帕金森病患者纹状体多巴胺耗竭与功能连接改变相关

Atsushi Shima, Rika Inano, Hayato Tabu, Tomohisa Okada, Yuji Nakamoto, Ryosuke Takahashi, Nobukatsu Sawamoto
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引用次数: 1

摘要

我们旨在阐明早期帕金森病(PD)后背纹状体的多巴胺耗竭是否会改变皮质-基底神经节运动回路的同步活动。总之,14名PD患者和16名匹配的健康对照(HC)接受了[11C]-2-β-碳甲氧基-3-β-(4-氟苯基)tropane正电子发射断层扫描,以确定纹状体多巴胺缺失区域。将识别的图谱应用于功能磁共振成像(fMRI),以发现PD患者在停药状态下相对于HC的运动任务和休息状态下功能连接(FC)的异常。纹状体多巴胺缺失区形成了同步的fMRI活动,这在很大程度上与皮质-基底神经节运动回路相对应。组间比较显示,纹状体多巴胺耗竭区在运动任务期间与内侧运动前皮层以及休息状态下与内侧、外侧运动前皮层和初级运动皮层的FC均下降。纹状体多巴胺耗竭区也表明运动任务和休息状态下PD患者丘脑下核(STN)的FC减少。纹状体多巴胺耗竭区表现出FC减少的STN区域仅在休息状态下表现出外侧运动前皮层和初级运动皮层的FC过多。我们的研究结果表明,纹状体多巴胺枯竭区与运动皮质和STN的同步活动减少,这反过来又导致PD区域之间耦合的异常增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Altered functional connectivity associated with striatal dopamine depletion in Parkinson's disease.

We aimed to clarify whether dopamine depletion in the posterior dorsal striatum in early-stage Parkinson's disease (PD) alters synchronized activity in the cortico-basal ganglia motor circuit. In sum, 14 PD patients and 16 matched healthy controls (HC) underwent [11C]-2-β-carbomethoxy-3-β-(4-fluorophenyl) tropane positron emission tomography to identify striatal dopamine-depleted areas. The identified map was applied to functional magnetic resonance imaging (fMRI) to discover abnormalities in functional connectivity (FC) during motor-task and rest-state in PD patients in the drug-off state relative to HC. Striatal dopamine-depleted areas formed synchronized fMRI activity that largely corresponded to the cortico-basal ganglia motor circuit. Group comparisons revealed that striatal dopamine-depleted areas exhibited decreased FC with the medial premotor cortex during motor-task and with the medial, lateral premotor and primary motor cortices during rest-state. Striatal dopamine-depleted areas also elucidated decreased FC in the subthalamic nucleus (STN) in PD both during motor-task and rest-state. The STN regions that exhibited reduced FC with striatal dopamine-depleted areas demonstrated excessive FC with the lateral premotor and primary motor cortices in PD only during rest-state. Our findings suggest that striatal dopamine-depleted area reduced synchronized activity with the motor cortices and STN, which, in turn, induces an abnormal increase in coupling between the areas in PD.

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