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Uric Acid Potential Role in Systemic Inflammation and Negative Symptoms After Acute Antipsychotic Treatment in Schizophrenia

Bibliographic Data

ID15526421
AuthorsMilica Borovčanin (0000-0002-2992-814X, University of Kragujevac), Milica M Borovcanin, Slavica Minic Janicijevic (University of Kragujevac), Nataša R Mijailović (0000-0002-2125-0565, University of Kragujevac), Ivan Jovanovic (0000-0002-1169-2378, University of Kragujevac), Ivan P Jovanovic, Nebojša Arsenijević (0000-0002-2107-3490, University of Kragujevac), Nebojsa N Arsenijevic, Katarina Vesić (0000-0001-8861-4987, University of Kragujevac, corresponding author)
Year2022
Volume12
Pages822579-822579
Publication date2022-02-14
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueFrontiers in Psychiatry (JOURNAL)
Journal identifiersISSN: 1664-0640 • E-ISSN: 1664-0640
PublisherFrontiers Media (PUBLISHER • CH)
DOI10.3389/fpsyt.2021.822579
PMID35237183
OpenAlexW4212931726
LanguageEN
Citations received2
References cited47

Uric acid (UA) has been shown to have neuroprotective or neurotoxic properties, in relation to specific tissues and diseases that have been studied. Previous studies provided contradictory results on the role of UA in schizophrenia as a neurodegenerative disorder. The aim of this brief report was an additional analysis of UA sera levels in different phases of schizophrenia. Here, 86 patients with first-episode psychosis (FEP) vs. 45 patients with schizophrenia in relapse (SC in relapse) vs. 35 healthy control subjects (HC) were studied before and 1 month after antipsychotic therapy. Further, we aimed to explore the possible correlation of UA with scores presenting clinical features and with serum concentrations of the proinflammatory cytokines interleukin (IL)-6 and IL-17. When comparing the data between all three groups, we did not find significant differences in UA levels, either before or after the applied therapy. Also, comparing sera concentrations of UA in every single group, the analysis did not reveal statistically significant differences between FEP patients, but statistically, a significant difference was found in SC in relapse before and after treatment (334.71 ± 116.84 vs. 289.37 ± 109.15 μmol/L, p = 0.05). Uric acid serum levels correlated with negative sub-score ( p = 0.001, r = 0.306), general sub-score ( p = 0.015, r = 0.236), and total PANSS score ( p = 0.009, r = 0.3) after 1 month of therapy. We have established a statistically significant positive correlation between serum concentrations of UA and IL-6 in exacerbation ( p = 0.01, r = 0.220) and with IL-17 after treatment and in the stabilization of psychosis ( p = 0.01, r = 0.34), suggesting potential cascades in different phases of schizophrenia that potentiate inflammation

Antipsychotic · Exacerbation · Inflammation · Proinflammatory cytokine · Psychiatry · Psychosis · Schizophrenia (object-oriented programming · Uric acid · Inflammasome and immune disorders · Medicine · Schizophrenia research and treatment · Tryptophan and brain disorders · Gastroenterology · Internal Medicine

  • IL-17 and TNF-β

    Open Access•Lijun Ouyang, David Li et al.•Frontiers in Psychiatry•2022

  • Role of uric acid as a biomarker of cognitive function in schizophrenia during maintenance period

    Open Access•Zelin Yuan, Huamin Liu et al.•Frontiers in Psychiatry•2023

  • The Positive and Negative Syndrome Scale (PANSS) for Schizophrenia

    Stanley R Kay, Abraham Fiszbein et al.•Schizophrenia Bulletin•1987

  • Insulin Resistance and Oxidative Stress

    Open Access•Tao Qi, Qi Tao et al.•Frontiers in Psychiatry•2020

Unique citing works2
Citations per year0,5
Citation span2022 - 2023 (2)
Citation velocityhistorical
Highly citedNo
Citation typesNeutral: 2

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