Brain structural damage networks at different stages of schizophrenia

被引:0
|
作者
Xu, Ruoxuan [1 ,2 ,3 ,4 ]
Zhang, Xiaohan [1 ,2 ,3 ,4 ]
Zhou, Shanlei [5 ]
Guo, Lixin [1 ,2 ,3 ,4 ]
Mo, Fan [1 ,2 ,3 ,4 ]
Ma, Haining [1 ,2 ,3 ,4 ]
Zhu, Jiajia [1 ,2 ,3 ,4 ]
Qian, Yinfeng [1 ,2 ,3 ,4 ]
机构
[1] Anhui Med Univ, Affiliated Hosp 1, Dept Radiol, Hefei 230022, Peoples R China
[2] Res Ctr Clin Med Imaging, Hefei 230032, Anhui, Peoples R China
[3] Anhui Prov Inst Translat Med, Hefei 230032, Peoples R China
[4] Anhui Prov Key Lab Brain Bank Construct & Resource, Hefei 230032, Peoples R China
[5] Anhui Med Univ, Affiliated Hosp 1, Dept Endocrinol, Hefei 230022, Peoples R China
基金
中国国家自然科学基金;
关键词
chronic; first episode; functional connectivity network mapping; gray matter; high risk; schizophrenia; CLINICAL HIGH-RISK; 1ST-EPISODE SCHIZOPHRENIA; BIPOLAR DISORDER; PSYCHOSIS; STATE; SYMPTOMS; METAANALYSIS; ABNORMALITIES; LOCALIZATION; STIMULATION;
D O I
10.1017/S0033291724003088
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Background: Neuroimaging studies have documented brain structural changes in schizophrenia at different stages of the illness, including clinical high-risk (cHR), genetic high-risk (gHR), first-episode schizophrenia (FES), and chronic schizophrenia (ChS). There is growing awareness that neuropathological processes associated with a disease fail to map to a specific brain region but do map to a specific brain network. We sought to investigate brain structural damage networks across different stages of schizophrenia. Methods: We initially identified gray matter alterations in 523 cHR, 855 gHR, 2162 FES, and 2640 ChS individuals relative to 6963 healthy controls. By applying novel functional connectivity network mapping to large-scale discovery and validation resting-state functional magnetic resonance imaging datasets, we mapped these affected brain locations to four specific networks. Results: Brain structural damage networks of cHR and gHR had limited and non-overlapping spatial distributions, with the former mainly involving the frontoparietal network and the latter principally implicating the subcortical network, indicative of distinct neuropathological mechanisms underlying cHR and gHR. By contrast, brain structural damage networks of FES and ChS manifested as similar patterns of widespread brain areas predominantly involving the somatomotor, ventral attention, and subcortical networks, suggesting an emergence of more prominent brain structural abnormalities with illness onset that have trait-like stability over time. Conclusions: Our findings may not only provide a refined picture of schizophrenia neuropathology from a network perspective, but also potentially contribute to more targeted and effective intervention strategies for individuals at different schizophrenia stages.
引用
收藏
页码:4809 / 4819
页数:11
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