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Turek, Aleksander

https://orcid.org/0000-0002-4327-252X

Mayo Clinic

Jagiellonian University

Citations 2

Association of Blood Metabolomics Biomarkers with Brain Metabolites and Patient-Reported Outcomes as a New Approach in Individualized Diagnosis of Schizophrenia
Krzyściak, Wirginia , Bystrowska, Beata , Karcz, Paulina , Chrzan, Robert , Bryll, Amira, Turek, Aleksander , Mazur, Paulina , Śmierciak, Natalia , Szwajca, Marta , Donicz, Paulina , Furman, Katarzyna, Pilato, Fabio , Kozicz, Tamás , Pilecki, Maciej , Kozicz, Tamas , Popiela, Tadeusz

International Journal of Molecular Sciences | February 15, 2024 | Volume: 25 | Issue: 4 | Pages: 2294

10.3390/ijms25042294 Get It

Given its polygenic nature, there is a need for a personalized approach to schizophrenia. The aim of the study was to select laboratory biomarkers from blood, brain imaging, and clinical assessment, with an emphasis on patients’ self-report questionnaires. Metabolomics studies of serum samples from 51 patients and 45 healthy volunteers, based on the liquid chromatography-electrospray ionization-mass spectrometry (LC-ESI-MS/MS), led to the identification of 3 biochemical indicators (cortisol, glutamate, lactate) of schizophrenia. These metabolites were sequentially correlated with laboratory tests results, imaging results, and clinical assessment outcomes, including patient self-report outcomes. The hierarchical cluster analysis on the principal components (HCPC) was performed to identify the most homogeneous clinical groups. Significant correlations were noted between blood lactates and 11 clinical and 10 neuroimaging parameters. The increase in lactate and cortisol were significantly associated with a decrease in immunological parameters, especially with the level of reactive lymphocytes. The strongest correlations with the level of blood lactate and cortisol were demonstrated by brain glutamate, N-acetylaspartate and the concentrations of glutamate and glutamine, creatine and phosphocreatine in the prefrontal cortex. Metabolomics studies and the search for associations with brain parameters and self-reported outcomes may provide new diagnostic evidence to specific schizophrenia phenotypes.
The Association of the Oral Microbiota with the Effects of Acid Stress Induced by an Increase of Brain Lactate in Schizophrenia Patients
Krzyściak, Wirginia , Karcz, Paulina , Bystrowska, Beata , Szwajca, Marta , Bryll, Amira, Śmierciak, Natalia , Ligezka, Anna N. , Turek, Aleksander , Kozicz, Tamás , Skalniak, Anna , Jagielski, Paweł , Pilecki, Maciej , Ligęzka, Anna , Skalniak, Anna E , Popiela, Tadeusz J , Kozicz, Tamas , Popiela, Tadeusz

Biomedicines | January 18, 2023 | Volume: 11 | Issue: 2 | Pages: 240

10.3390/biomedicines11020240 Get It

The altered cerebral energy metabolism central to schizophrenia can be linked to lactate accumulation. Lactic acid is produced by gastrointestinal bacteria, among others, and readily crosses the blood–brain barrier, leading to the brain acidity. This study aimed to examine the association of the oral microbiota with the effects of acid stress induced by an increase of brain lactate in schizophrenia patients. The study included patients with a diagnosis of acute polyphasic psychotic disorder meeting criteria for schizophrenia at 3-month follow-up. Results: Individuals with a significantly higher total score on the Positive and Negative Syndrome Scale had statistically significantly lower lactate concentrations compared to those with a lower total score and higher brain lactate. We observed a positive correlation between Actinomyces and lactate levels in the anterior cingulate cap and a negative correlation between bacteria associated with lactate metabolism and some clinical assessment scales. Conclusions: Shifts in the oral microbiota in favour of lactate-utilising bacterial genera may represent a compensatory mechanism in response to increased lactate production in the brain. Assessment of neuronal function mediated by ALA-LAC-dependent NMDA regulatory mechanisms may, thus, support new therapies for schizophrenia, for which acidosis has become a differentiating feature of individuals with schizophrenia endophenotypes.