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绘制帕金森病伴持续认知障碍患者纹状体功能梯度及相关基因表达图谱。

Mapping striatal functional gradients and associated gene expression in Parkinson's disease with continuous cognitive impairment.

作者信息

Li Xiaolu, Bu Shuting, Pang Huize, Yu Hongmei, Zhao Mengwan, Wang Juzhou, Liu Yu, Fan Guoguang

机构信息

Department of Radiology, The First Hospital of China Medical University, Liaoning, China.

Department of Neurology, The First Hospital of China Medical University, Liaoning, China.

出版信息

NPJ Parkinsons Dis. 2025 May 28;11(1):138. doi: 10.1038/s41531-025-01002-2.

Abstract

Cognitive impairment in Parkinson's disease is closely tied to striatal dysfunction, yet the neurobiological interface between macroscale connectivity and molecular signatures remains unexplored. This study characterizes striatal gradient organization and its genetic underpinnings across PD cognitive trajectories. We analyzed functional connectivity gradients in 126 PD patients (spanning the cognitive spectrum from normal cognition to dementia) and 40 healthy controls, correlating spatial patterns with neurotransmitter architecture and transcriptomic profiles. Three distinct striatal gradients emerged: Gradient 1 remains stable throughout disease progression and partially aligns with canonical striatal subdivisions. Gradient 2 represents a spatial continuum closely linked to dopaminergic innervation and becomes most pronounced in the dementia stage. Gradient 3 corresponds to cortico-striatal connectivity patterns implicated in both early and advanced cognitive deficits. Spatial transcriptomic and neuroimaging correlation analyses identified significant associations between cortico-striatal gradient disruptions and specific gene expression patterns. These findings provide valuable insights into striatal macro- and microstructural changes in PD and their role in cognitive impairment.

摘要

帕金森病中的认知障碍与纹状体功能障碍密切相关,但宏观连接性与分子特征之间的神经生物学界面仍未得到探索。本研究描述了整个帕金森病认知轨迹中的纹状体梯度组织及其遗传基础。我们分析了126例帕金森病患者(涵盖从正常认知到痴呆的认知范围)和40名健康对照者的功能连接梯度,将空间模式与神经递质结构和转录组谱相关联。出现了三种不同的纹状体梯度:梯度1在疾病进展过程中保持稳定,并部分与经典的纹状体细分区域一致。梯度2代表与多巴胺能神经支配密切相关的空间连续体,在痴呆阶段最为明显。梯度3对应于与早期和晚期认知缺陷均有关的皮质-纹状体连接模式。空间转录组学和神经影像学相关性分析确定了皮质-纹状体梯度破坏与特定基因表达模式之间的显著关联。这些发现为帕金森病中纹状体的宏观和微观结构变化及其在认知障碍中的作用提供了有价值的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/60e7/12117062/7aafbbdd0cc8/41531_2025_1002_Fig1_HTML.jpg

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