Literature DB >> 23360651

Circulating levels of sTNFR1 as a marker of severe clinical course in schizophrenia.

Cristiano Noto1, Ary Gadelha, Síntia I Belangero, Letícia M Spindola, Natália Pessoa Rocha, Aline Silva de Miranda, Antônio Lúcio Teixeira, Marília Arruda Cardoso Smith, Jair de Jesus Mari, Rodrigo Affonseca Bressan, Elisa Brietzke.   

Abstract

BACKGROUND: Schizophrenia (SZ) has been associated with an imbalance in the inflammatory cytokine TNF-α. The objectives of this study were to compare TNF-α and its soluble receptors' serum levels in individuals with SZ with the levels found in a group of healthy volunteers and to investigate the possible association between these biomarkers and the dimensions and severity of symptoms, clinical outcomes and response to treatment in patients with SZ.
METHODS: Fifty-four chronically medicated SZ outpatients and 118 healthy controls were included in the study. TNF-α levels were measured by Cytometric Bead Assay (CBA), and serum levels of soluble tumor necrosis factor receptor 1 (sTNFR1) and soluble tumor necrosis factor receptor 2 (sTNFR2) were measured by ELISA.
RESULTS: sTNFR1 and sTNFR2 were significantly elevated in patients with SZ as compared to the healthy control group. In the group of individuals with SZ, the levels of both types of soluble TNF receptors showed a negative correlation with global functioning. sTNFR1 levels were higher in the treatment-resistant patients as compared to the non-treatment-resistant patients and the controls. sTNFR1 levels were also heightened in patients with SZ and concomitant depression.
CONCLUSION: Our findings reinforce that SZ is associated with an inflammatory profile and suggest that sTNFR1 is a marker of a treatment-resistance and severe clinical course in SZ.
Copyright © 2013 Elsevier Ltd. All rights reserved.

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Year:  2013        PMID: 23360651     DOI: 10.1016/j.jpsychires.2012.12.010

Source DB:  PubMed          Journal:  J Psychiatr Res        ISSN: 0022-3956            Impact factor:   4.791


  14 in total

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Journal:  Mol Psychiatry       Date:  2016-02-23       Impact factor: 15.992

Review 3.  Recent Reports on Redox Stress-Induced Mitochondrial DNA Variations, Neuroglial Interactions, and NMDA Receptor System in Pathophysiology of Schizophrenia.

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Journal:  Schizophr Bull       Date:  2022-01-21       Impact factor: 7.348

5.  Depression, Cytokine, and Cytokine by Treatment Interactions Modulate Gene Expression in Antipsychotic Naïve First Episode Psychosis.

Authors:  Cristiano Noto; Vanessa Kiyomi Ota; Marcos Leite Santoro; Eduardo Sauerbronn Gouvea; Patricia Natalia Silva; Leticia Maria Spindola; Quirino Cordeiro; Rodrigo Affonseca Bressan; Ary Gadelha; Elisa Brietzke; Sintia Iole Belangero; Michael Maes
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7.  Effects of risperidone on cytokine profile in drug-naïve first-episode psychosis.

Authors:  Cristiano Noto; Vanessa Kiyomi Ota; Eduardo S Gouvea; Lucas B Rizzo; Leticia M N Spindola; Pedro H S Honda; Quirino Cordeiro; Sintia Iole Belangero; Rodrigo Affonseca Bressan; Ary Gadelha; Michael Maes; Elisa Brietzke
Journal:  Int J Neuropsychopharmacol       Date:  2014-10-31       Impact factor: 5.176

8.  Association Study of Tumor Necrosis Factor Receptor 1 (TNFR1) Gene Polymorphisms with Schizophrenia in the Polish Population.

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Journal:  Mediators Inflamm       Date:  2017-11-29       Impact factor: 4.711

9.  The Clinical Challenge of Autoimmune Psychosis: Learning from Anti-NMDA Receptor Autoantibodies.

Authors:  Pierre Ellul; Laurent Groc; Ryad Tamouza; Marion Leboyer
Journal:  Front Psychiatry       Date:  2017-04-19       Impact factor: 4.157

Review 10.  A critical review of pro-cognitive drug targets in psychosis: convergence on myelination and inflammation.

Authors:  Rune A Kroken; Else-Marie Løberg; Tore Drønen; Renate Grüner; Kenneth Hugdahl; Kristiina Kompus; Silje Skrede; Erik Johnsen
Journal:  Front Psychiatry       Date:  2014-02-04       Impact factor: 4.157

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