Identify Potential Causal Relationships Between Cortical Thickness, Mismatch Negativity, Neurocognition, and Psychosocial Functioning in Drug-Naïve First-Episode Psychosis Patients

被引:0
|
作者
Li, Xiaojing [1 ,2 ,3 ,4 ,5 ,6 ]
Wei, Wei [1 ,2 ,3 ,4 ,5 ,6 ]
Wang, Qiang [7 ,8 ]
Deng, Wei [1 ,2 ,3 ,4 ,5 ,6 ]
Li, Mingli [7 ,8 ]
Ma, Xiaohong [7 ,8 ]
Zeng, Jinkun [1 ,2 ]
Zhao, Liansheng [7 ,8 ]
Guo, Wanjun [1 ,2 ,3 ,4 ,5 ,6 ]
Hall, Mei-Hua [9 ]
Li, Tao [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Zhejiang Univ, Affiliated Mental Hlth Ctr, Sch Med, Hangzhou 310058, Zhejiang, Peoples R China
[2] Zhejiang Univ, Hangzhou Peoples Hosp 7, Sch Med, Hangzhou 310058, Zhejiang, Peoples R China
[3] Nanhu Brain Comp Interface Inst, Hangzhou 311100, Peoples R China
[4] Zhejiang Univ, MOE Frontier Sci Ctr Brain Sci & Brain Machine In, Liangzhu Lab, State Key Lab Brain Machine Intelligence, 1369 West Wenyi Rd, Hangzhou 311121, Peoples R China
[5] Zhejiang Univ, NHC, Hangzhou 310058, Peoples R China
[6] Zhejiang Univ, CAMS Key Lab Med Neurobiol, Hangzhou 310058, Peoples R China
[7] Sichuan Univ, Mental Hlth Ctr, West China Hosp, Chengdu 610041, Sichuan, Peoples R China
[8] Sichuan Univ, Psychiat Lab, West China Hosp, Chengdu 610041, Sichuan, Peoples R China
[9] Harvard Med Sch, McLean Hosp, Psychosis Neurobiol Lab, 115 Mill St, Belmont, MA 02478 USA
基金
中国国家自然科学基金;
关键词
first-episode psychosis; drug-naive; cortical thickness; mismatch negativity; neurocognition; psychosocial function; PROGRESSIVE BRAIN CHANGES; 1-YEAR FOLLOW-UP; AUDITORY HALLUCINATIONS; MATTER ABNORMALITIES; CLINICAL RISK; SURFACE-AREA; SCHIZOPHRENIA; VOLUME; METAANALYSIS; ASSOCIATION;
D O I
10.1093/schbul/sbae026
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Background: Cortical thickness (CT) alterations, mismatch negativity (MMN) reductions, and cognitive deficits are robust findings in first-episode psychosis (FEP). However, most studies focused on medicated patients, leaving gaps in our understanding of the interrelationships between CT, MMN, neurocognition, and psychosocial functioning in unmedicated FEP. This study aimed to employ multiple mediation analysis to investigate potential pathways among these variables in unmedicated drug-nai<spacing diaeresis> ve FEP. Methods: We enrolled 28 drug-naive FEP and 34 age and sex-matched healthy controls. Clinical symptoms, neurocognition, psychosocial functioning, auditory duration MMN, and T1 structural magnetic resonance imaging data were collected. We measured CT in the superior temporal gyrus (STG), a primary MMN-generating region. Results: We found a significant negative correlation between MMN amplitude and bilateral CT of STG (CT_STG) in FEP (left: r = -.709, P < .001; right: r = -.612, P = .008). Multiple mediation models revealed that a thinner left STG cortex affected functioning through both direct (24.66%) and indirect effects (75.34%). In contrast, the effects of the right CT_STG on functioning were mainly mediated through MMN and neurocognitive pathways. Conclusions: Bilateral CT_STG showed significant association with MMN, and MMN plays a mediating role between CT and cognition. Both MMN alone and its interaction with cognition mediated the effects of structural alterations on psychosocial function. The decline in overall function in FEP may stem from decreased CT_STG, leading to subsequent MMN deficits and neurocognitive dysfunction. These findings underline the crucial role of MMN in elucidating how subtle structural alterations can impact neurocognition and psychosocial function in FEP.
引用
收藏
页码:827 / 838
页数:12
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