Chang Xin, Yang Zhihuan, Tang Yingjie, Sun Xiaoying, Luo Cheng, Yao Dezhong
The Clinical Hospital of Chengdu Brain Science Institute, MOE Key Lab for Neuroinformation, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 611731, P. R. China.
Research Unit of NeuroInformation, Chinese Academy of Medical Sciences, 2019RU035, Chengdu 611731, P. R. China.
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2025 Apr 25;42(2):293-299. doi: 10.7507/1001-5515.202401053.
In different stages of schizophrenia (SZ), alterations in gray matter volume (GMV) of patients are normally regulated by various pathological mechanisms. Instead of analyzing stage-specific changes, this study employed a multivariate structural covariance model and sliding-window approach to investigate the illness duration-related developmental trajectory of GMV in SZ. The trajectory is defined as a sequence of brain regions activated by illness duration, represented as a sparsely directed matrix. By applying this approach to structural magnetic resonance imaging data from 145 patients with SZ, we observed a continuous developmental trajectory of GMV from cortical to subcortical regions, with an average change occurring every 0.208 years, covering a time window of 20.176 years. The starting points were widely distributed across all networks, except for the ventral attention network. These findings provide insights into the neuropathological mechanism of SZ with a neuroprogressive model and facilitate the development of process for aided diagnosis and intervention with the starting points.
在精神分裂症(SZ)的不同阶段,患者灰质体积(GMV)的改变通常受多种病理机制调控。本研究未分析特定阶段的变化,而是采用多变量结构协方差模型和滑动窗口方法,来研究SZ中与病程相关的GMV发育轨迹。该轨迹被定义为由病程激活的一系列脑区,以稀疏有向矩阵表示。通过将此方法应用于145例SZ患者的结构磁共振成像数据,我们观察到GMV从皮质区域到皮质下区域的连续发育轨迹,平均每0.208年发生一次变化,覆盖时间窗口为20.176年。起始点广泛分布于所有网络,腹侧注意网络除外。这些发现通过神经进展模型为SZ的神经病理机制提供了见解,并有助于以起始点为依据开发辅助诊断和干预流程。