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[氧化应激对首发精神分裂症认知功能损害的影响]

[Effects of oxidative stress on cognitive impairment in first episode schizophrenia].

作者信息

Wang Y P, Zhang P F, Yuan X X, Liu Y F, Li H H, Tao Q, Li X, Pang L J, Song X Q

机构信息

Department of Psychiatry, the First Affiliated Hospital of Zhengzhou University, Zhengzhou 450052, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2019 Jan 1;99(1):9-13. doi: 10.3760/cma.j.issn.0376-2491.2019.01.003.

Abstract

To observe the relationship between serum oxidative stress as well as brain-derived neurotrophic factor (BDNF) and cognitive function in first-episode drug-free schizophrenics, and to explore the possible effect of oxidative stress in cognitive impairment of first-episode schizophrenia. A total of 125 first-episode drug-free schizophrenics (schizophrenia group) from the First Affiliated Hospital of Zhengzhou University and 80 healthy individuals (control group) were enrolled. The serum concentration of oxidized glutathione (GSSG) was measured by the Microenzyme method the serum concentration of nitric oxide (NO) was measured by one-step method, the BDNF level was measured by enzyme linked immunosorbent assay and Matrics Consensus Cognitive Battery(MCCB) was used to evaluate the cognitive function. (1)The serum level of BDNF in schizophrenia group (2 763±1 728 pg/ml) was significantly lower than that in control group (4 165±1 299 pg/ml)(0.001). And the serum levels of GSSG and NO in schizophrenia group ((36±9), (81±65) μmol/L) were significantly higher than that in control group ((27±11), (24±16) μmol/L) (0.001). In comparison with the control group scores were significantly lower in the seven domains of cognitive function in the schizophrenia group (all 0.001). (2)After controlling the confounding factors like age, gender, cultural differences and course of disease by partial correlation analysis, the correlation analysis showed that: serum level of BDNF in schizophrenia group had positive correlation with Information processing rate T points, attentional facilitating T points, working memory T points and Reasoning and problem solving T points (0.417, 0.206, 0.247, 0.318, all 0.05). In schizophrenia group the serum level of GSSG had a negative correlation with information processing rate T points and reasoning and problem solving T points (-0.321, -0.231, all 0.05). The serum level of NO was negatively related to Information processing rate T points working memory T points Verbal learning T points(-0.201, -0.193, -0.237, all 0.05). Oxidative stress may be involved in the cognitive impairment of schizophrenia Oxidation products are risk factors for cognitive impairment of schizophrenia and BDNF is a protective factor of cognitive function.

摘要

观察首发未用药精神分裂症患者血清氧化应激及脑源性神经营养因子(BDNF)与认知功能的关系,探讨氧化应激在首发精神分裂症认知损害中的可能作用。选取郑州大学第一附属医院125例首发未用药精神分裂症患者(精神分裂症组)和80例健康个体(对照组)。采用微量酶法测定血清氧化型谷胱甘肽(GSSG)浓度,一步法测定血清一氧化氮(NO)浓度,酶联免疫吸附测定法检测BDNF水平,并用矩阵共识认知成套测验(MCCB)评估认知功能。(1)精神分裂症组BDNF血清水平(2763±1728 pg/ml)显著低于对照组(4165±1299 pg/ml)(P<0.001)。精神分裂症组GSSG和NO血清水平((36±9),(81±65)μmol/L)显著高于对照组((27±11),(24±16)μmol/L)(P<0.001)。与对照组相比,精神分裂症组认知功能七个领域的得分均显著降低(均P<0.001)。(2)经偏相关分析控制年龄、性别、文化差异和病程等混杂因素后,相关性分析显示:精神分裂症组BDNF血清水平与信息处理率T分、注意力促进T分、工作记忆T分及推理与问题解决T分呈正相关(0.417、0.206、0.247、0.318,均P<0.05)。精神分裂症组GSSG血清水平与信息处理率T分及推理与问题解决T分呈负相关(-0.321、-0.231,均P<0.055)。NO血清水平与信息处理率T分、工作记忆T分、言语学习T分呈负相关(-0.201、-0.193、-0.237,均P<0.05)。氧化应激可能参与精神分裂症的认知损害,氧化产物是精神分裂症认知损害的危险因素,BDNF是认知功能的保护因素。

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