Więdłocha Magdalena, Zborowska Natalia, Marcinowicz Piotr, Dębowska Weronika, Dębowska Marta, Zalewska Anna, Maciejczyk Mateusz, Waszkiewicz Napoleon, Szulc Agata
Department of Psychiatry, Faculty of Health Sciences, Medical University of Warsaw, 02-091 Warsaw, Poland.
Experimental Dentistry Laboratory, Medical University of Bialystok, 15-089 Bialystok, Poland.
Brain Sci. 2023 Mar 14;13(3):490. doi: 10.3390/brainsci13030490.
Finding the associations between schizophrenia symptoms and the biomarkers of inflammation, oxidative stress and the kynurenine pathway may lead to the individualization of treatment and increase its effectiveness.
The study group included 82 schizophrenia inpatients. The Positive and Negative Symptoms Scale (PANSS), the Brief Assessment of Cognition in Schizophrenia (BACS) and the Calgary Depression in Schizophrenia Scale were used for symptom evaluation. Biochemical analyses included oxidative stress parameters and brain-derived neurotrophic factor (BDNF).
Linear models revealed the following: (1) malondiadehyde (MDA), N-formylkynurenine (N-formKYN), advanced oxidation protein products (AOPP), advanced glycation end-products of proteins (AGE) and total oxidative status (TOS) levels are related to the PANSS-total score; (2) MDA, reduced glutathione (GSH) and BDNF levels are related to the PANSS-negative score; (3) TOS and kynurenine (KYN) levels are related to the PANSS-positive score; (4) levels of total antioxidant status (TAS) and AOPP along with the CDSS score are related to the BACS-total score; (5) TAS and N-formKYN levels are related to the BACS-working memory score.
Oxidative stress biomarkers may be associated with the severity of schizophrenia symptoms in positive, negative and cognitive dimensions. The identification of biochemical markers associated with the specific symptom clusters may increase the understanding of biochemical profiles in schizophrenia patients.
探寻精神分裂症症状与炎症、氧化应激及犬尿氨酸途径生物标志物之间的关联,可能会实现治疗的个体化并提高其有效性。
研究组包括82名精神分裂症住院患者。采用阳性和阴性症状量表(PANSS)、精神分裂症认知功能简评量表(BACS)以及精神分裂症卡尔加里抑郁量表进行症状评估。生化分析包括氧化应激参数和脑源性神经营养因子(BDNF)。
线性模型显示如下结果:(1)丙二醛(MDA)、N-甲酰犬尿氨酸(N-formKYN)、晚期氧化蛋白产物(AOPP)、蛋白质晚期糖基化终产物(AGE)以及总氧化状态(TOS)水平与PANSS总分相关;(2)MDA、还原型谷胱甘肽(GSH)和BDNF水平与PANSS阴性评分相关;(3)TOS和犬尿氨酸(KYN)水平与PANSS阳性评分相关;(4)总抗氧化状态(TAS)和AOPP水平以及CDSS评分与BACS总分相关;(5)TAS和N-formKYN水平与BACS工作记忆评分相关。
氧化应激生物标志物可能与精神分裂症症状在阳性、阴性和认知维度的严重程度相关。识别与特定症状簇相关的生化标志物,可能会增进对精神分裂症患者生化特征的理解。