Finke C, Schlichting J, Papazoglou S, Scheel M, Freing A, Soemmer C, Pech L M, Pajkert A, Pfüller C, Wuerfel J T, Ploner C J, Paul F, Brandt A U
Department of Neurology, Charité - Universitätsmedizin Berlin, Germany/Equal contribution
NeuroCure Clinical Research Center, Charité - Universitätsmedizin Berlin, Germany/Equal contribution.
Mult Scler. 2015 Jun;21(7):925-34. doi: 10.1177/1352458514555784. Epub 2014 Nov 12.
Fatigue is one of the most frequent and disabling symptoms in multiple sclerosis, but its pathophysiological mechanisms are poorly understood. It is in particular unclear whether and how fatigue relates to structural and functional brain changes.
We aimed to analyse the association of fatigue severity with basal ganglia functional connectivity, basal ganglia volumes, white matter integrity and grey matter density.
In 44 patients with relapsing-remitting multiple sclerosis and 20 age- and gender-matched healthy controls, resting-state fMRI, diffusion tensor imaging and voxel-based morphometry was performed.
In comparison with healthy controls, patients showed alteration of grey matter density, white matter integrity, basal ganglia volumes and basal ganglia functional connectivity. No association of fatigue severity with grey matter density, white matter integrity and basal ganglia volumes was observed within patients. In contrast, fatigue severity was negatively correlated with functional connectivity of basal ganglia nuclei with medial prefrontal cortex, precuneus and posterior cingulate cortex in patients. Furthermore, fatigue severity was positively correlated with functional connectivity between caudate nucleus and motor cortex.
Fatigue is associated with distinct alterations of basal ganglia functional connectivity independent of overall disability. The pattern of connectivity changes suggests that disruption of motor and non-motor basal ganglia functions, including motivation and reward processing, contributes to fatigue pathophysiology in multiple sclerosis.
疲劳是多发性硬化症中最常见且致残的症状之一,但其病理生理机制尚不清楚。尤其不清楚疲劳是否以及如何与大脑结构和功能变化相关。
我们旨在分析疲劳严重程度与基底节功能连接、基底节体积、白质完整性和灰质密度之间的关联。
对44例复发缓解型多发性硬化症患者和20名年龄及性别匹配的健康对照者进行静息态功能磁共振成像、扩散张量成像和基于体素的形态测量。
与健康对照相比,患者的灰质密度、白质完整性、基底节体积和基底节功能连接均有改变。在患者中未观察到疲劳严重程度与灰质密度、白质完整性和基底节体积之间的关联。相反,患者的疲劳严重程度与基底节核与内侧前额叶皮质、楔前叶和后扣带回皮质的功能连接呈负相关。此外,疲劳严重程度与尾状核和运动皮质之间的功能连接呈正相关。
疲劳与基底节功能连接的明显改变相关,且独立于整体残疾情况。连接变化模式表明,运动和非运动基底节功能的破坏,包括动机和奖赏处理,在多发性硬化症疲劳病理生理过程中起作用。