Proteomics in Schizophrenia: A Gateway to Discover Potential Biomarkers of Psychoneuroimmune Pathways
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Frontiers Media
Abstract
Schizophrenia is a severe and disabling psychiatric disorder with a complex and
multifactorial etiology. The lack of consensus regarding the multifaceted dysfunction of this
ailment has increased the need to explore new research lines. This research makes use
of proteomics data to discover possible analytes associated with psychoneuroimmune
signaling pathways in schizophrenia. Thus, we analyze plasma of 45 patients [10 patients
with first-episode schizophrenia (FES) and 35 patients with chronic schizophrenia] and
43 healthy subjects by label-free liquid chromatography–tandem mass spectrometry. The
analysis revealed a significant reduction in the levels of glia maturation factor beta (GMF-
β), the brain-derived neurotrophic factor (BDNF), and the 115-kDa isoform of the Rab3
GTPase-activating protein catalytic subunit (RAB3GAP1) in patients with schizophrenia
as compared to healthy volunteers. In conclusion, GMF-β, BDNF, and 115-kDa isoform of
RAB3GAP1 showed significantly reduced levels in plasma of patients with schizophrenia,
thus making them potential biomarkers in schizophrenia.
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Rodrigues-Amorim D, Rivera-Baltanás T, Vallejo-Curto MdC, Rodriguez-Jamardo C, de las Heras E, Barreiro-Villar C, Blanco-Formoso M, Fernández-Palleiro P, Álvarez-Ariza M, López M, García-Caballero A, Olivares JM and Spuch C (2019) Proteomics in Schizophrenia: A Gateway to Discover Potential Biomarkers of Psychoneuroimmune Pathways. Front. Psychiatry 10:885. doi: 10.3389/fpsyt.2019.00885
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https://doi.org/10.3389/fpsyt.2019.00885Sponsors
This work was financially backed by the Foundation for Science and Technology (FCT, Fundação para a Ciência e Tecnologia) within the framework of grant SFRH/BD/135623/2018 awarded to Daniela Rodrigues- Amorim, and another grant of Fundación Tatiana Pérez de Guzmanel Bueno provided to Carlos Spuch. Our research was further supported by the Carlos III Health Institute (ISCIII, Instituto Carlos III) through grant P16/00405
and co-funding awarded by the Spanish Foundation of Rare Diseases (FEDER, Fundación Española de Enfermedades Raras) to José Manuel Olivares
Rights
Copyright © 2019 Rodrigues-Amorim, Rivera-Baltanás, Vallejo-Curto, Rodriguez- Jamardo, de las Heras, Barreiro-Villar, Blanco-Formoso, Fernández-Palleiro, Álvarez- Ariza, López, García-Caballero, Olivares and Spuch. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms



