首发精神分裂症、超高风险人群和健康人群的框架网络研究

IF 4.1 Q2 PSYCHIATRY
Zhenmei Zhang, Xiaoqian Ma, Lijun Ouyang, Zongchang Li, Weiqing Liu, Ying He, Jingyan Lv, Xiaogang Chen, Liu Yuan
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摘要

精神分裂症是一种复杂的神经精神疾病,在其早期阶段大脑网络的异常仍然不完全清楚。先前,我们在健康个体中发现了一个稳定的高强度功能网络,称为“框架网络”,并观察了其在精神分裂症患者中的畸变。本研究旨在利用该网络探索早期精神分裂症的断开异常。本研究比较了drug-naïve首发精神分裂症患者(FES, n = 83)、精神分裂症超高风险患者(UHR, n = 65)和匹配的健康对照(HC, n = 67)。跨组分析框架网络,并使用来自两个公共数据集中稳定连接的健康人(HP)网络评估差异。基于网络的统计(NBS)-预测疾病分类模型的识别连接。将FES患者分为两个亚型,并使用基于连接体的预测模型(CPM)识别与阴性症状相关的连接。与对照组相比,UHR和FES患者的框架连接异常增加。HP和FES框架网络有效地区分了群体。在前额运动皮层中发现了对分类至关重要的连接。分为两种亚型的患者表现出不同的病理表现。框架网络能有效预测负面症状。根据症状严重程度,观察到视觉和前额皮质等区域的变化,表明精神分裂症临床异质性中存在多种潜在的联系差异。我们的研究结果表明,框架网络异常可能在精神分裂症的早期病理过程中发挥重要作用,并有望作为疾病分类和症状预后的生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A frame network study of first-episode schizophrenia, ultra-high risk, and healthy populations.

A frame network study of first-episode schizophrenia, ultra-high risk, and healthy populations.

A frame network study of first-episode schizophrenia, ultra-high risk, and healthy populations.

A frame network study of first-episode schizophrenia, ultra-high risk, and healthy populations.

Schizophrenia is a complex neuropsychiatric disorder, and the abnormalities in brain networks during its early stages remain incompletely understood. Previously, we identified a stable high-intensity functional network, termed the "Frame Network," in healthy individuals and observed its aberrations in schizophrenia patients. This study aimed to utilize this network to explore disconnection abnormalities in early-stage schizophrenia. This study compared drug-naïve first-episode schizophrenia patients (FES, n = 83), ultra-high risk of schizophrenia (UHR, n = 65), and matched healthy controls (HC, n = 67). Frame networks were analyzed across groups, and differences were assessed using networks from healthy people (HP) derived from stable connections in two public datasets. Network-Based Statistics (NBS)-predict identified connections for a disease classification model. FES patients were divided into two subtypes, and connections related to negative symptoms were identified using Connectome-based Predictive Modeling (CPM). UHR and FES patients showed increasing abnormalities in frame connections compared to controls. HP and FES frame networks effectively differentiated groups. Connections crucial for classification were found in the prefrontal motor cortex. Patients divided into two subtypes showed distinct pathological presentations. Frame networks predicted negative symptoms effectively. Variations in regions such as the visual and prefrontal cortex were observed based on symptom severity, indicating diverse underlying connection differences in the clinical heterogeneity of schizophrenia. Our findings indicate that Frame Network abnormalities likely play a significant role in early-stage pathological processes of schizophrenia and show promise as biomarkers for disease classification and symptom prognosis.

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