Shishegar Rosita, Harding Ian H, Selvadurai Louisa P, Corben Louise A, Delatycki Martin B, Egan Gary F, Georgiou-Karistianis Nellie
School of Psychological Sciences and Turner Institute for Brain and Mental Health, Monash University, Melbourne, VIC, 3800, Australia.
Monash Biomedical Imaging, Monash University, Melbourne, VIC, Australia.
Brain Struct Funct. 2022 Apr;227(3):809-819. doi: 10.1007/s00429-021-02413-6. Epub 2021 Oct 23.
Friedreich ataxia (FRDA) is a progressive autosomal recessive disease. While motor dysfunction is the primary neurological hallmark, little is known about the underlying neurobiological changes associated with motor deficits over the course of disease. We investigated the hypothesis that progressive functional changes in both the cerebellum and cerebrum are related to longitudinal changes in performance on complex motor tasks in individuals with FRDA. Twenty-two individuals with FRDA and 28 controls participated over 24 months. The longitudinal investigation included finger tapping tasks with different levels of complexity (i.e., visually cued, multi-finger; self-paced, single finger), performed in conjunction with fMRI acquisitions, to interrogate changes in the neurobiology of motor and attentional brain networks including the cerebellum and cerebrum. We demonstrated evidence for significant longitudinal decreased cerebral fMRI activity over time in individuals with FRDA, relative to controls, during an attentionally-demanding motor task (visually cued tapping of multiple fingers) in six cerebral regions: right and left superior frontal gyri, right superior temporal gyrus, right primary somatosensory area, right anterior cingulate cortex, and right medial frontal gyrus. Importantly, longitudinal decreased activity was associated with more severe disease status at baseline, higher GAA1 repeat length and earlier age of onset. These findings suggest a dynamic pattern of neuronal activity in motor, attention and executive control networks over time in individuals with FRDA, which is associated with increased disease severity at baseline, increased GAA1 repeat length and earlier age at onset.
弗里德赖希共济失调(FRDA)是一种进行性常染色体隐性疾病。虽然运动功能障碍是主要的神经学特征,但对于疾病过程中与运动缺陷相关的潜在神经生物学变化知之甚少。我们研究了这样一种假设,即小脑和大脑的进行性功能变化与FRDA患者复杂运动任务表现的纵向变化有关。22名FRDA患者和28名对照者参与了为期24个月的研究。纵向调查包括不同复杂程度的手指敲击任务(即视觉提示的多手指任务;自主节奏的单手指任务),并结合功能磁共振成像(fMRI)采集,以探究包括小脑和大脑在内的运动和注意力脑网络的神经生物学变化。我们发现,相对于对照者,在一项对注意力要求较高的运动任务(视觉提示的多手指敲击)中,FRDA患者随着时间推移大脑fMRI活动在六个脑区显著纵向下降,这六个脑区分别是:左右额上回、右颞上回、右初级躯体感觉区、右前扣带回皮质和右内侧额回。重要的是,纵向活动下降与基线时更严重的疾病状态、更长的GAA1重复长度和更早的发病年龄相关。这些发现表明,FRDA患者运动、注意力和执行控制网络中的神经元活动随时间呈现动态模式,这与基线时疾病严重程度增加、GAA1重复长度增加和发病年龄更早有关。