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. 2023 Jul:111:270-276.
doi: 10.1016/j.bbi.2023.05.001. Epub 2023 May 5.

Systemic inflammation and cortical neurochemistry in never-medicated first episode-psychosis individuals

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Systemic inflammation and cortical neurochemistry in never-medicated first episode-psychosis individuals

Pablo León-Ortiz et al. Brain Behav Immun. 2023 Jul.

Abstract

Studies of cellular and cytokine profiles have contributed to the inflammation hypothesis of schizophrenia; however, precise markers of inflammatory dysfunction remain elusive. A number of proton magnetic resonance spectroscopy (1H-MRS) studies in patients with first-episode psychosis (FEP) have shown higher brain levels of metabolites such as glutamate, myo-inositol (mI) and choline-containing compounds (tCho), suggesting neuroinflammation. Here, we present peripheral inflammatory profiles in antipsychotic-naive FEP patients and age-and-sex matched healthy controls, as well as cortical glutamate, mI and tCho levels using 1H-MRS. Inflammatory profiles were analyzed using cytokine production by peripheral blood mononuclear cells, that were either spontaneous or stimulated, in 48 FEP patients and 23 controls. 1H-MRS of the medial prefrontal cortex was obtained in 29 FEP patients and 18 controls. Finally, 16 FEP patients were rescanned after 4 weeks of treatment (open-label) with Risperidone. FEP patients showed a higher proportion of proinflammatory Th1/Th17 subset, and an increased spontaneous production of Interleukin (IL)-6, IL-2 and IL-4 compared with the control group. Results obtained from 1H-MRS showed no significant difference in either glutamate, mI or tCho between FEP and control groups. At baseline, CD8% showed a negative correlation with glutamate in FEP patients; after 4 weeks of risperidone treatment, the FEP group exhibited a decrease in glutamate levels which positively correlated with CD4 + T cells. Nevertheless, these correlations did not survive correction for multiple comparisons. FEP patients show evidence of immune dysregulation, affecting both the innate and adaptive immune response, with a predominantly Th2 signature. These findings, along with the changes produced by antipsychotic treatment, could be associated with both systemic and central inflammatory processes in schizophrenia.

Keywords: Cytokines; Inflammation; Magnetic resonance spectroscopy; Peripheral blood mononuclear cells; Psychosis.

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Conflict of interest statement

Declaration of Competing Interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests: Pablo León-Ortiz and Francisco Reyes-Madrigal have received speaking fees from Janssen (Johnson & Johnson) outside the submitted work. The rest of the authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Figures

Figure 1.
Figure 1.
Scatter plots of a) Inflammatory markers of never medicated first episode of psychosis subjects compared to healthy controls. b) Inflammatory markers of first episode of psychosis before and after 4 weeks of risperidone treatment. FEP, first-episode psychosis group; Th1, Type 1 helper T cells; Th17, T helper 17 cells; IL-6, interleukin 6; IL-4, interleukin 4; IL-2, interleukin 2; Th2, Type 2 helper T cells; TNF, Tumor necrosis factor. Data shown in the Figure has been log transformed for a better visualization. * p < 0.05.

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