[Illness duration-related developmental trajectory of progressive cerebral gray matter changes in schizophrenia].

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.

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Publication Details

Journal
PubMed
Published
2025-04-25
DOI
https://doi.org/10.7507/1001-5515.202401053
Primary Topic
Diet and metabolism studies
Type
article
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[Illness duration-related developmental trajectory of progressive cerebral gray matter changes in schizophrenia].

Cheng Luo, Yingjie Tang, Xin Chang, Zhihuan Yang et al.
PubMed
Diet and metabolism studies
article

[Illness duration-related developmental trajectory of progressive cerebral gray matter changes in schizophrenia].

Cheng Luo, Yingjie Tang, Xin Chang, Zhihuan Yang, Dezhong Yao, Xiaoying Sun
article en

Abstract

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.

PubMedVol. 42(2)
University of Electronic Science and Technology of China (CN)
Good health and well-being
Diet and metabolism studies
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