Publications by authors named "Irina A Mednova"

Metabolic syndrome (MetS) is common among schizophrenia patients, and one of MetS's causes may be an imbalance in nitric oxide regulation. In this study, we examined associations of three polymorphic variants of the nitric oxide synthase 1 adapter protein () gene with MetS in schizophrenia. NOS1AP regulates neuronal nitric oxide synthase, which controls intracellular calcium levels and may influence insulin secretion.

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Depressive disorder is a multifactorial disease that is based on dysfunctions in mental and biological processes. The search for biomarkers can improve its diagnosis, personalize therapy, and lead to a deep understanding of the biochemical processes underlying depression. The purpose of this work was a metabolomic analysis of blood serum to classify patients with depressive disorders and healthy individuals using Compound Discoverer software.

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Machine learning and artificial intelligence technologies are known to be a convenient tool for analyzing multi-domain data in precision psychiatry. In the case of schizophrenia, the most commonly used data sources for such purposes are neuroimaging, voice and language patterns, and mobile phone data. Data on peripheral markers can also be useful for building predictive models.

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Article Synopsis
  • The study examined how typical (first-generation) and atypical (second-generation) antipsychotic treatments affected these antibodies and serum cytokine levels in 40 schizophrenia patients.
  • Results showed that atypical antipsychotics altered levels of pro-inflammatory cytokines and significantly decreased myelin basic protein (MBP)-hydrolyzing activity, suggesting a link between these changes and the immune response in schizophrenia.
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  • - The study explores the role of growth factors, important molecules in cell development, in the development of schizophrenia symptoms, proposing it as a neurodevelopmental disorder.
  • - Researchers analyzed serum levels of six growth factors in 236 schizophrenia patients and 102 healthy individuals, finding higher levels of TGF-α and PDGF-AA in patients.
  • - The findings showed that the duration of schizophrenia correlates positively with FGF-2 levels, suggesting the need for combined biomarker screening to improve diagnosis and management of severe mental illnesses.
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Metabolic syndrome (MetS) is a common comorbidity of schizophrenia and significantly shortens life expectancy of the patients. Intercellular (ICAM), vascular (VCAM), and neural (NCAM) cell adhesion molecules (CAMs) mediate neuroinflammatory processes, and their soluble forms (e.g.

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Chemokines are known to be immunoregulatory proteins involved not only in lymphocyte chemotaxis to the site of inflammation, but also in neuromodulation, neurogenesis, and neurotransmission. Multiple lines of evidence suggest a peripheral proinflammatory state and neuroinflammation in at least a third of patients with schizophrenia. Therefore, chemokines can be active players in these processes.

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Article Synopsis
  • Immune activation and neuroinflammation are significant factors in the development of schizophrenia, supported by various studies and reviews.
  • A study measured levels of 22 cytokines in 236 schizophrenia patients and 103 healthy individuals, finding several cytokines elevated in patients with schizophrenia.
  • The research highlighted differences in cytokine levels based on sex and the duration of illness, suggesting that cytokine imbalances relate to both clinical features and the severity of schizophrenia symptoms.
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  • Metabolic syndrome (MetS) is prevalent among individuals with schizophrenia, particularly worsened by long-term use of atypical antipsychotic medications.
  • A study of 195 schizophrenia patients found that those with MetS had significantly higher leptin levels and lower ghrelin levels compared to those without MetS.
  • Insulin levels showed no significant difference between the two groups, and while some correlations between hormone levels and body characteristics were observed, they were more common in individuals without MetS, highlighting the distinct hormonal influences in this condition.
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  • * In a study of 112 paranoid schizophrenia patients, 39 were identified with MetS; those with MetS had elevated levels of specific acylcarnitines and branched-chain amino acids compared to those without MetS.
  • * The research indicated lower levels of certain carnitines in schizophrenia patients versus healthy individuals, suggesting that antipsychotic medications might impact energy metabolism by affecting a key enzyme responsible for fat metabolism.
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This study aimed to evaluate the superoxide dismutase (SOD) activity of IgG in patients with schizophrenia. After signing informed consent, we included 67 patients with schizophrenia (34 people with acute schizophrenia and 33 individuals were on outpatient treatment in therapeutic remission) and 14 healthy volunteers. IgGs from blood serum were isolated by affinity chromatography.

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  • Metabolic syndrome is common among schizophrenia patients on long-term antipsychotic treatment, which can result from the effects of dopamine D2 receptors.
  • The study analyzed 517 schizophrenia patients in Siberia, focusing on two specific genetic variations in the DRD2 gene and their link to metabolic syndrome.
  • Findings suggest that a particular variation (rs1799732) is associated with drug-induced metabolic syndrome in women, pointing to the potential for targeted genetic treatments to improve patient outcomes.
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Objectives: Because alcohol use disorder (AUD) is often accompanied by mood disorder (MD) and both alcoholism and depression result in activation of the immune system, this study compares serum cytokine levels in the presence of co-morbidity with those in either AUD or MD alone.

Methods: In this naturalistic prospective study the levels of 15 different cytokines were measured in serum samples of patients with MD ( = 43), participants with combined AUD-MD ( = 44) and AUD without MD ( = 42). The levels were compared cross-sectionally among themselves and with those in 50 healthy volunteers.

