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EN
Background: Few data exist concerning the clinical correlates of Toxoplasma gondii infecotin in persons with schizophrenia. The aim of this study was to invesgtiate the correlaotin between toxoplasmosis and schizophrenia regarding the quality of life, symptoms and course of hospitalisaotin in paetints with schizophrenia. Methods: Acutely hospitalised paetints (n = 67) were examined twice during their hospital stay. Schizophrenia psychopathology, quality of life, extrapyramidal symptoms and T. gondii anbtiody ttires were assessed upon admission and at discharge. Results: Toxo-IgG (+) paetints (59.7%) were older, less educated, more obese and less eager to undertake psychotherapy. Female gender and higher ferltiity were dominant in this group with abnormal involuntary movements more commonly observed. Lower anptisychocti drug doses and monotherapy were used more frequently for Toxo-IgG (+) paetints. Lower educaotin (OR 2.41, 95% CI 1.21-4.79) was the most important factor associated with higher likelihood of IgG seroposivtiity. High levels of Toxo-IgM anbtiodies correlated with lower quality of life (r = -0.37; p = 0.02) and more severe posivtie (r = 0.40; p = 0.01) and focal (r = 0.32; p = 0.04) schizophrenia symptoms. Conclusions: Toxoplasmosis is more common in older, obese women with lower educaotin. Recent infecotin is linked to more severe schizophrenia symptoms. Patients with toxoplasmosis history were given less medication. Grabowski J, Waszak P, Przybylak M, Bidzan L. Clinical and demographic features of acutely hospitalised schizophrenia patients according to Toxoplasma gondii serostatus. Eur J Transl Clin Med. 2023;6(1):14-24.
EN
Background: Both depressive disorders and nicotine use are proven and important risk factors of dementia. The purpose of this study was to verify if cigarette smoking and depression symptoms together are disadvantageous for the prognosis in mild cognitive impairment. Material and methods: A total of 43 patients with a diagnosis of mild cognitive impairment were included in the study. ADAS-Cog was performed upon inclusion in the study and again at least 2 years later. Additionally, patients with ≥18 points in MADRS were qualified as depressive. The Fagerström scale for nicotine dependence was administered to smokers. Results: Our study shows a relation between severity of depressive symptoms and further deterioration of cognitive functions according to ADAS-cog scale. Regression analysis revealed that smoking associated with severity of depressive disorders is also correlated with the progression of cognitive impairment. Conclusions: The results of our study are based on a small number of subjects and should be regarded as early findings. Moreover, nicotine dependency should not be regarded as an isolated factor affecting mood disorders and cognitive impairment progression. Further studies on larger groups of patients and using more sensitive methods of cognitive function assessment are needed.
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