Systematically mapping gray matter abnormal patterns in drug-naïve first-episode schizophrenia from childhood to adolescence.


Journal

Cerebral cortex (New York, N.Y. : 1991)
ISSN: 1460-2199
Titre abrégé: Cereb Cortex
Pays: United States
ID NLM: 9110718

Informations de publication

Date de publication:
07 02 2023
Historique:
received: 06 02 2022
revised: 23 03 2022
accepted: 24 03 2022
pubmed: 10 4 2022
medline: 18 2 2023
entrez: 9 4 2022
Statut: ppublish

Résumé

Schizophrenia originates early in neurodevelopment, underscoring the need to elaborate on anomalies in the still maturing brain of early-onset schizophrenia (EOS). Gray matter (GM) volumes were evaluated in 94 antipsychotic-naïve first-episode EOS patients and 100 typically developing (TD) controls. The anatomical profiles of changing GM deficits in EOS were detected using 2-way analyses of variance with diagnosis and age as factors, and its timing was further charted using stage-specific group comparisons. Interregional relationships of GM alterations were established using structural covariance network analyses. Antagonistic interaction results suggested dynamic GM abnormalities of the left fusiform gyrus, inferior occipital gyrus, and lingual gyrus in EOS. These regions comprise a dominating part of the ventral stream, a ventral occipitotemporal (vOT) network engaged in early social information processing. GM abnormalities were mainly located in the vOT regions in childhood-onset patients, whereas in the rostral prefrontal cortex (rPFC) in adolescent-onset patients. Moreover, compared with TD controls, patients' GM synchronization with the ventral stream was disrupted in widespread high-order social perception regions including the rPFC and salience network. The current findings reveal age-related anatomical abnormalities of the social perception system in pediatric patients with schizophrenia.

Sections du résumé

BACKGROUND
Schizophrenia originates early in neurodevelopment, underscoring the need to elaborate on anomalies in the still maturing brain of early-onset schizophrenia (EOS).
METHODS
Gray matter (GM) volumes were evaluated in 94 antipsychotic-naïve first-episode EOS patients and 100 typically developing (TD) controls. The anatomical profiles of changing GM deficits in EOS were detected using 2-way analyses of variance with diagnosis and age as factors, and its timing was further charted using stage-specific group comparisons. Interregional relationships of GM alterations were established using structural covariance network analyses.
RESULTS
Antagonistic interaction results suggested dynamic GM abnormalities of the left fusiform gyrus, inferior occipital gyrus, and lingual gyrus in EOS. These regions comprise a dominating part of the ventral stream, a ventral occipitotemporal (vOT) network engaged in early social information processing. GM abnormalities were mainly located in the vOT regions in childhood-onset patients, whereas in the rostral prefrontal cortex (rPFC) in adolescent-onset patients. Moreover, compared with TD controls, patients' GM synchronization with the ventral stream was disrupted in widespread high-order social perception regions including the rPFC and salience network.
CONCLUSIONS
The current findings reveal age-related anatomical abnormalities of the social perception system in pediatric patients with schizophrenia.

Identifiants

pubmed: 35396845
pii: 6565623
doi: 10.1093/cercor/bhac148
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1452-1461

Informations de copyright

© The Author(s) 2022. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Yun-Shuang Fan (YS)

Sichuan Provincial Center for Mental Health, The Center of Psychosomatic Medicine of Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu 611731, China.
School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 611731, China.

Yong Xu (Y)

Department of Psychiatry, First Hospital/First Clinical Medical College of Shanxi Medical University, Taiyuan 030000, China.

Qiang Li (Q)

Department of Psychiatry, First Hospital/First Clinical Medical College of Shanxi Medical University, Taiyuan 030000, China.

Yuyan Chen (Y)

School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 611731, China.
MOE Key Lab for Neuroinformation; High-Field Magnetic Resonance Brain Imaging Key Laboratory of Sichuan Province, University of Electronic Science and Technology of China, Chengdu 611731, China.

Xiaonan Guo (X)

School of Information Science and Engineering, Yanshan University, Qinhuangdao 066004, China.

Siqi Yang (S)

School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 611731, China.
MOE Key Lab for Neuroinformation; High-Field Magnetic Resonance Brain Imaging Key Laboratory of Sichuan Province, University of Electronic Science and Technology of China, Chengdu 611731, China.

Jing Guo (J)

School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 611731, China.
MOE Key Lab for Neuroinformation; High-Field Magnetic Resonance Brain Imaging Key Laboratory of Sichuan Province, University of Electronic Science and Technology of China, Chengdu 611731, China.

Wei Sheng (W)

School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 611731, China.
MOE Key Lab for Neuroinformation; High-Field Magnetic Resonance Brain Imaging Key Laboratory of Sichuan Province, University of Electronic Science and Technology of China, Chengdu 611731, China.

Chong Wang (C)

School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 611731, China.
MOE Key Lab for Neuroinformation; High-Field Magnetic Resonance Brain Imaging Key Laboratory of Sichuan Province, University of Electronic Science and Technology of China, Chengdu 611731, China.

Qing Gao (Q)

MOE Key Lab for Neuroinformation; High-Field Magnetic Resonance Brain Imaging Key Laboratory of Sichuan Province, University of Electronic Science and Technology of China, Chengdu 611731, China.

Huafu Chen (H)

Sichuan Provincial Center for Mental Health, The Center of Psychosomatic Medicine of Sichuan Provincial People's Hospital, University of Electronic Science and Technology of China, Chengdu 611731, China.
School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu 611731, China.
MOE Key Lab for Neuroinformation; High-Field Magnetic Resonance Brain Imaging Key Laboratory of Sichuan Province, University of Electronic Science and Technology of China, Chengdu 611731, China.

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