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Background: Metabolic syndrome (MetS) is a common complication of long-term treatment of persons with schizophrenia taking (atypical) antipsychotics. In this study, we investigated the existence of an association with polymorphisms of genes for four hormones that regulate energy metabolism.

Methods: We recruited 517 clinically admitted white patients (269M/248F) with a verified diagnosis of schizophrenia (ICD-10) and with a stable physical condition.

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Purpose: Metabolic syndrome (MetS) is characterized by abdominal obesity, hyperglycaemia, dyslipidaemia and hypertension. FTO gene has been implicated in the pathogenesis of obesity, but the available scientific data concerning their relationship to antipsychotic drug-induced obesity and metabolic syndrome is still incomplete and inconsistent, which indicates that continuing the investigation of this gene's role is necessary.

Patients And Methods: In the present study, 517 patients with schizophrenia underwent antipsychotic drug treatment, and two groups were identified: patients with MetS and without MetS.

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The purpose of this study was to compare the prevalence of MetS and the associated sociodemographic, clinical, and pharmacotherapeutic characteristics of patients with schizophrenia in three psychiatric hospitals in the West Siberian region. Patients with a clinical diagnosis of schizophrenia (ICD-10: F20) and an age between 18 and 60 years were included in the study after giving informed consent. Metabolic syndrome was diagnosed according to the International Diabetes Federation criteria.

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The present study aims at comparing the change in cytokine levels in schizophrenia patients treated with atypical antipsychotics, with or without metabolic syndrome (MetS). The study included 101 patients with schizophrenia, 38 with and 63 without MetS, who received risperidone, quetiapine, olanzapine or aripiprazole for six weeks. We analyzed the concentration of 21 cytokines in the serum patients.

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Background: Antipsychotic-induced metabolic syndrome (MetS) is a multifactorial disease with a genetic predisposition. Serotonin and its receptors are involved in antipsychotic-drug-induced metabolic disorders. The present study investigated the association of nine polymorphisms in the four 5-hydroxytryptamine receptor () genes , , , and and the gene encoding for the serotonin transporter with MetS in patients with schizophrenia.

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Amino acids and acylcarnitines play an important role as substrates and intermediate products in most of pathways involved in schizophrenia development such as mitochondrial dysfunction, inflammation, lipid oxidation, DNA damage, oxidative stress, and apoptosis. It seems relevant to use an integrated approach with 'omics' technology to study their contribution. The aim of our study was to investigate serum amino acid and acylcarnitine levels in antipsychotics-treated patients with chronic schizophrenia compared with healthy donors.

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The adipokines leptin, adiponectin, tumor necrosis factor-alpha (TNF-α), and interleukin 6 (IL-6) might be associated with metabolic syndrome (MetS) in patients with schizophrenia. In the present study, we attempted to confirm the results of previous reports and assessed their MetS-related correlation with body fat composition and biochemical parameters. We measured in 46 patients with schizophrenia and MetS serum levels of adiponectin insulin, leptin, TNF-α and IL-6 and compared these levels to those of patients with schizophrenia without MetS.

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Article Synopsis
  • The study investigates the relationship between body fat, glucose and lipid levels, and thyroid hormone levels in schizophrenia patients from the Tomsk region, looking specifically at whether they have metabolic syndrome (MetS) or not.
  • It includes 156 patients with schizophrenia—56 with MetS and 100 without—compared against reference groups of both individuals with MetS who do not have schizophrenia and healthy individuals.
  • Findings show that schizophrenia patients with MetS had higher levels of thyroid hormones (FT3 and FT4) compared to those without MetS, indicating significant associations with MetS, sex, age, and lipid/glucose levels.
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Background: Both dehydroepiandrosterone (DHEAS) and cortisol are secreted by the adrenal glands and may modulate metabolic syndrome (MetS), which often affects the health of patients with schizophrenia. The relationship between the serum levels of these hormones and MetS has not been established.

Purpose: In this pilot study, we investigated the serum levels in schizophrenia patients with and without MetS and compared them with those in healthy volunteers.

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This work is the first to demonstrate that class G immunoglobulins (IgGs) in patients with multiple sclerosis and healthy individuals have the ability to catalyze the dismutation reaction of the superoxide anion radical. Thus, superoxide dismutase (SOD) activity is an intrinsic property of antibodies, which is confirmed by a number of stringent criteria. SOD activity of IgGs in patients with multiple sclerosis statistically significantly exceeds such activity in healthy individuals by 2-4 times.

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Metabolic syndrome (MetS) is a common problem in schizophrenia patients and associated with increased mortality due to cardiovascular disease. Second-generation antipsychotics (SGAs) play an important role in facilitating MetS. The study aimed to assess weight changes and alterations of indicators of body fat composition and lipid-glucose metabolism induced by reinitiating atypical antipsychotics in patients with schizophrenia when with or without MetS.

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Background: Schizophrenia is associated with a lowered life expectancy due to cardiovascular disease. This is, at least in part, related to an increased vulnerability to the development of metabolic syndrome (MetS) in patients with schizophrenia. The dysregulation of apolipoproteins (Apos) may also play a role in the pathogenesis of schizophrenia via their effect on cerebral cholesterol processing.

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