精神分裂症患者小脑经颅磁刺激后小脑Glx/GABA和小脑丘脑皮质连通性的即时改变。

IF 3 Q2 PSYCHIATRY
Chenyang Yao, Youjin Zhao, Qian Zhang, Ziyuan Zhao, Kai Ai, Bo Zhang, Su Lui
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引用次数: 0

摘要

小脑功能障碍是精神分裂症的一个关键方面,小脑-丘脑-皮质(CTC)超连接是一种神经特征。γ -氨基丁酸(GABA)和谷氨酸+谷氨酰胺(Glx)水平的异常也有助于这种病理。应用于小脑的经颅磁刺激(TMS)显示出减轻精神分裂症症状的潜力,可能通过调节功能连接或神经递质水平。本研究旨在探讨经颅磁刺激对小脑CTC回路和神经递质水平的直接影响,以阐明其治疗精神分裂症的机制。该研究包括19名稳定型精神分裂症患者和26名健康对照者,根据DSM-V标准诊断,并使用阳性和阴性综合征量表(PANSS)评估症状严重程度。经颅磁刺激前后分别进行MRI扫描,检测CTC功能连通性、GABA、Glx和Glx/GABA的变化。采用线性混合效应模型(LMEM)和双样本检验分析这些变量从基线到经颅磁刺激后的变化。采用Pearson相关分析来检验这些变量之间的关系及其与PANSS评分的关系。采用中介分析来研究GABA和/或Glx是否作为精神分裂症患者CTC超连通性的潜在中介。精神分裂症患者表现出CTC超连通性,小脑经颅磁刺激后CTC超连通性保持在相对稳定的水平。与健康对照组相比,精神分裂症患者小脑GABA水平显著升高,小脑GABA对患者CTC超连通性具有显著的调节作用。Glx/GABA比值与患者临床症状的严重程度相关,小脑经颅磁刺激部分使该比值正常化。我们的研究结果表明,异常的小脑GABA水平有助于精神分裂症患者的CTC超连通性。此外,我们的研究表明,经颅磁刺激可增加精神分裂症患者小脑Glx水平,导致Glx/GABA比值正常化,这可能有助于经颅磁刺激对精神分裂症的治疗效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The immediate alteration of cerebellar Glx/GABA and cerebello-thalamo-cortical connectivity in patients with schizophrenia after cerebellar TMS.

Cerebellar dysfunction is a key aspect of schizophrenia, with the cerebello-thalamo-cortical (CTC) hyperconnectivity serving as a neural signature. Abnormalities in gamma-aminobutyric acid (GABA) and glutamate + glutamine (Glx) levels also contribute to this pathology. Transcranial magnetic stimulation (TMS) applied to the cerebellum shows potential in alleviating schizophrenia symptoms, possibly by modulating functional connectivity or neurotransmitter levels. This study aims to explore the immediate effects of cerebellar TMS on CTC circuitry and neurotransmitter levels to elucidate its therapeutic mechanisms in schizophrenia.The study involved 19 stable schizophrenia patients and 26 healthy controls, diagnosed according to DSM-V criteria and assessed for symptom severity using the Positive and Negative Syndrome Scale (PANSS). MRI scans were conducted pre- and post-TMS to detect changes in CTC functional connectivity, GABA, Glx, and Glx/GABA. Linear Mixed-Effects Model (LMEM) and two-sample tests were employed to analyze changes in these variables from baseline to post-TMS. Pearson's correlation analysis was conducted to examine the relationships among these variables and their association with PANSS scores. Mediation analyses were employed to investigate whether GABA and/or Glx serve as potential mediators of CTC hyperconnectivity in patients with schizophrenia. Schizophrenia patients exhibit CTC hyperconnectivity, which remains at a relatively stable level after cerebellar TMS. Compared to healthy controls, schizophrenia patients have significantly higher cerebellar GABA levels, and cerebellar GABA has a significant mediation effect on CTC hyperconnectivity in patients. The Glx/GABA ratio was associated with the severity of clinical symptoms in patients, and cerebellar TMS partially normalized this ratio. Our findings demonstrate that aberrant cerebellar GABA levels contribute to CTC hyperconnectivity in schizophrenia. Additionally, our study shows that cerebellar TMS can increase Glx levels in schizophrenia patients, leading to the normalization of the Glx/GABA ratio, which may contribute to the therapeutic effects of TMS in schizophrenia.

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