Publications by authors named "Tomasz Grazlewski"

Dysregulation of the hypothalamic-pituitary-adrenal (HPA) axis has been implicated in the development of psychosis and subthreshold psychotic symptoms commonly referred to as psychotic-like experiences (PLEs). The exact mechanisms linking the HPA axis responses with the emergence of PLEs remain unknown. The present study aimed to explore real-life associations between stress, negative affect, salivary cortisol levels (a proxy of the HPA axis activity) as well as PLEs together with their underlying cognitive biases (i.

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Background: Several studies have shown that social isolation and loneliness are associated with the occurrence of psychotic experiences. However, dynamics of these phenomena in people with subclinical experiences, commonly referred to as psychotic-like experiences (PLEs), remains largely unknown. Therefore, in this study we performed a temporal network analysis to model dynamic predictions between social isolation, loneliness, negative affect, social stress, and PLEs.

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Aim: It has been observed that deficit and non-deficit schizophrenia (SCZ-D and SCZ-ND) might be characterized by different risk factors. Therefore, the present study aimed to assess as to whether previously reported risk factors of schizophrenia are specifically associated with SCZ-D and SCZ-ND.

Method: This study was based on a cohort of 118 stable outpatients with schizophrenia.

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Previous studies have shown that neurodevelopmental characteristics of adverse childhood experiences (ACEs), such as their accumulation and minimal age at exposure, might moderate their impact on clinical expression of psychosis. However, it remains unknown as to whether specific neurodevelopmental characteristics of ACEs are associated with biological alterations observed in psychosis. In this study, we tested the hypothesis that younger minimal age at exposure as well as greater accumulation and severity of ACEs are associated with systemic biological dysregulations captured by the allostatic load (AL) index in patients with psychosis.

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Article Synopsis
  • - The study investigates how stem cells and immune factors like the complement cascade influence the development of schizophrenia, focusing on comparing levels of specific molecules in patients at various stages of psychosis and healthy controls.
  • - Researchers measured levels of certain immune components in the blood of 49 individuals, finding that those at ultra-high risk and those experiencing their first episode of psychosis had higher levels of a complement factor (C3a) compared to healthy individuals.
  • - They observed a significant correlation between a type of stem cell (VSELs) and negative symptoms in first-episode psychosis patients, suggesting that both regenerative and inflammatory processes may play a role in schizophrenia, but further research is needed to confirm these findings.
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Impairments in cognitive functions are one of the main features of schizophrenia. A variety of factors can influence the extent of cognitive deficits. In our study, we examined the severity of cognitive deficits at different stages of the disease and the relationship between psychopathological symptoms and cognitive functions.

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Altered methylation of the gene has been observed in various mental disorders and attributed to the effects of adverse childhood experiences (ACEs). However, the level of methylation has not been investigated in patients with psychotic disorders. Therefore, in this study we aimed to determine the methylation in patients with psychosis and controls, taking into account the effects of ACEs.

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