Duarte João Valente, Faustino Ricardo, Lobo Mercês, Cunha Gil, Nunes César, Ferreira Carlos, Januário Cristina, Castelo-Branco Miguel
Institute for Biomedical Imaging and Life Sciences (IBILI) - Faculty of Medicine, University of Coimbra, Portugal.
Institute of Nuclear Sciences Applied to Health (ICNAS) - University of Coimbra, Brain Imaging Network of Portugal, Portugal.
Hum Brain Mapp. 2016 Oct;37(10):3656-68. doi: 10.1002/hbm.23266. Epub 2016 Jun 7.
Machado-Joseph Disease, inherited type 3 spinocerebellar ataxia (SCA3), is the most common form worldwide. Neuroimaging and neuropathology have consistently demonstrated cerebellar alterations. Here we aimed to discover whole-brain functional biomarkers, based on parametric performance-level-dependent signals. We assessed 13 patients with early SCA3 and 14 healthy participants. We used a combined parametric behavioral/functional neuroimaging design to investigate disease fingerprints, as a function of performance levels, coupled with structural MRI and voxel-based morphometry. Functional magnetic resonance imaging (fMRI) was designed to parametrically analyze behavior and neural responses to audio-paced bilateral thumb movements at temporal frequencies of 1, 3, and 5 Hz. Our performance-level-based design probing neuronal correlates of motor coordination enabled the discovery that neural activation and behavior show critical loss of parametric modulation specifically in SCA3, associated with frequency-dependent cortico/subcortical activation/deactivation patterns. Cerebellar/cortical rate-dependent dissociation patterns could clearly differentiate between groups irrespective of grey matter loss. Our findings suggest functional reorganization of the motor network and indicate a possible role of fMRI as a tool to monitor disease progression in SCA3. Accordingly, fMRI patterns proved to be potential biomarkers in early SCA3, as tested by receiver operating characteristic analysis of both behavior and neural activation at different frequencies. Discrimination analysis based on BOLD signal in response to the applied parametric finger-tapping task significantly often reached >80% sensitivity and specificity in single regions-of-interest.Functional fingerprints based on cerebellar and cortical BOLD performance dependent signal modulation can thus be combined as diagnostic and/or therapeutic targets in hereditary ataxia. Hum Brain Mapp 37:3656-3668, 2016. © 2016 Wiley Periodicals, Inc.
马查多-约瑟夫病,即遗传性3型脊髓小脑共济失调(SCA3),是全球最常见的类型。神经影像学和神经病理学一直显示存在小脑改变。在此,我们旨在基于参数化的与表现水平相关的信号发现全脑功能生物标志物。我们评估了13例早期SCA3患者和14名健康参与者。我们采用了参数化行为/功能神经影像学联合设计,以研究疾病特征,该特征是表现水平的函数,并结合了结构MRI和基于体素的形态学测量。功能磁共振成像(fMRI)旨在对1、3和5Hz时间频率下音频驱动的双侧拇指运动的行为和神经反应进行参数化分析。我们基于表现水平的设计探究运动协调的神经元相关性,从而发现神经激活和行为在SCA3中表现出参数调制的关键缺失,这与频率依赖性皮质/皮质下激活/失活模式相关。小脑/皮质速率依赖性解离模式能够明确区分不同组,而与灰质损失无关。我们的研究结果提示运动网络的功能重组,并表明fMRI作为监测SCA3疾病进展工具的可能作用。因此,通过对不同频率下行为和神经激活的接受者操作特征分析测试,fMRI模式被证明是早期SCA3的潜在生物标志物。基于对应用的参数化手指轻敲任务的响应中BOLD信号的判别分析,在单个感兴趣区域中通常显著达到>80%的敏感性和特异性。基于小脑和皮质BOLD表现依赖性信号调制的功能特征因此可作为遗传性共济失调的诊断和/或治疗靶点。《人类大脑图谱》37:3656 - 3668,2016年。©2016威利期刊公司。