Interconnected Cognitive and Neuroimmune Impairments in Schizophrenia: Modulating Effects of Antipsychotic Type, Illness Duration, and Symptom Severity.

Thiago P Fernandes, Zeke Degraff, Fatima M Felisberti, Alisa Viktorovna Karlova, Givago S Souza, Irina I Shoshina, Milena E C Oliveira, Linnea N Dahlgren, Natanael A Santos
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引用次数: 0

Abstract

Objective: Cognitive impairment in schizophrenia (SCZ) is associated with neuroinflammation and neurotrophic dysregulation. The role of pro-inflammatory interleukins and brain-derived neurotrophic factor (BDNF) in cognitive deficits remains unclear. We aimed to examine the associations between IL-1β, IL-2, IL-6, BDNF, and cognitive function in patients with SCZ with typical or atypical antipsychotics.

Methods: Participants included 162 healthy controls (mean age = 33.6 ± 2.0 years), 88 patients with SCZ receiving typical antipsychotics (36.4 ± 6.4 years), and 62 receiving atypical antipsychotics (34.0 ± 4.0 years). Cognitive performance was evaluated using a battery of attentional, executive, and visuospatial working memory tasks. Data were analyzed using machine-learning approaches, multivariate statistics, and structural equation modeling.

Results: SCZ Patients exhibited marked cognitive impairments alongside lower BDNF concentrations and elevated interleukin levels, with the greatest deviations observed among those receiving typical antipsychotic treatment. Higher medication dosages and longer illness duration were associated with greater cognitive decline and stronger neuroimmune dysregulation.

Conclusions: The findings indicate that elevated cytokines and reduced neurotrophic support may contribute to cognitive impairment, whereas persistent cognitive dysfunction can further amplify inflammatory activity. This complexity suggests the need to broaden current assessment approaches and systematically examine biomarkers together with clinical features.

精神分裂症中相互关联的认知和神经免疫损伤:抗精神病药物类型、病程和症状严重程度的调节作用。
目的:精神分裂症患者的认知功能障碍与神经炎症和神经营养失调有关。促炎白介素和脑源性神经营养因子(BDNF)在认知缺陷中的作用尚不清楚。我们的目的是研究IL-1β、IL-2、IL-6、BDNF与服用典型或非典型抗精神病药物的SCZ患者认知功能之间的关系。方法:健康对照162例(平均年龄33.6±2.0岁),典型抗精神病药物治疗组88例(36.4±6.4岁),非典型抗精神病药物治疗组62例(34.0±4.0岁)。认知表现是通过一系列注意力、执行力和视觉空间工作记忆任务来评估的。数据分析使用机器学习方法,多元统计和结构方程建模。结果:SCZ患者表现出明显的认知障碍,同时BDNF浓度降低,白细胞介素水平升高,在接受典型抗精神病药物治疗的患者中观察到最大的偏差。较高的药物剂量和较长的疾病持续时间与更大的认知能力下降和更强的神经免疫失调有关。结论:研究结果表明,细胞因子升高和神经营养支持减少可能导致认知功能障碍,而持续的认知功能障碍可进一步放大炎症活动。这种复杂性表明需要扩大当前的评估方法,并系统地检查生物标志物与临床特征。
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