Genetic Contribution of Synapse-Associated Protein 97 to Orbitofrontal-Striatal-Thalamic Circuitry Connectivity Changes in First-Episode Schizophrenia.

SAP97 deterministic tractography resting state functional connectivity rs3915512 schizophrenia

Journal

Frontiers in psychiatry
ISSN: 1664-0640
Titre abrégé: Front Psychiatry
Pays: Switzerland
ID NLM: 101545006

Informations de publication

Date de publication:
2021
Historique:
received: 09 04 2021
accepted: 15 06 2021
entrez: 5 8 2021
pubmed: 6 8 2021
medline: 6 8 2021
Statut: epublish

Résumé

Functional and structural disturbances in the orbitofrontal-striatal-thalamic circuitry are thought to be associated with mental symptoms and neurocognitive impairments in schizophrenia. This study tested whether synapse-associated protein 97 (SAP97), a reasonable candidate gene for schizophrenia, is related to orbitofrontal-striatal-thalamic connection changes in first-episode schizophrenia (FES) patients and the clinical performance of schizophrenic patients by affecting this integrity. Fifty-two FES patients and 52 matched healthy controls were recruited. All subjects underwent genotyping via the improved multiplex ligation detection reaction technique and scanning with magnetic resonance imaging (MRI) to provide orbitofrontal-striatal-thalamic functional and structural imaging data. A two-way analysis of covariance model was employed to examine abnormal brain connectivities, and Spearman correlations were applied to estimate the relationships between brain connectivity and clinical manifestations. In the FES group, those with the SAP97 rs3915512 TT genotype showed lower structural and functional connectivity than A allele carriers between the orbitofrontal gyrus and striatum/thalamus. In the FES group, negative correlations were found between resting-state functional connectivity (RSFC) in the orbitofrontal gyrus and thalamus, and positive symptoms between structural connections in the orbitofrontal gyrus and striatum and cognitive functions, and positive correlations were suggested between RSFC in the orbitofrontal gyrus and thalamus and negative symptoms. Our findings suggested that the SAP97 rs3915512 polymorphism may be involved in mental symptoms and cognitive dysfunction in FES patients by influencing structural and functional connectivity of the orbitofrontal-striatal and orbitofrontal-thalamic regions.

Identifiants

pubmed: 34349683
doi: 10.3389/fpsyt.2021.691007
pmc: PMC8326367
doi:

Types de publication

Journal Article

Langues

eng

Pagination

691007

Informations de copyright

Copyright © 2021 Xu, Luo, Wen, Wang, Yin, Luo, He, Liang, Xiong, Zhu, Fu, Lv, Dai, Lin, Li, Lin, Chen, Luo, Wang and Ma.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Xusan Xu (X)

Institute of Neurology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.
Maternal and Children's Health Research Institute, Shunde Women and Children's Hospital, Guangdong Medical University, Foshan, China.

Shucun Luo (S)

Department of Radiology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

Xia Wen (X)

Institute of Neurology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

Xiaoxia Wang (X)

Institute of Neurology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

Jingwen Yin (J)

Department of Psychiatry, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

Xudong Luo (X)

Department of Psychiatry, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

Bin He (B)

Department of Radiology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

Chunmei Liang (C)

Institute of Neurology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

Susu Xiong (S)

Department of Psychiatry, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

Dongjian Zhu (D)

Department of Psychiatry, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

Jiawu Fu (J)

Institute of Neurology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

Dong Lv (D)

Department of Psychiatry, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

Zhun Dai (Z)

Department of Psychiatry, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

Juda Lin (J)

Department of Psychiatry, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

You Li (Y)

Institute of Neurology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

Zhixiong Lin (Z)

Department of Psychiatry, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

Wubiao Chen (W)

Department of Radiology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

Zebin Luo (Z)

Department of Radiology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.

Yajun Wang (Y)

Maternal and Children's Health Research Institute, Shunde Women and Children's Hospital, Guangdong Medical University, Foshan, China.

Guoda Ma (G)

Institute of Neurology, Affiliated Hospital of Guangdong Medical University, Zhanjiang, China.
Maternal and Children's Health Research Institute, Shunde Women and Children's Hospital, Guangdong Medical University, Foshan, China.

Classifications MeSH