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首发精神分裂症患者三重网络功能与结构及儿茶酚-O-甲基转移酶缬氨酸多态性之间的关联

Association between function and structure of the triple network and catechol-O-methyltransferase valmet polymorphism in the first episode schizophrenia.

作者信息

Kang Yafei, Huang Kexin, Cai Suping, Wang Haidong, Liu Jixin, Wang Yubo, Lv Yahui, Zhang Wei, Wang Qiang, Huang Liyu, Wang Jijun, Tian Jie

机构信息

School of Life Sciences and Technology, Xidian University, Xi'an, Shaanxi 710071, People's Republic of China.

Department of Anesthesiology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, People's Republic of China.

出版信息

Neurosci Lett. 2018 Nov 20;687:65-70. doi: 10.1016/j.neulet.2018.09.033. Epub 2018 Sep 18.

DOI:10.1016/j.neulet.2018.09.033
PMID:30240822
Abstract

The aberrant orchestration between the triple networks has been suggested as a backbone for some cognitive and clinical features of schizophrenia. The salience network (SN) plays a general role in switching between the central executive network (CEN) and the default mode network (DMN) mediated by dopamine activity. Whether the disease state and dopamine associated gene, catechol-O-methyltransferase (COMT), has an interactive effect on the function and structure of the triple network has not been understood. To this end, independent component analysis was used to identify the triple network. Then, cortical thickness and inter-regional resting state functional connectivity (RSFC) of the triple network was investigated in 55 first episode schizophrenia (FES) patients and 53 age-, gender-, and education- matched healthy controls. Finally, we investigated if there exist interactive effect between disease and COMT gene variation on the abnormal brain structure and function. Our results show that patients with FES exhibited significantly increased RSFC between anterior cingulate cortex and left dorsolateral prefrontal cortex (DLPFC) compared with healthy controls. The cortical thickness of the left DLPFC was thinner in FES patients. Significant interaction effect between COMT and disease was found in cortical thickness of the left DLPFC. Specifically, cortical thinning in this region was evident with the val homozygotes group of the COMT gene in FES. This findings suggest abnormal RSFC between CEN and SN and thinker cortical thickness in FES. And the val homozygotes of COMT may contribute to further cortical thinning in FES patients.

摘要

三重网络之间异常的协调被认为是精神分裂症某些认知和临床特征的基础。突显网络(SN)在由多巴胺活动介导的中央执行网络(CEN)和默认模式网络(DMN)之间的切换中起一般作用。疾病状态和与多巴胺相关的基因——儿茶酚-O-甲基转移酶(COMT)——是否对三重网络的功能和结构有交互作用尚不清楚。为此,采用独立成分分析来识别三重网络。然后,在55例首发精神分裂症(FES)患者和53例年龄、性别和教育程度匹配的健康对照中,研究了三重网络的皮质厚度和区域间静息态功能连接(RSFC)。最后,我们研究了疾病和COMT基因变异之间是否对异常脑结构和功能存在交互作用。我们的结果表明,与健康对照相比,FES患者前扣带回皮质和左侧背外侧前额叶皮质(DLPFC)之间的RSFC显著增加。FES患者左侧DLPFC的皮质厚度更薄。在左侧DLPFC的皮质厚度中发现了COMT与疾病之间的显著交互作用。具体而言,在FES患者中,COMT基因的缬氨酸纯合子组在该区域的皮质变薄明显。这些发现表明FES患者中CEN和SN之间存在异常的RSFC以及皮质变薄。并且COMT的缬氨酸纯合子可能导致FES患者进一步的皮质变薄。

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