributionof proteomics and multiplex immunoassays. Expert Review of Proteomics. 2016;13(12):1141-1155.

Publication Date

2016-12-01

Publisher

Taylor & Francis Group

PubMed ID

27771981

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