Institute of Neuroscience and Medicine, Brain & Behaviour (INM-7), Research Centre Jülich, 52428 Jülich, Germany.
Institute of Systems Neuroscience, Medical Faculty & University Hospital Düsseldorf, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany.
Brain. 2023 Aug 1;146(8):3319-3330. doi: 10.1093/brain/awad043.
Structural grey and white matter changes precede the manifestation of clinical signs of Huntington's disease by many years. Conversion to clinically manifest disease therefore likely reflects not merely atrophy but a more widespread breakdown of brain function. Here, we investigated the structure-function relationship close to and after clinical onset, in important regional brain hubs, particularly caudate nucleus and putamen, which are central to maintaining normal motor behaviour. In two independent cohorts of patients with premanifest Huntington's disease close to onset and very early manifest Huntington's disease (total n = 84; n = 88 matched controls), we used structural and resting state functional MRI. We show that measures of functional activity and local synchronicity within cortical and subcortical regions remain normal in the premanifest Huntington's disease phase despite clear evidence of brain atrophy. In manifest Huntington's disease, homeostasis of synchronicity was disrupted in subcortical hub regions such as caudate nucleus and putamen, but also in cortical hub regions, for instance the parietal lobe. Cross-modal spatial correlations of functional MRI data with receptor/neurotransmitter distribution maps showed that Huntington's disease-specific alterations co-localize with dopamine receptors D1 and D2, as well as dopamine and serotonin transporters. Caudate nucleus synchronicity significantly improved models predicting the severity of the motor phenotype or predicting the classification into premanifest Huntington's disease or motor manifest Huntington's disease. Our data suggest that the functional integrity of the dopamine receptor-rich caudate nucleus is key to maintaining network function. The loss of caudate nucleus functional integrity affects network function to a degree that causes a clinical phenotype. These insights into what happens in Huntington's disease could serve as a model for what might be a more general relationship between brain structure and function in neurodegenerative diseases in which other brain regions are vulnerable.
结构灰质和白质的变化先于亨廷顿病的临床症状出现多年。因此,向临床显性疾病的转化可能不仅反映了萎缩,还反映了更广泛的大脑功能崩溃。在这里,我们研究了接近和在临床发病后,在重要的区域性大脑中枢(特别是尾状核和壳核)的结构-功能关系,这些区域对于维持正常运动行为至关重要。在两个独立的亨廷顿病前驱期和早期显性亨廷顿病患者队列中(总共 n = 84;n = 88 名匹配的对照),我们使用了结构和静息状态功能 MRI。我们表明,尽管有明确的脑萎缩证据,但在亨廷顿病前驱期,皮质和皮质下区域的功能活动和局部同步性的测量值仍然正常。在显性亨廷顿病中,尽管存在皮质下中枢区域(如尾状核和壳核)以及皮质中枢区域(如顶叶)的同步性稳态破坏,但同步性的稳定性也被破坏。功能磁共振成像数据与受体/神经递质分布图谱的跨模态空间相关性表明,亨廷顿病特异性改变与多巴胺受体 D1 和 D2 以及多巴胺和 5-羟色胺转运体共定位。尾状核的同步性显著改善了预测运动表型严重程度或预测分类为亨廷顿病前驱期或运动显性亨廷顿病的模型。我们的数据表明,富含多巴胺受体的尾状核的功能完整性是维持网络功能的关键。尾状核功能完整性的丧失会在一定程度上影响网络功能,从而导致临床表型。这些关于亨廷顿病中发生的事情的见解可以作为一个模型,说明在其他易受影响的神经退行性疾病中,大脑结构和功能之间可能存在更普遍的关系。