精神分裂症的神经炎症和犬尿氨酸:对认知的影响取决于认知功能以及与认知矫正和有氧运动有关的调节特性

IF 2.3 Q2 PSYCHIATRY Schizophrenia Research-Cognition Pub Date : 2024-08-29 DOI:10.1016/j.scog.2024.100328
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引用次数: 0

摘要

背景近十年来,犬尿氨酸通路(Kynurenine pathway,KP)在精神分裂症认知障碍的发病机制中越来越受到关注,因为它处于神经炎症与谷氨酸能和胆碱能神经递质之间的十字路口。然而,临床研究结果稀少且相互矛盾,这两个系统对认知症状神经生物学的具体贡献也远未阐明。本研究根据认知障碍的严重程度将 72 名精神分裂症患者分为两组,目的是评估炎症生物标志物和 KP 代谢物对认知功能的影响。结果神经炎症似乎对认知功能较强的患者的认知能力产生了更明显的影响,而 KP 的激活则对认知功能较弱的患者产生了更大的影响。治疗后认知能力的改善与 TNF-α 水平呈负相关,而与 3-羟基犬尿氨酸(3-HK)/犬尿氨酸(KYN)比率(犬尿氨酸-3-单氧化酶(KMO)酶活性指数)呈正相关。结论总之,这些发现为精神分裂症认知障碍的生物学基础提供了新的证据,指出神经炎症和 KP 代谢物在诱发认知障碍方面的不同作用取决于认知储备和预测康复后的结果。
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Neuroinflammation and kynurenines in schizophrenia: Impact on cognition depending on cognitive functioning and modulatory properties in relation to cognitive remediation and aerobic exercise

Background

In the last decade, the kynurenine pathway (KP) has gained attention in the pathogenesis of cognitive impairment in schizophrenia being at the croassroad between neuroinflammation and glutamatergic and cholinergic neurotransmission. However, clinical findings are scarse and conflicting, and the specific contributions of these two systems to the neurobiology of cognitive symptoms are far from being elucidated. Furthermore, little is known about the molecular underpinnings of non-pharmacological interventions for cognitive improvement, including rehabilitation strategies.

Methods

The current study examined 72 patients with schizophrenia, divided in two clusters depending on the severity of the cognitive impairment, with the aim to evaluate the impact of inflammatory biomarkers and KP metabolites depending on cognitive functioning. Moreover, we studied their possible link to the cognitive outcome in relation to sessions of cognitive remediation therapy (CRT) and aerobic exercise (AE) in a longitudinal arm of 42 patients.

Results

Neuroinflammation appeared to exert a more pronounced influence on cognition in patients exhibiting a higher cognitive functioning, contrasting with the activation of the KP, which had a greater impact on individuals with a lower cognitive profile. Cognitive improvements after the treatments were negatively predicted by levels of TNF-α and positively predicted by the 3-hydroxykynurenine (3−HK)/kynurenine (KYN) ratio, an index of the kynurenine-3-monooxygenase (KMO) enzyme activity.

Conclusion

Overall, these findings add novel evidence on the biological underpinnings of cognitive impairment in schizophrenia pointing at a differential role of neuroinflammation and KP metabolites in inducing cognitive deficits depending on the cognitive reserve and predicting outcomes after rehabilitation.

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来源期刊
CiteScore
5.60
自引率
10.70%
发文量
54
审稿时长
67 days
期刊最新文献
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