Altered amygdala-based functional connectivity in individuals with attenuated psychosis syndrome and first-episode schizophrenia

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作者
Woo-Sung Kim
Guangfan Shen
Congcong Liu
Nam-In Kang
Keon-Hak Lee
Jing Sui
Young-Chul Chung
机构
[1] Jeonbuk National University,Department of Psychiatry, Medical School
[2] Jeonbuk National University Hospital,Department of Psychiatry
[3] Research Institute of Clinical Medicine of Jeonbuk National University-Biomedical Research Institute of Jeonbuk National University Hospital,Department of Psychiatry
[4] Maeumsarang Hospital,Brainnetome Center and National Laboratory of Pattern Recognition, Institute of Automation
[5] Chinese Academy of Sciences,University of Chinese Academy of Sciences, CAS Center for Excellence in Brain Science and Intelligence Technology
[6] Chinese Academy of Sciences,undefined
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Altered resting-state functional connectivity (FC) of the amygdala (AMY) has been demonstrated to be implicated in schizophrenia (SZ) and attenuated psychosis syndrome (APS). Specifically, no prior work has investigated FC in individuals with APS using subregions of the AMY as seed regions of interest. The present study examined AMY subregion-based FC in individuals with APS and first-episode schizophrenia (FES) and healthy controls (HCs). The resting state FC maps of the three AMY subregions were computed and compared across the three groups. Correlation analysis was also performed to examine the relationship between the Z-values of regions showing significant group differences and symptom rating scores. Individuals with APS showed hyperconnectivity between the right centromedial AMY (CMA) and left frontal pole cortex (FPC) and between the laterobasal AMY and brain stem and right inferior lateral occipital cortex compared to HCs. Patients with FES showed hyperconnectivity between the right superficial AMY and left occipital pole cortex and between the left CMA and left thalamus compared to the APS and HCs respectively. A negative relationship was observed between the connectivity strength of the CMA with the FPC and negative-others score of the Brief Core Schema Scales in the APS group. We observed different altered FC with subregions of the AMY in individuals with APS and FES compared to HCs. These results shed light on the pathogenetic mechanisms underpinning the development of APS and SZ.
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