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前额叶亚区的结构协方差与多巴胺相关基因共表达及精神分裂症选择性相关。

Structural covariances of prefrontal subregions selectively associate with dopamine-related gene coexpression and schizophrenia.

机构信息

Department of Radiology and Tianjin Key Laboratory of Functional Imaging, Tianjin Medical University General Hospital, Tianjin 300052, China.

Department of Radiology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin's Clinical Research Center for Cancer, Tianjin, China.

出版信息

Cereb Cortex. 2023 Jun 8;33(12):8035-8045. doi: 10.1093/cercor/bhad096.

Abstract

Evidence highlights that dopamine (DA) system dysregulation and prefrontal cortex (PFC) dysfunction may underlie the pathophysiology of schizophrenia. However, the associations among DA genes, PFC morphometry, and schizophrenia have not yet been fully clarified. Based on the brain gene expression dataset from Allen Human Brain Atlas and structural magnetic resonance imaging data (NDIS = 1727, NREP = 408), we first identified 10 out of 22 PFC subregions whose gray matter volume (GMV) covariance profiles were reliably associated with their DA genes coexpression profiles, then four out of the identified 10 PFC subregions demonstrated abnormally increased GMV covariance with the hippocampus, insula, and medial frontal areas in schizophrenia patients (NCASE = 100; NCONTROL = 102). Moreover, based on a schizophrenia postmortem expression dataset, we found that the DA genes coexpression of schizophrenia was significantly reduced between the middle frontal gyrus and hippocampus, in which 21 DA genes showed significantly unsynchronized expression changes, and the 21 genes' brain expression were enriched in brain activity invoked by working memory, reward, speech production, and episodic memory. Our findings indicate the DA genes selectively regulate the structural covariance of PFC subregions by their coexpression profiles, which may underlie the disrupted GMV covariance and impaired cognitive functions in schizophrenia.

摘要

证据表明,多巴胺(DA)系统失调和前额叶皮层(PFC)功能障碍可能是精神分裂症病理生理学的基础。然而,DA 基因、PFC 形态和精神分裂症之间的关联尚未完全阐明。基于艾伦人类大脑图谱的大脑基因表达数据集和结构磁共振成像数据(NDIS = 1727,NREP = 408),我们首先确定了 22 个 PFC 亚区中的 10 个,其灰质体积(GMV)协方差谱与其 DA 基因共表达谱可靠相关,然后在精神分裂症患者中,识别出的 10 个 PFC 亚区中的 4 个与海马体、脑岛和内侧前额叶区域的 GMV 协方差异常增加(NCASE = 100;NCONTROL = 102)。此外,基于精神分裂症的尸检表达数据集,我们发现精神分裂症的 DA 基因共表达在中间额回和海马体之间显著减少,其中 21 个 DA 基因的表达变化明显不同步,这 21 个基因的大脑表达在工作记忆、奖励、言语产生和情景记忆等大脑活动中得到了丰富。我们的研究结果表明,DA 基因通过共表达谱选择性地调节 PFC 亚区的结构协方差,这可能是精神分裂症中 GMV 协方差紊乱和认知功能受损的基础。

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